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对与卡波西肉瘤相关的T细胞中克隆性抗原受体基因重排的分析。

Analysis of clonal antigen receptor gene rearrangements in T-cells involved with Kaposi's sarcoma.

作者信息

Alaibac M, Congedo M, Barbarossa G, Bottiglieri A, Fillippi E D, Marzullo F, Quarta G, Schittulli F

机构信息

Laboratory of Experimental Oncology, National Oncology Institute, Bari, Italy.

出版信息

Anticancer Res. 1997 Mar-Apr;17(2A):1205-7.

PMID:9137472
Abstract

Kaposi's sarcoma (KS) is a multifocal neoplasm of unknown origin. All forms of KS are composed of spindle-shaped cells with elongated nuclei and sheets of endothelial-like cells. The proliferation of spindle cells is accompanied by the presence of an inflammatory infiltrate composed predominantly of T-cells. It has been suggested that this infiltrate might consist of a virally stimulated clonal population of T-lymphocytes which can produce growth factors initiating and substaining the proliferation of spindle-shaped cells. In this study we analyzed for clonal T-cell receptor gama gene rearrangements the T-cell populations present in the cutaneous infiltrate of seven cases of classical Kaposi's sarcoma using a polymerase chain reaction-based approach. Our data demonstrate the lack of a significant clonal population of T-cells in the cutaneous infiltrates of KS. This finding is indicative of a reactive polyclonal response of T-cells to the spindle-shaped cells and supports the contention that spindle-shaped cells are pathogenetically the central cell type in the disease. Our data also indicate that the anti-KS T-cell response, being polyclonal in nature, does not result from clonal expansion of T-cells targeting tumor-associated antigenic peptides.

摘要

卡波西肉瘤(KS)是一种起源不明的多灶性肿瘤。所有类型的KS均由具有细长细胞核的梭形细胞和成片的内皮样细胞组成。梭形细胞的增殖伴随着主要由T细胞组成的炎性浸润。有人提出,这种浸润可能由病毒刺激的T淋巴细胞克隆群体组成,这些T淋巴细胞可产生启动和维持梭形细胞增殖的生长因子。在本研究中,我们使用基于聚合酶链反应的方法,分析了7例经典卡波西肉瘤皮肤浸润中存在的T细胞群体的克隆性T细胞受体γ基因重排。我们的数据表明,KS皮肤浸润中缺乏显著的T细胞克隆群体。这一发现表明T细胞对梭形细胞的反应是反应性多克隆反应,并支持梭形细胞在发病机制上是该疾病核心细胞类型的观点。我们的数据还表明,抗KS T细胞反应本质上是多克隆的,并非由靶向肿瘤相关抗原肽的T细胞克隆性扩增所致。

相似文献

1
Analysis of clonal antigen receptor gene rearrangements in T-cells involved with Kaposi's sarcoma.对与卡波西肉瘤相关的T细胞中克隆性抗原受体基因重排的分析。
Anticancer Res. 1997 Mar-Apr;17(2A):1205-7.
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Heterogeneity of spindle cells in Kaposi's sarcoma: comparison of cells in lesions and in culture.卡波西肉瘤中梭形细胞的异质性:病变组织与培养细胞的比较
J Acquir Immune Defic Syndr Hum Retrovirol. 1995 Nov 1;10(3):295-305.
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Kaposi's sarcoma: a model of both malignancy and chronic inflammation.卡波西肉瘤:恶性肿瘤与慢性炎症的一个模型。
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AIDS-related Kaposi's sarcoma is a clonal neoplasm.
Clin Cancer Res. 1995 Mar;1(3):257-60.
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Expression of costimulatory molecules CD80 and/or CD86 by a Kaposi's sarcoma tumor cell line induces differential T-cell activation and proliferation.卡波西肉瘤肿瘤细胞系共刺激分子CD80和/或CD86的表达诱导不同的T细胞活化和增殖。
Clin Immunol. 1999 Jun;91(3):345-53. doi: 10.1006/clim.1999.4712.
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Vascular endothelial growth factor and basic fibroblast growth factor present in Kaposi's sarcoma (KS) are induced by inflammatory cytokines and synergize to promote vascular permeability and KS lesion development.卡波西肉瘤(KS)中存在的血管内皮生长因子和碱性成纤维细胞生长因子由炎性细胞因子诱导产生,并协同作用以促进血管通透性和卡波西肉瘤病变发展。
Am J Pathol. 1998 Jun;152(6):1433-43.
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Oxytocin is a growth factor for Kaposi's sarcoma cells: evidence of endocrine-immunological cross-talk.催产素是卡波西肉瘤细胞的生长因子:内分泌-免疫相互作用的证据。
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Identification of a clonal form of HIV in early Kaposi's sarcoma: evidence for a novel model of oncogenesis, "sequential neoplasia".早期卡波西肉瘤中一种克隆形式的艾滋病毒的鉴定:一种新的肿瘤发生模型“序贯瘤变”的证据
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Spindle cells and their role in Kaposi's sarcoma.梭形细胞及其在卡波西肉瘤中的作用。
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Kaposi's sarcoma cells of different etiologic origins respond to HIV-Tat through the Flk-1/KDR (VEGFR-2): relevance in AIDS-KS pathology.不同病因起源的卡波西肉瘤细胞通过Flk-1/KDR(血管内皮生长因子受体2)对HIV-Tat作出反应:在艾滋病相关卡波西肉瘤病理学中的意义
Biochem Biophys Res Commun. 2000 Jun 24;273(1):267-71. doi: 10.1006/bbrc.2000.2941.

引用本文的文献

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Single-Cell Transcriptomic Analysis of Kaposi Sarcoma.卡波西肉瘤的单细胞转录组分析
PLoS Pathog. 2025 Apr 1;21(4):e1012233. doi: 10.1371/journal.ppat.1012233. eCollection 2025 Apr.
2
CD4+ and CD8+ T-cell skewness in classic Kaposi sarcoma.经典型卡波西肉瘤中的 CD4+ 和 CD8+ T 细胞偏斜。
Neoplasia. 2012 Jun;14(6):487-94. doi: 10.1596/neo.11646.