Interferon-Gamma Responses to Chlamydia trachomatis Vaccine Candidate Proteins in Chlamydia-Infected Women with Different Chlamydia Outcomes.

Chlamydia trachomatis ELISPOT chlamydia interferon gamma spontaneous clearance vaccine

Journal

The Journal of infectious diseases
ISSN: 1537-6613
Titre abrégé: J Infect Dis
Pays: United States
ID NLM: 0413675

Informations de publication

Date de publication:
23 Feb 2024
Historique:
received: 27 10 2023
revised: 31 01 2024
accepted: 20 02 2024
medline: 23 2 2024
pubmed: 23 2 2024
entrez: 23 2 2024
Statut: aheadofprint

Résumé

Chlamydia trachomatis (CT) testing and treatment strategies have not decreased infection rates, justifying need for a CT vaccine. A murine study showed that a vaccine consisting of MOMP and 4 polymorphic membrane proteins (Pmps E, F, G, H) elicited protective immunity; studies on human cellular immune responses to Pmps are sparse. Interferon gamma (IFN-γ) responses to these 5 CT proteins were measured by ELISPOT in PBMCs from women returning for treatment of a positive CT screening test. Responses were compared in those with spontaneous CT clearance vs. persisting infection at baseline and no reinfection vs. reinfection at a 3-month follow-up visit. IFN-γ response to one or more proteins was detected in 39% at baseline and 51.5% at follow-up; PmpE and MOMP most often elicited positive responses. IFN-γ responses to MOMP were detected less often at follow-up vs. baseline in women with reinfection, but were maintained in those without reinfection. Women with spontaneous clearance had a higher magnitude of IFN-γ response to PmpE and MOMP. IFN-γ responses to these 5 CT vaccine candidate proteins were heterogenous and primarily directed against MOMP and PmpE. Spontaneous clearance of infection and absence of reinfection may be clinical correlates of protection.

Sections du résumé

BACKGROUND BACKGROUND
Chlamydia trachomatis (CT) testing and treatment strategies have not decreased infection rates, justifying need for a CT vaccine. A murine study showed that a vaccine consisting of MOMP and 4 polymorphic membrane proteins (Pmps E, F, G, H) elicited protective immunity; studies on human cellular immune responses to Pmps are sparse.
METHODS METHODS
Interferon gamma (IFN-γ) responses to these 5 CT proteins were measured by ELISPOT in PBMCs from women returning for treatment of a positive CT screening test. Responses were compared in those with spontaneous CT clearance vs. persisting infection at baseline and no reinfection vs. reinfection at a 3-month follow-up visit.
RESULTS RESULTS
IFN-γ response to one or more proteins was detected in 39% at baseline and 51.5% at follow-up; PmpE and MOMP most often elicited positive responses. IFN-γ responses to MOMP were detected less often at follow-up vs. baseline in women with reinfection, but were maintained in those without reinfection. Women with spontaneous clearance had a higher magnitude of IFN-γ response to PmpE and MOMP.
CONCLUSIONS CONCLUSIONS
IFN-γ responses to these 5 CT vaccine candidate proteins were heterogenous and primarily directed against MOMP and PmpE. Spontaneous clearance of infection and absence of reinfection may be clinical correlates of protection.

Identifiants

pubmed: 38394609
pii: 7613391
doi: 10.1093/infdis/jiae092
pii:
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Informations de copyright

© The Author(s) 2024. Published by Oxford University Press on behalf of Infectious Diseases Society of America. All rights reserved. For permissions, please e-mail: journals.permissions@oup.com.

Auteurs

Jacob Dziadula (J)

Departments of Medicine and Biostatistics, University of Alabama at Birmingham, Birmingham, AL, USA.

Steffanie Sabbaj (S)

Departments of Medicine and Biostatistics, University of Alabama at Birmingham, Birmingham, AL, USA.

Kanupriya Gupta (K)

Departments of Medicine and Biostatistics, University of Alabama at Birmingham, Birmingham, AL, USA.

Gary Cutter (G)

Biostatistics, University of Alabama at Birmingham, Birmingham, AL, USA.

Hong Yu (H)

British Columbia Centre for Disease Control, University of British Columbia, Vancouver, BC, Canada.

Robert C Brunham (RC)

British Columbia Centre for Disease Control, University of British Columbia, Vancouver, BC, Canada.

William M Geisler (WM)

Departments of Medicine and Biostatistics, University of Alabama at Birmingham, Birmingham, AL, USA.

Classifications MeSH