Nature Medicine, volume 25, issue 6, pages 977-987
IFN-γ-independent immune markers of Mycobacterium tuberculosis exposure
Lenette L. Lu
1, 2
,
Malisa T. Smith
3
,
Krystle K Q Yu
3
,
Corinne Luedemann
2
,
Todd J Suscovich
2
,
Patricia S. Grace
2
,
Adam Cain
2
,
Wen-Han Yu
2, 4
,
Tanya R Mckitrick
5
,
Douglas Lauffenburger
4
,
Richard D Cummings
5
,
Harriet Mayanja-Kizza
6
,
Thomas R. Hawn
3
,
W. Henry Boom
7
,
Catherine M. Stein
7, 8
,
Sarah A Fortune
1, 2
,
Chetan Seshadri
3
,
Galit Alter
2
5
Publication type: Journal Article
Publication date: 2019-05-20
Journal:
Nature Medicine
scimago Q1
SJR: 19.045
CiteScore: 100.9
Impact factor: 58.7
ISSN: 10788956, 1546170X, 17447933
General Biochemistry, Genetics and Molecular Biology
General Medicine
Abstract
Exposure to Mycobacterium tuberculosis (Mtb) results in heterogeneous clinical outcomes including primary progressive tuberculosis and latent Mtb infection (LTBI). Mtb infection is identified using the tuberculin skin test and interferon-γ (IFN-γ) release assay IGRA, and a positive result may prompt chemoprophylaxis to prevent progression to tuberculosis. In the present study, we report on a cohort of Ugandan individuals who were household contacts of patients with TB. These individuals were highly exposed to Mtb but tested negative by IFN-γ release assay and tuberculin skin test, ‘resisting’ development of classic LTBI. We show that ‘resisters’ possess IgM, class-switched IgG antibody responses and non-IFN-γ T cell responses to the Mtb-specific proteins ESAT6 and CFP10, immunologic evidence of exposure to Mtb. Compared to subjects with classic LTBI, ‘resisters’ display enhanced antibody avidity and distinct Mtb-specific IgG Fc profiles. These data reveal a distinctive adaptive immune profile among Mtb-exposed subjects, supporting an expanded definition of the host response to Mtb exposure, with implications for public health and the design of clinical trials. New immune biomarkers of exposure to tuberculosis may require a rethink of evidence of Mycobacterium tuberculosis infection and control.
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