AUCTORES
Chat with usReview | DOI: https://doi.org/10.31579/2693-4779/075
Department of Cardiothoracic Surgery, St Paul’s Hospital, Causeway Bay, Hong Kong
*Corresponding Author: JSM Leung. Department of Cardiothoracic Surgery, St Paul’s Hospital, Causeway Bay, Hong Kong.
Citation: JSM Leung. (2022) Major problems confronting the COVID-19 pandemic. Clinical Research and Clinical Trials. 5(3); DOI: 10.31579/2693-4779/075
Copyright: © 2022 JSM Leung, This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
Received: 27 November 2021 | Accepted: 07 January 2022 | Published: 18 February 2022
Keywords: Covid-19; black death
Beginning from December 2019, the present COVID-19 has ravaged the world for almost two years. While it appears to have peaked in many countries, it is still not under control in other areas. Worse still, new mutations of the virus continue to drive new waves of infection which manage to break through natural and human measures of defence.
Beginning from December 2019, the present COVID-19 has ravaged the world for almost two years. While it appears to have peaked in many countries, it is still not under control in other areas. Worse still, new mutations of the virus continue to drive new waves of infection which manage to break through natural and human measures of defence. In the following brief review, we shall attempt to analyse the problems confronting this pandemic from the historical, social-psychological, geopolitical, biological, and medical perspective.
Idemics date back to the beginning of human history and often shaped the course of history [1]. The term epidemics appeared in ancient Egyptian, Indian and Chinese languages over 4,000 years ago. In ancient Greece, it sealed the fate of the Athenians in their war with the Spartans in 430 B.C.
It was probably one of the factors that halted the conquest of Alexander the Great, who seemed to die prematurely in 323 B.C. of an infection caught in one of his campaigns. It ravaged China during the beginning of the first century eliminating a quarter of the population and again in the third century eliminating a third of the population. Around the same time similar epidemics broke out in the Roman Empire in the West, raising speculations that this was probably a pandemic. The situation was repeated during the 13th century when an epidemic coincided with the Mongolian conquest sweeping over most of Asia and half of Europe. Evidence was not strong as the “Black Death” did not appear to afflict Mongolia itself. In modern times, we have seen many epidemics come and gone, including small pox, cholera, typhoid fever, scarlet fever, poliomyelitis. Other infections have kept resurfacing, defying various temporarily successful measures. These include influenza, malaria, tuberculosis, syphilis etc. Still others we seem to be gaining control as typified by HIV and the viral hepatitis B and C. So, in this fight against the coronavirus SARS-CoV2 why is victory so elusive? We shall approach the problems according to the conventional factors in an epidemic.
Zootic Reservoir
One of the early hints that infections could be perpetuated in animals and jump species to affect humans was documented in ancient China when in 476 A.D. silk worms were first found to die in large numbers, followed by cattle and finally humans, with the epidemic sweeping down the course of the Yellow River from West to East [1]. In the 19th century [1], Patrick Mansion, researching in Hong Kong and Southern China, discovered the transmission of filaria by the mosquito. He finally convinced Ronald Ross that mosquitoes could transmit the pathogen and solved the mystery of malaria, which has a reservoir in forest animals including monkeys, an intermediate host in mosquitoes, which ultimately pass the infection to humans [2]. The notorious pandemic in 1919 originated in U.S.A., extended to Europe, where it was misnamed the “Spanish Flu”, and swept over the world causing the most massive and lethal disaster of the 20th century [3]. With the advancement of molecular science, the causative influenza virus H1N1 was found to have considerable resemblance to the swine influenza virus and probably originated from a pig reservoir. More recently, the first SARS epidemic in 2002-2003 was traced to coronavirus perpetuated in animal hosts like bats and civet cats and passed further on to humans. Similarly, subsequent repeated outbreaks of coronavirus infections, the MERS, arose from the Middle East and was traced to reservoirs in the bats with the camels as intermediate hosts.
The early stage of the pandemic and its control – lock-down and isolation
The present pandemic has been traced to zootic reservoirs in bats with the pangolin as one of the known intermediate hosts. The causative virus, SARS-COV2, bears strong resemblance to the first SARS pandemic but also important differences which are reflected in the transmission trajectory, the clinical course and the problems of control and treatment. Evidence exists which suggests sporadic infections in various places within or outside China [4]. Some infections passed as “influenza” due to lack of recognition, while others failed to develop into epidemics and simply died out [5]. The fact remains that the first confirmed infection appears in December 2019 in Wuhan, China. There was some delay in the recognition of the gravity of the infection. Most health workers believed that it was like another “bird flu”, serious if not lethal, but mainly an infection passed from the pangolin to human, with little risk of human-to-human transmission. There was no cover-up of the infection as subsequently alleged by various other countries, but a definite failure to recognize the full nature and gravity of the infection. This is understandable since it was due to an entirely new virus unknown to mankind.
By mid-January 2020, the true nature of the epidemic was recognized. The action of the Chinese leadership was swift, resolute and painful. The methodology of lock-down and isolation to control an epidemic is long established based on centuries of past experience [1]. As early as the year 2 A.D., a Chinese Emperor ordered to fight an epidemic in Eastern China by, “Empty out some premises and put (isolate) the sick people there, yet make sure they are looked after by physicians and well-supplied with medicine.” Remarkably, the Emperor was only nine years old and had to handle the crisis all alone, as his maternal uncle and prime minister was too busy lobbying for popular support for his own plan to usurp the throne, and he couldn’t be bothered with any distraction by the epidemic. Another Emperor of the Han Dynasty, (himself an ardent musician and played the flute), in facing another epidemic ordered, “Dissolve the imperial orchestra, close the imperial stable and dispose of the stallions; cut the imperial banquets; let all my subjects do likewise, and divert the resources to fight the epidemic.” Traditionally, in the face of an epidemic the top priority of a Chinese leader has always been health over wealth. A lock-down was slapped on Wuhan,6 the greatest industrial centre in China. It was the eve of the traditional Chinese New Year and hundreds of thousands of travellers were stranded on their homeward journey to celebrate the annual family reunion. It was also a great blow to the booming Chinese economy which was not on the way to catch up with U.S.A. as viewed by the West but only trying to shrug off poverty in reality. (The West only look at the sum-total GDP figures, but if you divide it by the huge population, the per capita income for many Chinese people is still barely trying to get over the poverty line.) And so, with a huge setback in economy and an immensely unpopular lockdown decision, China achieved early control of the pandemic [6].
A similar and even more remarkable example of infection control is seen in Macau [7]. The small peninsula with a population of half a million, flanked by two small adjacent islands on the Southern Coast of China. It was occupied by the Portuguese for four centuries but returned to China in 1999. In late January 2020, Macau enforced a strict lock-down immediately following Mainland China and closed all its casinos and tourism as well as putting on hold all its manufacturing industry (which depends heavily on factories and labour force in Mainland China). The territory sacrificed all its major source of revenue in putting health as top priority. Today, as one of the smallest and most densely populated cities in the world, Macau stands out as the only one with a minimal number of infection (77 cases in 18 months), no mortality and zero new indigenous COVID-19 cases for over a whole year. But this policy may not be easily generalized to other territories who are not based on the casino industry. As soon as the pandemic is under control tourist gamblers are expected to rapidly return and a rapid economic recovery is anticipated. The same may not be expected of most other industries. This is the first and most important problem confronting the world today, the question of priority which boils down to the choice between health and wealth.
