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57例外周T细胞淋巴瘤中α/β和γ/δ T细胞受体的表达。γ/δ T细胞淋巴瘤一个亚群的鉴定。

Expression of the alpha/beta and gamma/delta T-cell receptors in 57 cases of peripheral T-cell lymphomas. Identification of a subset of gamma/delta T-cell lymphomas.

作者信息

Gaulard P, Bourquelot P, Kanavaros P, Haioun C, Le Couedic J P, Divine M, Goossens M, Zafrani E S, Farcet J P, Reyes F

机构信息

Department of Tissular and Cellular Pathology, Henri Mondor Hospital, Créteil, France.

出版信息

Am J Pathol. 1990 Sep;137(3):617-28.

Abstract

Fifty-seven cases of peripheral T-cell lymphoma were studied for cell expression of the T-cell receptor (TCR) chains, using monoclonal antibodies specific for the beta chain (beta F1) of the alpha/beta TCR, and for the delta chain (anti-TCR delta-1) of the gamma/delta TCR. Three different patterns were demonstrated: in 39 cases (69%), the phenotype (CD3+beta F1+TCR delta-1-) was that of most normal T cells. A second pattern was found on six cases (10%), which were of CD3+beta F1-TCR delta-1+ phenotype, and in which DNA analysis showed a clonal rearrangement of the delta locus in the five cases studied. It is suggested that these cases are the neoplastic counterpart of the small subpopulation of normal T cells that express gamma delta receptor. It is of considerable interest that these gamma delta lymphomas had unusual clinicopathologic presentations, as one case corresponded to a lethal midline granuloma and the five others to hepatosplenic lymphomas with a sinusal/sinusoidal infiltration in spleen, marrow, and liver. The fact that the distribution of the neoplastic gamma delta cells in the splenic red pulp resembles that of normal gamma delta cells reinforces the concept of a preferential homing of gamma delta T cells to this tissue. A third pattern (CD3 +/- beta F1-TCR delta-1-) was seen in 12 cases (21%), in which, by contrast to normal post-thymic T cells, no evidence of either alpha beta or gamma delta T cell receptor was found.

摘要

对57例外周T细胞淋巴瘤进行了研究,以检测T细胞受体(TCR)链的细胞表达情况,所用单克隆抗体分别针对α/β TCR的β链(βF1)以及γ/δ TCR的δ链(抗-TCR δ-1)。结果显示出三种不同模式:39例(69%)的表型(CD3+βF1+TCR δ-1-)与大多数正常T细胞相同。在6例(10%)中发现了第二种模式,其表型为CD3+βF1-TCR δ-1+,并且在所研究的5例中,DNA分析显示δ基因座存在克隆性重排。提示这些病例是表达γδ受体的正常T细胞小亚群的肿瘤对应物。相当有趣的是,这些γδ淋巴瘤具有不寻常的临床病理表现,其中1例对应致死性中线肉芽肿,另外5例对应脾、骨髓和肝呈窦状/窦样浸润的肝脾淋巴瘤。肿瘤性γδ细胞在脾红髓中的分布与正常γδ细胞相似,这一事实强化了γδ T细胞优先归巢至该组织的概念。12例(21%)呈现出第三种模式(CD3+/-βF1-TCR δ-1-),与正常胸腺后T细胞相比,在这些病例中未发现αβ或γδ T细胞受体的证据。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/78a8/1877506/4b0ec511b170/amjpathol00105-0137-a.jpg

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