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浸润皮肤黑色素瘤的淋巴细胞的T细胞受体库以正常人皮肤T细胞中存在的Vα特异性为主。

T-cell receptor repertoire of lymphocytes infiltrating cutaneous melanoma is predominated by V alpha specificities present in T-cells of normal human skin.

作者信息

Strohal R, Paucz L, Pehamberger H, Stingl G

机构信息

Division of Immunology, Allergy and Infectious Diseases, University of Vienna Medical School, Austria.

出版信息

Cancer Res. 1994 Sep 1;54(17):4734-9.

PMID:8062272
Abstract

Lymphocytes infiltrating solid tumors can be propagated in vitro with interleukin 2 and are then capable, as CD8+ cytotoxic T-cells, of specific lysis of autologous tumor targets in a class I-restricted manner. Since the specificity of these cells is determined by their T-cell receptor (TCR) configuration, the aim of this study was to delineate the TCR V alpha repertoire of tumor-infiltrating lymphocytes within 24 melanoma specimens and to compare these data with the TCR expression pattern of unaffected peritumoral and normal human skin. While lymphocytes within all skin specimens tested expressed a substantial, albeit limited, heterogeneity of V alpha specificities with an average number of 9.0 different V alpha gene segments, the V alpha repertoire within cutaneous melanoma lesions was significantly more restricted (mean of V alpha expression, 3.86; P < 0.001) with a predominance of only 3 V alpha families (V alpha 13, V alpha 15, and V alpha 16), all of which were also found to be expressed within normal skin. Collectively, the fact that the TCR V alpha repertoire in melanoma is skewed toward the predominance of only a few V alpha regions may be indicative of a limited number of melanoma-associated antigenic determinants being involved in the anti-tumor immune response.

摘要

浸润实体瘤的淋巴细胞可在白细胞介素2作用下于体外增殖,随后作为CD8 + 细胞毒性T细胞,能够以I类限制性方式特异性裂解自体肿瘤靶标。由于这些细胞的特异性由其T细胞受体(TCR)构型决定,本研究的目的是描绘24例黑色素瘤标本中肿瘤浸润淋巴细胞的TCR Vα谱,并将这些数据与未受影响的瘤周和正常人类皮肤的TCR表达模式进行比较。虽然所有测试皮肤标本中的淋巴细胞均表现出Vα特异性的显著异质性(尽管有限),平均有9.0个不同的Vα基因片段,但皮肤黑色素瘤病变中的Vα谱明显更受限(Vα表达平均值为3.86;P < 0.001),仅3个Vα家族(Vα13、Vα15和Vα16)占主导地位,所有这些家族在正常皮肤中也有表达。总体而言,黑色素瘤中的TCR Vα谱偏向于仅少数Vα区域占主导地位这一事实,可能表明参与抗肿瘤免疫反应的黑色素瘤相关抗原决定簇数量有限。

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