Masks, face shields, hand hygiene, quarantine
Lock-down is to break the transmission of virus at the level of society. Transmission should also be blocked at the personal level. The most obvious and important tool is the face mask. Originally used by 19th century European surgeons to reduce wound contamination during operations, surgical masks were refined by the Chinese epidemiologist Wu Lien-teh in fighting the plague epidemic in Northern China in 1910 [8]. Dr. Wu was able to prove scientifically that the bacteria spread from the lymph node (bubonic plague) to the blood stream (septicaemic plague) and from the blood to the lungs (pneumonic plague). Once the lungs were infected the infection spread rapidly among humans via sputum, droplets and aerosol trajectories. Wu followed his common-sense logics and redesigned the surgical mask to break the transmission chain of the plague. In 1910, China was withering in a sub-colonial status. All major public services were headed by Europeans including the health service. His European superior remained entrenched in the old concept of bubonic plague and was biased against this “Chinaman’s new unorthodox idea” of pneumonic plague as well as the use of the facial mask. Dr. Wu was laid off and the plague raged on. But very soon this senior European doctor caught the infection himself and died within days. Dr. Wu could now carry out his anti-epidemic measures without hindrance, and the mask was instrumental in bringing the highly lethal pneumonic plague under control. The mask has since established its critically important role in subsequent air-borne and droplet-borne epidemics. Sadly, in 2002 the health system in Hong Kong was caught off-guard by the first SARS pandemic, all equipments were in short supply. Administrators were slow to apply remedial measures, and frontline health workers were forced to reuse disposable masks and gowns resulting in substantial tolls. Such tragic experience was repeated in 2020 in some health management organizations in Western countries, with the administrators covering their ineptitude by high-handedly suppressing the complaints of front-line health workers. This is the second major problem confronting our fight against any epidemic including the present pandemic, the biased refusal to accept the crucial importance of the facial masks and other simple and common-sense measures and the administrators putting other considerations above the safety of frontline workers.
Another common problem with masking is objection from the lay people. In spite of ample scientific evidence on the efficacy of masking and its common usage in East Asia, there were strong objections from certain sectors in the West based on individual interpretation or misinterpretation of personal freedom and human rights. There were also objections to social and physical distancing. Some churches refused to close congregations of worship. Some choirs continued to hold singing sessions. Some men and women continued to seek pleasure among various partners and spread the virus. Some people continued to travel and the airplane cabin and tourist cruises provided many opportunities of contact and spread of the virus. Offices, schools and shopping centres continued to open or started to reopen before the disease was under control.
It has been shown that, after shedding from the patient, the coronavirus could remain viable with infection potential for up to 48 hours. So, cleaning of fomites and hand hygiene is important. A less common portal of entry for the virus is through the eyes and it is shown that wearing eyeglasses (but not contact lens) confers some protection. For those not wearing glasses, a transparent face shield should be a good, if not better, substitute [9].
Caps, gowns, masks, face shields, hand-scrubs, gloves are all inexpensive items. The problem is they are used on a disposable basis and daily costs do add up to significant figures and impact on the budget. Once again, administrative interference may come into play. If administrators put profit as top priority, the safety of health workers will be compromised.
Characteristics peculiar to COVID-19
The next problem is asymptomatic transmission. COVID-19 could easily boast as being one of the most incomprehensible and intangible infections [10]. The clinical features present problems at almost every step and every corner [6]. To begin with, it is almost impossible to calculate the incubation period which varies from one or two days to a few weeks. For asymptomatic patients, we shall never be able to find out. In certain communities like the antenatal clinics a population-wide study showed up to 40% asymptomatic carriers. But this may not apply to the general population.
More importantly, the timing of virus shredding determines the infectivity of the patient and the risk of the contacts. It also indirectly determines the fate of the pandemic and the human race under its ravage. For the first SARS pandemic virus shedding began from the first two days of symptoms rising to a peak around day 5 and then declined. That was why it tended to infect health workers more than other contacts because by day 5 the patient was usually seeking medical help or hospitalized. So, once the disease was well-recognized it would have been isolated in hospital and the infection chain broken. Thus, the pandemic rapidly faded off after the first few months [11].
Not so with the new COVID-19, virus shedding starts within one to two days after virus entry and peaks one to two days before symptoms appear. The disease spreads freely and unknowingly at the pre-symptomatic or asymptomatic stage, evading conventional methods of screening such as taking temperature, checking clinical history and contact history and even blood tests and chest X-ray films. The only way to sort out such asymptomatic and pre-symptomatic carriers is to do complete virus screening for the whole population at the first hint of a new wave of infection. This in fact, has been the practice in Macau and undoubtedly contributed to their success.
Once again, the problem of personal freedom and human rights comes into play. The individual may argue that since she/he has no symptoms, the screening tests are unnecessary and infringes on his personal liberty and human rights. There could also be a subconscious bias against something like the anti-infection mask and the stringent lock-down measures, developed in a country historically well known for its poverty and backward status.
Problem of Hospital Beds
COVID-19 may hit a community with widely waxing and waning severity. At its height the number of patients may overwhelm any apparently well-equipped and well-staffed medical establishment [12]. China, based on previous experience with SARS has devised methods to build instant hospitals and large number of hospital beds by conversion of indoor stadiums and exhibition halls into make-shift hospitals. When the pandemic subsided, these facilities are returned to their original purpose. Again, such conversions may not be palatable or acceptable in other countries.
Problem of Medications (see Table 1)
A number of medications have evolved since the appearance of COVID19, some have since been delisted as useless or even deleterious (see Table 1). A few have shown marginal benefits. None has come to any high efficacy for cure. Even if a new drug were to succeed, it would probably come at a price beyond the budget of the average low or middle-low income country. Our best hope may lie with the repurpose of established old drugs (see Table 1).
