Suppr超能文献

异源共轭抗体增强体外肿瘤浸润淋巴细胞的细胞毒性

Enhancement of in vitro tumor-infiltrating lymphocyte cytotoxicity by heteroconjugated antibodies.

作者信息

Reid I, Lundy J, Donohue J H

机构信息

Department of Surgery, Mayo Clinic, Rochester, MN 55905.

出版信息

J Immunol. 1992 Apr 15;148(8):2630-5.

PMID:1532818
Abstract

Tumor-infiltrating lymphocytes (TIL) were obtained from a mouse melanoma cell line (CL 62) transfected with the gene for the human melanoma Ag p97. TIL were cultured with anti-CD3 antibody and IL-2 for up to 38 days. Flow cytometry identified these TIL as Thy-1.2 + ve/CD4-ve/CD8 + ve cells. A heteroconjugated antibody 500A2 x 96.5, specific for both the CD3 Ag on TIL and the p97 Ag on CL 62 melanoma cells, was prepared using N-succinimidyl-3-(2-pyridyldithio)-propionate as a linking agent. TIL alone demonstrated low levels of cytotoxicity against autologous CL 62 tumor and also against the parental K1735 tumor and an allogeneic murine melanoma (B16). The addition of 500A2 x 96.5 heteroconjugated antibody enhanced TIL-mediated lysis of CL 62 tumor, but not of the K1735 or B16 tumors. This enhanced cytotoxicity was elicited at E:T ratios as low as 0.4:1, and in TIL cultured for 7 to 38 days. These results suggest that hetero-conjugated antibody may enhance the anti-tumor effect of TIL in vivo.

摘要

肿瘤浸润淋巴细胞(TIL)取自转染了人黑色素瘤抗原p97基因的小鼠黑色素瘤细胞系(CL 62)。TIL与抗CD3抗体和白细胞介素-2一起培养长达38天。流式细胞术将这些TIL鉴定为Thy-1.2阳性/CD4阴性/CD8阳性细胞。使用N-琥珀酰亚胺基-3-(2-吡啶二硫基)-丙酸酯作为连接剂,制备了对TIL上的CD3抗原和CL 62黑色素瘤细胞上的p97抗原均具有特异性的异源共轭抗体500A2×96.5。单独的TIL对自体CL 62肿瘤以及亲本K1735肿瘤和同种异体小鼠黑色素瘤(B16)表现出低水平的细胞毒性。添加500A2×96.5异源共轭抗体增强了TIL介导的CL 62肿瘤细胞裂解,但对K1735或B16肿瘤没有作用。这种增强的细胞毒性在低至0.4:1的效靶比下即可引发,并且在培养7至38天的TIL中也可引发。这些结果表明,异源共轭抗体可能会增强TIL在体内的抗肿瘤作用。

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