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完全人源化的HLA-DR特异性单克隆抗体可有效诱导恶性淋巴细胞的程序性死亡。

Fully human, HLA-DR-specific monoclonal antibodies efficiently induce programmed death of malignant lymphoid cells.

作者信息

Nagy Zoltan A, Hubner Bernd, Löhning Corinna, Rauchenberger Robert, Reiffert Silke, Thomassen-Wolf Elisabeth, Zahn Stefan, Leyer Sigmar, Schier Eva M, Zahradnik Angelika, Brunner Christoph, Lobenwein Kurt, Rattel Benno, Stanglmaier Michael, Hallek Michael, Wing Mark, Anderson Steve, Dunn Matt, Kretzschmar Titus, Tesar Michael

机构信息

GPC Biotech AG, Martinsried/Munich, Germany.

出版信息

Nat Med. 2002 Aug;8(8):801-7. doi: 10.1038/nm736. Epub 2002 Jul 8.

Abstract

The Human Combinatorial Antibody Library (HuCAL) was screened for antibodies specific to human leukocyte antigen-DR (HLA-DR) that induce programmed death of lymphoma/leukemia cells expressing the target antigen. The active Fab fragments were affinity-matured, and engineered to IgG(4) antibodies of sub-nanomolar affinity. The antibodies exhibited potent in vitro tumoricidal activity on several lymphoma and leukemia cell lines and on chronic lymphocytic leukemia patient samples. They were also active in vivo in xenograft models of non-Hodgkin lymphoma. Cell death occurred rapidly, without the need for exogenous immunological effector mechanisms, and was selective to activated/tumor-transformed cells. Although the expression of HLA-DR on normal hematopoietic cells is a potential safety concern, the antibodies caused no long-lasting hematological toxicity in primates, in vivo. Such monoclonal antibodies offer the potential for a novel therapeutic approach to lymphoid malignancies.

摘要

对人组合抗体文库(HuCAL)进行筛选,以寻找对人白细胞抗原-DR(HLA-DR)具有特异性的抗体,这些抗体可诱导表达靶抗原的淋巴瘤/白血病细胞发生程序性死亡。对活性Fab片段进行亲和力成熟,并将其工程化为具有亚纳摩尔亲和力的IgG(4)抗体。这些抗体在几种淋巴瘤和白血病细胞系以及慢性淋巴细胞白血病患者样本上表现出强大的体外杀瘤活性。它们在非霍奇金淋巴瘤的异种移植模型中也具有体内活性。细胞死亡迅速发生,无需外源性免疫效应机制,并且对活化/肿瘤转化细胞具有选择性。尽管HLA-DR在正常造血细胞上的表达是一个潜在的安全问题,但这些抗体在灵长类动物体内并未引起持久的血液学毒性。此类单克隆抗体为淋巴恶性肿瘤提供了一种新型治疗方法的潜力。

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