首页> 外文期刊>Annals of hematology >Induction of molecular remission by using anti-CC-chemokine receptor 4 (anti-CCR4) antibodies for adult T cell leukemia: A risk of opportunistic infection after treatment with anti-CCR4 antibodies
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Induction of molecular remission by using anti-CC-chemokine receptor 4 (anti-CCR4) antibodies for adult T cell leukemia: A risk of opportunistic infection after treatment with anti-CCR4 antibodies

机译:使用抗CC趋化因子受体4(抗CCR4)抗体诱导成人T细胞白血病的分子缓解:抗CCR4抗体治疗后有机会感染的风险

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摘要

Human T cell leukemia virus type I (HTLV-I) is a human retrovirus that is an etiologic agent of adult T cell leukemia/lymphoma (ATL/ATLL) [1]. Adult ATL/ATLL is an aggressive lymphoid neoplasm associated with HTLV-1 [2]. The CC-chemokine receptor 4 (CCR4) is expressed in almost all ATLL cells [3, 4]. Thus, anti-CCR4 antibodies can be used as a treatment strategy for ATLL. Mogamulizumab (MOG), which is a defucosylated anti-CCR4 monoclonal antibody, showed good results even in patients with recurrent ATLL in phase I or II studies [5, 6]. In a phase II study of MOG for ATLL, the overall response rate was 50 % and progression-free survival and overall survival were also significantly improved [5].
机译:I型人类T细胞白血病病毒(HTLV-1)是一种人类逆转录病毒,是成人T细胞白血病/淋巴瘤(ATL / ATLL)的病原体[1]。成人ATL / ATLL是与HTLV-1相关的侵袭性淋巴瘤[2]。 CC趋化因子受体4(CCR4)在几乎所有ATLL细胞中表达[3,4]。因此,抗CCR4抗体可以用作ATLL的治疗策略。 Mogamulizumab(MOG)是一种去岩藻糖基化的抗CCR4单克隆抗体,即使在I或II期研究中复发ATLL的患者中也显示了良好的结果[5,6]。在一项针对ATLL的MOG的II期研究中,总缓解率为50%,无进展生存期和总生存期也得到了显着改善[5]。

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