Heparin-Binding Haemagglutinin, a New Tool for the Detection of Latent Mycobacterium tuberculosis Infection in Hemodialysis Patients
Patients with end-stage renal disease (ESRD) and latently infected with Mycobacterium tuberculosis (LTBI) are at higher risk to develop tuberculosis (TB) than healthy subjects. Interferon-gamma release assays (IGRAs) were reported to be more sensitive than tuberculin skin tests for the detection of...
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Published in | PloS one Vol. 8; no. 8; p. e71088 |
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Main Authors | , , , , , , , , , |
Format | Journal Article |
Language | English |
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United States
Public Library of Science
05.08.2013
Public Library of Science (PLoS) |
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ISSN | 1932-6203 1932-6203 |
DOI | 10.1371/journal.pone.0071088 |
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Abstract | Patients with end-stage renal disease (ESRD) and latently infected with Mycobacterium tuberculosis (LTBI) are at higher risk to develop tuberculosis (TB) than healthy subjects. Interferon-gamma release assays (IGRAs) were reported to be more sensitive than tuberculin skin tests for the detection of infected individuals in dialysis patients.
On 143 dialysis patients prospectively enrolled, we compared the results from the QuantiFERON®-TB Gold assay (QFT), to those of an IGRA in response to in vitro stimulation of circulating mononuclear cells with the mycobacterial latency antigen Heparin-Binding Haemagglutinin purified from Mycobacterium bovis BCG (native HBHA, nHBHA).
Seven patients had a past history of active TB and 1 had an undetermined result with both IGRAs. Among the other 135 patients, 94 had concordant results with the QFT and nHBHA-IGRA, 40.0% being negative and therefore not latently infected, and 29.6% being positive and thus LTBI. Discrepant results between these tests were found for 36 patients positive only with the nHBHA-IGRA and 5 only with the QFT.
The nHBHA-IGRA is more sensitive than the QFT for the detection of LTBI dialysis patients, and follow-up of the patients will allow us to define the clinical significance of discrepant results between the nHBHA-IGRA and the QFT. |
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AbstractList | BACKGROUND: Patients with end-stage renal disease (ESRD) and latently infected with Mycobacterium tuberculosis (LTBI) are at higher risk to develop tuberculosis (TB) than healthy subjects. Interferon-gamma release assays (IGRAs) were reported to be more sensitive than tuberculin skin tests for the detection of infected individuals in dialysis patients. METHODS: On 143 dialysis patients prospectively enrolled, we compared the results from the QuantiFERON®-TB Gold assay (QFT), to those of an IGRA in response to in vitro stimulation of circulating mononuclear cells with the mycobacterial latency antigen Heparin-Binding Haemagglutinin purified from Mycobacterium bovis BCG (native HBHA, nHBHA). RESULTS: Seven patients had a past history of active TB and 1 had an undetermined result with both IGRAs. Among the other 135 patients, 94 had concordant results with the QFT and nHBHA-IGRA, 40.0% being negative and therefore not latently infected, and 29.6% being positive and thus LTBI. Discrepant results between these tests were found for 36 patients positive only with the nHBHA-IGRA and 5 only with the QFT. CONCLUSIONS: The nHBHA-IGRA is more sensitive than the QFT for the detection of LTBI dialysis patients, and follow-up of the patients will allow us to define the clinical significance of discrepant results between the nHBHA-IGRA and the QFT. On 143 dialysis patients prospectively enrolled, we compared the results from the QuantiFERON®-TB Gold assay (QFT), to those of an IGRA in response to in vitro stimulation of circulating mononuclear cells with the