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IDEC-C2B8抗CD20单克隆抗体对CD20阳性B淋巴瘤细胞系的生长抑制作用。

Growth inhibition of CD20-positive B lymphoma cell lines by IDEC-C2B8 anti-CD20 monoclonal antibody.

作者信息

Taji H, Kagami Y, Okada Y, Andou M, Nishi Y, Saito H, Seto M, Morishima Y

机构信息

Department of Hematology and Chemotherapy, Aichi Cancer Center Hospital, Nagoya.

出版信息

Jpn J Cancer Res. 1998 Jul;89(7):748-56. doi: 10.1111/j.1349-7006.1998.tb03280.x.

Abstract

Treatment with IDEC-C2B8 (C2B8), the chimeric anti-CD20 antibody, was shown in a phase I-II study to be very effective for the treatment of low-grade B-cell lymphoma, in contrast to the results of most previous immunotherapies with monoclonal antibodies. In a study designed to elucidate the reason for this efficacy, two cell lines derived from lymphomas with BCL2 gene rearrangement (SU-DHL-4 and SU-DHL-6) showed remarkable growth inhibition and cell-death, and two other cell lines derived from a diffuse lymphoma (RC-K8) and a mantle cell lymphoma (SP-49) showed moderate growth inhibition, but neither a CD20 weakly positive cell line (NALL-1) nor a negative cell line (MOLT-4) showed any growth inhibition. An examination of the intensity of cell-surface CD20 expression showed no correlation between intensity and degree of growth inhibition among the four cell lines showing growth inhibition. Morphological examination revealed condensed and fragmented nuclei and budding of the plasma membrane, both characteristic of apoptosis, with some cells in these cell lines showing growth inhibition by C2B8. Such apoptosis was also confirmed by flow cytometric analysis, suggesting that, at least in part, apoptosis plays a role in this growth inhibition. This growth-inhibitory mechanism may thus account for the effectiveness of C2B8 antibody therapy.

摘要

在一项I-II期研究中,嵌合抗CD20抗体IDEC-C2B8(C2B8)治疗被证明对低度B细胞淋巴瘤的治疗非常有效,这与大多数先前单克隆抗体免疫疗法的结果形成对比。在一项旨在阐明这种疗效原因的研究中,来自具有BCL2基因重排的淋巴瘤的两个细胞系(SU-DHL-4和SU-DHL-6)显示出显著的生长抑制和细胞死亡,另外两个来自弥漫性淋巴瘤(RC-K8)和套细胞淋巴瘤(SP-49)的细胞系显示出中度生长抑制,但CD20弱阳性细胞系(NALL-1)和阴性细胞系(MOLT-4)均未显示出任何生长抑制。对细胞表面CD20表达强度的检查表明,在显示出生长抑制的四个细胞系中,强度与生长抑制程度之间没有相关性。形态学检查发现细胞核浓缩和碎片化以及质膜出芽,这都是凋亡的特征,这些细胞系中的一些细胞显示出被C2B8抑制生长。流式细胞术分析也证实了这种凋亡,表明凋亡至少在一定程度上参与了这种生长抑制。因此,这种生长抑制机制可能解释了C2B8抗体治疗的有效性。

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