Plasma Inflammatory Proteome Profile in a Cohort of Patients with Recurrent Vulvovaginal Candidiasis in Kenya

Author:

Rosati Diletta1ORCID,Ricaño Ponce Isis1,Omosa-Manyonyi Gloria S.23,Bruno Mariolina1ORCID,Kamau Nelly W.3ORCID,Jaeger Martin1ORCID,Kumar Vinod14ORCID,Netea Mihai G.15,van der Ven Andre J. A. M.1ORCID,ten Oever Jaap1

Affiliation:

1. Department of Internal Medicine, Radboud Center for Infectious Diseases, Radboud University Medical Center, 6525 GA Nijmegen, The Netherlands

2. Department of Medical Microbiology & Immunology, Faculty of Health Sciences, University of Nairobi, Nairobi P.O. Box 19676, Kenya

3. KAVI-Institute of Clinical Research (KAVI-ICR), Faculty of Health Sciences, University of Nairobi, Nairobi P.O. Box 19676, Kenya

4. Department of Genetics, University Medical Center Groningen, University of Groningen, Hanzeplein 1, 9713 GZ Groningen, The Netherlands

5. Department of Immunology and Metabolism, Life and Medical Sciences Institute (LIMES), University of Bonn, 53115 Bonn, Germany

Abstract

Vulvovaginal candidiasis (VVC) affects up to 75% of women at least once during their lifetime, and up to 8% of women suffer from frequent recurrent episodes of VVC (RVVC). A lack of a protective host response underlies vaginal Candida infections, while a dysregulated hyperinflammatory response may drive RVVC. This study aimed to investigate the systemic inflammatory protein profile in women with RVVC in an African population, considering the potential influence of hormonal contraceptive use on systemic inflammation. Using multiplex Proximity Extension Assay technology, we measured 92 circulatory inflammatory proteins in plasma samples from 158 RVVC patients and 92 asymptomatic women (controls). Hormonal contraceptive use was not found to have a statistically significant correlation with a systemic inflammatory protein profile in either RVVC patients or the asymptomatic women. RVVC women had lower circulating Fibroblast Growth Factor 21 (FGF-21) concentrations compared with healthy controls (adjusted p value = 0.028). Reduced concentrations of FGF-21 may be linked to the immune pathology observed in RVVC cases through IL-1β. This study may help to identify new biomarkers for the diagnosis and future development of novel immunomodulatory treatments for RVVC.

Funder

U.S. President’s Emergency Plan for AIDS Relief (PEPFAR) through United States Agency for International Development

FunHoMic ITN grant of the Horizon 2020 program

ERC Advanced

Spinoza grant of the Netherlands Organization for Scientific Research

Publisher

MDPI AG

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