Pirofski L A
Divn of Infectious Diseases, Room 709 Forchheimer Bldg, Albert Einstein College of Medicine, 1300 Morris Park Avenue, Bronx, NY 10461, USA.
Trends Microbiol. 2001 Sep;9(9):445-51. doi: 10.1016/s0966-842x(01)02134-5.
Vaccination is a rational alternative to treatment for Cryptococcus neoformans infections, as these infections are currently intractable in immunocompromised (including HIV-infected) individuals. Vaccines composed of the cryptococcal capsular polysaccharide glucuronoxylomannan (GXM), the key C. neoformans virulence factor, elicit protective antibodies in mice, although deleterious antibodies can also be induced. By contrast, polysaccharides are poor immunogens in HIV-infected humans and others with B-cell defects. Peptide mimotopes of GXM can induce protective immunity to C. neoformans in mice, however, our knowledge of the mechanisms of mimotope-induced protection is incomplete and further work is needed if polysaccharide- or mimotope-based vaccines are to be used to manage C. neoformans infection.
接种疫苗是治疗新型隐球菌感染的一种合理替代方法,因为这些感染目前在免疫功能低下(包括艾滋病毒感染)的个体中难以治疗。由新型隐球菌关键毒力因子荚膜多糖葡糖醛酸木聚糖甘露聚糖(GXM)组成的疫苗可在小鼠中引发保护性抗体,不过也会诱导有害抗体产生。相比之下,多糖在艾滋病毒感染的人类和其他B细胞缺陷者中是较差的免疫原。GXM的肽模拟表位可在小鼠中诱导对新型隐球菌的保护性免疫,然而,我们对模拟表位诱导保护机制的了解并不完整,如果要使用基于多糖或模拟表位的疫苗来控制新型隐球菌感染,还需要进一步的研究。