» Articles » PMID: 9528901

Cellular Immunity in Recurrent Vulvovaginal Candidiasis

Overview
Date 1998 Apr 7
PMID 9528901
Citations 11
Authors
Affiliations
Soon will be listed here.
Abstract

Impaired T cell function has been reported to predispose women to recurrent vulvovaginal candidiasis, but conflicting results have been noted in the literature. Most clinical episodes occur in the late luteal phase, suggesting hormonal influence on host resistance. The present study assesses the cellular immune responses of 28 women with recurrent vaginal candidiasis (patients) and 25 control women (controls), noting results in relation to whether the women were in the follicular or luteal phase of the menstrual cycle at the time of sampling. Candida-stimulated peripheral blood lymphocyte proliferation was significantly reduced in patients compared with controls. Interferon-gamma (IFN-gamma) production in response to both Candida and purified protein derivative (PPD) stimulation was significantly lower in patients compared with controls. Skin test responses were comparable in both groups. A significant reduction in Candida-stimulated IFN-gamma production was seen in patients but not controls in the follicular phase compared with those in the luteal phase. There was also a trend towards lower proliferation in response to Candida in patients but not controls in the follicular phase compared with patients in the luteal phase. These results suggest that there is a partial T cell dysregulation in recurrent vaginal candidiasis which may be exacerbated by the hormonal balance present during the follicular phase, correlating with the risk of clinical infection.

Citing Articles

Catamenial Hyperpigmentation: A Review.

Mobasher P, Foulad D, Raffi J, Zachary C, Fackler N, Zohuri N J Clin Aesthet Dermatol. 2020; 13(6):18-21.

PMID: 32884614 PMC: 7442313.


Recurrent Vulvovaginal Candidiasis: Could It Be Related to Cell-Mediated Immunity Defect in Response to Candida Antigen?.

Talaei Z, Sheikhbahaei S, Ostadi V, Ganjalikhani Hakemi M, Meidani M, Naghshineh E Int J Fertil Steril. 2017; 11(3):134-141.

PMID: 28868834 PMC: 5582140. DOI: 10.22074/ijfs.2017.4883.


Is human Dectin-1 Y238X gene polymorphism related to susceptibility to recurrent vulvovaginal candidiasis?.

Zahedi N, Abedian Kenari S, Mohseni S, Aslani N, Ansari S, Badali H Curr Med Mycol. 2017; 2(3):15-19.

PMID: 28681024 PMC: 5490285. DOI: 10.18869/acadpub.cmm.2.3.15.


Prospects for development of a vaccine to prevent and control vaginal candidiasis.

Fidel Jr P, Cutler J Curr Infect Dis Rep. 2011; 13(1):102-7.

PMID: 21308461 PMC: 3062364. DOI: 10.1007/s11908-010-0143-y.


Increased levels of Candida albicans mannan-specific T-cell-derived antigen binding molecules in patients with invasive candidiasis.

Kosonen J, Rantala A, Little C, Lintu P, Harjamaki P, Georgiou G Clin Vaccine Immunol. 2006; 13(4):467-74.

PMID: 16603614 PMC: 1459633. DOI: 10.1128/CVI.13.4.467-474.2006.


References
1.
Wira C, Rossoll R . Antigen-presenting cells in the female reproductive tract: influence of sex hormones on antigen presentation in the vagina. Immunology. 1995; 84(4):505-8. PMC: 1415167. View

2.
Hobbs J, Brigden D, Davidson F, Kahan M, OATES J . Immunological aspects of candidal vaginitis. Proc R Soc Med. 1977; 70 Suppl 4:11-14. PMC: 1543207. View

3.
McDermott M, Clark D, Bienenstock J . Evidence for a common mucosal immunologic system. II. Influence of the estrous cycle on B immunoblast migration into genital and intestinal tissues. J Immunol. 1980; 124(6):2536-9. View

4.
Wira C, Sandoe C . Sex steroid hormone regulation of IgA and IgG in rat uterine secretions. Nature. 1977; 268(5620):534-6. DOI: 10.1038/268534a0. View

5.
Kinsman O, Pitblado K, Coulson C . Effect of mammalian steroid hormones and luteinizing hormone on the germination of Candida albicans and implications for vaginal candidosis. Mycoses. 1988; 31(12):617-26. DOI: 10.1111/j.1439-0507.1988.tb04416.x. View