Agents | Mechanism of action | Remarks |
47D11 | Neutralizing mAb, human | Stops infection in vitro, also can develop into an Ab-based test for the virus |
α1-antitrypsin plasma infusion | To counter the damaging trypsin | Esp. in α1-antitrypsin deficient/AATD patient |
Acalabrutinib | BTK inhib., macrophage downreg | reduce macrophage’s drive on many cytokines |
ACEIs & ARBs ongoing admin. | Possibly acting as virus trap | Reduce mortality, OR ACEI 0.55, ARB 0.58 |
(Anakinra) | IL-1 receptor inhibitor; benefit resp failure w/no rising LDH | Reduce CRS, for resp failures reduce mortality HR 0.45, but w/rising LDH HR 1.006, no benefit |
Androgen deprivation ADT | Reduces AR stim of TMPRSS2* *cleaves S & cause virus-cell fus. | Explains the low incidence 4/5273, morbidity & 0 mortality in Ca prostate under ADT; potential Rx? |
Antibody, mAb LY-CoV555 | Virus-neutralizing mAb | Give day2 –6, by day29 hosp adm 1.6 vs 6.3 |
Anti-cancer drugs (off target antiviral effect) | ACE2-lowering drugs +/- direct toxicity/growth inhibition on virus | mTOR/PI3K inhibitors: temsirolimus everolimus, alpelisib anti-metabolites: gemcitabine, decitabine BCR-ABL, KIT inhibitor: dasatinib, ALK, ROS1, MET inhibitor: crizotinib Rate of COVID test +ve 7 vs 12 for those Ca pts not on these Rx |
Apilimod [STA-5326] (originally for Ebola, Crohn’s & NHL) | inhibitor of PIKfyve kinase, TLR & its products IL-12,13 | Inhibits CoV-2 replication in cell line by 85 & also in a human lung explant model |
ARBs | Losartan in outpatients | AEs & viral loads no difference w/placebo |
Telmisartan in hospital patients | Mortality@ 30d 4.29 vs control 22.54 | |
(L)-Arginine food supplement | Improves endothelial function | Reduce resp.-support requirement by 71 in first 10 days of severe dis. vs 44 on placebo which catch up by 20th day, shorten ICU/hosp. |
Aspirin, daly low dose | Anti-platelet | aHR of ventilator 56, ICU O.57, mortality 0.53 |
Bamlanivimab [LY-CoV555] | Neutralizing mAb on S protein But Co-V2 variants tend to be less susceptible, combo preferred | Appr for prehosp/preO2 pts in 1st 10 days, reduce hosp to 2 vs placebo’s 10 (not significant), no reduction of viral load on day 11; as prophylaxis in skilled nursing homes w/>1 index case, infection rate cut to 8.5% fr placebo’s 15.2, mortality to zero vs placebo’s 5/587 |
Bamlanivimab + etesevimab
(NIH approved combination) | Stopped in mid-2021 bec of inefficacy against new mut virus | Sig. red. of viral load to 0.09 by day 11 vs 10 Log viral load -3.72 for 700mg, -4.08 for 2800mg, -3.49 for 7000mg vs -3.80 for placebo; significant reduction in viral load on day 11 |
Baricitinib-remdesivir | JAK1,2 inhibitor + Remdesivir vs remdesivir alone | For pts on O2, ventilator or ECMO, FDA appr., recovery time 7 vs 8 d, high O2 dependency 10 vs 18d, mortality 5.1 vs 7.8;@ 28d mortality 8 vs placebo 13, = 38.2 relative, 5 absolute reduction of all cause mortality |
Camostat, a serine protease inhibitor | TMPRSS2 inhibitor, cut cell entry | No sig benefit, 30d mortality HR 0.8 |
Casirivimab+ imdevimab [REGEN-COV] | 2 mAbs neutralizing viral spike protein @ 2 different domains | Reduces viral load >10x vs placebo by day 5 Given before hospitalization reduces medical visits from 6.5 to 2.5 by day 29reduces admission, but may cause worsening if given after hosp.,O2 Rx or ventilator (NIH appr combo mainly for contact prophylaxis e.g. in patient’s household) |
Colchicine | General anti-inflam agent | Numerical but not statistically significant benefit in reducing hospitalization and severity |
Convalescent plasma | Contains variable Ab for neutralization of virus | Improvement 51 vs placebo 36, mortality 15 vs 24, PCR neg 87 vs 37 “not significant” for n=101 study; benefit more sig in severe subgroup; by a large Indian study, reduce viral load & fatigue on day7 but OS no benefit |
COV2-2196 & COV2130 (c.f. REGN-COV2 double Ab) | Neutralizing mAbs binding non-overlapping sites on SRBD | Protects mice fr COVID-19 infection, synergistic SRBD=receptor-binding domains on Spike protein |
COV2-2381 | ACE2 blocking mAb | Protects Rhesus monkeys from COVID-19 infect. |
Cytokine filter | Cytosorbent®, Cytosorb | Reduce excess cytokines in dialysis for CRS |
Danoprevir | Repurposed from HCV Rx |
|
Darapladib | Repurposed fr atherosclerosis Rx | Developed in Israel |
Dexamethasone | Anti-inflammatory steroid | 17 relative, 2.8 absolute reduction in all-cause mortality @ 28d |
Eculizumab | Complement protein C5 mAb | Improves survival @day 15 fr 62.2 to 82.9 |
Etesevimab [LY-CoV016] | Viral Spike protein rec.hu.mAb | Significant reduction of log viral load when add to bamlanivimab @ day 11, -4.37 vs bamlanivimab alone’s -4.08 (best try) & placebo’s -3.80 |
Favipiravir [T-705] | Repurposed from Rx of flu, Ebola | Inhibitor of PB1 subunit of viral RNA polymerase |
Flumatinib | Repurposed from Rx of cancer | Developed in Israel |
Fluvoxamine | Anti-depressant repurposed, binds σ1receptor (as agonist) on immune cell | Downregulates inflammatory reaction, upregulates cytokine production, reduces hospitalization by50 when used in early mild cases in a small study; clinical deterioration 0/80 vs placebo 6/72 |
GSK3360825A | MAP2K3 inhibitor | Blocks CD14 – MAP2K3 pathway, reduces innate immune intensity & risk of cytokine crisis |
Ibrutinib | BTK inhibitor incl MYD88 pathways that upreg cytokines | First 6 six patients w/ lung failure benefited from full dose, but not reduced dose |
IFNβ-1a [SNG001]by nebulizer daily x 14d | Antiviral vs placebo tried in 100 patients | Clinical improvement OR 2x @15d, 3x @28d, disease severity & mortality down 79 |
IFNβ-1b add to antiviral drugs (vs antivirals only) | +ribavirin&/or lopinavir-ritonavir, interferon makes the difference | Reduces NPS+ve fr 12 to 7d., symptoms fr 8 to 4 d., median hospital-stay 15 to 9 d., no sig. AEs |
IFN-λ (peginterferon lambda) | Reduces viral load esp >106/ml | By day 7, 80 -ve vs placebo 63 -ve |
IFN-κ + TFF2 | Anti-viral expr’d in keratinocytes + a mucosa healing agent | Reduce RNA conversion by 3.6 days & resolution of CT by 2.55 days |
IL-7 | Increase lymphocytes, without increasing cytokines | Reduces viral load & 2y infection, counters the lymphopenic effect of CoV2 infection |
Imdevimab [REGN 10987] +casirivimab [REGN 10933] | 2 mAbs neutralizing viral proteins | Given before hosp.,reduces adm, but may cause worsening if given after hosp.,O2 or ventilator |
Infliximab [Remicade] (& other TNF-α antagonists) | TNF-α mAb, chimeric | reduce cytokine storm; may accouont for the 3 M&M in IBDs on TNF-α mAb vs 26 on steroid |
