Literature DB >> 28115506

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

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.
Copyright © 2017 American Society for Microbiology.

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


  44 in total

Review 1.  Immunology of tuberculosis.

Authors:  J L Flynn; J Chan
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Authors:  Helen McShane; Ansar A Pathan; Clare R Sander; Nilu P Goonetilleke; Helen A Fletcher; Adrian V S Hill
Journal:  Tuberculosis (Edinb)       Date:  2005-01-21       Impact factor: 3.131

3.  Comprehensive characterization of MHC class II haplotypes in Mauritian cynomolgus macaques.

Authors:  Shelby L O'Connor; Alex J Blasky; Chad J Pendley; Ericka A Becker; Roger W Wiseman; Julie A Karl; Austin L Hughes; David H O'Connor
Journal:  Immunogenetics       Date:  2007-03-24       Impact factor: 2.846

Review 4.  The protective immune response to Mycobacterium tuberculosis.

Authors:  A M Cooper; J L Flynn
Journal:  Curr Opin Immunol       Date:  1995-08       Impact factor: 7.486

5.  Modified vaccinia Ankara-expressing Ag85A, a novel tuberculosis vaccine, is safe in adolescents and children, and induces polyfunctional CD4+ T cells.

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Journal:  Eur J Immunol       Date:  2010-01       Impact factor: 5.532

Review 6.  Non-human primates: a model for tuberculosis research.

Authors:  J L Flynn; S V Capuano; D Croix; S Pawar; A Myers; A Zinovik; E Klein
Journal:  Tuberculosis (Edinb)       Date:  2003       Impact factor: 3.131

Review 7.  The innate immune response in human tuberculosis.

Authors:  Thomas R Lerner; Sophie Borel; Maximiliano G Gutierrez
Journal:  Cell Microbiol       Date:  2015-07-28       Impact factor: 3.715

8.  Intranasal mucosal boosting with an adenovirus-vectored vaccine markedly enhances the protection of BCG-primed guinea pigs against pulmonary tuberculosis.

Authors:  Zhou Xing; Christine T McFarland; Jean-Michel Sallenave; Angelo Izzo; Jun Wang; David N McMurray
Journal:  PLoS One       Date:  2009-06-10       Impact factor: 3.240

9.  Immunodominant tuberculosis CD8 antigens preferentially restricted by HLA-B.

Authors:  Deborah A Lewinsohn; Ervina Winata; Gwendolyn M Swarbrick; Katie E Tanner; Matthew S Cook; Megan D Null; Meghan E Cansler; Alessandro Sette; John Sidney; David M Lewinsohn
Journal:  PLoS Pathog       Date:  2007-09-21       Impact factor: 6.823

10.  Acute-phase CD8 T cell responses that select for escape variants are needed to control live attenuated simian immunodeficiency virus.

Authors:  Max Harris; Charles M Burns; Ericka A Becker; Andrew T Braasch; Emma Gostick; Randall C Johnson; Karl W Broman; David A Price; Thomas C Friedrich; Shelby L O'Connor
Journal:  J Virol       Date:  2013-06-19       Impact factor: 5.103

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  4 in total

1.  Acute-Phase CD4+ T Cell Responses Targeting Invariant Viral Regions Are Associated with Control of Live Attenuated Simian Immunodeficiency Virus.

Authors:  Matthew S Sutton; Amy Ellis-Connell; Ryan V Moriarty; Alexis J Balgeman; Dane Gellerup; Gabrielle Barry; Andrea M Weiler; Thomas C Friedrich; Shelby L O'Connor
Journal:  J Virol       Date:  2018-10-12       Impact factor: 5.103

2.  Preexisting Simian Immunodeficiency Virus Infection Increases Susceptibility to Tuberculosis in Mauritian Cynomolgus Macaques.

Authors:  Mark A Rodgers; Cassaundra Ameel; Amy L Ellis-Connell; Alexis J Balgeman; Pauline Maiello; Gabrielle L Barry; Thomas C Friedrich; Edwin Klein; Shelby L O'Connor; Charles A Scanga
Journal:  Infect Immun       Date:  2018-11-20       Impact factor: 3.441

3.  MAIT cells are functionally impaired in a Mauritian cynomolgus macaque model of SIV and Mtb co-infection.

Authors:  Amy L Ellis; Alexis J Balgeman; Erica C Larson; Mark A Rodgers; Cassaundra Ameel; Tonilynn Baranowski; Nadean Kannal; Pauline Maiello; Jennifer A Juno; Charles A Scanga; Shelby L O'Connor
Journal:  PLoS Pathog       Date:  2020-05-20       Impact factor: 6.823

Review 4.  Immunological Characterization of Proteins Expressed by Genes Located in Mycobacterium tuberculosis-Specific Genomic Regions Encoding the ESAT6-like Proteins.

Authors:  Abu Salim Mustafa
Journal:  Vaccines (Basel)       Date:  2021-01-07
  4 in total

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