mycobacterial latency antigen Heparin-Binding Haemagglutinin purified from Mycobacterium bovis BCG (native HBHA, nHBHA). Seven patients had a past history of active TB and 1 had an undetermined result with both IGRAs. Among the other 135 patients, 94 had concordant results with the QFT and nHBHA-IGRA, 40.0% being negative and therefore not latently infected, and 29.6% being positive and thus LTBI. Discrepant results between these tests were found for 36 patients positive only with the nHBHA-IGRA and 5 only with the QFT. The nHBHA-IGRA is more sensitive than the QFT for the detection of LTBI dialysis patients, and follow-up of the patients will allow us to define the clinical significance of discrepant results between the nHBHA-IGRA and the QFT. Patients with end-stage renal disease (ESRD) and latently infected with Mycobacterium tuberculosis (LTBI) are at higher risk to develop tuberculosis (TB) than healthy subjects. Interferon-gamma release assays (IGRAs) were reported to be more sensitive than tuberculin skin tests for the detection of infected individuals in dialysis patients.BACKGROUNDPatients with end-stage renal disease (ESRD) and latently infected with Mycobacterium tuberculosis (LTBI) are at higher risk to develop tuberculosis (TB) than healthy subjects. Interferon-gamma release assays (IGRAs) were reported to be more sensitive than tuberculin skin tests for the detection of infected individuals in dialysis patients.On 143 dialysis patients prospectively enrolled, we compared the results from the QuantiFERON®-TB Gold assay (QFT), to those of an IGRA in response to in vitro stimulation of circulating mononuclear cells with the mycobacterial latency antigen Heparin-Binding Haemagglutinin purified from Mycobacterium bovis BCG (native HBHA, nHBHA).METHODSOn 143 dialysis patients prospectively enrolled, we compared the results from the QuantiFERON®-TB Gold assay (QFT), to those of an IGRA in response to in vitro stimulation of circulating mononuclear cells with the mycobacterial latency antigen Heparin-Binding Haemagglutinin purified from Mycobacterium bovis BCG (native HBHA, nHBHA).Seven patients had a past history of active TB and 1 had an undetermined result with both IGRAs. Among the other 135 patients, 94 had concordant results with the QFT and nHBHA-IGRA, 40.0% being negative and therefore not latently infected, and 29.6% being positive and thus LTBI. Discrepant results between these tests were found for 36 patients positive only with the nHBHA-IGRA and 5 only with the QFT.RESULTSSeven patients had a past history of active TB and 1 had an undetermined result with both IGRAs. Among the other 135 patients, 94 had concordant results with the QFT and nHBHA-IGRA, 40.0% being negative and therefore not latently infected, and 29.6% being positive and thus LTBI. Discrepant results between these tests were found for 36 patients positive only with the nHBHA-IGRA and 5 only with the QFT.The nHBHA-IGRA is more sensitive than the QFT for the detection of LTBI dialysis patients, and follow-up of the patients will allow us to define the clinical significance of discrepant results between the nHBHA-IGRA and the QFT.CONCLUSIONSThe nHBHA-IGRA is more sensitive than the QFT for the detection of LTBI dialysis patients, and follow-up of the patients will allow us to define the clinical significance of discrepant results between the nHBHA-IGRA and the QFT. Patients with end-stage renal disease (ESRD) and latently infected with Mycobacterium tuberculosis (LTBI) are at higher risk to develop tuberculosis (TB) than healthy subjects. Interferon-gamma release assays (IGRAs) were reported to be more sensitive than tuberculin skin tests for the detection of infected individuals in dialysis patients. On 143 dialysis patients prospectively enrolled, we compared the results from the QuantiFERON®-TB Gold assay (QFT), to those of an IGRA in response to in vitro stimulation of circulating mononuclear cells