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Interferon-γ Responses to Chlamydia trachomatis Vaccine Candidate Proteins in Women With Different Chlamydia Outcomes.
- Source :
-
The Journal of infectious diseases [J Infect Dis] 2024 Sep 23; Vol. 230 (3), pp. 569-577. - Publication Year :
- 2024
-
Abstract
- Background: Chlamydia trachomatis testing and treatment strategies have not decreased infection rates, justifying need for a chlamydia vaccine. A murine study showed that a vaccine consisting of major outer membrane protein (MOMP) and polymorphic membrane proteins (Pmps) E, F, G, and H elicited protective immunity; studies on human cellular immune responses to Pmps are sparse.<br />Methods: Interferon gamma (IFN-γ) responses to these 5 proteins were measured by ELISPOT in peripheral blood mononuclear cells from women returning for treatment of a positive chlamydia test. Responses were compared in those with spontaneous chlamydia clearance versus persisting infection at baseline and no reinfection versus reinfection at a 3-month follow-up visit.<br />Results: IFN-γ response to 1 or more proteins was detected in 39% at baseline and 51.5% at follow-up, most often to PmpE and MOMP. IFN-γ responses to MOMP were detected less often at follow-up versus 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.<br />Conclusions: IFN-γ responses to these 5 C. trachomatis vaccine candidate proteins were heterogenous and primarily directed against MOMP and PmpE. Spontaneous chlamydia clearance and absence of reinfection may be clinical correlates of protection.<br />Competing Interests: Potential conflicts of interest. W. M. G. and R. C. B. report receiving consulting fees from Sanofi. G. C. reports receiving consulting fees from Merck, Roche, and Sanofi; participating on an Advisory Board for Merck/Serono and Roche; and participating on a Data Safety Monitoring Board for Merck and Sanofi. All other authors report no potential conflicts. All authors have submitted the ICMJE Form for Disclosure of Potential Conflicts of Interest. Conflicts that the editors consider relevant to the content of the manuscript have been disclosed.<br /> (© The Author(s) 2024. Published by Oxford University Press on behalf of Infectious Diseases Society of America. All rights reserved. For commercial re-use, please contact reprints@oup.com for reprints and translation rights for reprints. All other permissions can be obtained through our RightsLink service via the Permissions link on the article page on our site—for further information please contact journals.permissions@oup.com.)
- Subjects :
- Humans
Female
Young Adult
Adult
Adolescent
Bacterial Proteins immunology
Bacterial Outer Membrane Proteins immunology
Reinfection immunology
Reinfection prevention & control
Enzyme-Linked Immunospot Assay
Chlamydia trachomatis immunology
Chlamydia Infections immunology
Chlamydia Infections prevention & control
Interferon-gamma metabolism
Bacterial Vaccines immunology
Leukocytes, Mononuclear immunology
Subjects
Details
- Language :
- English
- ISSN :
- 1537-6613
- Volume :
- 230
- Issue :
- 3
- Database :
- MEDLINE
- Journal :
- The Journal of infectious diseases
- Publication Type :
- Academic Journal
- Accession number :
- 38394609
- Full Text :
- https://doi.org/10.1093/infdis/jiae092