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...

Full description

Saved in:
Bibliographic Details
Main Authors: Ralf Baumann, Susanne Kaempfer, Novel N. Chegou, Wulf Oehlmann, Ralf Spallek, André G. Loxton, Paul D. van Helden, Gillian F. Black, Mahavir Singh, Gerhard Walzl
Format: Article
Language:English
Published: Wiley 2015-01-01
Series:Mediators of Inflammation
Online Access:http://dx.doi.org/10.1155/2015/364758
Tags: Add Tag
No Tags, Be the first to tag this record!
_version_ 1832564176219799552
author Ralf Baumann
Susanne Kaempfer
Novel N. Chegou
Wulf Oehlmann
Ralf Spallek
André G. Loxton
Paul D. van Helden
Gillian F. Black
Mahavir Singh
Gerhard Walzl
author_facet Ralf Baumann
Susanne Kaempfer
Novel N. Chegou
Wulf Oehlmann
Ralf Spallek
André G. Loxton
Paul D. van Helden
Gillian F. Black
Mahavir Singh
Gerhard Walzl
author_sort Ralf Baumann
collection DOAJ
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.
format Article
id doaj-art-2066cf28d127438cb672f1aa3f5f8dfd
institution Kabale University
issn 0962-9351
1466-1861
language English
publishDate 2015-01-01
publisher Wiley
record_format Article
series Mediators of Inflammation
spelling doaj-art-2066cf28d127438cb672f1aa3f5f8dfd2025-02-03T01:11:36ZengWileyMediators of Inflammation0962-93511466-18612015-01-01201510.1155/2015/364758364758A Subgroup of Latently Mycobacterium tuberculosis Infected Individuals Is Characterized by Consistently Elevated IgA Responses to Several Mycobacterial AntigensRalf Baumann0Susanne Kaempfer1Novel N. Chegou2Wulf Oehlmann3Ralf Spallek4André G. Loxton5Paul D. van Helden6Gillian F. Black7Mahavir Singh8Gerhard Walzl9DST/NRF Centre of Excellence for Biomedical TB Research and MRC Centre for TB Research, Division of Molecular Biology and Human Genetics, Department of Biomedical Sciences, Faculty of Medicine and Health Sciences, Stellenbosch University, P.O. Box 19063, Tygerberg 7505, South AfricaLionex Diagnostics and Therapeutics, Salzdahlumer Straße 196, 38126 Braunschweig, GermanyDST/NRF Centre of Excellence for Biomedical TB Research and MRC Centre for TB Research, Division of Molecular Biology and Human Genetics, Department of Biomedical Sciences, Faculty of Medicine and Health Sciences, Stellenbosch University, P.O. Box 19063, Tygerberg 7505, South AfricaLionex Diagnostics and Therapeutics, Salzdahlumer Straße 196, 38126 Braunschweig, GermanyLionex Diagnostics and Therapeutics, Salzdahlumer Straße 196, 38126 Braunschweig, GermanyDST/NRF Centre of Excellence for Biomedical TB Research and MRC Centre for TB Research, Division of Molecular Biology and Human Genetics, Department of Biomedical Sciences, Faculty of Medicine and Health Sciences, Stellenbosch University, P.O. Box 19063, Tygerberg 7505, South AfricaDST/NRF Centre of Excellence for Biomedical TB Research and MRC Centre for TB Research, Division of Molecular Biology and Human Genetics, Department of Biomedical Sciences, Faculty of Medicine and Health Sciences, Stellenbosch University, P.O. Box 19063, Tygerberg 7505, South AfricaDST/NRF Centre of Excellence for Biomedical TB Research and MRC Centre for TB Research, Division of Molecular Biology and Human Genetics, Department of Biomedical Sciences, Faculty of Medicine and Health Sciences, Stellenbosch University, P.O. Box 19063, Tygerberg 7505, South AfricaLionex Diagnostics and Therapeutics, Salzdahlumer Straße 196, 38126 Braunschweig, GermanyDST/NRF Centre of Excellence for Biomedical TB Research and MRC Centre for TB Research, Division of Molecular Biology and Human Genetics, Department of Biomedical Sciences, Faculty of Medicine and Health Sciences, Stellenbosch University, P.O. Box 19063, Tygerberg 7505, South AfricaElevated 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.http://dx.doi.org/10.1155/2015/364758
