Distinct protective host defenses against oral and vaginal candidiasis

被引:81
作者
Fidel, PL
机构
[1] Louisiana State Univ, Hlth Sci Ctr, Dept Microbiol Immunol & Parasitol, New Orleans, LA 70112 USA
[2] Louisiana State Univ, Sch Dent, Ctr Excellence Oral & Craniofacial Biol, New Orleans, LA 70119 USA
关键词
Candida albicans; mucosal candidiasis; host defense mechanisms; vaginal candidiasis; oral candidiasis; immunosuppression;
D O I
10.1080/714031126
中图分类号
R51 [传染病];
学科分类号
100401 ;
摘要
Oral and vaginal candidiasis are the two most common forms of opportunistic fungal infections. However, the prevalence of each can be quite variable depending on the immune status of the host. While vulvovaginal candidiasis (VVC) is equally common in immunocompetent and immunocompromised women, oropharyngeal candidiasis (OPC) is infrequent except under immunocompromised states. Candida albicans, the causative agent in the majority of cases, is a commensal of the gastrointestinal and lower female reproductive tracts. Thus, most healthy individuals have protective Candida-specific immunity that normally prevents infection. Studies from animal models, women with recurrent VVC (RVVC) and HIV-infected individuals, however, suggest that distinct protective host defense mechanisms may function against OPC and VVC. While local and systemic cell-mediated immunity (CMI) appear important for protection against OPC, there is little evidence to indicate that either local or systemic CMI plays a role against VVC. Innate resistance is also considered distinct at both sites with considerably less activity at the vaginal mucosa, including the newfound anti-Candida activity by epithelial cells. Finally, the protective role of humoral immunity has been and remains uncertain. Taken together, the differential prevalence of VVC and OPC is directly proportional to the levels of demonstrable innate and adaptive host defenses at each site.
引用
收藏
页码:359 / 375
页数:17
相关论文
共 160 条
[1]   COMPARISON OF A LESION-INDUCING ISOLATE AND A NON-LESIONAL ISOLATE OF CANDIDA-ALBICANS IN AN IMMUNOSUPPRESSED RAT MODEL OF ORAL CANDIDIASIS [J].
ALLEN, CM ;
SAFFER, A ;
MEISTER, RK ;
BECK, FM ;
BRADWAY, S .
JOURNAL OF ORAL PATHOLOGY & MEDICINE, 1994, 23 (03) :133-139
[2]   NONINHIBITORY BINDING OF HUMAN INTERLEUKIN-2-ACTIVATED NATURAL-KILLER-CELLS TO THE GERM TUBE FORMS OF CANDIDA-ALBICANS [J].
ARANCIA, G ;
MOLINARI, A ;
CRATERI, P ;
STRINGARO, A ;
RAMONI, C ;
DUPUIS, ML ;
GOMEZ, MJ ;
TOROSANTUCCI, A ;
CASSONE, A .
INFECTION AND IMMUNITY, 1995, 63 (01) :280-288
[3]  
BALISH E, 1993, J MED VET MYCOL, V31, P143
[4]   CORRELATES OF CELL-MEDIATED-IMMUNITY IN CANDIDA-ALBICANS-COLONIZED GNOTOBIOTIC MICE [J].
BALISH, E ;
FILUTOWICZ, H ;
OBERLEY, TD .
INFECTION AND IMMUNITY, 1990, 58 (01) :107-113
[5]  
BALISH E, 1984, APPL ENVIRON MICROB, V47, P647, DOI 10.1128/AEM.47.4.647-652.1984
[6]   Growth inhibition of Candida albicans by human vaginal epithelial cells [J].
Barousse, MM ;
Steele, C ;
Dunlap, K ;
Espinosa, T ;
Boikov, D ;
Sobel, JD ;
Fidel, PL .
JOURNAL OF INFECTIOUS DISEASES, 2001, 184 (11) :1489-1493
[7]   GROWTH-INHIBITION OF CANDIDA-ALBICANS BY INTERLEUKIN-2-INDUCED LYMPH-NODE CELLS [J].
BENO, DWA ;
MATHEWS, HL .
CELLULAR IMMUNOLOGY, 1990, 128 (01) :89-100
[8]  
BENO DWA, 1995, J IMMUNOL, V154, P5273
[9]   Increased severity of Candida vaginitis in BALB/c nu/nu mice versus the parent strain is not abrogated by adoptive transfer of T cell enriched lymphocytes [J].
Black, CA ;
Eyers, FM ;
Russell, A ;
Dunkley, ML ;
Clancy, RL ;
Beagley, KW .
JOURNAL OF REPRODUCTIVE IMMUNOLOGY, 1999, 45 (01) :1-18
[10]   Acute neutropenia decreases inflammation associated with murine vaginal candidiasis but has no effect on the course of infection [J].
Black, CA ;
Eyers, FM ;
Russell, A ;
Dunkley, ML ;
Clancy, RL ;
Beagley, KW .
INFECTION AND IMMUNITY, 1998, 66 (03) :1273-1275