Paul Hunter, Professor of Medicine, University of East Anglia explains at The Conversation COVID-19 vaccines are probably less effective at preventing transmission than symptoms – here’s why. Excerpts in italics with my bolds.
Countries where COVID-19 vaccines have rolled out quickly, such as Israel and the UK, are starting to give an indication of how well they work. Their early results suggest the vaccines are highly effective at preventing people from being hospitalised or dying from the disease.
However, it’s less clear how good the vaccines are at stopping people from spreading the virus. But given what we know about how they work, we shouldn’t be surprised if they are less effective at stopping people transmit the virus than preventing them becoming ill. This is because the type of immunity they generate is likely to be better at fighting off severe rather than mild infections.
How immunity is created
There are a number of distinct phases in the course of a coronavirus infection. Usually the virus starts with what’s known as a “mucosal infection” because it infects the lining of the nose and throat, the nasopharyngeal mucosa.
This is the asymptomatic or pre-symptomatic phase. Mild symptoms such as cough or altered taste or smell may then develop. However, in a proportion of people, the infection then spreads down the respiratory tract to the lungs, causing more serious problems. Some may develop very severe illness, leading to respiratory and other organ failure. At this point, with the virus moving around the body and causing problems in multiple areas, the infection is “systemic”.
People are most infectious during the early stages of infection, when the virus is largely restricted to the nasopharyngeal mucosa. Indeed, it’s possible for people to be highly infectious without the virus spreading to other parts of the body or causing severe illness.
Importantly, the immune system responds differently to mucosal and systemic infections.
A systemic immune response, which works across large swathes of the body, is associated with creating one type of antibody, IgG. Immunity generated in the mucosa (also called secretory immunity) is associated with creating another, IgA. As a result, immunisations that focus on generating systemic immunity – which is what injected vaccines do – rarely induce mucosal immunity. This likely applies to all the COVID-19 vaccines currently available.
And yet, the nasopharyngeal mucosa is ground zero for most coronavirus infections. So while COVID-19 vaccines may generate a response that’s highly protective against systemic disease in the lungs and other organs, the vaccines are less likely to generate strong mucosal immunity that’s effective against the mild but infectious early stage of infection in the nose and throat. We should therefore expect some difference in the vaccines’ effects on preventing severe disease and blocking infection and transmission.
We don’t yet know if there’s a difference in the development of systemic and mucosal immunity for COVID-19. Emerging evidence suggests there might be, but it isn’t conclusive, and much of this research still needs to be fully reviewed.
Finally, it’s worth remembering that even if these vaccines don’t end up blocking infections to a high degree, that doesn’t mean they won’t make a major contribution to suppressing viral spread. Even if people still get infected, COVID-19 vaccines are likely to reduce the amount of virus generated during an infection, lowering what can be passed on.
1. The superiority of natural immunity to vaccine-induced immunity is not mentioned. Dr. Robert Clancy explains:
Another issue is the recognition that genetic vaccines have limited value. While doctors support the current vaccine roll-out, reported “danger signals” must be clarified. Both the DNA-vector vaccine (AstraZeneca) and mRNA vaccines (Pfizer and Moderna) behave as predicted by biology relevant to airways’ protection (something not understood by the vast majority of “experts”): short duration of protection limited to control of systemic inflammation, with little impact on infection of the airways.
Israel was used as a laboratory for the Pfizer vaccine. Six months after vaccination, there was essentially no protection against infection or mild disease, although protection against severe disease remained at 85-to-90 per cent. Thereafter came a rapid and progressive loss of protection against more severe disease. Infected vaccinated and unvaccinated subjects have similar viral loads and transmission capacity.
Immunity following natural infection is better and more durable than that induced by vaccination, so there is no sense in immunising those who have had COVID infection in the preceding six months.
2. Ivermectin Effectively Blocks viral entry at ACE-2 receptors in the nasal and oral cavity.
It has been reported that ACE2 is the main host cell receptor of 2019-nCoV and plays a crucial role in the entry of virus into the cell to cause the final infection. To investigate the potential route of 2019-nCov infection on the mucosa of oral cavity, bulk RNA-seq profiles from two public databases including The Cancer Genome Atlas (TCGA) and Functional Annotation of The Mammalian Genome Cap Analysis of Gene Expression (FANTOM5 CAGE) dataset were collected. RNA-seq profiling data of 13 organ types with para-carcinoma normal tissues from TCGA and 14 organ types with normal tissues from FANTOM5 CAGE were analyzed in order to explore and validate the expression of ACE2 on the mucosa of oral cavity. Further, single-cell transcriptomes from an independent data generated in-house were used to identify and confirm the ACE2-expressing cell composition and proportion in oral cavity. The results demonstrated that the ACE2 expressed on the mucosa of oral cavity. Interestingly, this receptor was highly enriched in epithelial cells of tongue. Preliminarily, those findings have explained the basic mechanism that the oral cavity is a potentially high risk for 2019-nCoV infectious susceptibility and provided a piece of evidence for the future prevention strategy in dental clinical practice as well as daily life.
Fig. 1 A schematic of the key cellular and biomolecular interactions between Ivermectin, host cell, and SARS-CoV-2 in COVID19 pathogenesis and prevention of complications.
Ivermectin; IVM (red block) inhibits and disrupts binding of the SARS-CoV-2 S protein at the ACE-2 receptors (green). The green dotted lines depict activation pathways and the red dotted lines depict the inhibition pathways.
Ivermectin also had the highest binding affinity for TMPRSS2. By binding so well to all three — the spike, the ACE2 receptor and the TMPRSS2 secateurs that prune or prime the spike, ivermectin makes it much harder for the virus to get inside a cell.
via Science Matters
November 23, 2021