Ivermectin | Repurposed from other viral & parasitic Rx | Blocker of (viral) integrase IN & (host) Importin IMP α/β1 interaction for nuclear import of virus; in mild cases s/s resolution shortened fr. 12 to 10d, mortality fr 24.5 to 13.3; but another trial showed no difference in mild COVID |
(IVIG) for pts on ventilator |
| No benefit, but increased DVT & PE 3x; should NOT be used! |
Leronlimab (compassionate use) | CCR5 mAb | To control cytokine storm in high IL-6 |
Lopinavir-ritonavir | Repurposed from HIV-1 Rx | Clinical benefit HR 1.24; 28d mort 25>19.2; time to improvement down 1d., no statistic significance |
LY-CoV555 | Virus-neutralizing mAb (2.8g iv) | Give day2 – 6, by day29 hosp adm 1.6 vs 6.3 |
Mavrilimumab (no statistically significant benefit) | GM-CSF receptor α-subunit (CSF2RA) mAb, GM-CSF block | In 13 cases on O2, mortality 0 vs 27, recovery 8 vs 19 days; in 40 cases @d14 57 off O2 vs 47 |
MDL-28170 | Cysteine protease inhibitor | Inhibits virus replication in cell line by 65% |
Metformin | Anti-diabetic, repurposed | HR for infection 0.8, mortality 0.87; -ve assoc. |
Molnupiravir [MK4482] | Prodrug of N4-hydroxycitidine | Introduce copying errors in viral RNA replication, Activity shown in influenza & corona virus; reduces mortality by 50 |
Niclosamide | Antiviral agent | New inhalation formulation promising in Phase I |
nNIF | neonatal neutrophil-extra- cellular-trap inhibitory factor | Reduces microvascular thrombosis (one of the major lethal factor in COVID & other infections |
Off-label drugs (beside those mentioned above) | (Azithromycin, Josamycin) | Macrolides may reduce inflam reaction & fibrosis |
(Chloroquine,hydroxychloroquine) | No firm proof, more harm | |
(Dipyridamole [Persantine]) | Antiplatelet, may benefit microvasc thrombosis | |
(Prazosin [Minipress]) | Alfa-adreneric blocker, may benefit vasc disoders | |
ONO-5334 | Cysteine protease inhibitor | Inhibits virus replication in cell line by 72 |
Opaganib [ABC294640] | Sphingosine kinase inhibitor | Potential in anti-Ca & anti-viral Rx |
(Oseltamivir) |
| Tried with no benefit at all |
Ranitidine bismuth citrate | (for gastroduodenal ulcer) | Reduces cellular CoV2 by 1,000 fold in hamsters |
REGN-COV2 Ab cocktail | See casirivimab + imdevimab |
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Remdesivir [Veklury] FDA appr. | Prodrug for RNA polymerase inhibitor; modest significant gains | ORR 68, recovery 15dà11d, severe adv events 27à21, mortality @ 14d 11.9aà7.1; x 5d more likely benefit than x10d, but not the timing; VA study: causes longer stay in hosp., OS no diff. |
Ribavirin | A broad spectrum antiviral | ? worth a try, effective in some trials but not others |
Sarilumab | IL-6R mAb | In COVID-19 pneumonia ICU ventilator rate kept @ 5.7; mortality reduced fr 36 to 22; some trials found no benefit |
[SARSHRC-PEG4]2-chol(esterol) | Blockade of virus-membrane fusion | Nasal sprays prevent COVID infection 100% in ferrets |
Statins & mortality reduction | Some meta-analysis found no benefit, even harm if concommit- tant confounding factor not considered; “don’t start or stop” | In DM in-patient lowers mortality 24 fr 39 In non-DM pts no significant difference; in Beijing cut mort.fr.9.4 to 5.2; in NYC fr.26.5 to 14.8; in MGH only >65 benefited |
Steroids & mortality reduction | OR vs placebo | Dexamethasone 0.64; hydrocortisone 0.69; methyl prednisolone 0.91 |
Synbiotic therapy | Corrects gut dysbiosis | Up pro-immune markers, reduce inflam markers; @wk 1, Ab+ in 88 vs control’s 10; @wk 2, Ab+ in 88 vs 63 |
TNF-α mAb (see infliximab) |
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Tocilizumab (or sarilumab) | IL-6 inhibitor
Benefit only in specific subgroups
maybe given in 24 h from first sign of deterioration requiring high O2 support | For cytokine storm w/very high IL-6 blood levels For ICU pts., cut mortality fr 36 to 28(22) but up infection from 26 to 54; for rising CRP or falling LDH cut mortality HR 0.99 & AE HR 0.98, for rising LDH mortality HR 1.006 REMAP-CAP, hosp mort 27 vs 36 w/std care; RECOVERY, mort @28d 31 vs 35 (biggest trial); COVACTA mortality @ 28d no difference; if CRP>15 NIV/IV rate 18 vs 57, 90-d mort. 9 vs 35; if CRP<15> |
Tocilizumab disadvantage | Blocks both stim of Ab production by IL-6 receptor +ve cells & inflam cytokines by receptor -ve immune cells. Ideal blockade should be at the latter, e.g. blocking the IL-6/gp130 interaction (see gene & marker) | |
Tofacitinib (Xeljanz) | JAK 1,3 inhibitor | Reduce cytokine storm when tocilizumab etc fails Mortality 2.8 vs placebo 5.5; TAE 26 vs 22 |
Treg cells (off-shelf) |
| Reduce cytokine storm |
Über antibodies | Side-steps Spike protein hotspots, targeting more conserved regions | Being developed, could be an answer to various evolving mutations |
Upamostat [WX671, Mesupron] | Urokinase/serine protease inhibitor, repurposed fr. Cancer Rx | Developed for Ca pancreas, inhibits metastasis; For non-hospitalized pts; targets serine protease |
Vacuolin-1 (originally for Ebola) | inhibitor of PIKfyve kinase, TLR & its products IL-12,13 | Inhibits CoV-2 replication in cell line by 85 & also in a human lung explant model |
VBY-825 | Cysteine protease inhibitors | Inhibits virus in cell line |
Vedolizumab | α4β7 integrin* mAb, *primary mediator of GI inflammation | Reduce cytokine storm when steroids fail |
Z LVG CHN2 | Cysteine protease inhibitors | Inhibits virus in cell line |
Table 1: A list of agents used or misused on COVID-19 patients
AATD, alfa-1-antitrypsin deficiency
DM, diabetes mellitus
Esp., especially
Fr., from
Hosp., hospital, hospitalization
HR, hazard ratio
OR, odds ratio
PIKfyve, phosphatidylinositol-3-phosphatase five kinase
Rec.hu, recombinant human
Rx, treatment
The problem of thrombosis
A well-known complication of COVID-19 is the risk of deep vein thrombosis and pulmonary embolism (PE) [13, 14]. In COVID-19, the blood marker D-dimer has 100 sensitivity but only 9 specificity for PE. Due to virus-induced endothelial inflammation the D-dimer will be always raised. Raising the threshold of D-dimer will improve specificity for PE but sacrifice its sensitivity. Thus, the test may not be helpful in COVID-19. Although a low value of D-dimer may exclude deep vein thrombosis and pulmonary embolism, it is rare to come by because the pathology of the infection itself would raise the value, while a high value might be due to other factors than deep vein thrombosis and pulmonary embolism. Other in-depth investigations such as ultrasound doppler, and pulmonary CT angiogram may be necessary.
The treatment of thrombosis is also problematic as heparin might induce PF4-related thrombotic thrombocytopenia and alternative anticoagulants might be necessary and it would be a delicate balance between the risk of bleeding and the risk of thrombosis.
