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本文引用的文献

1
Comparative kinetic analyses of gene profiles of naïve CD4+ and CD8+ T cells from young and old animals reveal novel age-related alterations.比较年轻和老年动物幼稚 CD4+ 和 CD8+ T 细胞的基因谱的动力学分析揭示了新的与年龄相关的变化。
Aging Cell. 2011 Oct;10(5):853-67. doi: 10.1111/j.1474-9726.2011.00730.x. Epub 2011 Aug 7.
2
Senescent cells as a source of inflammatory factors for tumor progression.衰老细胞作为肿瘤进展炎症因子的来源。
Cancer Metastasis Rev. 2010 Jun;29(2):273-83. doi: 10.1007/s10555-010-9220-9.
3
Prevention of infectious diseases in older adults through immunization: the challenge of the senescent immune response.通过免疫接种预防老年人传染病:衰老免疫反应的挑战。
Expert Rev Vaccines. 2009 May;8(5):593-606. doi: 10.1586/erv.09.12.
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The effect of aging on OX40 agonist-mediated cancer immunotherapy.衰老对OX40激动剂介导的癌症免疫治疗的影响。
Cancer Immunol Immunother. 2009 Dec;58(12):1941-7. doi: 10.1007/s00262-009-0687-6. Epub 2009 Mar 14.
5
OX40-enhanced tumor rejection and effector T cell differentiation decreases with age.随着年龄增长,OX40增强的肿瘤排斥和效应T细胞分化会降低。
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The mechanism of anti-CTLA-4 activity and the negative regulation of T-cell activation.抗CTLA-4活性机制及T细胞活化的负调控。
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7
Functional regulatory T cells accumulate in aged hosts and promote chronic infectious disease reactivation.功能性调节性T细胞在老年宿主中积累,并促进慢性传染病的重新激活。
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8
Implications of aging and self-tolerance on the generation of immune and antitumor immune responses.衰老和自身耐受性对免疫及抗肿瘤免疫反应产生的影响。
Cancer Res. 2008 Jul 1;68(13):5423-31. doi: 10.1158/0008-5472.CAN-07-6436.
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Regulatory T cells and immune tolerance.调节性T细胞与免疫耐受。
Cell. 2008 May 30;133(5):775-87. doi: 10.1016/j.cell.2008.05.009.
10
Inhibitory B7-family molecules in the tumour microenvironment.肿瘤微环境中的抑制性B7家族分子。
Nat Rev Immunol. 2008 Jun;8(6):467-77. doi: 10.1038/nri2326.

免疫、癌症与衰老:来自于小鼠模型的启示。

Immunity, cancer and aging: lessons from mouse models.

机构信息

Mayo Clinic College of Medicine, Department of Immunology, Mayo Clinic Arizona, USA.

出版信息

Aging Dis. 2011 Dec;2(6):512-23. Epub 2011 Dec 2.

PMID:22396898
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3295066/
Abstract

The deterioration of immune function with advancing age is associated with an increased incidence of cancer. Most of the studies to evaluate the effect of immunotherapy on cancer have been conducted in the young without considering the effect of age-associated changes in immune function. Studies from my laboratory and others groups indicate that immunotherapeutic interventions could be effective in young animals, but that the same therapies are not as effective in old animals. The present review summarizes some defects found in the old immune system affecting the activation of antitumor immune responses, the strategies used to activate a more robust antitumor immune response in the old and the description of a preclinical tumor model indicating possible strategies for optimization of immunotherapeutic interventions in the old.

摘要

随着年龄的增长,免疫功能的衰退与癌症发病率的增加有关。大多数评估免疫疗法对癌症影响的研究都是在年轻人中进行的,没有考虑到与年龄相关的免疫功能变化的影响。我的实验室和其他研究小组的研究表明,免疫治疗干预在年轻动物中可能是有效的,但在老年动物中,同样的疗法效果并不那么显著。本综述总结了一些在衰老免疫系统中发现的缺陷,这些缺陷影响了抗肿瘤免疫反应的激活,以及在老年中激活更强大的抗肿瘤免疫反应所使用的策略,并描述了一个临床前肿瘤模型,该模型为优化老年免疫治疗干预提供了可能的策略。