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  4. Tertiary Lymphoid Structures and B cells: Clinical impact and therapeutic modulation in cancer
 
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Tertiary Lymphoid Structures and B cells: Clinical impact and therapeutic modulation in cancer

Journal
Seminars in Immunology
Journal Volume
48
Date Issued
2020
Author(s)
Saut?s-Fridman C.
Verneau J.
Sun C.-M.
Moreira M.
WEI-WU CHEN  
Meylan M.
Petitprez F.
Fridman W.H.
DOI
10.1016/j.smim.2020.101406
URI
https://www.scopus.com/inward/record.uri?eid=2-s2.0-85097394323&doi=10.1016%2fj.smim.2020.101406&partnerID=40&md5=55c56bdd303b0f6bbc87fd5c0fb491ac
https://scholars.lib.ntu.edu.tw/handle/123456789/597536
Abstract
Tumors progression is under the control of a heterogeneous microenvironment composed of immune cells, fibroblasts, blood and lymphatic vessels, in which T cells have been demonstrated to be major actors, through their cytotoxic and cytokine producing effector functions and their long term memory that protects against metastasis. In this scenario, lessons from mouse models taught that B cells exert a protumoral role, via macrophage-dependent activation of inflammation. However, it became progressively evident from studies in patients with human cancers that the anti-tumor responses can be generated and controlled in tertiary lymphoid structures (TLS) that concentrate most of the intratumoral B cells and where B cells can differentiate into plasma cells and memory cells. Furthermore, recent studies demonstrated that the presence in tumors of B cells and TLS are associated with favorable outcome in patients treated by immunotherapy, unraveling TLS as a new predictive marker of anti-tumor response human cancers. This review encompasses the characteristics and functions of TLS and of B cells in human tumors, their prognostic and theranostic impact and summarizes the mouse models used to induce TLS neogenesis in tumors. ? 2020 Elsevier Ltd
Subjects
Adaptive anti-tumor response; B cells; Clinical outcome; Immunotherapy; Prognosis; Tertiary lymphoid structures
SDGs

[SDGs]SDG3

Other Subjects
antineoplastic agent; antineoplastic monoclonal antibody; chemokine; cytokine; pharmacological biomarker; tumor marker; B lymphocyte; cancer chemotherapy; cancer immunotherapy; cancer prognosis; carcinogenesis; cell function; clinical outcome; human; immunocompetent cell; immunomodulation; lymphocyte differentiation; malignant neoplasm; mouse model; neoadjuvant chemotherapy; nonhuman; preclinical study; Review; single cell RNA seq; stroma cell; T lymphocyte activation; tertiary lymphoid structure; animal; B lymphocyte; immunology; immunomodulation; immunotherapy; neoplasm; procedures; T lymphocyte; tertiary lymphoid structure; tumor microenvironment; Animals; B-Lymphocytes; Biomarkers, Pharmacological; Biomarkers, Tumor; Humans; Immunomodulation; Immunotherapy; Neoplasms; T-Lymphocytes; Tertiary Lymphoid Structures; Tumor Microenvironment
Publisher
Academic Press
Type
review

臺大位居世界頂尖大學之列,為永久珍藏及向國際展現本校豐碩的研究成果及學術能量,圖書館整合機構典藏(NTUR)與學術庫(AH)不同功能平台,成為臺大學術典藏NTU scholars。期能整合研究能量、促進交流合作、保存學術產出、推廣研究成果。

To permanently archive and promote researcher profiles and scholarly works, Library integrates the services of “NTU Repository” with “Academic Hub” to form NTU Scholars.

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開放取用是從使用者角度提升資訊取用性的社會運動,應用在學術研究上是透過將研究著作公開供使用者自由取閱,以促進學術傳播及因應期刊訂購費用逐年攀升。同時可加速研究發展、提升研究影響力,NTU Scholars即為本校的開放取用典藏(OA Archive)平台。(點選深入了解OA)

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