The problem of hypoxia
To begin with, severe hypoxia may develop deceptively with very little symptoms. Often diagnosis dependents on vigilance and liberal use of oximeter and blood gas analysis. Certain refinements on non-pharmacological intervention have developed since the first SARS pandemic. We are more experienced in applying the prone position in lung ventilation, in administering high flow oxygenation and non-invasive biphasic respiratory support. We have developed sophisticated enclosed methods of tracheal intubation and tracheostomy. Yet, we shall always have problems with the hospital administration whose first worry is about the safety of the staff and other patients from cross infection, and this goes with all positive pressure ventilation and aerosol generating manipulations. Advancing the ECMO (extra-corporal membrane oxygenator) from the third line to second line rescue of oxygen desaturation may be a solution. The problem is it will be against the guidelines which relegate the use of this advanced technology to a late and moribund stage of the disease [15].
Problems in convalescence
While most patients will recover at the end of two to three weeks, some will have lingering symptom and/or continue to shed the virus. Others might be virus negative for two or three tests and then become positive again. Such “Long COVID” patients often, but not invariably, come from the elderly or debilitated group and warrant prolonged monitoring and follow up.16
A more serious problem is “Multi-system Inflammatory Syndrome” (MIS), more common in children (MIS-C) [17] than adults (MSI-A) [18]. The disorder is most likely related to cytokine release and its pathogenesis and treatment is still evolving.
Vaccine and vaccine related problems (see Table 2)
A variety of COVID-19 have been produced at record speed. Some are based on conventional methods of production such as using inactivated virus or recombinant viral proteins. More important is the major technological breakthrough of using messenger RNA to direct the recipient’s own cells to produce the viral protein for eliciting antibodies from the recipients. This reduces the cost, time and labour of vaccine production as most of the work of production is passed from the manufacturer to the recipient’s own cells. The problem is the technology has no substantial past human experience to back up its safety. Even experimental animal study is scanty. Effects on the elderly, the very young, the pregnant mother and the unborn child are all unknown.
Vaccine | Producer | Nature | Efficacy | Ab speed | Side effects |
Ad5-nCoV | CanSinoBIO, China | Non-replic. Adenovirus 5 as vector for S-protein | T-cell response 14 days
| 28 days | High dose assoc w/ fever, myalgia fatigue |
Ad26.CoV2.S | J&J (USA) | recS protein full length in non-replicate adenovirus vector; cell receptor CD46 | Ph II, 76 dev T CD4+ @ d14, 90 dev Ab @ d29, 100 @ d57 | Single injection | GBS 4x general population CVST up |
BBIBP-CorV | SinoPharm (China) | Inactivated virus |
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BBV152 with Algel-IMDG/Covaxin | Bharat Biotech International (India) | Inactivated whole viron + TLR 7/8 agonist molecule-alum | Protection overall 77.8, against severe COVID 93.4, against asymp COVID 63.6, against delta 65.2 | 2nd dose 28thd 3rd dose 56thd Store @2-8C |
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BNT1621b1
| Pfizer & BioNTech, Germany
| mRNA vaccine targeting secreted RBD3SARS-CoV2 storage @ -70C | Ph II, Ab above convalescent pts; Ph III: RT-PCR+ 8 vs placebo 162, severe COVID 1 vs 9 | 14 d aft 1st , 7 days aft 2nd dose, in 95 | Fever, chills, headache, myalgia, anorexia, 3 anaphylaxis |
BNT1621b2/Comirnaty | Ditto | mRNA vaccine targeting membrane-bound full-length spike protein | Ditto, RBD3= trimeric receptor- binding domain, efficacy for B.117 down 1/2.6, for B.1351 down 1/4.9, B1617 down 1/5.8 vs w.t. Ex vivo tested effective on 3 clades: [B.1.429 S gene (B.1.429-spike–S13I, W152C, L452R, and D614G)]* [B.1.526 S gene (B.1.526-spike–L5F, T95I, D253G, E484K, D614G, and A701V)] [B.1.1.7 S gene plus the E484K substitution (B.1.1.7-spike+E484K–Δ69-70, Δ145, E484K, N501Y, A570D, D614G, P681H, T716I, S982A, and D1118H)]
| Ditto | Lower incidence & severity of MAE
*Neutralization a bit lower for B.1.429, still further lower for all strains w/ E484K
Post vaccination myocarditis |
CanSino | Beijing Instit. Biotech. | Vector carried vaccine | 91 protected |
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ChAdOx1 nCoV-19, a.k.a. AZD1222,former COVID vaccine AstraZ now Vaxzevria | Oxford University + AstraZeneca, UK | Attenuated adendovirus Modified to encode S-protein; cell receptor CAR/ Coxackie&adenoV receptor | T-cell response 14 days; best w/ ½ dose 1st inj. w/90 protection, but full dose x 2 inj. yield only 60 protection – need to clarify; S African variant not covered | Efficacy up by delaying 2nd dose from 3 to 4 weeks, 90 protected | Headache, fatigue, VITT, CVST Failed to protect against B.1.351 var. |
ChAdOx1 nCoV-19, intranasal vaccine | AstraZeneca, UK | Same as i.m. but given to nose | Confer immunity on nasal mucosa & stop virus hitchhiking there to infect others | Elicit higher Ab level than i.m. vaccine | More effective to stop the transmission than i.m.vaccines |
Intranasal live attenua RSV expressing CoV-2 S instead of RSV membrane protein | Meissa Vaccines, Red Wood City, California |
| In monkey expt. 0/4 vaccinated animals got infected vs 3/4 unvaccinated got infected |
| virus in nasal shedding of vaccinated monkeys reduced by 200x |
Intranasal Parainfluenza virus 5(PIV5) encoding the virus antigens | CyanVac LLC, Georgia & California | Intranasal vaccine as primary immunization, then an i.m. boost w/various mutant vaccine like particles | Plan to deal with all kinds of COVID mutants in future |
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AdCOVID intranasal vaccine | Altimmune, Maryland |
| Failed to elicit adequate response in human in spite of promising results in animals |
| But blood level of Ab may not reflect extent of nasal immunity |
CoronaVac 2 doses/2-3 wk | Sinovac Life Science, Beijing | Chemical-inactivated virus | Just over 50 protection for mild infection but near 100 for M&M. Effective for P.1, E484K(Ab evader) | 90@14d 100 28d | Could be the answer to vaccine evader virus |
WIVO4 (strain fr a Wuhan pt.) |
| 5/4.5μg virus fr 2 Wuhan pts, grown & inactivated w/ β-propanolide, adsorbed on 0.5/0.45mg alum | Protection 72.8, fr severe 100; RT-PCR+ve +/- symptoms 42pts | Alum-only RT -PCR 116pts+ AE 46.5 | Seroconversion 99.3; AE any grade 44.2 |
HBO2 (strain fr another Wuhan pt.) |
| Protection 78.1, fr severe 100; RT-PCR+ve +/- symptoms 31pts | Seroconversion 100; AE any grade 41.7* | ||
COVAXIN | Oxford U+AstraZeneca Bharat Biotec, Councel of Med. Research, India |
