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一种抗肿瘤单克隆抗体免疫反应性组分的评估

Evaluation of the immunoreactive fraction of an anti-tumour monoclonal antibody.

作者信息

Mantovani L, Ménard S, Mezzanzanica D, Miotti S, Pupa S M, Colnaghi M I

机构信息

Division of Experimental Oncology E. Istituto Nazionale per lo Studio e la Cura dei Tumori, Milan, Italy.

出版信息

Br J Cancer Suppl. 1990 Jul;10:15-7.

Abstract

Over a period of approximately 1 year, the immunoreactivity of the anti-ovary carcinoma MAb MOv18 was evaluated after radiolabelling with 125I on two different ovarian carcinoma cell lines, OvCa432 and IGROV1. A high variability of the immunoreactive values was observed by analysing different preparations of radiolabelled MOv18 (from 12 to 21% on OvCa432 and from 22 to 56% on IGROV1) and by using the same radiolabelled preparation (12% on OvCa432 and 51% on IGROV1). Since the variability could be due to the target cells, we set up an alternative binding assay using the anti-idiotypic MAb anti-Id18.1 directed against a private idiotype closely associated with the MOv18 paratope. Three different experiments carried out with the anti-idiotypic MAb gave reproducible results with an immunoreactive range from 71 to 83%. A direct comparison between the reactivity of the same 125I-MOv18 preparation on anti-Id18.1 and on IGROV1 confirmed the higher value of the immunoreactive fraction estimated on the more homogeneous anti-idiotypic reagent (71%), rather than on the tumour cells (56%). These data suggest that anti-idiotypic MAbs could represent suitable reagents for the evaluation of the immunoreactivity of an antibody preparation after radiolabelling and before in vivo administration.

摘要

在大约1年的时间里,用125I对两种不同的卵巢癌细胞系OvCa432和IGROV1进行放射性标记后,评估抗卵巢癌单克隆抗体MOv18的免疫反应性。通过分析放射性标记的MOv18的不同制剂(OvCa432上为12%至21%,IGROV1上为22%至56%)以及使用相同的放射性标记制剂(OvCa432上为12%,IGROV1上为51%),观察到免疫反应值存在高度变异性。由于这种变异性可能是由于靶细胞引起的,我们建立了一种替代结合试验,使用针对与MOv18互补位密切相关的独特型的抗独特型单克隆抗体anti-Id18.1。用抗独特型单克隆抗体进行的三项不同实验给出了可重复的结果,免疫反应范围为71%至83%。对同一125I-MOv18制剂在anti-Id18.1和IGROV1上的反应性进行直接比较,证实了在更均匀的抗独特型试剂上估计的免疫反应部分的值(71%)高于在肿瘤细胞上的值(56%)。这些数据表明,抗独特型单克隆抗体可能是评估放射性标记后和体内给药前抗体制剂免疫反应性的合适试剂。

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