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Nat Med. 2019 Feb;25(2):255-262. doi: 10.1038/s41591-018-0319-9. Epub 2019 Jan 21.

Prevention of tuberculosis infection and disease by local BCG in repeatedly exposed rhesus macaques.

Author information

1
Biomedical Primate Research Centre, Rijswijk, the Netherlands. dijkman@bprc.nl.
2
Biomedical Primate Research Centre, Rijswijk, the Netherlands.
3
Department of Infectious Diseases, Leiden University Medical Centre, Leiden, the Netherlands.
4
Biomedical Primate Research Centre, Rijswijk, the Netherlands. verreck@bprc.nl.

Abstract

Tuberculosis (TB) remains the deadliest infectious disease1, and the widely used Bacillus Calmette-Guérin (BCG) vaccine fails to curb the epidemic. An improved vaccination strategy could provide a cost-effective intervention to break the transmission cycle and prevent antimicrobial resistance2,3. Limited knowledge of the host responses critically involved in protective immunity hampers the development of improved TB vaccination regimens. Therefore, assessment of new strategies in preclinical models to select the best candidate vaccines before clinical vaccine testing remains indispensable. We have previously established in rhesus macaques (Macaca mulatta) that pulmonary mucosal BCG delivery reduces TB disease where standard intradermal injection fails4,5. Here, we show that pulmonary BCG prevents infection by using a repeated limiting-dose Mycobacterium tuberculosis challenge model and identify polyfunctional T-helper type 17 (TH17) cells, interleukin-10 and immunoglobulin A as correlates of local protective immunity. These findings warrant further research into mucosal immunization strategies and their translation to clinical application to more effectively prevent the spread of TB.

PMID:
30664782
DOI:
10.1038/s41591-018-0319-9
[Indexed for MEDLINE]

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