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一种将高活性肿瘤浸润淋巴细胞与高敏感性抗肿瘤药物联合应用于晚期恶性肿瘤的新实验和临床方法。

A new experimental and clinical approach of combining usage of highly active tumor-infiltrating lymphocytes and highly sensitive antitumor drugs for the advanced malignant tumor.

作者信息

Li B R, Tong S Q, Zhang X H, Lu J, Gu Q L, Lu D Y

机构信息

Department of Microbiology, Shanghai Second Medical University.

出版信息

Chin Med J (Engl). 1994 Nov;107(11):803-7.

PMID:7867384
Abstract

In recent years, tumor-infiltrating lymphocytes (TILs) have been reported to be effective for tumors in experimental and clinical research. In order to increase the therapeutical effect, we modified some steps of Rosenberg's approach: a. cold digestion with collagenase at 4 degrees C for 24 hours; b. sedimentation instead of centrifugation; c. elimination of tumor cells before the cultivation procedure. Compared with the original approach, the proliferation, activity and cytotoxicity of TILs obtained by the modified procedure were much improved. TILs' expansion-fold was greater than that with the original approach. Cytotoxicity against tumor cells was more potent. Increased TILs' subsets were CD3 and CD8 cells. Meanwhile, we took tumor cells from tumor tissues to test their in vitro chemosensitivities to different drugs in order to select highly sensitive antitumor drugs for treatment of cases with advanced tumors. According to the design of using highly active TILs and highly sensitive drugs (H & H therapy), preliminary clinical results of 50 cases showed higher response rates than those in treatment with TIL/IL2, LAK/IL2 and TIL+IL2+CTX. Less toxic side effects were observed in 14 patients.

摘要

近年来,在实验和临床研究中,肿瘤浸润淋巴细胞(TILs)已被报道对肿瘤有效。为了提高治疗效果,我们改进了罗森伯格方法的一些步骤:a. 在4℃用胶原酶冷消化24小时;b. 采用沉降而非离心;c. 在培养程序前消除肿瘤细胞。与原始方法相比,通过改进程序获得的TILs的增殖、活性和细胞毒性有了很大提高。TILs的扩增倍数大于原始方法。对肿瘤细胞的细胞毒性更强。增加的TILs亚群是CD3和CD8细胞。同时,我们从肿瘤组织中获取肿瘤细胞,检测它们对不同药物的体外化疗敏感性,以便为晚期肿瘤患者选择高敏感性抗肿瘤药物。根据使用高活性TILs和高敏感性药物的设计(H & H疗法),50例患者的初步临床结果显示,其有效率高于TIL/IL2、LAK/IL2和TIL+IL2+CTX治疗。14例患者观察到较少的毒副作用。

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