NORMAL UTERINE CERVIX - CHARACTERIZATION OF ISOLATED LYMPHOCYTE PHENOTYPES AND IMMUNOGLOBULIN SECRETION

被引:51
作者
CROWLEYNOWICK, PA
BELL, M
EDWARDS, RP
MCCALLISTER, D
GORE, H
KANBOURSHAKIR, A
MESTECKY, J
PARTRIDGE, EE
机构
[1] UNIV PITTSBURGH,INST CANC,DEPT OBSTET GYNECOL & REPROD SCI,PITTSBURGH,PA
[2] UNIV ALABAMA,DEPT OBSTET GYNECOL,BIRMINGHAM,AL
[3] UNIV BIRMINGHAM,DEPT PATHOL,BIRMINGHAM,AL
[4] UNIV PITTSBURGH,DEPT PATHOL,PITTSBURGH,PA
[5] UNIV BIRMINGHAM,DEPT MICROBIOL,BIRMINGHAM,AL
来源
AMERICAN JOURNAL OF REPRODUCTIVE IMMUNOLOGY | 1995年 / 34卷 / 04期
关键词
ELISPOT; TISSUE LYMPHOCYTES; CERVICAL IGG; IGA; IGM;
D O I
10.1111/j.1600-0897.1995.tb00948.x
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
PROBLEM: Isolation of viable cervical lymphocyte populations and characterization of their function in healthy tissue is necessary to understand immunity in the genital tract. METHODS: Normal, cervical tissue was digested using a multi-enzymatic digestion procedure. Lymphocytes were characterized using FAGS analysis and ELISPOT analysis for immunoglobulin secreting cells. RESULTS: Following the digestion procedure, 0.16 x 10(6) +/- 0.8 cells/g of tissue with a viability of 90-98% were isolated from normal cervical tissue, FAGS analysis determined that B lymphocytes were the predominant cell type in normal cervical tissue representing a significantly higher percentage than that found in peripheral blood (P = 0.015). T lymphocytes and NK cells represented a significantly lower percentage than that found in peripheral blood (P = 0.0001 and 0.026, respectively). The largest percentage of immunoglobulin secreting cells isolated were secreting IgG followed by IgA. A limited number of IgM secreting cells were detected. IgA2 secreting cells represented 34.46 +/- 4.6% of the total number of IgA plasma cells. CONCLUSION: These studies represent the first analysis of viable mononuclear cells isolated from normal cervical tissue. The results form a baseline from which it will now be possible to compare changes that occur at the cervical squamocolumnar junction in response to infection or neoplasia.
引用
收藏
页码:241 / 247
页数:7
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