首页> 外文期刊>The Journal of Immunology: Official Journal of the American Association of Immunologists >Immunotoxins Containing Recombinant Anti-CTLA-4 Single-Chain Fragment Variable Antibodies and Saporin: In Vitro Results and In Vivo Effects in an Acute Rejection Model
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Immunotoxins Containing Recombinant Anti-CTLA-4 Single-Chain Fragment Variable Antibodies and Saporin: In Vitro Results and In Vivo Effects in an Acute Rejection Model

机译:包含重组抗CTLA-4单链片段可变抗体和Saporin的免疫毒素:急性排斥模型的体外结果和体内效应

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摘要

Immunotoxins containing recombinant human-derived single-chain fragment variable (scFv) reagents (83 and 40) against CTLA-4(CD152) linked to saporin, a ribosome-inactivating protein, were prepared and tested on CD3/CD28-activated T lymphocytes, MLRs, CTLA-4-positive cell lines, and hemopoietic precursors. Immunotoxins inducedapoptosis in activated T lymphocytes and were able to specifically inhibit MLR between T lymphocytes and dendritic cells. The 83-saporin immunotoxin also inhibited the T cell activation in an MLR between T lymphocytes and an EBV-positive lymphoblastoid B cell line. Toxicity tests on hemopoietic precursors showed little or no effects in inhibiting colonies' growth. As the 83 scFv Ab was reactive also with activated mouse T lymphocytes, 83-saporin was tested in a model of tumor rejection consisting of C57BL/6 mice bearing a murine H.end endothelioma cell line, derived from DBA/2 mice. The lymphoid infiltration due to the presence of the tumor was reduced to a high extent, demonstrating that the immunotoxin was actually available and active in vivo. Thus, taking the results altogether, this study might represent a new breakthrough for immunotherapy, showing the possibility of targeting CTLA-4 to kill activated T cells, using conjugates containing scFv Abs and type 1 ribosome-inactivating protein.
机译:制备了含有重组人源性抗CTLA-4(CD152)的重组人源性单链片段可变(scFv)试剂(83和40)的免疫毒素,该试剂与saporin(一种核糖体失活蛋白)连接并在CD3 / CD28激活的T淋巴细胞上进行了测试, MLR,CTLA-4阳性细胞系和造血前体。免疫毒素诱导活化的T淋巴细胞凋亡,并能够特异性抑制T淋巴细胞与树突状细胞之间的MLR。 83-saporin免疫毒素还抑制T淋巴细胞和EBV阳性淋巴母细胞B细胞系之间的MLR中的T细胞活化。对造血前体的毒性试验显示,抑制菌落生长的作用很小或没有。由于83 scFv Ab也可与活化的小鼠T淋巴细胞反应,因此在肿瘤排斥模型中测试了83皂甙,该模型由C57BL / 6小鼠组成,该小鼠带有源自DBA / 2小鼠的鼠肝内皮细胞瘤细胞系。由于肿瘤的存在,淋巴样浸润在很大程度上减少了,这表明免疫毒素实际上是可利用的并且在体内具有活性。因此,总的来说,这项研究可能代表了免疫治疗的新突破,表明使用包含scFv Abs和1型核糖体失活蛋白的结合物靶向CTLA-4杀死活化的T细胞的可能性。

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