Comparative immunogenicity and reactogenicity of heterologous ChAdOx1-nCoV-19-priming and BNT162b2 or mRNA-1273-boosting with homologous COVID-19 vaccine regimens

被引:37
作者
Klemis, Verena [1 ]
Schmidt, Tina [1 ]
Schub, David [1 ]
Mihm, Janine [2 ,5 ]
Marx, Stefanie [1 ]
Abu-Omar, Amina [1 ]
Ziegler, Laura [1 ]
Hielscher, Franziska [1 ]
Guckelmus, Candida [1 ]
Urschel, Rebecca [1 ]
Wagenpfeil, Stefan [3 ]
Schneitler, Sophie [4 ]
Becker, Soeren L. [4 ]
Gaertner, Barbara C. [4 ]
Sester, Urban [2 ,5 ]
Sester, Martina [1 ]
机构
[1] Saarland Univ, Dept Transplant & Infect Immunol, Homburg, Germany
[2] Saarland Univ, Dept Internal Med 4, Homburg, Germany
[3] Saarland Univ, Inst Med Stat Epidemiol & Med Informat, Campus Homburg Saar, Homburg, Germany
[4] Saarland Univ, Inst Med Microbiol & Hyg, D-66421 Homburg, Germany
[5] SHG Kliniken, Volklingen, Germany
关键词
CHADOX1; NCOV-19; MESSENGER-RNA; PHASE-2; SAFETY;
D O I
10.1038/s41467-022-32321-0
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Comparative analyses of the immunogenicity and reactogenicity of homologous and heterologous SARS-CoV-2 vaccine-regimens will inform optimized vaccine strategies. Here we analyze the humoral and cellular immune response following heterologous and homologous vaccination strategies in a convenience cohort of 331 healthy individuals. All regimens induce immunity to the vaccine antigen. Immunity after vaccination with ChAdOx1-nCoV-19 followed by either BNT162b2 (n = 66) or mRNA-1273 (n = 101) is equivalent to or more pronounced than homologous mRNA-regimens (n = 43 BNT162b2, n = 59 mRNA-1273) or homologous ChAdOx1-nCoV-19 vaccination (n = 62). We note highest levels of spike-specific CD8 T-cells following both heterologous regimens. Among mRNA-containing combinations, spike-specific CD4 T-cell levels in regimens including mRNA-1273 are higher than respective combinations with BNT162b2. Polyfunctional T-cell levels are highest in regimens based on ChAdOx1-nCoV-19-priming. All five regimens are well tolerated with most pronounced reactogenicity upon ChAdOx1-nCoV-19-priming, and ChAdOx1-nCoV-19/mRNA-1273-boosting. In conclusion, we present comparative analyses of immunogenicity and reactogenicity for heterologous vector/mRNA-boosting and homologous mRNA-regimens.
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页数:11
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