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T cell-recruiting triplebody 19-3-19 mediates serial lysis of malignant B-lymphoid cells by a single T cell

机译:募集T细胞的三体19-3-19通过单个T细胞介导恶性B淋巴细胞的系列裂解

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摘要

Triplebody 19-3-19, an antibody-derived protein, carries three single chain fragment variable domains in tandem in a single polypeptide chain. 19-3-19 binds CD19-bearing lymphoid cells via its two distal domains and primary T cells via its CD3-targeting central domain in an antigen-specific manner. Here, malignant B-lymphoid cell lines and primary cells from patients with B cell malignancies were used as targets in cytotoxicity tests with pre-stimulated allogeneic T cells as effectors. 19-3-19 mediated up to 95% specific lysis of CD19-positive tumor cells and, at picomolar EC50 doses, had similar cytolytic potency as the clinically successful agent BlinatumomabTM. 19-3-19 activated resting T cells from healthy unrelated donors and mediated specific lysis of both autologous and allogeneic CD19-positive cells. 19-3-19 led to the elimination of 70% of CD19-positive target cells even with resting T cells as effectors at an effector-to-target cell ratio of 1 : 10. The molecule is therefore capable of mediating serial lysis of target cells by a single T cell. These results highlight that central domains capable of engaging different immune effectors can be incorporated into the triplebody format to provide more individualized therapy tailored to a patient’s specific immune status.
机译:三体抗体19-3-19,一种抗体衍生的蛋白质,在一条多肽链中串联携带三个单链片段可变域。 19-3-19通过其两个远端结构域结合带有CD19的淋巴样细胞,并通过其靶向CD3的中央结构域以抗原特异性方式结合原代T细胞。在这里,恶性B淋巴样细胞系和来自B细胞恶性肿瘤患者的原代细胞被用作细胞毒性测试的靶标,并以预刺激的同种异体T细胞作为效应子。 19-3-19介导CD19阳性肿瘤细胞的特异性裂解率高达95%,在皮摩尔EC50剂量下,其溶细胞效力与临床上成功的药物Blinatumomab TM 相似。 19-3-19激活了健康无关供体的静息T细胞,并介导了自体和异体CD19阳性细胞的特异性裂解。 19-3-19导致消除了70%的CD19阳性靶细胞,即使静止的T细胞以效应子与靶细胞的比例为1:10也是如此。该分子因此能够介导靶标的系列裂解单个T细胞这些结果表明,能够结合不同免疫效应子的中枢结构域可以整合到三体抗体形式中,以提供针对患者特定免疫状况的个性化疗法。

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