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白细胞介素-7的作用机制及其在癌症免疫治疗中的潜在应用与局限性

Mechanism of Action of IL-7 and Its Potential Applications and Limitations in Cancer Immunotherapy.

作者信息

Gao Jianbao, Zhao Lintao, Wan Yisong Y, Zhu Bo

机构信息

Institute of Cancer, Xinqiao Hospital, Third Military Medical University, Chongqing 400037, China.

Lineberger Comprehensive Cancer Center, University of North Carolina at Chapel Hill, Chapel Hill, NC 27599, USA.

出版信息

Int J Mol Sci. 2015 May 6;16(5):10267-80. doi: 10.3390/ijms160510267.

Abstract

Interleukin-7 (IL-7) is a non-hematopoietic cell-derived cytokine with a central role in the adaptive immune system. It promotes lymphocyte development in the thymus and maintains survival of naive and memory T cell homeostasis in the periphery. Moreover, it is important for the organogenesis of lymph nodes (LN) and for the maintenance of activated T cells recruited into the secondary lymphoid organs (SLOs). The immune capacity of cancer patients is suppressed that is characterized by lower T cell counts, less effector immune cells infiltration, higher levels of exhausted effector cells and higher levels of immunosuppressive cytokines, such as transforming growth factor β (TGF-β). Recombinant human IL-7 (rhIL-7) is an ideal solution for the immune reconstitution of lymphopenia patients by promoting peripheral T cell expansion. Furthermore, it can antagonize the immunosuppressive network. In animal models, IL-7 has been proven to prolong the survival of tumor-bearing hosts. In this review, we will focus on the mechanism of action and applications of IL-7 in cancer immunotherapy and the potential restrictions for its usage.

摘要

白细胞介素-7(IL-7)是一种由非造血细胞产生的细胞因子,在适应性免疫系统中起核心作用。它促进胸腺中的淋巴细胞发育,并维持外周幼稚和记忆性T细胞稳态的存活。此外,它对淋巴结(LN)的器官发生以及募集到二级淋巴器官(SLO)中的活化T细胞的维持也很重要。癌症患者的免疫能力受到抑制,其特征是T细胞计数较低、效应免疫细胞浸润较少、耗竭效应细胞水平较高以及免疫抑制细胞因子(如转化生长因子β(TGF-β))水平较高。重组人IL-7(rhIL-7)是通过促进外周T细胞扩增来免疫重建淋巴细胞减少患者的理想解决方案。此外,它可以拮抗免疫抑制网络。在动物模型中,IL-7已被证明可延长荷瘤宿主的生存期。在本综述中,我们将重点关注IL-7在癌症免疫治疗中的作用机制和应用以及其使用的潜在限制。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b9f1/4463645/3a797f84b17f/ijms-16-10267-g001.jpg

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