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N-[-4-(5-硝基-2-呋喃基)-2-噻唑基]甲酰胺诱导的膀胱癌的免疫原性

Immunogenicity of N-[-4-(5-nitro-2-furyl)-2-thiazolyl]formamide-induced bladder cancer.

作者信息

Soloway M S, Martino C, Hyatt C, Marrone J C

出版信息

Natl Cancer Inst Monogr. 1978 Dec(49):293-300.

PMID:748783
Abstract

Five transplantable TCC initially induced by the carcinogen FANFT were systematically tested for individual immunogenicity and then for the presence of cross-reacting tumor antigens. The classic amputation challenge technique was used. Three of the 5 tumors were immunogenic, as determined by their ability to reduce the growth of a challenge tumor dose in mice immunized with the same bladder tumor. Prior immunization with one of the immunogenic tumors failed to reduce the incidence or growth of primary bladder tumors induced by the ingestion of 0.1% FANFT in C3H/HeJ mice. The lack of cross-reacting tumor antigens has important implications for the use of allogeneic tumor cells as an antigen source in immunotherapy.

摘要

对最初由致癌物FANFT诱导产生的5种可移植性移行细胞癌(TCC)进行了系统测试,以检测其个体免疫原性,随后检测交叉反应性肿瘤抗原的存在情况。采用了经典的截肢攻击技术。5种肿瘤中有3种具有免疫原性,这是根据它们在经相同膀胱肿瘤免疫的小鼠中减少攻击肿瘤剂量生长的能力来确定的。用其中一种免疫原性肿瘤进行预先免疫,未能降低C3H/HeJ小鼠摄入0.1% FANFT诱导的原发性膀胱肿瘤的发生率或生长。缺乏交叉反应性肿瘤抗原对于将同种异体肿瘤细胞用作免疫治疗中的抗原来源具有重要意义。

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