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干扰素和白细胞介素与放疗联合的抗肿瘤作用。第一部分:免疫学基础

[Antitumoral action of interferons and interleukins in combination with radiotherapy. Part I: immunologic basis].

作者信息

Herskind Carsten, Fleckenstein Katharina, Lohr Jens, Li Chuan-Yuan, Wenz Frederik, Lohr Frank

机构信息

Department of Experimental Clinical Oncology, Aarhus University Hospital, Aarhus, Dänemark.

出版信息

Strahlenther Onkol. 2004 Apr;180(4):187-93. doi: 10.1007/s00066-004-9119-x.

Abstract

BACKGROUND

During the last 2 decades, cytokines such as interferons (IFN) have been used to modulate tumor response in radiotherapy. Initially, the focus was on antiviral and radiosensitizing effects of interferons but increasingly, the function of interferons and interleukins (IL) within the immune response to tumor cells is becoming important.

METHOD

The cellular immune response toward tumor cells is reviewed. The role of cytokines in antigen presentation and activation of effector cells and their interactions with radiation are described. Preclinical strategies of the antitumor action of cytokines are presented and discussed based on the induction of IFN-gamma by IL-12.

RESULTS

Recent advances in immunology have demonstrated the importance of local interactions between antigen-presenting cells (APC) and effector cells such as natural killer (NK) cells and T-lymphocytes for an effective immune reaction against tumors. Interferons stimulate such interactions, while IL-2 plays a central role in the activation of NK cells and T-lymphocytes. The interactions between APC and effector cells are suppressed by many tumors but can be stimulated by irradiation. Since systemic application of interferons is quite toxic, present strategies aim at local expression, e. g., the induction of IFN-gamma expression in Th1 cells by IL-12.

CONCLUSION

The improved understanding of immunologic mechanisms has emphasized the role of the cytokine network in the interaction between tumor cells and effector cells such as NK cells and T-lymphocytes. This opens new possibilities for the application of cytokines as biological response modifiers, which may eventually help widening the therapeutic window in radiotherapy.

摘要

背景

在过去20年中,细胞因子如干扰素(IFN)已被用于调节放疗中的肿瘤反应。最初,重点是干扰素的抗病毒和放射增敏作用,但越来越多地,干扰素和白细胞介素(IL)在对肿瘤细胞的免疫反应中的功能变得重要起来。

方法

综述了针对肿瘤细胞的细胞免疫反应。描述了细胞因子在抗原呈递和效应细胞激活中的作用及其与辐射的相互作用。基于IL-12诱导IFN-γ,提出并讨论了细胞因子抗肿瘤作用的临床前策略。

结果

免疫学的最新进展表明,抗原呈递细胞(APC)与效应细胞如自然杀伤(NK)细胞和T淋巴细胞之间的局部相互作用对于针对肿瘤的有效免疫反应至关重要。干扰素刺激这种相互作用,而IL-2在NK细胞和T淋巴细胞的激活中起核心作用。APC与效应细胞之间的相互作用受到许多肿瘤的抑制,但可被辐射刺激。由于干扰素的全身应用毒性较大,目前的策略旨在局部表达,例如通过IL-12诱导Th1细胞中IFN-γ的表达。

结论

对免疫机制的进一步理解强调了细胞因子网络在肿瘤细胞与效应细胞如NK细胞和T淋巴细胞之间相互作用中的作用。这为将细胞因子作为生物反应调节剂应用开辟了新的可能性,最终可能有助于扩大放疗的治疗窗口。

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