Prior SARS‐CoV‐2 infection balances immune responses triggered by four EMA‐approved COVID‐19 vaccines: An observational study
Other authors have reported that in natural infection anti-Spike RBD IgA antibodies showed to be the major responsible of the neutralizing ability in early stages.2 Regarding the cellular response, CD4+ but not CD8+ T-cell activities against SARS-CoV-2 spike peptide pool (Supporting information Figu...
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Published in | Clinical and translational medicine Vol. 12; no. 5; pp. e869 - n/a |
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Main Authors | , , , , , , , , , , , , , , , , , , , , , , , |
Format | Journal Article |
Language | English |
Published |
United States
John Wiley & Sons, Inc
01.05.2022
John Wiley and Sons Inc Wiley |
Subjects | |
Online Access | Get full text |
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Summary: | Other authors have reported that in natural infection anti-Spike RBD IgA antibodies showed to be the major responsible of the neutralizing ability in early stages.2 Regarding the cellular response, CD4+ but not CD8+ T-cell activities against SARS-CoV-2 spike peptide pool (Supporting information Figure S2A) remained high at late-time points in naïve individuals immunized with the mRNA-type vaccines (Figures 2C and Supporting information Figure S2B). [...]when comparing humoral and cellular responses between naïve and COVID-19-recovered subjects, we found higher anti-spike RBD IgG and neutralizing antibodies levels in recovered individuals, but no differences in the cellular CD4+ T-cell response were found (Figure 4). Several studies performed in Spain confirm the impact of ratcheting up SARS-CoV-2 vaccination has had on declining COVID-19 hospitalizations and lethality rates, even though a lack of efficiency reducing the transmission rate was observed.3,4 Additionally, these high ranks of vaccination have supposed a reduction in the use of medical resources with a high social returns.5 Nevertheless, a comparison between the differential immune responses triggered by each vaccine is still lacking. |
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Bibliography: | Roberto Lozano‐Rodríguez and Verónica Terrón‐Arcos contributed equally to this work. SourceType-Scholarly Journals-1 ObjectType-Correspondence-1 content type line 14 content type line 23 ObjectType-Undefined-2 |
ISSN: | 2001-1326 2001-1326 |
DOI: | 10.1002/ctm2.869 |