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| Allegation of trial irreg. w/ some died after inj. |
Gam-COVID-Vac (Sputnik V) | Gamaleya NRCEM, Moscow | recAdv -based; storage -18C; -2 to -8C appr. | 91 protection, 1st dose rAd26-S, 2nd dose rAd5-S, 21 days apart |
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mRNA-1273 COVID-19 | Moderna + NIAID, USA | mRNA vaccine; storage @ -20C @ 2-8C stable 30 days | 94.5 protection, severe cases 0 vs placebo 11; trial no. 30,000 100ug induce Ab titre >25ug GMT geometric mean titre | day119 Ab > convalescent: GMT 182-109 for age 18-70 | Anaphylaxis 2.5/million; of 4.04 million 1st dose, 1266 AEs, 108 severe, VITT, 10 confirmed anaphylaxis |
MVC-COV1901 | Medigreen Vaccine Biologis, Taiwan | Recomb Spike S-2 protein + CPG 1018 & Alum hydroxide | Sero-conversion 99.8; nAb GMT@ 28d = 662.3IU/mL after 2 doses |
| Entering Phase III |
NDV-vector w S-protein | Microbiol dept., Mt Sinai, NY | Live nonpathogenic New Castle disease virus trans -fected with Spike gene | Successful protection in mice |
| Safe, inexpensive by virus culture in eggs |
NVX-CoV2373 | Novavax, USA | Recomb.S protein+Matrix-M adjuvant, nano-particulated, storage 2-8C | Phase 3, S Africa, 61 protection, 51 for B1351 clade (excl HIV pt) 49 protection incl HIV & all var. | Only 1 died of COVID in placebo gr., HIV pts also some protection; later UK trial for B117/α 86 protected,for non-α 96 | |
SCB-2019, S-trimer | Australia | Trimeric spike protein +2 adjuvants, either AS03 or CpG/Alum | 2 doses, 21 days apart |
| Phase 1 |
Sputnik V rAd26 & rAd5 | Russia | recombDNA encoding S delivered by AdV25 1st & AdV5 2nd dose | Avoid 2nd dose being neutralized by Ab from 1st dose |
| Infection rate down fr 1.3 to 0.1 |
ZyCov-D | Zydus Cadila, India | Plasmid w/DNA encoding S given by intradermal jet | 3 doses 28d apart | 28,000 volunteers, 67 protection for all symptomatic infection, 100 for lethal infection after 2 doses, 100 for moderate infection after 3 doses |
Table 2: A List of COVID-19 vaccines
Ab, antibody
Ad/AdV, adenovirus
CVST, cerebral venous sinus thrombosis
d, day
GBS, Guillain-Barre syndrome
GMT, geometric mean titre
MAE, major adverse event
NDV, New Castle disease virus
NVX, Novavax
RBD, receptor binding domain
Rec/recomb, recombinant
S, spike protein
VITT, vaccine-induced thrombotic thrombocytopenia
The next problem with COVID-19 vaccines is over-inflated expectation, so that the public is misled to believe vaccines would solve all problems of the pandemic. Anti-viral vaccines principally work by eliciting neutralizing antibodies that bind to specific sites (epitopes) on the Spike protein of the virus and stop its gaining attachment to receptors (ACE-2) on the human cells. There are 3 scenarios where this neutralization might fail. First, the level of antibodies might be inadequate due to its waning with time or inadequate original response of the recipient’s immune system from old age, debilitation or immune suppression from disease and/ or disease treatment. Second, the exposure of the individual is so severe that the number of virus overwhelms the level of antibodies. Third, the virus has mutated so that the antibodies could no longer effectively neutralize the invader. Vaccines should work along with other measures like masking, and reduction of exposure by social distancing and not replace them altogether. The time to relax our vigilance is when the disease is eliminated, not when the population is 70, 80 or 90 vaccinated.
By relaxing on lock-down measures, masking and social distancing, and relying exclusively on the vaccines we are creating a paradox in the infection trajectory. The vaccine will effectively protect the recipients from high mortality and morbidity but not entirely from asymptomatic infection. Instead of ensuring a clear interruption of virus transmission, our vaccines are creating an ever-increasing number of asymptomatic carriers, silently spreading the infection undetected and unhindered in our society.
Improving vaccine efficacy
The current method to improve vaccine efficacy is to add another booster dose. Already, a third dose has been applied on the elderly and those immunologically compromised in developed countries. In Israel they are going on to a fourth booster dose. For the ChAdOx vaccine it has been demonstrated that a higher antibody response could be elicited if the second dose of vaccine is given 4 weeks after the first dose instead of the officially recommended 3 weeks. However, such a delay would also expose the recipient to the risk of delay in achieving full protection. Choice of vaccine also may make a difference. E.g. BNT-162b2 is found to elicit a level of antibodies nine times that of SinoVac [11].
Intradermal versus intramuscular vaccine injection
The skin has been the route of administering vaccine for many years, being the site for small pox vaccine and the BCG against tuberculosis. The skin is endowed with a rich supply of dendritic cells to process the antigens [11]. Locked in a small intradermal blister, for the first 15 to 30 minutes, the vaccine has more time to interact with skin tissues, with no chance of accidentally entering a blood vessel or a nerve, both would result in grave consequences. In the case of HBV vaccine, intradermal vaccine has been shown to need only 1/10 of the standard dose to elicit a protection level higher than the intramuscular injection. Booster doses would put extra demand on vaccine supply and expenses. Changing to intradermal injection at reduced dosage would effectively expand the vaccine supply at no extra cost. Moreover, dose reduction implies risk reduction and might even change the attitude of some vaccine skeptics.
Here the problem is the rigidity of guidelines which stipulate that the vaccines have to be given by the intramuscular route and any change would have go through elaborate trials before official approval.
The problem of virus mutations (see Table 3)
The virus SARS-CoV-2 that causes this pandemic is a positive-sense single-stranded RNA virus. Because of this, its genome ranks among the most unstable among virus, surpassed only by the influenza virus which has the additional advantage of having its genome divided into eight segments and capable of reshuffling (like in a pack of cards). Nonetheless, the coronavirus CoV-2 already possesses great propensity to mutate. Such mutations have led to frequent emergence of new variants, some of which might give the new variants advantages in transmission, evasion from host immunity, resistance to treatment and, worst of all, increased pathogenicity. Certain virus variants are capable of overcoming immunity conferred by vaccines or previous infections. And the virus can mutate much faster than the development of new vaccines by humans.
