Comparative single-cell transcriptomic profile of hybrid immunity induced by adenovirus vector-based COVID-19 vaccines

In this study, antibody response and a single-cell RNA-seq analysis were conducted on peripheral blood mononuclear cells from five different groups: naïve subjects vaccinated with AZD1222 (AZ) or Ad5-nCoV (Cso), individuals previously infected and later vaccinated (hybrid) with AZD1222 (AZ-hb) or Ad...

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Veröffentlicht in:Genes and immunity 2024-04, Vol.25 (2), p.158-167
Hauptverfasser: García-Vega, Melissa, Wan, Hui, Reséndiz-Sandoval, Mónica, Hinojosa-Trujillo, Diana, Valenzuela, Olivia, Mata-Haro, Verónica, Dehesa-Canseco, Freddy, Solís-Hernández, Mario, Marcotte, Harold, Pan-Hammarström, Qiang, Hernández, Jesús
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Sprache:eng
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Zusammenfassung:In this study, antibody response and a single-cell RNA-seq analysis were conducted on peripheral blood mononuclear cells from five different groups: naïve subjects vaccinated with AZD1222 (AZ) or Ad5-nCoV (Cso), individuals previously infected and later vaccinated (hybrid) with AZD1222 (AZ-hb) or Ad5-nCoV (Cso-hb), and those who were infected and had recovered from COVID-19 (Inf). The results showed that AZ induced more robust neutralizing antibody responses than Cso. The single-cell RNA data revealed a high frequency of memory B cells in the Cso and Cso-hb. In contrast, AZ and AZ-hb groups exhibited the highest proportion of activated naïve B cells expressing CXCR4 . Transcriptomic analysis of CD4 + and CD8 + T cells demonstrated a heterogeneous response following vaccination, hybrid immunity, or natural infection. However, a single dose of Ad5-nCoV was sufficient to strongly activate CD4 + T cells (naïve and memory) expressing ANX1 and FOS , similar to the hybrid response observed with AZ. An interesting finding was the robust activation of a subset of CD8 + T cells expressing GZMB , GZMH , and IFNG genes in the Cso-hb group. Our findings suggest that both vaccines effectively stimulated the cellular immune response; however, the Ad5-nCoV induced a more robust CD8 + T-cell response in previously infected individuals.
ISSN:1476-5470
1466-4879
1476-5470
DOI:10.1038/s41435-024-00270-x