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由甲酰甲硫氨酰亮氨酰苯丙氨酸与抗人卵巢癌单克隆抗体偶联介导的单核细胞趋化作用。

Monocyte chemotaxis mediated by formyl-methionyl-leucyl-phenylalanine conjugated with monoclonal antibodies against human ovarian carcinoma.

作者信息

Obrist R, Reilly R, Leavitt T, Knapp R C, Bast R C

出版信息

Int J Immunopharmacol. 1983;5(4):307-14. doi: 10.1016/0192-0561(83)90033-4.

Abstract

Availability of a chemically defined chemoattractant (fMLP) and of appropriate monoclonal antibodies may permit local manipulation of the inflammatory response to human tumors. fMLP has been conjugated with two monoclonal antibodies (OC125 and OC133) which react with human ovarian carcinomas. Conjugates retained the ability to bind to a human ovarian carcinoma line (OVCA433) judged by indirect immunofluorescence and by radioimmunoassay. The fMLP conjugate was maximally chemotactic for human blood monocytes and human peritoneal macrophages at protein concentrations of 300-900 micrograms/ml. Conjugates stimulated chemotaxis rather than chemokinesis. After incubation with an fMLP-antibody conjugate, antigen positive OVCA433 cells released chemotactic activity and attracted monocytes in vitro, whereas an antigen-negative ovarian cell line failed to do so. As monocytes can be important effectors of antibody dependent cell mediated cytoxicity, fMLP conjugates might increase monocyte concentrations at tumor sites and potentiate serotherapy for certain human neoplasms.

摘要

化学合成趋化因子(fMLP)和合适的单克隆抗体的存在,可能使对人类肿瘤的炎症反应进行局部调控成为可能。fMLP已与两种与人卵巢癌发生反应的单克隆抗体(OC125和OC133)结合。通过间接免疫荧光和放射免疫测定判断,结合物保留了与人类卵巢癌细胞系(OVCA433)结合的能力。fMLP结合物在蛋白质浓度为300 - 900微克/毫升时,对人血单核细胞和人腹膜巨噬细胞具有最大趋化活性。结合物刺激的是趋化作用而非趋动作用。用fMLP - 抗体结合物孵育后,抗原阳性的OVCA433细胞释放趋化活性并在体外吸引单核细胞,而抗原阴性的卵巢细胞系则无此作用。由于单核细胞可能是抗体依赖性细胞介导细胞毒性的重要效应细胞,fMLP结合物可能会增加肿瘤部位的单核细胞浓度,并增强对某些人类肿瘤的血清疗法。

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