抗原
单克隆抗体
白血病
抗体
分子生物学
T细胞
生物
T淋巴细胞
B细胞
慢性淋巴细胞白血病
B-1电池
T细胞白血病
抗原提呈细胞
免疫学
免疫系统
作者
Malek Kamoun,M. Kadin,Paul J. Martin,J Nettleton,JA Hansen
出处
期刊:Journal of Immunology
[American Association of Immunologists]
日期:1981-09-01
卷期号:127 (3): 987-991
被引量:126
标识
DOI:10.4049/jimmunol.127.3.987
摘要
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.
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