TY - JOUR
T1 - Pan-vaccine analysis reveals innate immune endotypes predictive of antibody responses to vaccination
AU - The Human Immunology Project Consortium (HIPC)
AU - Fourati, Slim
AU - Tomalin, Lewis E.
AU - Mulè, Matthew P.
AU - Chawla, Daniel G.
AU - Gerritsen, Bram
AU - Rychkov, Dmitry
AU - Henrich, Evan
AU - Miller, Helen E.R.
AU - Hagan, Thomas
AU - Diray-Arce, Joann
AU - Dunn, Patrick
AU - Deckhut-Augustine, Alison
AU - Haddad, Elias K.
AU - Hafler, David A.
AU - Harris, Eva
AU - Farber, Donna
AU - McElrath, Julie
AU - Montgomery, Ruth R.
AU - Peters, Bjoern
AU - Rahman, Adeeb
AU - Reed, Elaine F.
AU - Rouphael, Nadine
AU - Fernandez-Sesma, Ana
AU - Sette, Alessandro
AU - Stuart, Kenneth D.
AU - Togias, Alkis
AU - Levy, Ofer
AU - Gottardo, Raphael
AU - Sarwal, Minnie M.
AU - Tsang, John S.
AU - Suárez-Fariñas, Mayte
AU - Pulendran, Bali
AU - Kleinstein, Steven H.
AU - Sékaly, Rafick Pierre
N1 - Publisher Copyright:
© 2022, The Author(s).
PY - 2022/12
Y1 - 2022/12
N2 - Several studies have shown that the pre-vaccination immune state is associated with the antibody response to vaccination. However, the generalizability and mechanisms that underlie this association remain poorly defined. Here, we sought to identify a common pre-vaccination signature and mechanisms that could predict the immune response across 13 different vaccines. Analysis of blood transcriptional profiles across studies revealed three distinct pre-vaccination endotypes, characterized by the differential expression of genes associated with a pro-inflammatory response, cell proliferation, and metabolism alterations. Importantly, individuals whose pre-vaccination endotype was enriched in pro-inflammatory response genes known to be downstream of nuclear factor-kappa B showed significantly higher serum antibody responses 1 month after vaccination. This pro-inflammatory pre-vaccination endotype showed gene expression characteristic of the innate activation state triggered by Toll-like receptor ligands or adjuvants. These results demonstrate that wide variations in the transcriptional state of the immune system in humans can be a key determinant of responsiveness to vaccination.
AB - Several studies have shown that the pre-vaccination immune state is associated with the antibody response to vaccination. However, the generalizability and mechanisms that underlie this association remain poorly defined. Here, we sought to identify a common pre-vaccination signature and mechanisms that could predict the immune response across 13 different vaccines. Analysis of blood transcriptional profiles across studies revealed three distinct pre-vaccination endotypes, characterized by the differential expression of genes associated with a pro-inflammatory response, cell proliferation, and metabolism alterations. Importantly, individuals whose pre-vaccination endotype was enriched in pro-inflammatory response genes known to be downstream of nuclear factor-kappa B showed significantly higher serum antibody responses 1 month after vaccination. This pro-inflammatory pre-vaccination endotype showed gene expression characteristic of the innate activation state triggered by Toll-like receptor ligands or adjuvants. These results demonstrate that wide variations in the transcriptional state of the immune system in humans can be a key determinant of responsiveness to vaccination.
UR - http://www.scopus.com/inward/record.url?scp=85141085346&partnerID=8YFLogxK
U2 - 10.1038/s41590-022-01329-5
DO - 10.1038/s41590-022-01329-5
M3 - Article
C2 - 36316476
AN - SCOPUS:85141085346
SN - 1529-2908
VL - 23
SP - 1777
EP - 1787
JO - Nature Immunology
JF - Nature Immunology
IS - 12
ER -