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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...

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Autores principales: 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.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Society for Microbiology 2016
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.
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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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