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Tumor Antigen-Dependent and Tumor Antigen-Independent Activation of Antitumor Activity in T Cells by a Bispecific Antibody-Modified Tumor Vaccine

机译:双特异性抗体修饰的肿瘤疫苗在T细胞中的肿瘤抗原依赖性和肿瘤抗原非依赖性激活抗肿瘤活性

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New approaches of therapeutic cancer vaccination are needed to improve the antitumor activity of T cells from cancer patients. We studied over the last years the activation of human T cells for tumor attack. To this end, we combined the personalized therapeutic tumor vaccine ATV-NDV—which is obtained by isolation, short in vitro culture, irradiation, and infection of patient's tumor cells by Newcastle Disease Virus (NDV)—with bispecific antibodies (bsAbs) binding to this vaccine and introducing anti-CD3 (signal 1) and anti-CD28 (signal 2) antibody activities. This vaccine called ATV-NDV/bsAb showed the unique ability to reactivate a preexisting potentially anergized antitumor memory T cell repertoire. But it also activated naive T cells to have antitumor properties in vitro and in vivo . This innovative concept of direct activation of cancer patients' T cells via cognate and noncognate interactions provides potential for inducing strong antitumor activities aiming at overriding T cell anergy and tumor immune escape mechanisms.
机译:需要新的治疗性癌症疫苗接种方法,以改善癌症患者的T细胞的抗肿瘤活性。在过去的几年中,我们研究了人类T细胞对肿瘤攻击的激活作用。为此,我们将个性化的治疗性肿瘤疫苗ATV-NDV与双特异性抗体(bsAbs)结合,该疫苗是通过分离,短期体外培养,放射和通过新城疫病毒(NDV)感染患者的肿瘤细胞而获得的这种疫苗并引入了抗CD3(信号1)和抗CD28(信号2)抗体活性。这种称为ATV-NDV / bsAb的疫苗显示出独特的能力,可以重新激活预先存在的可能变质的抗肿瘤记忆T细胞库。但是它也可以激活天然T细胞在体内和体外具有抗肿瘤作用。通过同源和非同源相互作用直接激活癌症患者T细胞的这一创新概念为诱导强大的抗肿瘤活性提供了潜力,这些活性旨在超越T细胞无反应性和肿瘤免疫逃逸机制。

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