Candida vaginitis: virulence, host response and vaccine prospects

被引:53
作者
De Bernardis, Flavia [1 ]
Graziani, Sofia [1 ]
Tirelli, Flavio [2 ]
Antonopoulou, Stavroula [3 ,4 ]
机构
[1] Ist Super Sanita, Dept Infect Dis, Viale Regina Elena 299, I-00161 Rome, Italy
[2] Univ Cattolica Sacro Cuore, Largo F Vito 1, I-00168 Rome, Italy
[3] G Gennimatas Gen Hosp, Dept Clin Microbiol, 154 Ave Mesoge, Athens 11527, Greece
[4] Univ Athens, Dept Genet & Biotechnol, Fac Biol, Ave Oulof Palme, Athens 15784, Greece
关键词
Candida vaginitis; virulence factors; aspartyl-proteinase; immune-response; mucosal anti-Candida vaccine; VULVO-VAGINAL CANDIDIASIS; ALS GENE FAMILY; FLUCONAZOLE THERAPY; ALBICANS VAGINITIS; PATHOGENICITY MECHANISMS; ASPARTYL PROTEINASES; IMMUNE-RESPONSES; FUNGAL DISEASES; RAT MODEL; IN-VIVO;
D O I
10.1093/mmy/myx139
中图分类号
R51 [传染病];
学科分类号
100401 ;
摘要
Vulvovaginal candidiasis is a common mucosal infection affecting a large proportion of women with some of them affected by recurrent often intractable forms of the disease. Thus, there is an increasing interest in understanding the pathogenesis of this disease. The aim of our work was to characterize, in animal models of vaginal candidiasis, the components of the host-fungus interaction at the mucosal level. The evidence of an immune response in the vaginal compartment was very encouraging to identify the proper targets for new strategies for vaccination or immunotherapy of vaginal candidiasis. Aspartyl-proteinase (Sap2), which is an important immunodominant antigens and virulence factors of C. albicans acting inmucosal infections, was assembled with virosomes and a vaccine PEV7 was obtained. The results obtained in the mouse model and in the clinical trial conducted by Pevion on women have evidenced that the vaccine PEV7, intravaginally administered, has an encouraging therapeutic potential for the treatment of recurrent vulvovaginal candidiasis. This opens the way to a modality for anti-Candida protection at mucosal level.
引用
收藏
页码:S26 / S31
页数:6
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