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低度恶性淋巴瘤。发育调控性B细胞抗原的表达。

Low-grade lymphomas. Expression of developmentally regulated B-cell antigens.

作者信息

Cossman J, Neckers L M, Hsu S, Longo D, Jaffe E S

出版信息

Am J Pathol. 1984 Apr;115(1):117-24.

Abstract

A series of low-grade B-cell lymphomas was analyzed for a battery of immunologic determinants by flow cytometry and immunohistochemistry. Histologically distinctive subclasses of these lymphomas, well-differentiated lymphocytic (WDL), intermediately differentiated lymphocytic (IDL), and follicular center cell (FCC) lymphoma, were found to be readily distinguishable by their expression of immunologic determinants that are known to be developmentally regulated in normal B cells. Although all cases expressed monoclonal surface immunoglobulin (sIg), HLA-DR, and the surface membrane proteins recognized by antibodies B1 (p32) and BA1, staining with other monoclonal antibodies revealed unique immunologic phenotypes for each subclass: WDL p65 (Leu 1)+, p24 (BA2)-; IDL p65+, p24+; FCC p65-, p24-. Additionally, the fluorescence intensities (number of determinants per cell) obtained for sIg, BA-1, and B1, but not HLA-DR, were significantly different among the three lymphoma subclasses. The relative fluorescence intensities of each of these three markers followed the same pattern: FCC greater than IDL greater than WDL. Taken together, these distinguishing features suggest that low-grade B-cell lymphomas represent arrested, and possibly sequential, stages of B-cell differentiation.

摘要

通过流式细胞术和免疫组织化学对一系列低度B细胞淋巴瘤进行了一组免疫决定簇分析。这些淋巴瘤在组织学上有明显区别的亚类,即高分化淋巴细胞性(WDL)、中分化淋巴细胞性(IDL)和滤泡中心细胞(FCC)淋巴瘤,通过它们对已知在正常B细胞发育过程中受调控的免疫决定簇的表达,很容易区分。尽管所有病例均表达单克隆表面免疫球蛋白(sIg)、HLA-DR以及被抗体B1(p32)和BA1识别的表面膜蛋白,但用其他单克隆抗体染色显示每个亚类具有独特的免疫表型:WDL p65(Leu 1)+,p24(BA2)-;IDL p65+,p24+;FCC p65-,p24-。此外,在三个淋巴瘤亚类中,sIg、BA-1和B1(而非HLA-DR)的荧光强度(每个细胞的决定簇数量)有显著差异。这三种标志物各自的相对荧光强度遵循相同模式:FCC大于IDL大于WDL。综上所述,这些区别特征表明低度B细胞淋巴瘤代表B细胞分化的停滞阶段,且可能是连续阶段。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/47cb/1900345/51f3551f9206/amjpathol00181-0125-a.jpg

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