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Development of a Bispecific Antibody Targeting CD30 and CD137 on Hodgkin and Reed-Sternberg Cells

机译:在霍奇金和里德-斯特恩伯格细胞上靶向CD30和CD137的双特异性抗体的发展。

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摘要

Hodgkin Lymphoma (HL) is a malignancy that frequently affects young adults. Although, there are effective treatments not every patient responds, necessitating the development of novel therapeutic approaches, especially for relapsed and refractory cases. The two TNF receptor family members CD30 and CD137 are expressed on Hodgkin and Reed Sternberg (HRS) cells, the malignant cells in HL. We found that this co-expression is specific for HRS cells. Based on this discovery we developed a bispecific antibody that binds preferentially to the CD30, CD137-double positive HRS cells. The CD30, CD137 bispecific antibody gets internalized into HRS cells opening up the possibility to use it as a carrier for a toxin. This antibody also induces antibody-dependent, cell-mediated cytotoxicity in CD30, CD137-double positive HRS cells. The enhances specificity of the CD30, CD137 bispecific antibody to HRS cells makes it a promising candidate for development as a novel HL treatment.
机译:霍奇金淋巴瘤(HL)是一种恶性肿瘤,经常影响年轻人。尽管有有效的治疗方法,但并不是每位患者都能做出反应,因此有必要开发新的治疗方法,尤其是对于复发和难治性病例。在HL的恶性细胞Hodgkin和Reed Sternberg(HRS)细胞上表达了两个TNF受体家族成员CD30和CD137。我们发现这种共表达是专门针对HRS细胞的。基于这一发现,我们开发了一种优先结合CD30,CD137-双阳性HRS细胞的双特异性抗体。 CD30,CD137双特异性抗体被内化到HRS细胞中,从而打开了将其用作毒素载体的可能性。该抗体还在CD30,CD137-双阳性HRS细胞中诱导抗体依赖性细胞介导的细胞毒性。 CD30,CD137双特异性抗体对HRS细胞的特异性增强,使其成为一种有望作为新型HL治疗药物开发的候选药物。

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