Suppr超能文献

宫颈原位及浸润性鳞状细胞癌中的细胞介导细胞毒性

Cell-mediated cytotoxicity in preinvasive and invasive squamous cell carcinoma of the cervix.

作者信息

Dini M M, Jafari K, Faiferman I

出版信息

Obstet Gynecol. 1980 Jun;55(6):728-31.

PMID:7383460
Abstract

Cell-mediated immunity was tested by coincubation of target cell line (2043) of human squamous cell carcinoma and peripheral blood leukocytes (PBL) of 22 patients with squamous cell neoplasia of the uterine cervix, 9 patients with other tumors, and 9 normal females. The percentage of cell reduction in mild dysplasia was 90.1 +/- 6.8% (.001 less than P less than .005), in moderate dysplasia was 91.1 +/- 6.4% (.001 less than P less than .005), in severe dysplasia was 91.6 +/- 15.6% (P less than .001), in carcinoma in situ was 85.0 +/ 2.6% (P less than .001), and in invasive squamous cell carcinoma of the cervix was 85.0 +/- 6.9% (P less than .001). Peripheral blood leukocytes of patients with squamous neoplasia did not show any significant cytocoxicity against cell line SKOV-3, developed from an ovarian adenocarcinoma, nor did the PBL of patients with "other tumors" show any significant cytotoxicity against cell line 2043. This study shows that even in early stages of preinvasive squamous cell carcinoma of the cervix, the PBL are sensitized against the neoplastic process, confirming that different stages of cervical intraepithelial neoplasia and invasive squamous cell carcinoma are different intensities of the same biologic process.

摘要

通过将人鳞状细胞癌靶细胞系(2043)与22例宫颈鳞状上皮瘤变患者、9例其他肿瘤患者及9例正常女性的外周血白细胞(PBL)共同孵育来检测细胞介导的免疫。轻度发育异常时细胞减少百分比为90.1±6.8%(.001<P<.005),中度发育异常时为91.1±6.4%(.001<P<.005),重度发育异常时为91.6±15.6%(P<.001),原位癌时为85.0±2.6%(P<.001),宫颈浸润性鳞状细胞癌时为85.0±6.9%(P<.001)。鳞状上皮瘤变患者的外周血白细胞对源自卵巢腺癌的SKOV-3细胞系未显示出任何显著的细胞毒性,“其他肿瘤”患者的PBL对2043细胞系也未显示出任何显著的细胞毒性。本研究表明,即使在宫颈浸润前鳞状细胞癌的早期阶段,PBL对肿瘤形成过程也已致敏,证实宫颈上皮内瘤变和浸润性鳞状细胞癌的不同阶段是同一生物学过程的不同强度表现。

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验