Anti-Treponema pallidum IgA response as a potential diagnostic marker of syphilis.


Journal

Clinical microbiology and infection : the official publication of the European Society of Clinical Microbiology and Infectious Diseases
ISSN: 1469-0691
Titre abrégé: Clin Microbiol Infect
Pays: England
ID NLM: 9516420

Informations de publication

Date de publication:
Dec 2023
Historique:
received: 20 04 2023
revised: 15 08 2023
accepted: 16 08 2023
medline: 29 11 2023
pubmed: 24 8 2023
entrez: 23 8 2023
Statut: ppublish

Résumé

Serological tests for syphilis detect mainly total Ig, IgM or IgG antibodies. We aimed to evaluate the specific IgA response in syphilis patients according to disease stage. A serum IgA-enzyme immunoassay was developed using commercially available microplates coated with recombinant treponemal antigens and an anti-IgA-conjugate. To define a cut-off, we used 91 syphilis positive and 136 negative sera previously defined by the rapid plasma reagin and the Treponema pallidum particle agglutination results. Then we determined the intra- and inter-assay precisions, diagnostic sensitivity according to the clinical stage (in 66, 55 and 42 sera from primary, secondary and latent syphilis patients, respectively) and specificity (in 211 sera from people with conditions different to syphilis). IgA values were further measured in 71 sera from patients with previously treated syphilis. The newly developed IgA-enzyme immunoassay showed a good discrimination between negative and positive samples with intra- and inter-assay variation coefficients <20%. The sensitivity was 80.3% (95% CI, 70.0-90.6), 100.0% (95% CI, 99.1-100.0) and 95.2% (95% CI, 87.6-100.0) in primary, secondary and latent syphilis, respectively, and the specificity was 98.1% (95% CI, 96.0-100.0). Further, IgA values were negative in 61.3% (38/62) of patients with previously treated syphilis. Our findings suggest serum IgA as a sensitive and specific marker of syphilis and its detection could be used as a screening assay for active infection. Further evaluation is needed in prospective longitudinal field studies.

Identifiants

pubmed: 37611864
pii: S1198-743X(23)00398-1
doi: 10.1016/j.cmi.2023.08.015
pii:
doi:

Substances chimiques

anti-IgA 0
Immunoglobulin A 0
Antibodies, Bacterial 0

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

1603.e1-1603.e4

Informations de copyright

Copyright © 2023 The Authors. Published by Elsevier Ltd.. All rights reserved.

Auteurs

Islay Rodríguez (I)

National Reference Laboratory of Treponemes and Special Pathogens, Tropical Medicine Institute "Pedro Kourí", Havana, Cuba. Electronic address: islay@ipk.sld.cu.

Angel A Noda (AA)

National Reference Laboratory of Treponemes and Special Pathogens, Tropical Medicine Institute "Pedro Kourí", Havana, Cuba.

Philipp P Bosshard (PP)

Department of Dermatology, University Hospital Zurich, University of Zurich, Zurich, Switzerland.

Reto Lienhard (R)

ADMed Microbiology, La Chaux de Fonds, Switzerland.

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Classifications MeSH