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肿瘤诱导的前哨淋巴结免疫调节

Tumour-induced immune modulation of sentinel lymph nodes.

作者信息

Cochran Alistair J, Huang Rong-Rong, Lee Jonathan, Itakura Eijun, Leong Stanley P L, Essner Richard

机构信息

Department of Pathology and Laboratory Medicine, David Geffen School of Medicine at the University of California at Los Angeles, California 90095, USA.

出版信息

Nat Rev Immunol. 2006 Sep;6(9):659-70. doi: 10.1038/nri1919.

Abstract

Sentinel lymph nodes (SLNs), being the first nodes to receive lymph from a primary tumour and the preferential site of initial tumour metastases, are intensively exposed to the bioactive products of tumour cells and other associated cells. This makes them ideal for studies of the factors that determine selective tissue susceptibility to metastases. We postulate that tumour-induced immune modulation of SLNs facilitates lymph-node metastases by inhibiting the generation of tumour-specific cytotoxic T cells that are active against tumour cells of primary and metastatic melanomas. Immune modulation of the lymph nodes can be reversed by granulocyte/macrophage colony-stimulating factor (GM-CSF), a finding that has implications for the future therapy of lymph-node metastases.

摘要

前哨淋巴结(SLN)作为首个接收来自原发肿瘤淋巴液的淋巴结以及肿瘤最初转移的优先部位,会大量接触肿瘤细胞和其他相关细胞的生物活性产物。这使得它们成为研究决定组织对转移选择性易感性因素的理想对象。我们推测,肿瘤对前哨淋巴结的免疫调节通过抑制针对原发性和转移性黑色素瘤肿瘤细胞具有活性的肿瘤特异性细胞毒性T细胞的产生,促进了淋巴结转移。淋巴结的免疫调节可通过粒细胞/巨噬细胞集落刺激因子(GM-CSF)逆转,这一发现对淋巴结转移的未来治疗具有重要意义。

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