| Literature DB >> 30794328 |
Jean-Louis Palgen1,2, Nicolas Tchitchek1,2, Nicolas Huot2,3, Jamila Elhmouzi-Younes1,2, Cécile Lefebvre2,4, Pierre Rosenbaum1,2, Nathalie Dereuddre-Bosquet1,2, Frédéric Martinon1,2, Hakim Hocini2,4, Antonio Cosma1,2, Michaela Müller-Trutwin2,3, Yves Lévy2,4, Roger Le Grand1,2, Anne-Sophie Beignon1,2.
Abstract
A better understanding of innate responses induced by vaccination is critical for designing optimal vaccines. Here, we studied the diversity and dynamics of the NK cell compartment after prime-boost immunization with the modified vaccinia virus Ankara using cynomolgus macaques as a model. Mass cytometry was used to deeply characterize blood NK cells. The NK cell subphenotype composition was modified by the prime. Certain phenotypic changes induced by the prime were maintained over time and, as a result, the NK cell composition prior to boost differed from that before prime. The key phenotypic signature that distinguished NK cells responding to the boost from those responding to the prime included stronger expression of several cytotoxic, homing, and adhesion molecules, suggesting that NK cells at recall were functionally distinct. Our data reveal potential priming or imprinting of NK cells after the first vaccine injection. This study provides novel insights into prime-boost vaccination protocols that could be used to optimize future vaccines. ©2019 Society for Leukocyte Biology.Entities:
Keywords: MVA; NHP; NK cells; innate lymphoid immunity; mass cytometry; prime-boost; transcriptomics; vaccination
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Year: 2019 PMID: 30794328 DOI: 10.1002/JLB.4A1018-391RR
Source DB: PubMed Journal: J Leukoc Biol ISSN: 0741-5400 Impact factor: 4.962