Type Here to Get Search Results !

Pfizer releases more data indicating omicron boosters are better than old Covid shots

Pfizer and BioNTech released more human data Friday indicating the omicron BA.5 boosters perform better than the old Covid shots. People older than 55 who received the new booster had about four times more antibodies targeting omicron BA.5 than people in the same age group who received the old vaccine, according to the companies. Antibodies are a key part of the body’s defense system that block the virus from invading cells. The study compared 36 people older than 55 who received the omicron booster as their fourth dose with 40 people from the same age group who received the original vaccine as their fourth shot. In addition, people ages 18 to 55 who received the booster had 9.5 times more antibodies targeting omicron BA.5 than they did before receiving the shot. These participants weren’t compared with people of the same age who received the old vaccines. Pfizer and BioNTech also found that people with and without prior Covid infections had a significant increase in their antibody levels after the omicron boosters. But those who had no prior infection had a greater increase in their antibodies, according to the companies. Pfizer and BioNTech released the first human data in October showing the omicron boosters trigger a better immune response. But two small, independent studies from Columbia and Harvard cast doubt on whether the shots really were a significant improvement. They found the new boosters and the old shots performed about the same against omicron BA.5. The Food and Drug Administration said the Columbia and Harvard studies were too small to draw any definitive conclusions about the boosters. The scientific community and public health officials are closely following data on the boosters because the FDA authorized them without direct human data. The FDA relied instead on human data from a similar shot that targeted the original version of omicron, BA.1, as well as animal studies that directly examined the BA.5 shot. Pfizer and Moderna were originally developing BA.1 shots, but the FDA asked them to switch gears over the summer and develop a booster targeting BA.5 because it had become the dominant variant. As a consequence, there wasn’t enough time for the companies to launch clinical trials and deliver data before FDA authorization.

Post a Comment

0 Comments
* Please Don't Spam Here. All the Comments are Reviewed by Admin.