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肿瘤微环境与抗肿瘤治疗在淋巴增殖性综合征中的免疫效应。

Tumor microenvironment and immune effects of antineoplastic therapy in lymphoproliferative syndromes.

作者信息

Alvaro Tomás, de la Cruz-Merino Luis, Henao-Carrasco Fernando, Villar Rodríguez José Luis, Vicente Baz David, Codes Manuel de Villena Manuel, Provencio Mariano

机构信息

Pathology Department, Hospital de Tortosa Verge de la Cinta, 41300 Tortosa, Spain.

出版信息

J Biomed Biotechnol. 2010;2010. doi: 10.1155/2010/846872. Epub 2010 Aug 12.

DOI:10.1155/2010/846872
PMID:20814546
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC2931385/
Abstract

Lymphomas represent a wide group of heterogenic diseases with different biological and clinical behavior. The underlying microenvironment-specific composition seems to play an essential role in this scenario, harboring the ability to develop successful immune responses or, on the contrary, leading to immune evasion and even promotion of tumor growth. Depending on surrounding lymphoid infiltrates, lymphomas may have different prognosis. Moreover, recent evidences have emerged that confer a significant impact of main lymphoma's treatment over microenvironment, with clinical consequences. In this review, we summarize these concepts from a pathological and clinical perspective. Also, the state of the art of lymphoma's anti-idiotype vaccine development is revised, highlighting the situations where this strategy has proven to be successful and eventual clues to obtain better results in the future.

摘要

淋巴瘤是一大类具有不同生物学和临床行为的异质性疾病。潜在的微环境特异性组成似乎在这种情况下起着至关重要的作用,它具有引发成功免疫反应的能力,或者相反,导致免疫逃逸甚至促进肿瘤生长。根据周围的淋巴细胞浸润情况,淋巴瘤可能有不同的预后。此外,最近有证据表明,主要淋巴瘤治疗对微环境有重大影响,并产生临床后果。在本综述中,我们从病理学和临床角度总结了这些概念。此外,还对淋巴瘤抗独特型疫苗的发展现状进行了综述,强调了该策略已被证明成功的情况以及未来取得更好结果的潜在线索。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/387d/2931385/f6dc77f4cf0d/JBB2010-846872.001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/387d/2931385/f6dc77f4cf0d/JBB2010-846872.001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/387d/2931385/f6dc77f4cf0d/JBB2010-846872.001.jpg

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本文引用的文献

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Tumor-reactive CD4(+) T cells develop cytotoxic activity and eradicate large established melanoma after transfer into lymphopenic hosts.肿瘤反应性 CD4(+) T 细胞在转移到淋巴耗竭宿主后会发展出细胞毒性活性,并根除已建立的大型黑色素瘤。
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