spellingShingle Ralf Baumann
Susanne Kaempfer
Novel N. Chegou
Wulf Oehlmann
Ralf Spallek
André G. Loxton
Paul D. van Helden
Gillian F. Black
Mahavir Singh
Gerhard Walzl
A Subgroup of Latently Mycobacterium tuberculosis Infected Individuals Is Characterized by Consistently Elevated IgA Responses to Several Mycobacterial Antigens
Mediators of Inflammation
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
url http://dx.doi.org/10.1155/2015/364758
work_keys_str_mv AT ralfbaumann asubgroupoflatentlymycobacteriumtuberculosisinfectedindividualsischaracterizedbyconsistentlyelevatedigaresponsestoseveralmycobacterialantigens
AT susannekaempfer asubgroupoflatentlymycobacteriumtuberculosisinfectedindividualsischaracterizedbyconsistentlyelevatedigaresponsestoseveralmycobacterialantigens
AT novelnchegou asubgroupoflatentlymycobacteriumtuberculosisinfectedindividualsischaracterizedbyconsistentlyelevatedigaresponsestoseveralmycobacterialantigens
AT wulfoehlmann asubgroupoflatentlymycobacteriumtuberculosisinfectedindividualsischaracterizedbyconsistentlyelevatedigaresponsestoseveralmycobacterialantigens
AT ralfspallek asubgroupoflatentlymycobacteriumtuberculosisinfectedindividualsischaracterizedbyconsistentlyelevatedigaresponsestoseveralmycobacterialantigens
AT andregloxton asubgroupoflatentlymycobacteriumtuberculosisinfectedindividualsischaracterizedbyconsistentlyelevatedigaresponsestoseveralmycobacterialantigens
AT pauldvanhelden asubgroupoflatentlymycobacteriumtuberculosisinfectedindividualsischaracterizedbyconsistentlyelevatedigaresponsestoseveralmycobacterialantigens
AT gillianfblack asubgroupoflatentlymycobacteriumtuberculosisinfectedindividualsischaracterizedbyconsistentlyelevatedigaresponsestoseveralmycobacterialantigens
AT mahavirsingh asubgroupoflatentlymycobacteriumtuberculosisinfectedindividualsischaracterizedbyconsistentlyelevatedigaresponsestoseveralmycobacterialantigens
AT gerhardwalzl asubgroupoflatentlymycobacteriumtuberculosisinfectedindividualsischaracterizedbyconsistentlyelevatedigaresponsestoseveralmycobacterialantigens
AT ralfbaumann subgroupoflatentlymycobacteriumtuberculosisinfectedindividualsischaracterizedbyconsistentlyelevatedigaresponsestoseveralmycobacterialantigens
AT susannekaempfer subgroupoflatentlymycobacteriumtuberculosisinfectedindividualsischaracterizedbyconsistentlyelevatedigaresponsestoseveralmycobacterialantigens
AT novelnchegou subgroupoflatentlymycobacteriumtuberculosisinfectedindividualsischaracterizedbyconsistentlyelevatedigaresponsestoseveralmycobacterialantigens
AT wulfoehlmann subgroupoflatentlymycobacteriumtuberculosisinfectedindividualsischaracterizedbyconsistentlyelevatedigaresponsestoseveralmycobacterialantigens
AT ralfspallek subgroupoflatentlymycobacteriumtuberculosisinfectedindividualsischaracterizedbyconsistentlyelevatedigaresponsestoseveralmycobacterialantigens
AT andregloxton subgroupoflatentlymycobacteriumtuberculosisinfectedindividualsischaracterizedbyconsistentlyelevatedigaresponsestoseveralmycobacterialantigens
AT pauldvanhelden subgroupoflatentlymycobacteriumtuberculosisinfectedindividualsischaracterizedbyconsistentlyelevatedigaresponsestoseveralmycobacterialantigens
AT gillianfblack subgroupoflatentlymycobacteriumtuberculosisinfectedindividualsischaracterizedbyconsistentlyelevatedigaresponsestoseveralmycobacterialantigens
AT mahavirsingh subgroupoflatentlymycobacteriumtuberculosisinfectedindividualsischaracterizedbyconsistentlyelevatedigaresponsestoseveralmycobacterialantigens
AT gerhardwalzl subgroupoflatentlymycobacteriumtuberculosisinfectedindividualsischaracterizedbyconsistentlyelevatedigaresponsestoseveralmycobacterialantigens