Chronic vulvovaginal Candida hypersensitivity: An underrecognized and undertreated disorder by allergists

被引:13
作者
Bernstein, Jonathan A. [1 ,3 ]
Seidu, Luqman [2 ]
机构
[1] Univ Cincinnati Coll Med, Div Immunol Allergy Sect, Dept Internal Med, Atlanta, GA USA
[2] Div Omni Allergy & Immunol, Atlanta, GA USA
[3] Univ Cincinnati Coll Med, 231 Albert Sabin Way,ML# 563, Cincinnati, OH 45267 USA
来源
ALLERGY & RHINOLOGY | 2015年 / 6卷 / 01期
关键词
D O I
10.2500/ar.2015.6.0113
中图分类号
R76 [耳鼻咽喉科学];
学科分类号
100213 ;
摘要
Vulvovaginal candidiasis infections are estimated to occur at least once during the lifetime of 75% of the female population. It has been proposed that some women with recurrent vulvovaginal candidiasis (RVVC) develop sensitization to Candida albicans and clinically improve in response to Candida immunotherapy. Here, we report a case series of 12 women diagnosed with chronic vulvovaginal Candida hypersensitivity subsequently treated with Candida immunotherapy and review potential systemic and localized host immune defense mechanisms involved in C. albicans overgrowth and sensitization. A retrospective review of vulvovaginal Candida hypersensitivity in women who were treated with C. albicans immunotherapy over the past eight years was conducted. Twelve women who qualified for a diagnosis of vulvovaginal Candida hypersensitivity were treated with Candida immunotherapy. Eleven of the 12 (92%) women reported clinical improvement after immunotherapy. The majority of these women were not sensitized to seasonal or perennial aeroallergens and clinically responded to lower concentrations of C. albicans allergen than what has been previously reported. In general, Candida immunotherapy was well tolerated. Chronic vulvovaginal Candida hypersensitivity is an underrecognized disorder by primary care physicians and therefore an undertreated disorder by allergists. A double-blinded, placebo-controlled randomized trial is necessary to firmly establish the efficacy of treatment with Candida immunotherapy. This investigation should be designed to include mechanistic studies that would help to better understand the etiology of this disorder.
引用
收藏
页码:E44 / E49
页数:6
相关论文
共 24 条
[1]  
BERNSTEIN JA, 1993, OBSTET GYNECOL, V82, P667
[2]   Partial protection against experimental vaginal candidiasis after mucosal vaccination with heat-killed Candida albicans and the mucosal adjuvant LT(R192G) [J].
Cárdenas-Freytag, L ;
Steele, C ;
Wormley, FL ;
Cheng, E ;
Clements, JD ;
Fidel, PL .
MEDICAL MYCOLOGY, 2002, 40 (03) :291-299
[3]  
De Knott HMR, 2005, CONTACT DERMATITIS, V53, P214, DOI 10.1111/j.0105-1873.2005.00685.x
[4]   A NOVEL CANDIDA-ALBICANS SKIN-TEST ANTIGEN - EFFICACY AND SAFETY IN MAN [J].
ESCH, RE ;
BUCKLEY, CE .
JOURNAL OF BIOLOGICAL STANDARDIZATION, 1988, 16 (01) :33-43
[5]   EFFECTS OF PREINDUCED CANDIDA-SPECIFIC CELL-MEDIATED-IMMUNITY ON EXPERIMENTAL VAGINAL CANDIDIASIS [J].
FIDEL, PL ;
LYNCH, ME ;
SOBEL, JD .
INFECTION AND IMMUNITY, 1994, 62 (03) :1032-1038
[6]   History and new insights into host defense against vaginal candidiasis [J].
Fidel, PL .
TRENDS IN MICROBIOLOGY, 2004, 12 (05) :220-227
[7]   Intravaginal live Candida challenge in humans leads to new hypotheses for the immunopathogenesis of vulvovaginal candidiasis [J].
Fidel, PL ;
Barousse, M ;
Espinosa, T ;
Ficarra, M ;
Sturtevant, J ;
Martin, DH ;
Quayle, AJ ;
Dunlap, K .
INFECTION AND IMMUNITY, 2004, 72 (05) :2939-2946
[8]   Gut Dysbiosis Promotes M2 Macrophage Polarization and Allergic Airway Inflammation via Fungi-Induced PGE2 [J].
Kim, Yun-Gi ;
Udayanga, Kankanam Gamage Sanath ;
Totsuka, Naoya ;
Weinberg, Jason B. ;
Nunez, Gabriel ;
Shibuya, Akira .
CELL HOST & MICROBE, 2014, 15 (01) :95-102
[9]  
KUDELKO NM, 1971, ANN ALLERGY, V29, P266
[10]  
MEECH RJ, 1985, NEW ZEAL MED J, V98, P1