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Pfizer, Moderna jab shows reduced antibody response to Indian mutants

Pfizer, Moderna jab shows reduced antibody response to Indian mutants

 


New Delhi : A preliminary laboratory study of the mRNA vaccine by Pfizer and Moderna showed reduced efficacy against double mutants found in India, the World Health Organization said in a memo. This is behind a multilateral agency that classifies mutant virus strain B.1.617 as a variant of concern.

“Preliminary laboratory studies awaiting peer review suggest a limited reduction in antibody-induced neutralization, but the actual effects may be limited,” he said.

The WHO memo mainly described the features of B.1.617. It was classified as a “variant of concern” earlier this week. That is, mutant strains and their substrains (B.1.617.1, B.1.617.2, and B.1.617.3) were infected, including a sharp increase in prevalence in multiple countries. The rate seems to be high. So far, the strain has been found in 44 countries since it was first discovered in Maharashtra in October.

Indeed, laboratory data suggest that these vaccines may show lower efficacy against mutant strains, but the question is determined until studies are conducted in the actual setting. Not the target.

The Global Health Agency cited three studies showing that the antibodies produced by the vaccine developed by Pfizer and Moderna significantly reduced the ability to neutralize the mutant virus and its substrains.

Meanwhile, we cited another non-peer-reviewed study that showed that covaxin was largely effective against mutant strains of the virus.

One of the studies was conducted jointly by researchers at Emory University School of Medicine, Stanford University School of Medicine, and the National Institute of Allergy and Infectious Diseases Vaccine Research Center in Georgia, USA. The study tested sera from 24 people who recovered from covid-19, 15 people who received the Moderna vaccine, and 10 people who received the Pfizer vaccine.

When compared to the original strain isolated in the United States, this study found that the Indian variant was neutralized by serum in persons who were previously infected with covid-19, or who were vaccinated with either jab. I concluded that it was not easily affected. However, despite high resistance from mutant strains, the majority of sera from infected individuals and all vaccinated individuals were still able to neutralize the mutant, the study said. ..

Other studies cited by WHO, conducted by the University of Cambridge, the National Center for Disease Control, and the CSIR Institute for Genome Integrated Biology, also showed a reduction in the neutralizing activity produced by vaccines against the virus.

The third study, cited by the agency, was conducted by German researchers, with approximately one-third reduction in plasma neutralization activity from Pfizer’s 15 recipients against Indian variants, and convalescent sera. Reported a limited half reduction due to. Severe covid-19.

The three studies will be conducted when the Government of India has agreed to provide a rapid licensing process for vaccines that have already been approved by the US, UK, Japan, European Union, and WHO regulators. Indian regulators also allow state and private sector organizations to import these vaccines directly, subject to import registration and certification, even before they have been licensed in India. ..

Pfizer’s vaccine has been approved by all top regulators and is keen to supply the vaccine to the government, but has not yet applied for approval.

A third study also showed resistance to Eli Lilly’s monoclonal antibody gamlanivimab, which was effectively inhibited by the monoclonal antibody cocktail of regenerone kacilibimab and imdebimab.

Last week, Indian regulators granted Regeneron’s partner Roche an urgent license for antibody cocktails, but the US FDA last month revoked Eli Lilly monoclonal antibody approval due to resistance of mutants to the drug.

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