Pan-vaccine analysis reveals innate immune endotypes predictive of antibody responses to vaccination

Slim Fourati(Emory University), Lewis E. Tomalin(Icahn School of Medicine at Mount Sinai), Matthew P. Mulè(Bridge University), Daniel G. Chawla(Yale University), Bram Gerritsen(Yale University), Dmitry Rychkov(University of California, San Francisco), Evan Henrich(Fred Hutch Cancer Center), Helen E. R. Miller(Fred Hutch Cancer Center), Thomas Hagan(Stanford University), Joann Diray‐Arce(Boston Children's Hospital), Patrick Dunn, Alison Deckhut-Augustine, Elias K. Haddad(Drexel University), David A. Hafler(Yale University), Eva Harris(Berkeley Public Health Division), Donna L. Färber(Columbia University Irving Medical Center), Julie McElrath(Fred Hutch Cancer Center), Ruth R. Montgomery(Fred Hutch Cancer Center), Bjoern Peters(La Jolla Institute for Immunology), Adeeb Rahman(Icahn School of Medicine at Mount Sinai), Elaine F. Reed(University of California, Los Angeles), Nadine Rouphael(Emory University), Ana Fernández-Sesma(Icahn School of Medicine at Mount Sinai), Alessandro Sette(La Jolla Institute for Immunology), Kenneth Stuart, Alkis Togias, Ofer Levy(Boston Children's Hospital), Raphaël Gottardo(SIB Swiss Institute of Bioinformatics), Minnie Sarwal(University of California, San Francisco), John S. Tsang, Mayte Suárez‐Fariñas(Icahn School of Medicine at Mount Sinai), Bali Pulendran(Stanford University), Steven H. Kleinstein(Yale University), Rafick‐Pierre Sékaly(Emory University)
Nature Immunology
October 31, 2022
Cited by 137Open Access
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Abstract

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.


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