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Serological Evidence of Immune Priming by Group A Streptococci in Patients with Acute Rheumatic Fever

Acute rheumatic fever (ARF) is an autoimmune response to Group A Streptococcus (GAS) infection. Repeated GAS exposures are proposed to ‘prime’ the immune system for autoimmunity. This notion of immune-priming by multiple GAS infections was first postulated in the 1960s, but direct experimental evide...

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Autores principales: Raynes, Jeremy M., Frost, Hannah R. C., Williamson, Deborah A., Young, Paul G., Baker, Edward N., Steemson, John D., Loh, Jacelyn M., Proft, Thomas, Dunbar, P. R., Atatoa Carr, Polly E., Bell, Anita, Moreland, Nicole J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4957554/
https://www.ncbi.nlm.nih.gov/pubmed/27499748
http://dx.doi.org/10.3389/fmicb.2016.01119
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author Raynes, Jeremy M.
Frost, Hannah R. C.
Williamson, Deborah A.
Young, Paul G.
Baker, Edward N.
Steemson, John D.
Loh, Jacelyn M.
Proft, Thomas
Dunbar, P. R.
Atatoa Carr, Polly E.
Bell, Anita
Moreland, Nicole J.
author_facet Raynes, Jeremy M.
Frost, Hannah R. C.
Williamson, Deborah A.
Young, Paul G.
Baker, Edward N.
Steemson, John D.
Loh, Jacelyn M.
Proft, Thomas
Dunbar, P. R.
Atatoa Carr, Polly E.
Bell, Anita
Moreland, Nicole J.
author_sort Raynes, Jeremy M.
collection PubMed
description Acute rheumatic fever (ARF) is an autoimmune response to Group A Streptococcus (GAS) infection. Repeated GAS exposures are proposed to ‘prime’ the immune system for autoimmunity. This notion of immune-priming by multiple GAS infections was first postulated in the 1960s, but direct experimental evidence to support the hypothesis has been lacking. Here, we present novel methodology, based on antibody responses to GAS T-antigens, that enables previous GAS exposures to be mapped in patient sera. T-antigens are surface expressed, type specific antigens and GAS strains fall into 18 major clades or T-types. A panel of recombinant T-antigens was generated and immunoassays were performed in parallel with serum depletion experiments allowing type-specific T-antigen antibodies to be distinguished from cross-reactive antibodies. At least two distinct GAS exposures were detected in each of the ARF sera tested. Furthermore, no two sera had the same T-antigen reactivity profile suggesting that each patient was exposed to a unique series of GAS T-types prior to developing ARF. The methods have provided much-needed experimental evidence to substantiate the immune-priming hypothesis, and will facilitate further serological profiling studies that explore the multifaceted interactions between GAS and the host.
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spelling pubmed-49575542016-08-05 Serological Evidence of Immune Priming by Group A Streptococci in Patients with Acute Rheumatic Fever Raynes, Jeremy M. Frost, Hannah R. C. Williamson, Deborah A. Young, Paul G. Baker, Edward N. Steemson, John D. Loh, Jacelyn M. Proft, Thomas Dunbar, P. R. Atatoa Carr, Polly E. Bell, Anita Moreland, Nicole J. Front Microbiol Microbiology Acute rheumatic fever (ARF) is an autoimmune response to Group A Streptococcus (GAS) infection. Repeated GAS exposures are proposed to ‘prime’ the immune system for autoimmunity. This notion of immune-priming by multiple GAS infections was first postulated in the 1960s, but direct experimental evidence to support the hypothesis has been lacking. Here, we present novel methodology, based on antibody responses to GAS T-antigens, that enables previous GAS exposures to be mapped in patient sera. T-antigens are surface expressed, type specific antigens and GAS strains fall into 18 major clades or T-types. A panel of recombinant T-antigens was generated and immunoassays were performed in parallel with serum depletion experiments allowing type-specific T-antigen antibodies to be distinguished from cross-reactive antibodies. At least two distinct GAS exposures were detected in each of the ARF sera tested. Furthermore, no two sera had the same T-antigen reactivity profile suggesting that each patient was exposed to a unique series of GAS T-types prior to developing ARF. The methods have provided much-needed experimental evidence to substantiate the immune-priming hypothesis, and will facilitate further serological profiling studies that explore the multifaceted interactions between GAS and the host. Frontiers Media S.A. 2016-07-22 /pmc/articles/PMC4957554/ /pubmed/27499748 http://dx.doi.org/10.3389/fmicb.2016.01119 Text en Copyright © 2016 Raynes, Frost, Williamson, Young, Baker, Steemson, Loh, Proft, Dunbar, Atatoa Carr, Bell and Moreland. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) or licensor are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Microbiology
Raynes, Jeremy M.
Frost, Hannah R. C.
Williamson, Deborah A.
Young, Paul G.
Baker, Edward N.
Steemson, John D.
Loh, Jacelyn M.
Proft, Thomas
Dunbar, P. R.
Atatoa Carr, Polly E.
Bell, Anita
Moreland, Nicole J.
Serological Evidence of Immune Priming by Group A Streptococci in Patients with Acute Rheumatic Fever
title Serological Evidence of Immune Priming by Group A Streptococci in Patients with Acute Rheumatic Fever
title_full Serological Evidence of Immune Priming by Group A Streptococci in Patients with Acute Rheumatic Fever
title_fullStr Serological Evidence of Immune Priming by Group A Streptococci in Patients with Acute Rheumatic Fever
title_full_unstemmed Serological Evidence of Immune Priming by Group A Streptococci in Patients with Acute Rheumatic Fever
title_short Serological Evidence of Immune Priming by Group A Streptococci in Patients with Acute Rheumatic Fever
title_sort serological evidence of immune priming by group a streptococci in patients with acute rheumatic fever
topic Microbiology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4957554/
https://www.ncbi.nlm.nih.gov/pubmed/27499748
http://dx.doi.org/10.3389/fmicb.2016.01119
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