AI Article Synopsis

  • - Various studies suggest pneumococcal vaccines may help protect against both symptomatic SARS-CoV-2 infections and related deaths, potentially due to cross-reactivity between vaccine proteins and SARS-CoV-2 antigens.
  • - While a comparison of the glycosylation structures showed no clear similarities, pneumococcal vaccines contain proteins that have significant similarities to SARS-CoV-2 proteins, which could explain their protective effect.
  • - New vaccines targeting highly antigenic proteins like PspA and PspC from pneumococcal vaccines are being tested in clinical trials to confirm their effectiveness against SARS-CoV-2.

Article Abstract

Various studies indicate that vaccination, especially with pneumococcal vaccines, protects against symptomatic cases of SARS-CoV-2 infection and death. This paper explores the possibility that pneumococcal vaccines in particular, but perhaps other vaccines as well, contain antigens that might be cross-reactive with SARS-CoV-2 antigens. Comparison of the glycosylation structures of SARS-CoV-2 with the polysaccharide structures of pneumococcal vaccines yielded no obvious similarities. However, while pneumococcal vaccines are primarily composed of capsular polysaccharides, some are conjugated to cross-reacting material CRM197, a modified diphtheria toxin, and all contain about three percent protein contaminants, including the pneumococcal surface proteins PsaA, PspA and probably PspC. All of these proteins have very high degrees of similarity, using very stringent criteria, with several SARS-CoV-2 proteins including the spike protein, membrane protein and replicase 1a. CRM197 is also present in (Hib) and meningitis vaccines. Equivalent similarities were found at lower rates, or were completely absent, among the proteins in diphtheria, tetanus, pertussis, measles, mumps, rubella, and poliovirus vaccines. Notably, PspA and PspC are highly antigenic and new pneumococcal vaccines based on them are currently in human clinical trials so that their effectiveness against SARS-CoV-2 disease is easily testable.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC7712751PMC
http://dx.doi.org/10.3390/vaccines8040559DOI Listing

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