Researchers in the United States have conducted a study showing that the coronavirus disease 2019 (COVID-19) vaccines developed by Pfizer-BioNTech and Moderna generate a coordinated adaptive immune response that is capable of eliciting recall responses to future infection with severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2).

The team from the University of California found that immunization with either Pfizer-BioNTech’s BNT162b2 or Moderna’s mRNA-1273 vaccine-induced enrichment of spike-specific B cells.

The viral spike protein mediates the initial stage of the SARS-CoV-2 infection process and is the primary target of antibodies following natural infection or vaccination.

Ilhem Messaoudi and colleagues say that vaccination also activated CD4 T cells and induced robust antigen-specific polyfunctional CD4 T cell responses.

Furthermore, clonally expanded CD8 T cells were observed in all vaccine recipients.

A pre-print version of the research paper is available on the bioRxiv* server, while the article undergoes peer review.

Vaccination and infection provide two different pathways to immunity

Since the COVID-19 outbreak first began in December 2019 in Wuhan, China, intense global efforts to rapidly develop effective vaccines against the causative agent SARS-CoV-2 have led to the emergency use authorization of several vaccines.

These include the messenger RNA- (mRNA) based vaccines developed by Pfizer (BNT162b2) and Moderna (mRNA-1273). Findings from clinical trials indicated that a 95% maximal protection is achieved within 1 to 2 months following the second dose of either vaccine, including protection against several circulating SARS-CoV-2 variants of concern.

However, the mechanisms by which these vaccines elicit long-lasting cellular immune responses to the virus remain poorly understood.

Natural infection and vaccination provide two different pathways to immunity, which studies have previously shown to be characterized by distinct T and B cell responses.

“Additional studies that integrate functional, transcriptional, and repertoire analysis of the memory immune cell response to COVID-19 mRNA vaccination are needed,” writes Messaoudi and colleagues.

What did the researchers do?

The team used single-cell RNA sequencing and functional assays to assess humoral (antibody) and cellular responses to two doses of either the Pfizer-BioNTech or Moderna mRNA vaccine (14 days following a second dose) in four individuals. The results were compared with the immune responses observed in three convalescent individuals who had experienced asymptomatic or mild infection.

What did the study find?

Both infection and vaccination induced anti-SARS-CoV-2 binding and neutralizing antibodies.

These antibodies were detected as early as two weeks following a first vaccine dose, with levels increasing several-fold after a second dose.

While neutralizing antibody titers following the first vaccine dose were comparable to those among convalescent individuals, significantly higher levels were observed in the vaccinees following the booster dose.

However, several important B cell adaptations were shared between vaccinees and convalescent individuals.

Analysis by flow cytometry revealed a reduction in the level of naïve B cells, but an expansion of memory B cells in both groups.

Additionally, single-cell RNA sequencing showed a reduction in IgA+ memory B cells following vaccination, a finding that has recently been described for convalescent individuals.

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