抗cd40激动剂抗体:临床前和临床经验

Magi Khalil, Robert H. Vonderheide
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引用次数: 67

摘要

细胞表面分子CD40是肿瘤坏死因子受体超家族的一员,广泛调控免疫激活并介导肿瘤凋亡。CD40由抗原呈递细胞(APC)表达,其天然配体与T细胞结合可激活APC,包括树突状细胞和B细胞。在小鼠T细胞介导免疫模型中,激动性CD40抗体已被证明可以替代CD4+淋巴细胞提供的T细胞帮助。在携带肿瘤的宿主中,CD40激动剂可触发针对肿瘤相关抗原的有效免疫反应。相反,CD40也在许多肿瘤细胞上表达,在这种情况下,它的结扎介导了直接的细胞毒性作用。CD40作用于肿瘤细胞导致体外细胞凋亡和体内肿瘤生长受损。这些观察结果促使人们努力使用激动性CD40抗体来治疗癌症患者,初步临床结果很有希望。
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Anti-CD40 agonist antibodies: Preclinical and clinical experience

The cell-surface molecule CD40, a member of the tumor necrosis factor receptor superfamily, broadly regulates immune activation and mediates tumor apoptosis. CD40 is expressed by antigen-presenting cells (APC) and engagement of its natural ligand on T cells activates APC including dendritic cells and B cells. Agonistic CD40 antibodies have been shown to substitute for T cell help provided by CD4+ lymphocytes in murine models of T cell-mediated immunity. In tumor-bearing hosts, CD40 agonists trigger effective immune responses against tumor-associated antigens. In contrast, CD40 is also expressed on many tumor cells and its ligation in this setting mediates a direct cytotoxic effect. Engagement of CD40 on tumor cells results in apoptosis in vitro and impaired tumor growth in vivo. These observations have prompted efforts to use agonistic CD40 antibodies for the treatment of cancer patients and initial clinical results have been promising.

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