细胞溶解
月经周期
子宫
子宫内膜
CTL公司*
生物
CD3型
子宫颈
CD8型
卵泡期
男科
内分泌学
内科学
医学
免疫学
细胞毒性T细胞
激素
免疫系统
癌症
体外
生物化学
作者
H D White,K M Crassi,Alice L. Givan,Judy E. Stern,Jorge Luis Valdés González,Vincent A. Memoli,W R Green,Charles R. Wira
出处
期刊:Journal of Immunology
[The American Association of Immunologists]
日期:1997-03-15
卷期号:158 (6): 3017-3027
被引量:212
标识
DOI:10.4049/jimmunol.158.6.3017
摘要
The human female reproductive tract (RT) has been analyzed by others with respect to NK cell cytolytic activity, but not CD3+ T cell (CTL) cytolytic activity. Here, we describe the cytolytic capacity of mucosal CD3+ T cells both longitudinally within the RT (Fallopian tube, uterine endometrium, endocervix, ectocervix, and vaginal mucosa) and temporally throughout the menstrual cycle, using a redirected lysis assay system. Cytolysis by CD3+ CD8+ T cells is found throughout the RT and appears to be hormonally regulated, since in the uterine endometrium, the capacity for CD3+ T cell cytolytic activity is present during the proliferative phase of the menstrual cycle and absent during the subsequent secretory (postovulatory) phase. In contrast, in postmenopausal women the entire RT, including the uterus, retains the capacity for strong CD3+ T cell cytolytic activity. These findings suggest that the high levels of estradiol and progesterone present during days 14 to 28 of the menstrual cycle down-regulate CTL activity in the uterus. As a consequence, the absence of this activity may allow implantation of a semiallogeneic embryo that would otherwise be rejected. Further, these studies indicate that CTL activity is regulated differentially in different regions of the RT, persisting in the cervix and vagina throughout the menstrual cycle.
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