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一种新型人类T细胞抗原,优先表达于成熟T细胞,且在高分化和低分化B细胞白血病及淋巴瘤中均有表达。

A novel human T cell antigen preferentially expressed on mature T cells and shared by both well and poorly differentiated B cell leukemias and lymphomas.

作者信息

Kamoun M, Kadin M E, Martin P J, Nettleton J, Hansen J A

出版信息

J Immunol. 1981 Sep;127(3):987-91.

PMID:6790625
Abstract

A new lymphocyte differentiation antigen shared by all normal T cells and some malignant B cells was defined by a monoclonal antibody designated 12.1. This antibody reacted with all peripheral blood T cells but not with normal B cells and B cell lines. Analysis with a fluorescence activated cell sorter showed that the expression of 12.1 antigen changes during T cell maturation. Most thymocytes, blasts of acute T cell leukemia, and cells from established leukemic T cell lines bear a small amount of 12.1 antigen. In contrast the majority of peripheral blood T cells, activated T cells, and leukemic T cells of the Sezary syndrome bear a large amount of 12.1 antigen. Unexpectedly, antibody 12.1 reacted with leukemic cells from most patients with B-type chronic lymphocytic leukemia (CLL) and some patients with lymphosarcoma cell leukemia (LSCL). Among these leukemias, expression of the 12.1 antigen was not correlated with the stage of B cell maturation, with the amount of surface immunoglobulin on the cells, or with the presence or absence of monoclonal gammapathy. In a comparative serologic analysis the antigen defined by antibody 12.1 was distinct from the p67 T cell antigen (defined by monoclonal antibody 10.2) that is also known to be expressed by B-type CLL cells.

摘要

一种由名为12.1的单克隆抗体所界定的新型淋巴细胞分化抗原,为所有正常T细胞及部分恶性B细胞所共有。该抗体与所有外周血T细胞发生反应,但不与正常B细胞及B细胞系发生反应。通过荧光激活细胞分选仪分析显示,12.1抗原的表达在T细胞成熟过程中发生变化。大多数胸腺细胞、急性T细胞白血病母细胞以及已建立的白血病T细胞系的细胞带有少量12.1抗原。相比之下,大多数外周血T细胞、活化T细胞以及Sezary综合征的白血病T细胞带有大量12.1抗原。出乎意料的是,抗体12.1与大多数B型慢性淋巴细胞白血病(CLL)患者及部分淋巴肉瘤细胞白血病(LSCL)患者的白血病细胞发生反应。在这些白血病中,12.1抗原的表达与B细胞成熟阶段、细胞表面免疫球蛋白的量或单克隆丙种球蛋白病的有无均无关联。在一项比较血清学分析中,抗体12.1所界定的抗原与同样已知由B型CLL细胞表达的p67 T细胞抗原(由单克隆抗体10.2所界定)不同。

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