Subtype Variants | Mutations | Characterization & Remarks | ||||
Early variants in China | CoVid-2019 virus L-type a.k.a. SARS CoV2-L | CT haplotype, T28,144 | This SNP being in the codon of Leucine, a newer subtype, more aggressive, 70 in initial pandemic, diminishing because it attracts more evolutionary pressure fr. Rx | |||
CoVid-2019 virus S-type a.k.a. SARS CoV2-S | TC haplotype, C28,144 | This SNP being in the codon of Serine, an older subtype, less aggressive, 30 in initial pandemic, increasing because of less quarantine & treatment pressure | ||||
SARS-CoV-2 | Spike protein S-2P var. 614D (Asp) | The Wuhan virus predominant genotype less stable and less infectious binding ACE2 | ||||
Early variant in Europe/USA | D614G (Gly) | The USA & world-wide predominant genotype, more stable & infectious in binding ACE2, but its stability made it more targetable by Ab from host or vaccination | ||||
α, alfa sub-type | Lineage B.1.1.7, a.k.a. 501Y.V1 by phylogenetic cluster | N501Y @ receptor-binding domain D614G | S England, Binds ACE2 w/higher affinity & tighter, higher viral load, 56 more contagious, more lethal, mortality up 61, covered by current vaccines, but theoretically might be missed by some diagnostic tests creating false negatives. Topol: 1st variant of concern in USA Convalescent serum & vaccines effective; BioNTec induced NAb efficacy down to 1/2.6 vs w.t. | |||
β, beta | S Africa variant (B.1.351)/501Y.V2 | N501Y, E484K*, K417N triple var also the common D614G ACE2 affinity up many times A promising candidate to produce vaccines cross-reactive w/other str. | Appear even more contagious than (α) B.1.1.7, infects even COVD recovered pts, ChAdOx1 vac 10.4 protection – ineffective NVX-CoV2373 49.4 protection, 100 for severe cases; Ad26.CoV2.S J&J 64 protection, 82 for severe cases; BNT162b2 72 protect’n, 97.4 for severe cases, NAb efficacy dropped to 1/4.9 vs w.t. Convalescent serum and vaccines fr other strains 9-14x less effective on this strain, but its Ab highly effective against other strains like P.1 fr Brazil - *E484K confers Ab evasion | |||
γ, gamma | Brazil P.1 variant/b.1.1.28.1 | K417T, E484K*+N501Y RBD, D614G total 17 mutations
| Double mutation in receptor domain spreading from Manaus, Amazona, Brazil to 6 countries; ACE2 affinity up 9x more contagious; convalescent serum and vaccinated serum 2-3x less effective,*E484K confers Ab evasion, γ-infection broke out when 76 of Manaus have Ab’s. (Topol: 2nd var of concern in USA, Sinovac effective); BNT162b2 NAb efficacy down 60 | |||
δ, delta | Indian variant B1617.2 (typo 1167 some reports) | T19R, Δ157-158, L452R, T478K, D614G, P681R, D950N | Possibly more infectious and Ab-evasive, had spread to Singapore and other neighbours; BioNTec vaccine induced NAb efficacy dropped to 1/5.8 vs w.t. | |||
δ plus | Nepal variant of δ | + K417N | Could be more infectious than delta | |||
ε, epsilon | California var. CAL.20C | S131I, W152C, L452R | B.1,427 | + 4 specific mutations | Emerged in S California w/ increased transmission/Ab resistance; eventually out-competed by the alfa variant | |
B.1.429 | + 3 specific mutations | |||||
ζ, zeta | Lineage P.2 | E484K,D614G,V1176F,+/-F565L | Evolved in Rio de Janeiro independent of the γ variant, WHO: a var of interest now delisted | |||
η, eta | Lineage B.1.525, VUI-21FEB-03,UK1188,21D | First found in UK & Nigeria & spread to 23 countries F888L is unique to eta variant. | ||||
θ, theta | Lineage P.3 | E484K,N501Y,D614G,P681H, E1092K,H1101Y,V1176F,K2G | First found in Philippines, spread to Japan, more resistant to Ab’s fr. vaccines | |||
ι, iota | B1526,a pangolin lineage | S477N, E484K, L5F, T95I, D253G, D614G & A701V | A variant first found in NY City, more likely in neighbourhood than in metropolitan area S477N binds tightly to human cells, E484K confers immune escape & Ab evasion | |||
κ, kappa | B1617.1 | E484Q, L452R, D614G | Increase in transmission but decrease in virulence | |||
λ, lambda | lineage C.37 | G75V, T76I, Δ246-252, L452Q, F490S, D614G, T859N | First in Peru, April 2021, now all over the world, but mainly prevalent in S America, possibly more infectious and vaccine-resistant than α or γ subtypes | |||
μ, mu | B.1.621, a variant of interest | N501Y, E484K >9SNPs (cf β & γ), T95I, YY144-145TSN, R346K, E484K, N501Y, D614G, P681H, D950N | From Columbia, S America, Jan 2021, spreading to 39 countries, @<0> More Ab-resistant than β variant by 2.0x (natural Ab) & 1.5x (BNT-162b2 induced Ab) | |||
Italy var. Spike protein | N501T;N501T+Q403K double mut | The double mut might alter receptor binding domain RBD such as to affect ACE2 affinity | ||||
Netherland-Denmark mink variant | Y453F @ receptor-binding domain | Binds mink ACE2 with increased efficacy, may create another zootic reservoir | ||||
Denmark 3 additional human mut | I692V, M1229I, del69_70 | No increased transmission or pathogenicity but reduce neutralization activity of Ab | ||||
Danish ‘cluster 5’ var adds 3muts | Del69_70, I692V, M12299I | 11pts in Netherlands infected, modest reduction in convalescent Ab neutralization response | ||||
USA-WA1/2020 |
| One of the first virus species sequenced in USA fr someone back fr Wuhan used as reference | ||||
c.1.2 variant (as yet un-named) | Carries mut of α, β, γ, δ + 3 VOIs | From S Africa May 2021 w/mut enabling immune escape | ||||
COVID vaccine break-through mut in 417 vaccinees: Moderna 19d & Pfizer 36d after 2nd dose w/in vitro effective neutralizing Ab present! | E484K, A570D, P796H | Found in 1st patient, but E484K shared by β, γ, μ & assoc w/greatest resistance to natural Ab’s | ||||
P681H, | Found in 1st pt., & in heterozygosity in 2nd pt | |||||
T95I, del142-144, D614G | Found in both patients | |||||
F220I, R237K, R246T, D614G | Found in 2nd patient only | |||||
L452R, N501Y | Not detected in 1st pt. undetermined in 2nd | |||||
S477N, A701V | Not detected in 1st pt., partial heterozygosity in 2nd | |||||
H655Y | Not detected in either pt. | |||||
Other mut | N439K, L452R, |
| ||||
Mut that enhance ACE2 binding | Spike D614G, N501Y | Characterize the alfa virus, N501Y also in beta virus | ||||
Mut that enhance transmission | D614R, P681R |
| ||||
Mut that reduce Ab neutralization | L452R | A variation in delta virus | ||||
Mut that further Ab escape | K417N | In beta and delta plus virus | ||||
Mut Ab escape commonest among var. | E484K | In β, γ, μ, also assoc w/greatest reduction in sensitivity to Ab fr natural infection | ||||
Experimental mut in mice | Q493K, Q498H | Significantly increase affinity to mouse ACE2; resiquimod effective in Rx | ||||
Mut that reduce virus ferocity | nsp-14 mut (nonstructural protein) | Virus use nsp-14 to inhibit host IL-1instigated defence & to regulate/repair its own genetic damage, nsp-14 mut/LOF lead to rapid replication & increase of deleterious mut w/initial out- competing other viral variants but ultimate self-extinction – Ituro Inoue on Japan’s 5th wave | ||||
Table 3: A list of some of the more important mutations in the SARS-CoV-2 virus
Ab, antibody
Assoc., associate or associated
fr., from
mut, mutation(s)
NAb, neutralizing antibody
nsp, non-structural protein
pt., pts, patient, patients
w/, with
Can virus mutation help mankind to solve the COVID-19 problem?
