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用抗独特型抗体治疗淋巴细胞白血病时遇到的肿瘤细胞逃逸机制。

Mechanisms of tumour cell escape encountered in treating lymphocytic leukaemia with anti-idiotypic antibody.

作者信息

Gordon J, Abdul-Ahad A K, Hamblin T J, Stevenson F K, Stevenson G T

出版信息

Br J Cancer. 1984 May;49(5):547-57. doi: 10.1038/bjc.1984.88.

Abstract

Four patients with chronic lymphocytic leukaemia were treated by one or more infusions of polyclonal antibody specific for the immunoglobulin idiotype expressed on their leukaemic cells. The antibody was in the form of IgG from sheep antiserum. Three of the 4 cases showed a significant fall in blood lymphocyte count. On one occasion most of the residual circulating lymphocytes were apparently dead. However on all occasions the cell counts rebounded to near pre-infusion levels within one week. Viable lymphocytes recovered from the blood after infusion always showed evidence of antigenic modulation: a diminished level of surface idiotype in a patched distribution, with an accompanying refractoriness to lysis by anti-idiotype plus complement. When cultured in vitro blood lymphocytes from three of the four patients revealed an appreciable export of idiotypic Ig. These 3 patients showed plasma levels of idiotypic Ig up to 400 micrograms ml-1, reduced by plasma exchange prior to infusion. The fourth patient had a level of less than 4 micrograms ml-1, and was the only one in whom free antibody could be found in the plasma after infusion. These cases demonstrate two major factors which thwart antibody attack on leukaemic cells--extracellular antigen and antigenic modulation--as well as problems relating to sparseness of surface antigen, recruitment of effectors, and exhaustion of effectors.

摘要

4例慢性淋巴细胞白血病患者接受了一次或多次输注针对其白血病细胞上表达的免疫球蛋白独特型的多克隆抗体治疗。该抗体为来自绵羊抗血清的IgG形式。4例患者中有3例血液淋巴细胞计数显著下降。有一次,大部分残留的循环淋巴细胞明显死亡。然而,在所有情况下,细胞计数在一周内反弹至接近输注前水平。输注后从血液中回收的存活淋巴细胞总是显示出抗原调制的证据:表面独特型水平降低,呈斑块状分布,同时对抗独特型加补体的裂解具有抗性。在体外培养时,4例患者中有3例的血液淋巴细胞显示出明显的独特型Ig输出。这3例患者的血浆独特型Ig水平高达400微克/毫升,在输注前通过血浆置换降低。第4例患者的水平低于4微克/毫升,并且是输注后血浆中唯一能发现游离抗体的患者。这些病例证明了阻碍抗体攻击白血病细胞的两个主要因素——细胞外抗原和抗原调制——以及与表面抗原稀少、效应器募集和效应器耗竭相关的问题。

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