| Literature DB >> 28115506 |
Amy Ellis1, Alexis Balgeman1, Mark Rodgers2, Cassaundra Updike2, Jaime Tomko2, Pauline Maiello2, Charles A Scanga2, Shelby L O'Connor3,4.
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.Entities:
Keywords: CFP-10; ESAT-6; Mauritian cynomolgus macaque; T cells; T-cell immunity; adaptive immunity; epitope; macaque; major histocompatibility complex; tuberculosis
Mesh:
Substances:
Year: 2017 PMID: 28115506 PMCID: PMC5364300 DOI: 10.1128/IAI.01009-16
Source DB: PubMed Journal: Infect Immun ISSN: 0019-9567 Impact factor: 3.441