Characterization of T Cells Specific for CFP-10 and ESAT-6 in Mycobacterium tuberculosis-Infected Mauritian Cynomolgus Macaques

Author:

Ellis Amy1,Balgeman Alexis1,Rodgers Mark2,Updike Cassaundra2,Tomko Jaime2,Maiello Pauline2,Scanga Charles A.2,O'Connor Shelby L.13

Affiliation:

1. Department of Pathology and Laboratory Medicine, University of Wisconsin—Madison, Madison, Wisconsin, USA

2. Department of Microbiology and Molecular Genetics, University of Pittsburgh, Pittsburgh, Pennsylvania, USA

3. Wisconsin National Primate Research Center, University of Wisconsin—Madison, Madison, Wisconsin, USA

Abstract

ABSTRACT Nonhuman primates can be used to study host immune responses to Mycobacterium tuberculosis . Mauritian cynomolgus macaques (MCMs) are a unique group of animals that have limited major histocompatibility complex (MHC) genetic diversity, such that MHC-identical animals can be infected with M. tuberculosis . Two MCMs homozygous for the relatively common M1 MHC haplotype were bronchoscopically infected with 41 CFU of the M. tuberculosis Erdman strain. Four other MCMs, which had at least one copy of the M1 MHC haplotype, were infected with a lower dose of 3 CFU M. tuberculosis . All animals mounted similar T-cell responses to CFP-10 and ESAT-6. Two epitopes in CFP-10 were characterized, and the MHC class II alleles restricting them were determined. A third epitope in CFP-10 was identified but exhibited promiscuous restriction. The CFP-10 and ESAT-6 antigenic regions targeted by T cells in MCMs were comparable to those seen in cases of human M. tuberculosis infection. Our data lay the foundation for generating tetrameric molecules to study epitope-specific CD4 T cells in M. tuberculosis -infected MCMs, which may guide future testing of tuberculosis vaccines in nonhuman primates.

Funder

HHS | NIH | NIH Office of the Director

Publisher

American Society for Microbiology

Subject

Infectious Diseases,Immunology,Microbiology,Parasitology

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