2) The study aimed to understand how repeated vaccination with the ancestral SARS-CoV-2 mRNA vaccine induces antibodies that can neutralize Omicron variants, which have mutations that allow immune escape.
3) They analyzed blood samples from 41 individuals who received three doses of the BNT162b2 mRNA vaccine. Samples were collected at various time points to track the immune response.
4) Analysis of B-cell receptor repertoires found that after the third dose, specific B-cell clones accumulated mutations (somatic hypermutation) that allowed them to bind both the ancestral spike protein and Omicron spike protein.
5) Certain B-cell receptor clones became prevalent after the third dose, particularly clones using the IGHV3-53/IGHV3-66 genes. Accumulation of mutations in these clones increased their affinity for both ancestral and Omicron spike proteins.
6) Functional testing confirmed that antibodies produced by these mutated B-cell clones could neutralize not just the original virus strain but also Alpha, Beta, Gamma, Delta and early Omicron variants in vitro.
7) The accumulation of mutations after the third dose seemed to expand the specificity of the B-cell receptor repertoire to recognize newer Omicron subvariants that emerged later, like BA.1, BQ.1.1, XBB.1.5, and XBB.1.16.
In summary, repeated vaccination induced ...
8) ... somatic hypermutation of antibody-producing B-cells, which helped generate antibodies that could neutralize diverse Omicron variants through cross-reactive binding to the spike protein. This may be a protective immune mechanism against viral variants.
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It has been more than 1 year, since we sounded the alarm about the transmission of avian influenza to mammals.
The almost total indifference gave way to general excitement.
2) But, from one extreme to the other, there is a transmission timing. A tik tock ๐ญ as says my friend David @DavidJoffe64
3) On April 17, 2023, increased mortality was observed in a backyard poultry farm in Brescia, northern Italy. The farm was quarantined and samples were taken to test for avian influenza. Out of the 22 poultry on the farm, only the hens showed mortality ...
Being one of the most important studies we have read, we will take the time to explain all the concepts, one by one.
2) ๐๐๐๐ฉ ๐๐ง๐ ๐ผ๐ช๐ฉ๐ค๐ฅ๐๐๐๐ค๐จ๐ค๐ข๐๐จ ?
Autophagosomes are double-membrane vesicles formed during autophagy, that sequester cytoplasmic cargo like proteins, organelles and pathogens targeted for degradation.
Upon SARS-CoV-2 invasion, host cells induce autophagy ...
3) ...as an intrinsic antiviral defense mechanism. Autophagosomes capture invading viral particles and components.
Cargo-loaded autophagosomes then fuse with lysosomes. This degrades intact virions and disrupts infection.
โถ๏ธ SARS-COV-2 variants have independently adapted spike to escape IFITM3
โถ๏ธ IFITM3 deficiency facilitated infection of AVIAN INFLUENZA in multiple human cell types
2) Even if there is no a priori direct link between the adaptation of SARS-COV-2 to IFITM3 and the risk of IFITM3 deficiency for avian influenza, it seemed interesting to us to return to IFITM3.
2) GBP2 and GBP5 were found to inhibit infection of early SARS-CoV-2 isolates Wuhan-Hu-1 and VIC by blocking furin cleavage of spike and reducing spike processing/glycosylation. This decreased particle infectivity.
Maintaining non-pharmaceutical interventions like masking is essential to vaccination success, not a replacement.
@C_A_G0101 medrxiv.org/content/10.110โฆ
2) The study used a compartmental SEIIS model to simulate the course of a COVID epidemic both without and with vaccination interventions. Variables like vaccine hesitancy, vaccination speed, duration of immunity, and variants were tested.
3) Even a perfect vaccine that always provides sterilizing immunity can still allow high disease rates depending on factors like hesitation, slow rollout, dropping measures, and variants.
SARS-CoV-2, the virus that causes COVID-19, binds to the ACE2 receptor which is expressed in reproductive tissues like the ovaries, endometrium, testes, etc. This suggests the virus could potentially affect the female reproductive system.
3) Studies found SARS-CoV-2 RNA was not present in endometrial biopsy samples from infected women. The endometrium appears protected from infection via the ACE2/TMPRSS2 route.
2) This study describes the emergence of the SARS-CoV-2 Omicron subvariant JN.1 in Tamil Nadu, India between November and December 2023. JN.1 rapidly replaced the previously dominant XBB variant.
3) 66 JN.1 positive samples underwent whole genome sequencing. The majority of patients were middle-aged, with equal male/female representation. Over 50% had diabetes and 21% had hypertension