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The targeting of T-helper cells and tumourcidal macrophages to a B-cell lymphoma using a PPD-monoclonal antibody heteroconjugate.

机译:使用PPD单克隆抗体异源偶联物将T辅助细胞和杀肿瘤性巨噬细胞靶向B细胞淋巴瘤。

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摘要

This paper describes a T-cell targeting strategy based on the use of an antigen-monoclonal antibody heteroconjugate. A rat anti-idiotypic monoclonal antibody specific for a murine B-cell lymphoma was conjugated to the purified protein derivative (PPD) of tuberculin. This construct selectively delivered up to 4.5 x 10(4) molecules of PPD onto each tumour cell. Targeted PPD was internalized for endosomal processing and was presented in association with the I-A class II restriction element to PPD-reactive T-helper (Th) cells. Activated Th cells were demonstrated to proliferate and secrete significant levels of tumour necrosis factor (TNF). Such lymphokine secretion was observed at a PPD concentration as low as 1 ng/ml. Despite the secretion of TNF, the B-cell lymphoma was found to be resistant to autonomous Th-mediated cytotoxicity. Targeted Th cells did, however, activate tumourcidal macrophages that subsequently mediated significant tumour cytostasis. Based on this observation, it is proposed that the targeting system described may be exploited as the basis for a future immunotherapeutic strategy.
机译:本文介绍了基于使用抗原-单克隆抗体异源偶联物的T细胞靶向策略。将对鼠B细胞淋巴瘤具有特异性的大鼠抗独特型单克隆抗体与结核菌素的纯化蛋白衍生物(PPD)偶联。该构建体选择性地将多达4.5 x 10(4)个PPD分子传递到每个肿瘤细胞上。靶向的PPD已内化以用于内体加工,并与I-A类II限制元件结合提供给PPD反应性T辅助(Th)细胞。活化的Th细胞被证明能增殖并分泌大量的肿瘤坏死因子(TNF)。在PPD浓度低至1 ng / ml时观察到这种淋巴因子分泌。尽管TNF的分泌,发现B细胞淋巴瘤对自主Th介导的细胞毒性有抵抗力。然而,靶向的Th细胞确实激活了杀肿瘤的巨噬细胞,其随后介导了显着的肿瘤细胞停滞。基于该观察结果,提出可以将所述的靶向系统用作未来免疫治疗策略的基础。

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