Not all virus mutations are deleterious to mankind. Many are also deleterious to the virus itself.
Singapore has reported on the deletion of 382 nucleotides in a SARS-CoV-2 variant causing truncation at ORF 7b and elimination of ORF8 transcription [19]. This resulted in a milder form of infection with lower virus replication, less inflammatory cytokine production and reduced morbidity and mortality with none of the 29 infected patients requiring any oxygen supplement compared with oxygen requirement in 30 of patients infected with wild type virus.
Japan’s fifth wave of the pandemic following the summer Olympic Games was considerably milder than expected. Ituro Inoue recently offered a plausible explanation [20]. The virus non-structural protein nsp-14, under pressure of host APOBEC enzyme activity has gone through mutations that initially leads to much faster replication, but also to loss of capability to suppress host IL1-led anti-viral defence, and ultimately accumulation of a heavy load of mutations incompatible with the virus’ own survival. If substantiated, this mechanism would add a silver lining to the dark cloud hanging over the pandemic.
And it brings out a stark basic problem in this pandemic. While even the virus itself may be helping us with mutations that favour its own control, we humans continue to put other priorities above consideration of health. As late as the 20th century the US and the Soviet Union joined hands, put the Cold War aside, and developed vaccines that led to control of the polio pandemic. Today, all that cooperative spirit is buried under the obsession of a desire to stay on top of the world in terms of wealth and power.
This is the greatest problem confronting the present, the bias and lack of mutual trust and conjoint effort to fight the virus. What does it profit a nation if it gains the status as the “greatest” in the world but suffers the loss of the health of its own people?
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Dear editorial department: On behalf of our team, I hereby certify the reliability and superiority of the International Journal of Clinical Case Reports and Reviews in the peer review process, editorial support, and journal quality. Firstly, the peer review process of the International Journal of Clinical Case Reports and Reviews is rigorous, fair, transparent, fast, and of high quality. The editorial department invites experts from relevant fields as anonymous reviewers to review all submitted manuscripts. These experts have rich academic backgrounds and experience, and can accurately evaluate the academic quality, originality, and suitability of manuscripts. The editorial department is committed to ensuring the rigor of the peer review process, while also making every effort to ensure a fast review cycle to meet the needs of authors and the academic community. Secondly, the editorial team of the International Journal of Clinical Case Reports and Reviews is composed of a group of senior scholars and professionals with rich experience and professional knowledge in related fields. The editorial department is committed to assisting authors in improving their manuscripts, ensuring their academic accuracy, clarity, and completeness. Editors actively collaborate with authors, providing useful suggestions and feedback to promote the improvement and development of the manuscript. We believe that the support of the editorial department is one of the key factors in ensuring the quality of the journal. Finally, the International Journal of Clinical Case Reports and Reviews is renowned for its high- quality articles and strict academic standards. The editorial department is committed to publishing innovative and academically valuable research results to promote the development and progress of related fields. The International Journal of Clinical Case Reports and Reviews is reasonably priced and ensures excellent service and quality ratio, allowing authors to obtain high-level academic publishing opportunities in an affordable manner. I hereby solemnly declare that the International Journal of Clinical Case Reports and Reviews has a high level of credibility and superiority in terms of peer review process, editorial support, reasonable fees, and journal quality. Sincerely, Rui Tao.
Clinical Cardiology and Cardiovascular Interventions I testity the covering of the peer review process, support from the editorial office, and quality of the journal.
Clinical Cardiology and Cardiovascular Interventions, we deeply appreciate the interest shown in our work and its publication. It has been a true pleasure to collaborate with you. The peer review process, as well as the support provided by the editorial office, have been exceptional, and the quality of the journal is very high, which was a determining factor in our decision to publish with you.
The peer reviewers process is quick and effective, the supports from editorial office is excellent, the quality of journal is high. I would like to collabroate with Internatioanl journal of Clinical Case Reports and Reviews journal clinically in the future time.
Clinical Cardiology and Cardiovascular Interventions, I would like to express my sincerest gratitude for the trust placed in our team for the publication in your journal. It has been a true pleasure to collaborate with you on this project. I am pleased to inform you that both the peer review process and the attention from the editorial coordination have been excellent. Your team has worked with dedication and professionalism to ensure that your publication meets the highest standards of quality. We are confident that this collaboration will result in mutual success, and we are eager to see the fruits of this shared effort.
Dear Dr. Jessica Magne, Editorial Coordinator 0f Clinical Cardiology and Cardiovascular Interventions, I hope this message finds you well. I want to express my utmost gratitude for your excellent work and for the dedication and speed in the publication process of my article titled "Navigating Innovation: Qualitative Insights on Using Technology for Health Education in Acute Coronary Syndrome Patients." I am very satisfied with the peer review process, the support from the editorial office, and the quality of the journal. I hope we can maintain our scientific relationship in the long term.
Dear Monica Gissare, - Editorial Coordinator of Nutrition and Food Processing. ¨My testimony with you is truly professional, with a positive response regarding the follow-up of the article and its review, you took into account my qualities and the importance of the topic¨.
Dear Dr. Jessica Magne, Editorial Coordinator 0f Clinical Cardiology and Cardiovascular Interventions, The review process for the article “The Handling of Anti-aggregants and Anticoagulants in the Oncologic Heart Patient Submitted to Surgery” was extremely rigorous and detailed. From the initial submission to the final acceptance, the editorial team at the “Journal of Clinical Cardiology and Cardiovascular Interventions” demonstrated a high level of professionalism and dedication. The reviewers provided constructive and detailed feedback, which was essential for improving the quality of our work. Communication was always clear and efficient, ensuring that all our questions were promptly addressed. The quality of the “Journal of Clinical Cardiology and Cardiovascular Interventions” is undeniable. It is a peer-reviewed, open-access publication dedicated exclusively to disseminating high-quality research in the field of clinical cardiology and cardiovascular interventions. The journal's impact factor is currently under evaluation, and it is indexed in reputable databases, which further reinforces its credibility and relevance in the scientific field. I highly recommend this journal to researchers looking for a reputable platform to publish their studies.
Dear Editorial Coordinator of the Journal of Nutrition and Food Processing! "I would like to thank the Journal of Nutrition and Food Processing for including and publishing my article. The peer review process was very quick, movement and precise. The Editorial Board has done an extremely conscientious job with much help, valuable comments and advices. I find the journal very valuable from a professional point of view, thank you very much for allowing me to be part of it and I would like to participate in the future!”
Dealing with The Journal of Neurology and Neurological Surgery was very smooth and comprehensive. The office staff took time to address my needs and the response from editors and the office was prompt and fair. I certainly hope to publish with this journal again.Their professionalism is apparent and more than satisfactory. Susan Weiner
My Testimonial Covering as fellowing: Lin-Show Chin. The peer reviewers process is quick and effective, the supports from editorial office is excellent, the quality of journal is high. I would like to collabroate with Internatioanl journal of Clinical Case Reports and Reviews.