与非结缔组织增生黑色素瘤相比,结缔组织增生黑色素瘤的三级淋巴样结构具有更高的淋巴细胞密度、淋巴细胞增殖和与肿瘤的免疫串扰。

IF 7.2 2区 医学
Nicole L Edmonds, Sarah E Gradecki, Priya Katyal, Kevin T Lynch, Anne M Stowman, Alejandro A Gru, Victor H Engelhard, Craig L Slingluff, Ileana S Mauldin
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引用次数: 1

摘要

三级淋巴样结构(TLS)是一种异位淋巴样结构,可在人类癌症中出现,并与几种癌症(包括非结缔组织增生转移性黑色素瘤(NDMM))的总生存率(OS)和免疫检查点封锁(ICB)反应的改善有关。结缔组织增生性黑色素瘤(DM)对ICB的应答率最高,我们之前发现原发性DM (PDM)含有TLS。尽管TLS与生存和ICB应答相关,但尚不清楚TLS或相关免疫活性标志物在PDM和NDMM之间是否存在差异。我们假设PDM的TLS频率高于NDMM, PDM的TLS中T细胞和b细胞的密度和增殖率高于NDMM的TLS, PDM TLS中T细胞和b细胞的增殖率与肿瘤内淋巴细胞的增殖率一致。我们发现PDM中的TLS与NDMM中的TLS有四个不同之处。NDMM多发于肿瘤周围,PDM多发于肿瘤内。CD8+ t细胞和CD20+ b细胞密度和增殖分数在PDM TLS中高于NDMM TLS。此外,T细胞和b细胞的增殖分数在PDM的TLS和肿瘤部位之间是一致的,而在NDMM中是不一致的。总的来说,这些数据表明TLS和相关免疫标记物在黑色素瘤亚群中可能存在差异,并且表明与NDMM相比,PDM TLS可能具有更高的免疫活性,并且增强了肿瘤和TLS之间的免疫细胞运输。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Tertiary lymphoid structures in desmoplastic melanoma have increased lymphocyte density, lymphocyte proliferation, and immune cross talk with tumor when compared to non-desmoplastic melanomas.

Tertiary lymphoid structures in desmoplastic melanoma have increased lymphocyte density, lymphocyte proliferation, and immune cross talk with tumor when compared to non-desmoplastic melanomas.

Tertiary lymphoid structures in desmoplastic melanoma have increased lymphocyte density, lymphocyte proliferation, and immune cross talk with tumor when compared to non-desmoplastic melanomas.

Tertiary lymphoid structures in desmoplastic melanoma have increased lymphocyte density, lymphocyte proliferation, and immune cross talk with tumor when compared to non-desmoplastic melanomas.

Tertiary lymphoid structures (TLS) are ectopic lymphoid structures that can arise in human cancers and are associated with improved overall survival (OS) and response to immune checkpoint blockade (ICB) in several cancers, including non-desmoplastic metastatic melanoma (NDMM). Desmoplastic melanoma (DM) has one of the highest response rates to ICB, and we previously identified that primary DM (PDM) contains TLS. Despite the association of TLS with survival and ICB response, it is unknown whether TLS or associated markers of immune activity can differ between PDM and NDMM. We hypothesized that PDM would contain higher frequencies of TLS than NDMM, that T and B-cell densities and proliferation would be greater in TLS of PDM than TLS of NDMM, and that proliferation rates of T and B-cells in PDM TLS would be concordant with those of intratumoral lymphocytes. We found that four features of TLS in PDM distinguish them from TLS in NDMM. TLS were peritumoral in NDMM but intratumoral in PDM. CD8+ T-cell and CD20+ B-cell densities and proliferative fractions were higher in PDM TLS than NDMM TLS. Additionally, the proliferative fractions of T- and B-cells were concordant between the TLS and tumor site in PDM and discordant in NDMM. Collectively, these data suggest that TLS and associated immune markers can differ across melanoma subsets and suggest that PDM TLS may be more immunologically active and have enhanced immune cell trafficking between tumor and TLS compared to NDMM.

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来源期刊
Oncoimmunology
Oncoimmunology ONCOLOGY-IMMUNOLOGY
CiteScore
12.80
自引率
2.80%
发文量
276
期刊介绍: Tumor immunology explores the natural and therapy-induced recognition of cancers, along with the complex interplay between oncogenesis, inflammation, and immunosurveillance. In response to recent advancements, a new journal, OncoImmunology, is being launched to specifically address tumor immunology. The field has seen significant progress with the clinical demonstration and FDA approval of anticancer immunotherapies. There's also growing evidence suggesting that many current chemotherapeutic agents rely on immune effectors for their efficacy. While oncologists have historically utilized chemotherapeutic and radiotherapeutic regimens successfully, they may have unwittingly leveraged the immune system's ability to recognize tumor-specific antigens and control cancer growth. Consequently, immunological biomarkers are increasingly crucial for cancer prognosis and predicting chemotherapy efficacy. There's strong support for combining conventional anticancer therapies with immunotherapies. OncoImmunology will welcome high-profile submissions spanning fundamental, translational, and clinical aspects of tumor immunology, including solid and hematological cancers, inflammation, and both innate and acquired immune responses.
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