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一种双特异性 G 蛋白偶联受体家族 5 成员 D x CD3 T 细胞导向抗体,用于治疗多发性骨髓瘤。

A T-cell-redirecting bispecific G-protein-coupled receptor class 5 member D x CD3 antibody to treat multiple myeloma.

机构信息

Oncology, Janssen Research & Development, LLC, Spring House, PA.

Janssen Biotherapeutics, Janssen Research & Development, LLC, La Jolla, CA; and.

出版信息

Blood. 2020 Apr 9;135(15):1232-1243. doi: 10.1182/blood.2019003342.

DOI:10.1182/blood.2019003342
PMID:32040549
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7146017/
Abstract

T-cell-mediated approaches have shown promise in myeloma treatment. However, there are currently a limited number of specific myeloma antigens that can be targeted, and multiple myeloma (MM) remains an incurable disease. G-protein-coupled receptor class 5 member D (GPRC5D) is expressed in MM and smoldering MM patient plasma cells. Here, we demonstrate that GPRC5D protein is present on the surface of MM cells and describe JNJ-64407564, a GPRC5DxCD3 bispecific antibody that recruits CD3+ T cells to GPRC5D+ MM cells and induces killing of GPRC5D+ cells. In vitro, JNJ-64407564 induced specific cytotoxicity of GPRC5D+ cells with concomitant T-cell activation and also killed plasma cells in MM patient samples ex vivo. JNJ-64407564 can recruit T cells and induce tumor regression in GPRC5D+ MM murine models, which coincide with T-cell infiltration at the tumor site. This antibody is also able to induce cytotoxicity of patient primary MM cells from bone marrow, which is the natural site of this disease. GPRC5D is a promising surface antigen for MM immunotherapy, and JNJ-64407564 is currently being evaluated in a phase 1 clinical trial in patients with relapsed or refractory MM (NCT03399799).

摘要

T 细胞介导的方法在骨髓瘤治疗中显示出前景。然而,目前能够靶向的特定骨髓瘤抗原数量有限,多发性骨髓瘤(MM)仍然是一种不可治愈的疾病。G 蛋白偶联受体家族 5 成员 D(GPRC5D)在 MM 和冒烟型 MM 患者浆细胞中表达。在这里,我们证明 GPRC5D 蛋白存在于 MM 细胞表面,并描述了 JNJ-64407564,一种 GPRC5DxCD3 双特异性抗体,它可将 CD3+T 细胞募集到 GPRC5D+MM 细胞上,并诱导 GPRC5D+细胞的杀伤。在体外,JNJ-64407564 诱导了 GPRC5D+细胞的特异性细胞毒性,同时伴随着 T 细胞的激活,并在体外杀死了 MM 患者样本中的浆细胞。JNJ-64407564 可招募 T 细胞并诱导 GPRC5D+MM 鼠模型中的肿瘤消退,这与肿瘤部位的 T 细胞浸润相吻合。该抗体还能够诱导患者骨髓中原发性 MM 细胞的细胞毒性,这是该疾病的自然部位。GPRC5D 是 MM 免疫治疗的一个有前途的表面抗原,JNJ-64407564 目前正在复发或难治性 MM 患者的 I 期临床试验中进行评估(NCT03399799)。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8300/7146017/50ca635d9079/bloodBLD2019003342absf1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8300/7146017/50ca635d9079/bloodBLD2019003342absf1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8300/7146017/50ca635d9079/bloodBLD2019003342absf1.jpg

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N Engl J Med. 2019 May 2;380(18):1726-1737. doi: 10.1056/NEJMoa1817226.
3
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