Traditionally we hear about virus entering the exposed surface of the cell, like a bug flying in through the open window of a multi-apartment complex.
Now, imagine this bug burrowing through the walls into all the neighboring units. That essentially is cell-to-cell entry.
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The problem with this process is that our neutralising antibodies might not be able to stop it.
These antibodies are designed to stop the bug from entering through the window, but not from burrowing through the walls between adjacent apartments.
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Several viruses use this method. Apparently the SARS-CoV-2 virus is better than its predecessor the SARS virus (of 2003) at doing this. This means it is easily able to find its way deeper into tissues.
This research has implications on our strategies to fight the pandemic.
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Work from Gamaleya National Research Center for Epidemiology and Microbiology, Moscow showing that side-to-side cell entry of the SARS-CoV-2 virus is ~fully resistant to neutralizing antibodies. biorxiv.org/content/10.110…
Work from Anamika Basu et al from Gurudas College and Jadavpur University, Kolkata, India from over a year ago on the topic of cell-to cell transmission of the SARS-CoV-2 virus biorxiv.org/content/10.110…
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Covaxin tested against two variants B.1.617.2 (India) & B.1.351 (S Africa). Mild reduction in neutralization ability noted; 2.7 and 3-fold, which is a smaller loss compared to other vaccines, reports ICMR/NIV study.
See graph for comparison.
Thread. 1/n biorxiv.org/content/10.110…
Neutralizing ability is one of the parameters scientists use to measure a vaccine's firepower against a virus.
If the vaccine is very effective, then its ability will be 1 or close to 1 -that is, in comparison with how effective the same vaccine was against the old virus.
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If the virus has become so smart, it will then take several times the original "neutralising power" to kill it.
e.g. If the amount of vaccine required to kill the new variant is 10 times what it took to kill the old virus, we say the neutralising ability is 10-fold lower.
ICMR-NIV study on P.2, the variant originally found in Brazil since ~April 2020 (WHO). Also called B.1.1.28.2 or zeta, it is now being rapidly replaced by P.1 in Brazil.
ICMR/NIV observed its effects on hamsters in comparison with P.1.
Presenting some context first. This variant P.2 was only seen in 2 samples so far in India; from asymptomatic travelers who arrived from Brazil and UK.
In Brazil, it is also being phased out by P.1 (deeper colour in recent weeks of 2021, genomic data from Manaus, Brazil).
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Study from Brazil showing how P.2 is being phased out by P.1. The latter variant has the N501Y mutation in addition to E484K, among several others.
Traditionally D-dimer is elevated when there are fibrin degradation products associated with clots. But D dimer is also elevated in other inflammatory conditions, trauma, post-op state / malignancy.
In COVID-19, its role is primarily as a marker of severity & inflammation.
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Studies in COVID-19 patients have shown that unless there are specific clinical pointers to a clot (leg or lung), an elevated D-dimer value ALONE will not be worth pursuing: we might end up chasing a bird that was never there.
The latest COVID-19 guideline from Directorate General of Health Services at Ministry of Health & Family Welfare @MoHFW_INDIA, are pristine no-nonsense science.
Antibody titre 115 AU/ml for Covishield and 51 for covaxin.
27 breakthrough infections occurred (4.9%) after both doses: 25 were mild, 2 were moderate, no deaths.
Risk of breakthrough infection:
5.5% with covishield
2.2% with covaxin
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Listing some facts which will help understand the context of the study:
1. Anti Spike antibody is not the same as neutralising antibody. Its level is not known to reliably correlate with NAb, which is typically measured only in research labs. See my earlier tweet on this.
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