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Cell Rep DOI:10.1016/j.celrep.2021.110028

Single-cell transcriptomic profiles reveal changes associated with BCG-induced trained immunity and protective effects in circulating monocytes.

Publication TypeJournal Article
Year of Publication2021
AuthorsKong, L, Moorlag, SJCFM, Lefkovith, A, Li, B, Matzaraki, V, van Emst, L, Kang, HA, Latorre, I, Jaeger, M, Joosten, LAB, Netea, MG, Xavier, RJ
JournalCell Rep
Volume37
Issue7
Pages110028
Date Published2021 Nov 16
ISSN2211-1247
Abstract

Bacillus Calmette-Guérin (BCG) vaccine is one of the most widely used vaccines worldwide. In addition to protection against tuberculosis, BCG confers a degree of non-specific protection against other infections by enhancing secondary immune responses to heterologous pathogens, termed "trained immunity." To better understand BCG-induced immune reprogramming, we perform single-cell transcriptomic measurements before and after BCG vaccination using secondary immune stimulation with bacterial lipopolysaccharide (LPS). We find that BCG reduces systemic inflammation and identify 75 genes with altered LPS responses, including inflammatory mediators such as CCL3 and CCL4 that have a heightened response. Co-expression analysis reveals that gene modules containing these cytokines lose coordination after BCG. Other modules exhibit increased coordination, including several humanin nuclear isoforms that we confirm induce trained immunity in vitro. Our results link in vivo BCG administration to single-cell transcriptomic changes, validated in human genetics experiments, and highlight genes that are putatively responsible for non-specific protective effects of BCG.

DOI10.1016/j.celrep.2021.110028
Pubmed

https://www.ncbi.nlm.nih.gov/pubmed/34788625?dopt=Abstract

Alternate JournalCell Rep
PubMed ID34788625