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淋巴系统对癌症免疫和转移的调节。

Lymphatic system regulation of anti-cancer immunity and metastasis.

机构信息

Edwin L. Steele Laboratories for Tumor Biology, Department of Radiation Oncology, Massachusetts General Hospital Cancer Center, Massachusetts General Hospital and Harvard Medical School, Boston, MA, United States.

Department of Molecular Metabolism, Harvard T.H. Chan School of Public Health, Boston, MA, United States.

出版信息

Front Immunol. 2024 Aug 15;15:1449291. doi: 10.3389/fimmu.2024.1449291. eCollection 2024.


DOI:10.3389/fimmu.2024.1449291
PMID:39211044
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11357954/
Abstract

Cancer dissemination to lymph nodes (LN) is associated with a worse prognosis, increased incidence of distant metastases and reduced response to therapy. The LN microenvironment puts selective pressure on cancer cells, creating cells that can survive in LN as well as providing survival advantages for distant metastatic spread. Additionally, the presence of cancer cells leads to an immunosuppressive LN microenvironment, favoring the evasion of anti-cancer immune surveillance. However, recent studies have also characterized previously unrecognized roles for tumor-draining lymph nodes (TDLNs) in cancer immunotherapy response, including acting as a reservoir for pre-exhausted CD8+ T cells and stem-like CD8+ T cells. In this review, we will discuss the spread of cancer cells through the lymphatic system, the roles of TDLNs in metastasis and anti-cancer immune responses, and the therapeutic opportunities and challenges in targeting LN metastasis.

摘要

癌症向淋巴结(LN)的扩散与预后更差、远处转移发生率增加以及对治疗的反应降低有关。LN 微环境对癌细胞施加选择性压力,产生能够在 LN 中存活的细胞,并为远处转移扩散提供生存优势。此外,癌细胞的存在导致 LN 微环境的免疫抑制,有利于逃避抗肿瘤免疫监视。然而,最近的研究也描述了肿瘤引流淋巴结(TDLNs)在癌症免疫治疗反应中的先前未被认识的作用,包括作为耗尽的 CD8+T 细胞和类干细胞 CD8+T 细胞的储存库。在这篇综述中,我们将讨论癌细胞通过淋巴系统的扩散、TDLNs 在转移和抗肿瘤免疫反应中的作用,以及靶向 LN 转移的治疗机会和挑战。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0118/11357954/8ab6134758a3/fimmu-15-1449291-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0118/11357954/f451b4508032/fimmu-15-1449291-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0118/11357954/d32a0cf8a2be/fimmu-15-1449291-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0118/11357954/8ab6134758a3/fimmu-15-1449291-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0118/11357954/f451b4508032/fimmu-15-1449291-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0118/11357954/d32a0cf8a2be/fimmu-15-1449291-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0118/11357954/8ab6134758a3/fimmu-15-1449291-g003.jpg

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本文引用的文献

[1]
Delayed tumor-draining lymph node irradiation preserves the efficacy of combined radiotherapy and immune checkpoint blockade in models of metastatic disease.

Nat Commun. 2024-6-29

[2]
Targeting lymph nodes for enhanced cancer vaccination: From nanotechnology to tissue engineering.

Mater Today Bio. 2024-4-26

[3]
Durable lymph-node expansion is associated with the efficacy of therapeutic vaccination.

Nat Biomed Eng. 2024-10

[4]
Vitamin D regulates microbiome-dependent cancer immunity.

Science. 2024-4-26

[5]
Lymphatic vessels in the age of cancer immunotherapy.

Nat Rev Cancer. 2024-6

[6]
A call for accessible tools to unlock single-cell immunometabolism research.

Nat Metab. 2024-5

[7]
Omitting Axillary Dissection in Breast Cancer with Sentinel-Node Metastases.

N Engl J Med. 2024-4-4

[8]
Lymph-targeted high-density lipoprotein-mimetic nanovaccine for multi-antigenic personalized cancer immunotherapy.

Sci Adv. 2024-3-15

[9]
Anti-PD-1 therapy triggers Tfh cell-dependent IL-4 release to boost CD8 T cell responses in tumor-draining lymph nodes.

J Exp Med. 2024-4-1

[10]
Lymph Node-Targeted Vaccine Boosting of TCR T-cell Therapy Enhances Antitumor Function and Eradicates Solid Tumors.

Cancer Immunol Res. 2024-2-2

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