Immunogenicity and reactogenicity of heterologous ChAdOx1 nCoV-19/mRNA vaccination.
Immunogenicity and reactogenicity of heterologous ChAdOx1 nCoV-19/mRNA vaccination.
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DOI:
10.1038/s41591-021-01464-w
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发表时间:
2021-09
期刊:
影响因子:
82.9
通讯作者:
Sester M
中科院分区:
文献类型:
--
作者:
Schmidt T;Klemis V;Schub D;Mihm J;Hielscher F;Marx S;Abu-Omar A;Ziegler L;Guckelmus C;Urschel R;Schneitler S;Becker SL;Gärtner BC;Sester U;Sester M
Heterologous priming with the ChAdOx1 nCoV-19 vector vaccine followed by boosting with a messenger RNA vaccine (BNT162b2 or mRNA-1273) is currently recommended in Germany, although data on immunogenicity and reactogenicity are not available. In this observational study we show that, in healthy adult individuals (n = 96), the heterologous vaccine regimen induced spike-specific IgG, neutralizing antibodies and spike-specific CD4 T cells, the levels of which which were significantly higher than after homologous vector vaccine boost (n = 55) and higher or comparable in magnitude to homologous mRNA vaccine regimens (n = 62). Moreover, spike-specific CD8 T cell levels after heterologous vaccination were significantly higher than after both homologous regimens. Spike-specific T cells were predominantly polyfunctional with largely overlapping cytokine-producing phenotypes in all three regimens. Recipients of both the homologous vector regimen and the heterologous vector/mRNA combination reported greater reactogenicity following the priming vector vaccination, whereas heterologous boosting was well tolerated and comparable to homologous mRNA boosting. Taken together, heterologous vector/mRNA boosting induces strong humoral and cellular immune responses with acceptable reactogenicity profiles. In healthy adults, booster vaccination with an mRNA vaccine, irrespective of the vaccine used for the first dose, was well tolerated and elicited higher levels of spike-specific antibodies and spike-specific T cells than booster vaccination with ChAdOx1 nCov-19.
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DOI:
10.1016/s0140-6736(20)32661-1
发表时间:
2021-01-09
期刊:
Lancet (London, England)
影响因子:
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作者:
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10.1056/nejmoa2034577
发表时间:
2020-12-31
期刊:
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影响因子:
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通讯作者:
C4591001 Clinical Trial Group
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10.1056/nejmoa2104840
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2021-06-03
期刊:
The New England journal of medicine
影响因子:
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通讯作者:
Eichinger S
影响因子:
56.3
作者:
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通讯作者:
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2021-07-10
期刊:
Lancet (London, England)
影响因子:
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作者:
Borobia AM;Carcas AJ;Pérez-Olmeda M;Castaño L;Bertran MJ;García-Pérez J;Campins M;Portolés A;González-Pérez M;García Morales MT;Arana-Arri E;Aldea M;Díez-Fuertes F;Fuentes I;Ascaso A;Lora D;Imaz-Ayo N;Barón-Mira LE;Agustí A;Pérez-Ingidua C;Gómez de la Cámara A;Arribas JR;Ochando J;Alcamí J;Belda-Iniesta C;Frías J;CombiVacS Study Group
通讯作者:
CombiVacS Study Group