儿童非t、非b急性淋巴细胞白血病的免疫学亚分类。

Y Komada, E Azuma, S Tanaka, H Ochiai, M Sakurai
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引用次数: 6

摘要

采用抗ALL普通抗原(cALLa)、p24、p20和HLA-DR抗原的单克隆抗体对41例非t、非b急性淋巴细胞白血病(ALL)进行免疫学分类。41例患者中,cALLa、p24、p20和HLA-DR抗原分别阳性31例、34例、35例和41例。普通ALL组包括4例表达细胞质mu重链的病例。我们证明了大多数非t,非b ALL将来自b系细胞。p24和p20的表达之后是cALLa的表达和细胞质免疫球蛋白的合成。这些证据支持了cALLa、p24、p20和HLA-DR抗原在ALL细胞上的表达在美国、欧洲和日本是普遍存在的。尽管形态相同,但基于cALLa、p24、p20和HLA-DR抗原,非t、非b ALL病例可以细分为表型定义的亚组。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Immunological subclassification of non-T, non-B acute lymphoblastic leukaemia in childhood.

41 cases of non-T, non-B acute lymphoblastic leukaemia (ALL) were classified by immunological criteria using a panel of monoclonal antibodies against common ALL antigen (cALLa), p24, p20 and HLA-DR antigens. Out of 41 cases, cALLa, p24, p20 and HLA-DR antigens were positive in 31 cases, 34 cases, 35 cases and 41 cases, respectively. 4 cases expressing cytoplasmic mu heavy chains were included in the group of common ALL. We demonstrated that a majority of non-T, non-B ALL would be derived from B-lineage cells. The expression of p24 and p20 was followed by the expression of cALLa and the synthesis of cytoplasmic immunoglobulin. These items of evidence support the idea that the expression of cALLa, p24, p20 and HLA-DR antigens on ALL cells would be universal in the USA, Europe and Japan. Although morphologically identical, non-T, non-B ALL cases could be subdivided into phenotypically-defined subgroups on the basis of cALLa, p24, p20 and HLA-DR antigens.

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