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慢性B细胞疾病中MHC II类抗原的差异表达。

Differential expression of MHC class II antigens in chronic B-cell disorders.

作者信息

Drexler H G, Gignac S M, Brenner M K, Coustan-Smith E, Janossy G, Hoffbrand A V

机构信息

Department of Haematology, Royal Free Hospital, London, UK.

出版信息

Clin Exp Immunol. 1988 Feb;71(2):217-23.

Abstract

Cells from the peripheral blood of 22 patients with chronic B-cell disorders were examined for the expression of surface MHC class II antigens. We made use of well-characterized monoclonal antibodies (McAbs) specific for HLA-DP, -DQ and -DR molecules (B7/21, Tü22, RFDR1 and RFDR2) and of another McAb, RFD1, associated with the class II system. By using indirect immunofluorescence and flow cytometry we found both non-coordination and heterogeneity in expression of MHC class II antigens but generally with a hierarchy of positivity: DR greater than DQ greater than DP. This suggests a sequence of gradual acquisition of HLA-D antigens and indicates distinct differences in maturation arrest of the individual cases. However, after treatment with phorbol ester TPA and calcium ionophore A23187, all cases expressed the previously absent molecules indicating that the structural genes for these products remained intact. TPA and A23187 increased both the number of positive cells in most cases and the fluorescence staining intensities of all class II markers including RFD1. Thus, leukaemic cells may express different combinations of class II antigens reflecting: (i) a predetermined order of gradual acquisition of class II molecules; (ii) differences in the stages of maturation arrest; and (iii) in the cases of disordered expression a desynchronized regulation of these markers.

摘要

对22例慢性B细胞疾病患者外周血中的细胞进行了表面MHC II类抗原表达的检测。我们使用了针对HLA-DP、-DQ和-DR分子(B7/21、Tü22、RFDR1和RFDR2)的特性明确的单克隆抗体(McAbs)以及另一种与II类系统相关的单克隆抗体RFD1。通过间接免疫荧光和流式细胞术,我们发现MHC II类抗原的表达存在不协调和异质性,但通常存在阳性等级:DR大于DQ大于DP。这表明HLA-D抗原是逐步获得的,并表明个别病例在成熟停滞方面存在明显差异。然而,在用佛波酯TPA和钙离子载体A23187处理后,所有病例均表达了先前缺失的分子,这表明这些产物的结构基因保持完整。TPA和A23187在大多数情况下增加了阳性细胞的数量,并增加了包括RFD1在内的所有II类标记物的荧光染色强度。因此,白血病细胞可能表达不同组合的II类抗原,这反映了:(i)II类分子逐步获得的预定顺序;(ii)成熟停滞阶段的差异;以及(iii)在表达紊乱的情况下,这些标记物的不同步调节。

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