4.7 Article

Antibody-Dependent Natural Killer Cell Activation After Ebola Vaccination

期刊

JOURNAL OF INFECTIOUS DISEASES
卷 223, 期 7, 页码 1171-1182

出版社

OXFORD UNIV PRESS INC
DOI: 10.1093/infdis/jiz657

关键词

antibody; Ebola; vaccine; natural killer cell

资金

  1. MRC [G1000808] Funding Source: UKRI

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This study highlights the importance of antibody concentration and NK cell differentiation status in promoting Fc-mediated NK cell activation after Ebola virus vaccination, suggesting a potential role for antibody-mediated NK cell activation in vaccine-induced immune responses.
Background. Antibody Fc-mediated functions, such as antibody-dependent cellular cytotoxicity, contribute to vaccine-induced protection against viral infections. Fc-mediated function of anti-Ebola glycoprotein (GP) antibodies suggest that Fc-dependent activation of effector cells, including natural killer (NK) cells, could play a role in vaccination against Ebola virus disease. Methods. We analyzed the effect on primary human NK cell activation of anti-Ebola GP antibody in the serum of United Kingdom-based volunteers vaccinated with the novel 2-dose heterologous adenovirus type 26.ZEBOV, modified vaccinia AnkaraBN-Filo vaccine regimen. Results. We demonstrate primary human NK cell CD107a and interferon. expression, combined with down-regulation of CD16, in response to recombinant Ebola virus GP and post-vaccine dose 1 and dose 2 serum samples. These responses varied significantly with vaccine regimen, and NK cell activation was found to correlate with anti-GP antibody concentration. We also reveal an impact of NK cell differentiation phenotype on antibody-dependent NK cell activation, with highly differentiated CD56(dim)CD57(+) NK cells being the most responsive. Conclusions. These findings highlight the dual importance of vaccine-induced antibody concentration and NK cell differentiation status in promoting Fc-mediated activation of NK cells after vaccination, raising a potential role for antibody-mediated NK cell activation in vaccine-induced immune responses.

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