B.1.617, the double mutant variant of coronavirus that has emerged in India, entered certain types of lung and intestine cells with slightly increased efficiency.

However, this host cell entry was not blocked by the monoclonal antibody Bamlanivimab, which has received emergency use authorisation (EUA) as a Covid-19 treatment.
Finally, B.1.617 also partially evaded neutralisation by the antibodies induced through natural infection or immunization with the Pfizer-BioNTech BNT162b2 vaccine, a study that appeared in the pre-print repository medRxiv, suggested.
The researcher said that antibody evasion by B.1.617 may contribute to the rapid spread of this variant.
These include the RBD mutations L452R and E484Q, which are known to modulate antibody-mediated neutralisation.
To test whether B.1.617 is more adept at entering cells, the researchers infected eight cell lines with pseudotyped virus particles expressing spike protein from the original wild-type virus, the B.1.617 variant, or the B.1.351 variant.
Collectively, the study reveals that antibody evasion by B.1.617 may contribute to the rapid spread of this variant, the team noted.
Source-IANS
MEDINDIA














