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A Subgroup of Latently Mycobacterium tuberculosis Infected Individuals Is Characterized by Consistently Elevated IgA Responses to Several Mycobacterial Antigens

Elevated antibody responses to Mycobacterium tuberculosis antigens in individuals with latent infection (LTBI) have previously been linked to an increased risk for progression to active disease. Studies in the field focussed mainly on IgG antibodies. In the present study, IgA and/or IgG responses to...

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Autores principales: Baumann, Ralf, Kaempfer, Susanne, Chegou, Novel N., Oehlmann, Wulf, Spallek, Ralf, Loxton, André G., van Helden, Paul D., Black, Gillian F., Singh, Mahavir, Walzl, Gerhard
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi Publishing Corporation 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4546975/
https://www.ncbi.nlm.nih.gov/pubmed/26347586
http://dx.doi.org/10.1155/2015/364758
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author Baumann, Ralf
Kaempfer, Susanne
Chegou, Novel N.
Oehlmann, Wulf
Spallek, Ralf
Loxton, André G.
van Helden, Paul D.
Black, Gillian F.
Singh, Mahavir
Walzl, Gerhard
author_facet Baumann, Ralf
Kaempfer, Susanne
Chegou, Novel N.
Oehlmann, Wulf
Spallek, Ralf
Loxton, André G.
van Helden, Paul D.
Black, Gillian F.
Singh, Mahavir
Walzl, Gerhard
author_sort Baumann, Ralf
collection PubMed
description Elevated antibody responses to Mycobacterium tuberculosis antigens in individuals with latent infection (LTBI) have previously been linked to an increased risk for progression to active disease. Studies in the field focussed mainly on IgG antibodies. In the present study, IgA and/or IgG responses to the mycobacterial protein antigens AlaDH, NarL, 19 kDa, PstS3, and MPT83 were determined in a blinded fashion in sera from 53 LTBI controls, 14 healthy controls, and 42 active TB subjects. Among controls, we found that elevated IgA levels against all investigated antigens were not randomly distributed but concentrated on a subgroup of <30%—with particular high levels in a small subgroup of ~5% comprising one progressor to active TB. Based on a specificity of 100%, anti-NarL IgA antibodies achieved with 78.6% sensitivity the highest accuracy for the detection of active TB compared to healthy controls. In conclusion, the consistently elevated IgA levels in a subgroup of controls suggest higher mycobacterial load, a risk factor for progression to active TB, and together with high IgG levels may have prognostic potential and should be investigated in future large scale studies. The novel antigen NarL may also be promising for the antibody-based diagnosis of active TB cases.
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spelling pubmed-45469752015-09-07 A Subgroup of Latently Mycobacterium tuberculosis Infected Individuals Is Characterized by Consistently Elevated IgA Responses to Several Mycobacterial Antigens Baumann, Ralf Kaempfer, Susanne Chegou, Novel N. Oehlmann, Wulf Spallek, Ralf Loxton, André G. van Helden, Paul D. Black, Gillian F. Singh, Mahavir Walzl, Gerhard Mediators Inflamm Research Article Elevated antibody responses to Mycobacterium tuberculosis antigens in individuals with latent infection (LTBI) have previously been linked to an increased risk for progression to active disease. Studies in the field focussed mainly on IgG antibodies. In the present study, IgA and/or IgG responses to the mycobacterial protein antigens AlaDH, NarL, 19 kDa, PstS3, and MPT83 were determined in a blinded fashion in sera from 53 LTBI controls, 14 healthy controls, and 42 active TB subjects. Among controls, we found that elevated IgA levels against all investigated antigens were not randomly distributed but concentrated on a subgroup of <30%—with particular high levels in a small subgroup of ~5% comprising one progressor to active TB. Based on a specificity of 100%, anti-NarL IgA antibodies achieved with 78.6% sensitivity the highest accuracy for the detection of active TB compared to healthy controls. In conclusion, the consistently elevated IgA levels in a subgroup of controls suggest higher mycobacterial load, a risk factor for progression to active TB, and together with high IgG levels may have prognostic potential and should be investigated in future large scale studies. The novel antigen NarL may also be promising for the antibody-based diagnosis of active TB cases. Hindawi Publishing Corporation 2015 2015-08-10 /pmc/articles/PMC4546975/ /pubmed/26347586 http://dx.doi.org/10.1155/2015/364758 Text en Copyright © 2015 Ralf Baumann et al. https://creativecommons.org/licenses/by/3.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Baumann, Ralf
Kaempfer, Susanne
Chegou, Novel N.
Oehlmann, Wulf
Spallek, Ralf
Loxton, André G.
van Helden, Paul D.
Black, Gillian F.
Singh, Mahavir
Walzl, Gerhard
A Subgroup of Latently Mycobacterium tuberculosis Infected Individuals Is Characterized by Consistently Elevated IgA Responses to Several Mycobacterial Antigens
title A Subgroup of Latently Mycobacterium tuberculosis Infected Individuals Is Characterized by Consistently Elevated IgA Responses to Several Mycobacterial Antigens
title_full A Subgroup of Latently Mycobacterium tuberculosis Infected Individuals Is Characterized by Consistently Elevated IgA Responses to Several Mycobacterial Antigens
title_fullStr A Subgroup of Latently Mycobacterium tuberculosis Infected Individuals Is Characterized by Consistently Elevated IgA Responses to Several Mycobacterial Antigens
title_full_unstemmed A Subgroup of Latently Mycobacterium tuberculosis Infected Individuals Is Characterized by Consistently Elevated IgA Responses to Several Mycobacterial Antigens
title_short A Subgroup of Latently Mycobacterium tuberculosis Infected Individuals Is Characterized by Consistently Elevated IgA Responses to Several Mycobacterial Antigens
title_sort subgroup of latently mycobacterium tuberculosis infected individuals is characterized by consistently elevated iga responses to several mycobacterial antigens
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4546975/
https://www.ncbi.nlm.nih.gov/pubmed/26347586
http://dx.doi.org/10.1155/2015/364758
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