TY - JOUR
T1 - NK cell immune responses differ after prime and boost vaccination
AU - Palgen, Jean Louis
AU - Tchitchek, Nicolas
AU - Huot, Nicolas
AU - Elhmouzi-Younes, Jamila
AU - Lefebvre, Cécile
AU - Rosenbaum, Pierre
AU - Dereuddre-Bosquet, Nathalie
AU - Martinon, Frédéric
AU - Hocini, Hakim
AU - Cosma, Antonio
AU - Müller-Trutwin, Michaela
AU - Lévy, Yves
AU - Le Grand, Roger
AU - Beignon, Anne Sophie
N1 - Publisher Copyright:
©2019 Society for Leukocyte Biology
PY - 2019/5
Y1 - 2019/5
N2 - 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.
AB - 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.
KW - MVA
KW - NHP
KW - NK cells
KW - innate lymphoid immunity
KW - mass cytometry
KW - prime-boost
KW - transcriptomics
KW - vaccination
UR - http://www.scopus.com/inward/record.url?scp=85061963770&partnerID=8YFLogxK
U2 - 10.1002/JLB.4A1018-391RR
DO - 10.1002/JLB.4A1018-391RR
M3 - Article
C2 - 30794328
AN - SCOPUS:85061963770
SN - 0741-5400
VL - 105
SP - 1055
EP - 1073
JO - Journal of Leukocyte Biology
JF - Journal of Leukocyte Biology
IS - 5
ER -