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T细胞招募三体分子19-3-19介导单个T细胞对恶性B淋巴细胞的连续裂解。

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

作者信息

Roskopf Claudia C, Schiller Christian B, Braciak Todd A, Kobold Sebastian, Schubert Ingo A, Fey Georg H, Hopfner Karl-Peter, Oduncu Fuat S

机构信息

Klinikum der Universität München, Medizinische Klinik und Poliklinik IV, Haematology/Oncology, Munich, Germany.

Ludwig-Maximilians-Universität München, Department of Biochemistry/Gene Center, Munich, Germany.

出版信息

Oncotarget. 2014 Aug 15;5(15):6466-83. doi: 10.18632/oncotarget.2238.

Abstract

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 Blinatumomab. 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.

摘要

三体型19-3-19是一种源自抗体的蛋白质,在一条多肽链中串联携带三个单链可变区片段。19-3-19通过其两个远端结构域以抗原特异性方式结合携带CD19的淋巴细胞,并通过其靶向CD3的中央结构域结合原代T细胞。在这里,恶性B淋巴细胞系和B细胞恶性肿瘤患者的原代细胞被用作细胞毒性试验的靶标,预刺激的同种异体T细胞作为效应细胞。19-3-19介导了高达95%的CD19阳性肿瘤细胞的特异性裂解,并且在皮摩尔EC₅₀剂量下,具有与临床成功药物博纳吐单抗相似的细胞溶解效力。19-3-19激活了来自健康无关供体的静息T细胞,并介导了自体和同种异体CD19阳性细胞的特异性裂解。即使以1:10的效应细胞与靶细胞比例使用静息T细胞作为效应细胞,19-3-19也能导致70%的CD19阳性靶细胞被清除。因此,该分子能够介导单个T细胞对靶细胞的连续裂解。这些结果突出表明,能够与不同免疫效应器结合的中央结构域可以被纳入三体型形式,以提供更适合患者特定免疫状态的个性化治疗。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b3a1/4171644/00ec07299fc9/oncotarget-05-6466-g003.jpg

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