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白细胞介素-21 在癌症中的治疗潜力

英文原题:Therapeutic potential of interleukin-21 in cancer.

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Therapeutic potential of interleukin-21 in cancer.

PubMed 2024/04/04(内容时间) Front Immunol Q1 · IF 7(JCR 2025)

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中文摘要

白细胞介素-21(IL-21)是一种免疫刺激性细胞因子,属于共同γ链家族细胞因子。它在免疫细胞,特别是T细胞和自然杀伤(NK)细胞的发育、分化、增殖和活化中发挥重要作用。自2000年被发现以来,IL-21已被证明可调节适应性免疫应答和免疫应答,在抗病毒和抗肿瘤反应中具有关键作用。近期进展表明,IL-21是一个有前景的癌症治疗靶点,在临床前研究中获得了令人鼓舞的结果,这些研究探讨了IL-21单独或与其他疗法联合使用的效力,包括单克隆抗体、检查点抑制分子、溶瘤病毒治疗和过继性细胞转移。此外,在多项临床试验中,IL-21在晚期癌症患者的治疗中显示出抗肿瘤效果,且副作用极小。在本综述中,我们将概述IL-21研究的最新进展,重点介绍基于IL-21的疗法作为单药或与其他药物联合使用以提高癌症治疗效率的潜力。

展开英文摘要原文

Interleukin-21 (IL-21) is an immunostimulatory cytokine which belongs to the common gamma-chain family of cytokines. It plays an import role in the development, differentiation, proliferation, and activation of immune cells, in particular T and natural killer (NK) cells. Since its discovery in 2000, IL-21 has been shown to regulate both adaptive and immune responses associates with key role in antiviral and antitumor responses.

Recent advances indicate IL-21 as a promising target for cancer treatment and encouraging results were obtained in preclinical studies which investigated the potency of IL-21 alone or in combination with other therapies, including monoclonal antibodies, checkpoint inhibitory molecules, oncolytic virotherapy, and adoptive cell transfer.

Furthermore, IL-21 showed antitumor effects in the treatment of patients with advanced cancer, with minimal side effects in several clinical trials. In the present review, we will outline the recent progress in IL-21 research, highlighting the potential of IL-21 based therapy as single agent or in combination with other drugs to enhance cancer treatment efficiency.

论文信息

作者
Isvoranu G、Chiritoiu-Butnaru M
第一作者单位
Department of Animal Husbandry," Victor Babeș" National Institute of Pathology, Bucharest, Romania.Romania
通讯作者单位
Department of Molecular and Cell Biology, Institute of Biochemistry of the Romanian Academy, Bucharest, Romania.Italy
文献类型
综述 · 非美国政府资助研究
期刊
Frontiers in immunology2024
原文标识
PubMed 38638431 · DOI 10.3389/fimmu.2024.1369743