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A Subset of Protective γ(9)δ(2) T Cells Is Activated by Novel Mycobacterial Glycolipid Components
γ(9)δ(2) T cells provide a natural bridge between innate and adaptive immunity, rapidly and potently respond to pathogen infection in mucosal tissues, and are prominently induced by both tuberculosis (TB) infection and bacillus Calmette Guérin (BCG) vaccination. Mycobacterium-expanded γ(9)δ(2) T cel...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Society for Microbiology
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4995917/ https://www.ncbi.nlm.nih.gov/pubmed/27297390 http://dx.doi.org/10.1128/IAI.01322-15 |
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author | Xia, Mei Hesser, Danny C. De, Prithwiraj Sakala, Isaac G. Spencer, Charles T. Kirkwood, Jay S. Abate, Getahun Chatterjee, Delphi Dobos, Karen M. Hoft, Daniel F. |
author_facet | Xia, Mei Hesser, Danny C. De, Prithwiraj Sakala, Isaac G. Spencer, Charles T. Kirkwood, Jay S. Abate, Getahun Chatterjee, Delphi Dobos, Karen M. Hoft, Daniel F. |
author_sort | Xia, Mei |
collection | PubMed |
description | γ(9)δ(2) T cells provide a natural bridge between innate and adaptive immunity, rapidly and potently respond to pathogen infection in mucosal tissues, and are prominently induced by both tuberculosis (TB) infection and bacillus Calmette Guérin (BCG) vaccination. Mycobacterium-expanded γ(9)δ(2) T cells represent only a subset of the phosphoantigen {isopentenyl pyrophosphate [IPP] and (E)-4-hydroxy-3-methyl-but-2-enylpyrophosphate [HMBPP]}-responsive γ(9)δ(2) T cells, expressing an oligoclonal set of T cell receptor (TCR) sequences which more efficiently recognize and inhibit intracellular Mycobacterium tuberculosis infection. Based on this premise, we have been searching for M. tuberculosis antigens specifically capable of inducing a unique subset of mycobacterium-protective γ(9)δ(2) T cells. Our screening strategy includes the identification of M. tuberculosis fractions that expand γ(9)δ(2) T cells with biological functions capable of inhibiting intracellular mycobacterial replication. Chemical treatments of M. tuberculosis whole-cell lysates (MtbWL) ruled out protein, nucleic acid, and nonpolar lipids as the M. tuberculosis antigens inducing protective γ(9)δ(2) T cells. Mild acid hydrolysis, which transforms complex carbohydrate to monomeric residues, abrogated the specific activity of M. tuberculosis whole-cell lysates, suggesting that a polysaccharide was required for biological activity. Extraction of MtbWL with chloroform-methanol-water (10:10:3) resulted in a polar lipid fraction with highly enriched specific activity; this activity was further enriched by silica gel chromatography. A combination of mass spectrometry and nuclear magnetic resonance analysis of bioactive fractions indicated that 6-O-methylglucose-containing lipopolysaccharides (mGLP) are predominant components present in this active fraction. These results have important implications for the development of new immunotherapeutic approaches for prevention and treatment of TB. |
format | Online Article Text |
id | pubmed-4995917 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | American Society for Microbiology |
record_format | MEDLINE/PubMed |
spelling | pubmed-49959172016-09-06 A Subset of Protective γ(9)δ(2) T Cells Is Activated by Novel Mycobacterial Glycolipid Components Xia, Mei Hesser, Danny C. De, Prithwiraj Sakala, Isaac G. Spencer, Charles T. Kirkwood, Jay S. Abate, Getahun Chatterjee, Delphi Dobos, Karen M. Hoft, Daniel F. Infect Immun Microbial Immunity and Vaccines γ(9)δ(2) T cells provide a natural bridge between innate and adaptive immunity, rapidly and potently respond to pathogen infection in mucosal tissues, and are prominently induced by both tuberculosis (TB) infection and bacillus Calmette Guérin (BCG) vaccination. Mycobacterium-expanded γ(9)δ(2) T cells represent only a subset of the phosphoantigen {isopentenyl pyrophosphate [IPP] and (E)-4-hydroxy-3-methyl-but-2-enylpyrophosphate [HMBPP]}-responsive γ(9)δ(2) T cells, expressing an oligoclonal set of T cell receptor (TCR) sequences which more efficiently recognize and inhibit intracellular Mycobacterium tuberculosis infection. Based on this premise, we have been searching for M. tuberculosis antigens specifically capable of inducing a unique subset of mycobacterium-protective γ(9)δ(2) T cells. Our screening strategy includes the identification of M. tuberculosis fractions that expand γ(9)δ(2) T cells with biological functions capable of inhibiting intracellular mycobacterial replication. Chemical treatments of M. tuberculosis whole-cell lysates (MtbWL) ruled out protein, nucleic acid, and nonpolar lipids as the M. tuberculosis antigens inducing protective γ(9)δ(2) T cells. Mild acid hydrolysis, which transforms complex carbohydrate to monomeric residues, abrogated the specific activity of M. tuberculosis whole-cell lysates, suggesting that a polysaccharide was required for biological activity. Extraction of MtbWL with chloroform-methanol-water (10:10:3) resulted in a polar lipid fraction with highly enriched specific activity; this activity was further enriched by silica gel chromatography. A combination of mass spectrometry and nuclear magnetic resonance analysis of bioactive fractions indicated that 6-O-methylglucose-containing lipopolysaccharides (mGLP) are predominant components present in this active fraction. These results have important implications for the development of new immunotherapeutic approaches for prevention and treatment of TB. American Society for Microbiology 2016-08-19 /pmc/articles/PMC4995917/ /pubmed/27297390 http://dx.doi.org/10.1128/IAI.01322-15 Text en Copyright © 2016 Xia et al. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution 4.0 International license (http://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Microbial Immunity and Vaccines Xia, Mei Hesser, Danny C. De, Prithwiraj Sakala, Isaac G. Spencer, Charles T. Kirkwood, Jay S. Abate, Getahun Chatterjee, Delphi Dobos, Karen M. Hoft, Daniel F. A Subset of Protective γ(9)δ(2) T Cells Is Activated by Novel Mycobacterial Glycolipid Components |
title | A Subset of Protective γ(9)δ(2) T Cells Is Activated by Novel Mycobacterial Glycolipid Components |
title_full | A Subset of Protective γ(9)δ(2) T Cells Is Activated by Novel Mycobacterial Glycolipid Components |
title_fullStr | A Subset of Protective γ(9)δ(2) T Cells Is Activated by Novel Mycobacterial Glycolipid Components |
title_full_unstemmed | A Subset of Protective γ(9)δ(2) T Cells Is Activated by Novel Mycobacterial Glycolipid Components |
title_short | A Subset of Protective γ(9)δ(2) T Cells Is Activated by Novel Mycobacterial Glycolipid Components |
title_sort | subset of protective γ(9)δ(2) t cells is activated by novel mycobacterial glycolipid components |
topic | Microbial Immunity and Vaccines |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4995917/ https://www.ncbi.nlm.nih.gov/pubmed/27297390 http://dx.doi.org/10.1128/IAI.01322-15 |
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