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黑色素瘤患者前哨淋巴结中的朗格汉斯细胞。

Langerhans Cells in Sentinel Lymph Nodes from Melanoma Patients.

作者信息

Gerlini Gianni, Susini Pietro, Sestini Serena, Brandani Paola, Giannotti Vanni, Borgognoni Lorenzo

机构信息

Plastic and Reconstructive Surgery Unit, Regional Melanoma Referral Center and Melanoma & Skin Cancer Unit, Santa Maria Annunziata Hospital, 50012 Florence, Italy.

Plastic Surgery Unit, Department of Medicine, Surgery and Neuroscience, University of Siena, 53100 Siena, Italy.

出版信息

Cancers (Basel). 2024 May 16;16(10):1890. doi: 10.3390/cancers16101890.

Abstract

BACKGROUND

Langerhans cells (LCs) are professional Dendritic Cells (DCs) involved in immunoregulatory functions. At the skin level, LCs are immature. In response to tissue injuries, they migrate to regional Lymph Nodes (LNs), reaching a full maturation state. Then, they become effective antigen-presenting cells (APCs) that induce anti-cancer responses. Notably, melanoma patients present several DC alterations in the Sentinel Lymph Node (SLN), where primary antitumoral immunity is generated. LCs are the most represented DCs subset in melanoma SLNs and are expected to play a key role in the anti-melanoma response. With this paper, we aim to review the current knowledge and future perspectives regarding LCs and melanoma.

METHODS

A systematic review was carried out according to the PRISMA statement using the PubMed (MEDLINE) library from January 2004 to January 2024, searching for original studies discussing LC in melanoma.

RESULTS

The final synthesis included 15 articles. Several papers revealed significant LCs-melanoma interactions.

CONCLUSIONS

Melanoma immune escape mechanisms include SLN LC alterations, favoring LN metastasis arrival/homing and melanoma proliferation. The SLN LCs of melanoma patients are defective but not irreversibly, and their function may be restored by appropriate stimuli. Thus, LCs represent a promising target for future immunotherapeutic strategies and cancer vaccines.

摘要

背景

朗格汉斯细胞(LCs)是参与免疫调节功能的专职树突状细胞(DCs)。在皮肤层面,LCs不成熟。响应组织损伤时,它们迁移至区域淋巴结(LNs),达到完全成熟状态。然后,它们成为诱导抗癌反应的有效抗原呈递细胞(APCs)。值得注意的是,黑色素瘤患者在前哨淋巴结(SLN)中存在多种DC改变,而前哨淋巴结是产生原发性抗肿瘤免疫的部位。LCs是黑色素瘤前哨淋巴结中最具代表性的DC亚群,有望在抗黑色素瘤反应中发挥关键作用。本文旨在综述关于LCs与黑色素瘤的现有知识及未来展望。

方法

根据PRISMA声明,利用2004年1月至2024年1月的PubMed(MEDLINE)数据库进行系统综述,检索讨论黑色素瘤中LCs的原始研究。

结果

最终纳入15篇文章。多篇论文揭示了LCs与黑色素瘤之间存在显著相互作用。

结论

黑色素瘤免疫逃逸机制包括前哨淋巴结LCs改变,有利于淋巴结转移的到达/归巢及黑色素瘤增殖。黑色素瘤患者的前哨淋巴结LCs存在缺陷,但并非不可逆转,其功能可通过适当刺激恢复。因此,LCs是未来免疫治疗策略和癌症疫苗的一个有前景的靶点。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/98b8/11119378/e6014038466e/cancers-16-01890-g001.jpg

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