COVID-19 vaccination may protect against variants better than natural infection, study finds | News Center

The researchers compared the levels and types of antibodies to SARS-CoV-2 in participants in Stanford’s clinical trial of the BioNTech-Pfizer vaccine with those of COVID-19 patients treated at Stanford Medicine during the first months of the pandemic. These patients were treated before the widespread circulation of SARS-CoV-2 in the United States and were most likely infected with one of the earliest strains of the virus, known as Wuhan-Hu-1.

“When we compared antibody responses to infection with those from vaccination, we found that infected people generated variable levels of antibodies, which dropped steadily after infection,” Röltgen said. “In contrast, the response to vaccination was very uniform — all the study participants had a good response, with high levels of antibodies, although these also decreased over time.”

The mRNA-based vaccine generated the highest levels of antibodies in the researchers’ comparison of results from people studied at the Onom Foundation and Liver Center in Mongolia who had been vaccinated with one of three other globally available SARS-CoV-2 vaccines: the adenovirus -based vaccines produced by Cambridge-based AstraZeneca and the Russian vaccine Sputnik V, and an inactivated virus vaccine produced by the Chinese company Sinopharm. All of these vaccines work by exposing the immune systems to portions or all of the Wuhan-Hu-1 virus.

Vaccines generate broad range of antibodies

Each of the vaccines generated a broad range of antibodies. Although most antibodies targeted the viral spike protein of the Wuhan-Hu-1 virus, others could also bind to the spike proteins of nine other viral variants, including the delta variant that caused a surge in hospitalizations and deaths in the late summer and fall of 2021 in the United States. In contrast, unvaccinated patients infected with Wuhan-Hu-1 made a narrower range of antibodies, fewer of which could bind to the spike proteins of the variants.

“Our data indicates that infection with a particular viral variant gives an antibody response that is focused on the antigens from that variant, and it doesn’t have as much breadth of binding to different variants as the vaccine-induced antibody response,” Boyd said . “These results support and extend findings reported for certain viral mutations by previous studies.”

When the researchers examined the lymph nodes of vaccinated and infected people, they saw that the germinal centers in those who were vaccinated appeared to be potent antibody-generating factories for as long as eight weeks after vaccination. In contrast, the germinal centers of lymph nodes in people with severe COVID-19 were poorly formed and were missing key immune cell types, suggesting an impairment of their ability to make disease-fighting antibodies.

If you are hoping to avoid future infection with an as-yet-unknown variant, your best bet is to get vaccinated and boosted now.

The researchers also studied vaccinated and unvaccinated people who became infected with the alpha or delta variants that succeeded the original viral strain. They found that unvaccinated people infected with alpha or delta made antibodies that are specialized in binding to the viral spike protein of alpha or delta, respectively. Previously vaccinated people who were subsequently infected with alpha or delta variant viruses made a panel of antibodies that recognized the spike protein from the Wuhan-Hu-1 strain, which was first presented to them in the vaccine, as well as those of other variants, including alpha and delta.

In previously vaccinated people, “there is less bias of the antibody response toward the variant that has infected you,” Boyd said. This could mean that vaccinated people are better prepared than naturally infected people to fend off subsequent infections with other variants.

It’s unclear whether booster shots tailored to emerging new variants will also be effective in eliciting immune responses to future variants. If a variant arises that is significantly different from the Wuhan-Hu-1 strain used to make the currently available vaccines—and from the variants that preceded it—it may be useful to prime our immune systems with the new information, the researchers said.

In any case, the current vaccines generate broad protection from severe disease caused by variants — one that surpasses the effect of infection.

“In the case of SARS-CoV-2, the argument that infection is better than vaccination isn’t well-supported based on current evidence,” Boyd said. “It is clear that the current vaccines have saved many lives worldwide during this pandemic. If you are hoping to avoid future infection with an as-yet-unknown variant, your best bet is to get vaccinated and boosted now.”

The research was supported by the National Institutes of Health (grants R01AI127877, R01AI130398, U19AI057229, 1U54CA260517, HHSN272201700013C, P30AG019610-20S1), the Bill & Melinda Gates Foundation, the Crown Family Foundation, the American Heart Association, an Arnold O. Beckman Independence Award, the Swiss National Science Foundation, the National Science Foundation and an anonymous philanthropic donation to the Boyd laboratory.