with the mycobacterial latency antigen Heparin-Binding Haemagglutinin purified from Mycobacterium bovis BCG (native HBHA, nHBHA). Seven patients had a past history of active TB and 1 had an undetermined result with both IGRAs. Among the other 135 patients, 94 had concordant results with the QFT and nHBHA-IGRA, 40.0% being negative and therefore not latently infected, and 29.6% being positive and thus LTBI. Discrepant results between these tests were found for 36 patients positive only with the nHBHA-IGRA and 5 only with the QFT. The nHBHA-IGRA is more sensitive than the QFT for the detection of LTBI dialysis patients, and follow-up of the patients will allow us to define the clinical significance of discrepant results between the nHBHA-IGRA and the QFT. Background Patients with end-stage renal disease (ESRD) and latently infected with Mycobacterium tuberculosis (LTBI) are at higher risk to develop tuberculosis (TB) than healthy subjects. Interferon-gamma release assays (IGRAs) were reported to be more sensitive than tuberculin skin tests for the detection of infected individuals in dialysis patients. Methods On 143 dialysis patients prospectively enrolled, we compared the results from the QuantiFERON®-TB Gold assay (QFT), to those of an IGRA in response to in vitro stimulation of circulating mononuclear cells with the mycobacterial latency antigen Heparin-Binding Haemagglutinin purified from Mycobacterium bovis BCG (native HBHA, nHBHA). Results Seven patients had a past history of active TB and 1 had an undetermined result with both IGRAs. Among the other 135 patients, 94 had concordant results with the QFT and nHBHA-IGRA, 40.0% being negative and therefore not latently infected, and 29.6% being positive and thus LTBI. Discrepant results between these tests were found for 36 patients positive only with the nHBHA-IGRA and 5 only with the QFT. Conclusions The nHBHA-IGRA is more sensitive than the QFT for the detection of LTBI dialysis patients, and follow-up of the patients will allow us to define the clinical significance of discrepant results between the nHBHA-IGRA and the QFT. |
Audience | Academic |
Author | Nortier, Joëlle Mascart, Françoise Dratwa, Max Grandbastien, Bruno Pozdzik, Agnieszka Locht, Camille Dessein, Rodrigue Corbière, Véronique Lecher, Sophie Gastaldello, Karine |
AuthorAffiliation | 6 CNRS UMR8204, Lille, France Johns Hopkins University School of Medicine, United States of America 8 Service de Gestion du Risque Infectieux, des Vigilances et d’Infectiologie, CHRU, Lille, France 7 Université Lille Nord de France, Lille, France 1 Laboratory of Vaccinology and Mucosal Immunity, Université Libre de Bruxelles, Brussels, Belgium 3 Nephrology Department, Hôpital Brugmann, Université Libre de Bruxelles, Brussels, Belgium 5 Institut Pasteur de Lille, Center for Infection and Immunity of Lille, Lille, France 9 Immunobiology Clinic, Hôpital Erasme, Université Libre de Bruxelles, Brussels, Belgium 2 Nephrology Department, Hôpital Erasme, Université Libre de Bruxelles, Brussels, Belgium 4 INSERM, Lille, France |
AuthorAffiliation_xml | – name: Johns Hopkins University School of Medicine, United States of America – name: 5 Institut Pasteur de Lille, Center for Infection and Immunity of Lille, Lille, France – name: 7 Université Lille Nord de France, Lille, France – name: 4 INSERM, Lille, France – name: 6 CNRS UMR8204, Lille, France – name: 1 Laboratory of Vaccinology and Mucosal Immunity, Université Libre de Bruxelles, Brussels, Belgium – name: 8 Service de Gestion du Risque Infectieux, des Vigilances et d’Infectiologie, CHRU, Lille, France – name: 2 Nephrology Department, Hôpital Erasme, Université Libre de Bruxelles, Brussels, Belgium – name: 9 Immunobiology Clinic, Hôpital Erasme, Université Libre de Bruxelles, Brussels, Belgium – name: 3 Nephrology Department, Hôpital Brugmann, Université Libre de Bruxelles, Brussels, Belgium |
