CD99 tumor associated antigen is a potential target for antibody therapy of T-cell acute lymphoblastic leukemia.

Q3 Medicine
Exploration of targeted anti-tumor therapy Pub Date : 2024-01-01 Epub Date: 2024-02-19 DOI:10.37349/etat.2024.00207
Kamonporn Kotemul, Watchara Kasinrerk, Nuchjira Takheaw
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引用次数: 0

Abstract

Monoclonal antibodies (mAbs) are an effective drug for targeted immunotherapy in several cancer types. However, so far, no antibody has been successfully developed for certain types of cancer, including T-cell acute lymphoblastic leukemia (T-ALL). T-ALL is an aggressive hematologic malignancy. T-ALL patients who are treated with chemotherapeutic drugs frequently relapse and become drug resistant. Therefore, antibody-based therapy is promising for T-ALL treatment. To successfully develop an antibody-based therapy for T-ALL, antibodies that induce death in malignant T cells but not in nonmalignant T cells are required to avoid the induction of secondary T-cell immunodeficiency. In this review, CD99 tumor associated antigen, which is highly expressed on malignant T cells and lowly expressed on nonmalignant T cells, is proposed to be a potential target for antibody therapy of T-ALL. Since certain clones of anti-CD99 mAbs induce apoptosis only in malignant T cells, these anti-CD99 mAbs might be a promising antibody drug for the treatment of T-ALL with high efficiency and low adverse effects. Moreover, over the past 25 years, many clones of anti-CD99 mAbs have been studied for their direct effects on T-ALL. These outcomes are gathered here.

CD99 肿瘤相关抗原是 T 细胞急性淋巴细胞白血病抗体疗法的潜在靶点。
单克隆抗体(mAbs)是对多种癌症进行靶向免疫治疗的有效药物。然而,迄今为止,还没有针对某些类型癌症(包括 T 细胞急性淋巴细胞白血病(T-ALL))的抗体研发成功。T-ALL 是一种侵袭性血液恶性肿瘤。接受化疗药物治疗的 T-ALL 患者经常复发并产生耐药性。因此,抗体疗法在 T-ALL 治疗中大有可为。要成功开发出治疗 T-ALL 的抗体疗法,需要能诱导恶性 T 细胞死亡而非非恶性 T 细胞死亡的抗体,以避免诱导继发性 T 细胞免疫缺陷。在这篇综述中,CD99 肿瘤相关抗原被认为是 T-ALL 抗体治疗的潜在靶点,它在恶性 T 细胞中高表达,而在非恶性 T 细胞中低表达。由于某些克隆的抗 CD99 mAbs 只诱导恶性 T 细胞凋亡,因此这些抗 CD99 mAbs 有可能成为治疗 T-ALL 的高效、低不良反应的抗体药物。此外,在过去的 25 年中,许多克隆的抗 CD99 mAbs 都被研究过对 T-ALL 的直接作用。现将这些成果汇集于此。
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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来源期刊
CiteScore
2.80
自引率
0.00%
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审稿时长
13 weeks
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