Pathobiological link between CD30 and abnormal lymphocytes in adult T-cell leukemia/lymphoma.

IF 1.4
Ryouichi Horie, Mariko Watanabe, Reiko Furuta, Koji Miyazaki, Toshiki Watabnabe
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Abstract

Adult T-cell leukemia/lymphoma (ATLL) is a T-cell malignancy with poor prognosis caused by human T-cell leukemia virus type 1 (HTLV-1). ATLL is characterized by the emergence of abnormal lymphocytes, represented by the so called "flower cell". However, the mechanisms by which these cells contribute to tumorigenic processes associated with HTLV-1 infection are not well understood. Recent reports have suggested that CD30, tumor necrosis factor receptor superfamily 8 plays a role in the generation of these abnormal lymphocytes, providing insight into the involvement of CD30 in the tumorigenic process of HTLV-1-infected cells. Since CD30 can be targeted with brentuximab vedotin (BV), an anti-CD30 antibody linked with monomethyl auristatin E, a tubulin toxin, it is essential to gain a deeper understanding of the functions of CD30 in HTLV-1-infected cells in order to develop effective strategies for treating and preventing ATLL. This review describes the current understanding of how CD30 impacts the development of ATLL in cells infected with HTLV-1, with a specific emphasis on the connection between CD30 and the generation of abnormal lymphocytes.

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成人t细胞白血病/淋巴瘤中CD30与异常淋巴细胞的病理生物学联系
成人t细胞白血病/淋巴瘤(Adult T-cell leukemia/lymphoma, ATLL)是由人t细胞白血病病毒1型(HTLV-1)引起的一种预后较差的t细胞恶性肿瘤。ATLL的特点是出现异常淋巴细胞,以所谓的“花细胞”为代表。然而,这些细胞参与HTLV-1感染相关致瘤过程的机制尚不清楚。最近的报道表明,CD30,肿瘤坏死因子受体超家族8在这些异常淋巴细胞的产生中起作用,这为CD30参与htlv -1感染细胞的致瘤过程提供了新的见解。由于CD30可以被brentuximab vedotin (BV)靶向,BV是一种抗CD30抗体,与一种微管蛋白毒素monomethyl auristatin E连接,因此有必要更深入地了解CD30在htlv -1感染细胞中的功能,以便制定有效的治疗和预防ATLL的策略。本文综述了目前对CD30如何影响HTLV-1感染细胞ATLL发展的理解,并特别强调了CD30与异常淋巴细胞产生之间的联系。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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