Author_xml | – sequence: 1 givenname: Rodrigue surname: Dessein fullname: Dessein, Rodrigue – sequence: 2 givenname: Véronique surname: Corbière fullname: Corbière, Véronique – sequence: 3 givenname: Joëlle surname: Nortier fullname: Nortier, Joëlle – sequence: 4 givenname: Max surname: Dratwa fullname: Dratwa, Max – sequence: 5 givenname: Karine surname: Gastaldello fullname: Gastaldello, Karine – sequence: 6 givenname: Agnieszka surname: Pozdzik fullname: Pozdzik, Agnieszka – sequence: 7 givenname: Sophie surname: Lecher fullname: Lecher, Sophie – sequence: 8 givenname: Bruno surname: Grandbastien fullname: Grandbastien, Bruno – sequence: 9 givenname: Camille surname: Locht fullname: Locht, Camille – sequence: 10 givenname: Françoise surname: Mascart fullname: Mascart, Françoise |
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CitedBy_id | crossref_primary_10_1186_s12879_015_0796_0 crossref_primary_10_1186_s12882_020_01875_w crossref_primary_10_1007_s10157_021_02093_w crossref_primary_10_1097_QAI_0000000000000980 crossref_primary_10_3390_diagnostics12020453 crossref_primary_10_1097_QCO_0000000000000158 crossref_primary_10_3109_23744235_2015_1031173 crossref_primary_10_1016_j_jinf_2015_09_040 crossref_primary_10_1016_j_rmr_2018_08_015 |
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Notes | ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 14 content type line 23 Current address: Laboratoire de Bactériologie Hygiène, Institut de Microbiologie, Pôle de Biologie, Centre de Biologie et Pathologie, CHRU, Lille, France Conceived and designed the experiments: FM RD VC. Performed the experiments: RD VC. Analyzed the data: FM RD VC CL BG. Contributed reagents/materials/analysis tools: SL CL. Wrote the paper: RD VC CL FM. Patients inclusions: JN MD KG AP. Competing Interests: The authors have declared that no competing interests exist. |
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Snippet | Patients with end-stage renal disease (ESRD) and latently infected with Mycobacterium tuberculosis (LTBI) are at higher risk to develop tuberculosis (TB) than... Background Patients with end-stage renal disease (ESRD) and latently infected with Mycobacterium tuberculosis (LTBI) are at higher risk to develop tuberculosis... On 143 dialysis patients prospectively enrolled, we compared the results from the QuantiFERON®-TB Gold assay (QFT), to those of an IGRA in response to in vitro... BACKGROUND: Patients with end-stage renal disease (ESRD) and latently infected with Mycobacterium tuberculosis (LTBI) are at higher risk to develop... Background Patients with end-stage renal disease (ESRD) and latently infected with Mycobacterium tuberculosis (LTBI) are at higher risk to develop tuberculosis... |
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SubjectTerms | Aged Anticoagulants Antigens Antigens, Bacterial - immunology Bacillus Calmette-Guerin vaccine BCG Binding Biological response modifiers Biology Case-Control Studies Cells, Cultured Chronic kidney failure Comparative analysis Development and progression Dialysis End-stage renal disease Female Health aspects Health care Hemagglutinins Hemodialysis Heparin Humans Infections Interferon Interferon-gamma Release Tests Kidney diseases Kidney Failure, Chronic - complications Kidney Failure, Chronic - therapy Kidney transplantation Laboratories Latency Latent infection Latent Tuberculosis - diagnosis Latent Tuberculosis - microbiology Lectins - immunology Leukocytes (mononuclear) Leukocytes, Mononuclear - immunology Male Medicine Middle Aged Mycobacterium tuberculosis Mycobacterium tuberculosis - immunology Nephrology Patients Prospective Studies Reagent Kits, Diagnostic Renal Dialysis Skin tests Tuberculin Tuberculosis Vaccines |
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Title | Heparin-Binding Haemagglutinin, a New Tool for the Detection of Latent Mycobacterium tuberculosis Infection in Hemodialysis Patients |
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