de Préval C, Hadam M R, Mach B
Department of Microbiology, University of Geneva Medical School, Switzerland.
N Engl J Med. 1988 May 19;318(20):1295-300. doi: 10.1056/NEJM198805193182003.
HLA Class II-negative severe combined immunodeficiency (SCID) results from a congenital defect characterized by an absence of HLA Class II antigens. Patients with the disorder have no HLA-DR, DQ, or DP antigens or mRNAs in their peripheral-blood lymphocytes. The affected gene is a recessive, transacting regulatory gene that controls the expression of Class II genes. We studied the regulation of HLA Class II gene expression with the use of established Epstein-Barr virus-transformed B-cell lines and skin fibroblast lines from a group of patients with SCID. Lymphoblastoid B-cell lines from the patients contained no mRNA for HLA-DR, DQ, and DP alpha and beta polypeptides, but did express mRNA for the HLA-associated invariant chain, which is normally coregulated with HLA Class II antigens. In the B-cell line from one patient, a very low amount of DR mRNA could be detected, indicating some heterogeneity in SCID. The lymphokine gamma-interferon, a strong inducer of Class II genes in a variety of normal cells, did not restore Class II gene expression in any of the SCID B-cell lines. More important, gamma-interferon was unable to induce any Class II mRNA in fibroblast lines from patients with SCID, in contrast to the efficient induction observed in normal fibroblasts. The invariant-chain gene, however, was induced in the SCID fibroblasts, confirming a unique uncoupling in the regulation of invariant and Class II genes. Thus, the genetic defect in patients with SCID affects not only the B-cell lineage but also the inducible expression of HLA Class II genes that is normally observed in Class II-negative cells, such as fibroblasts. This unresponsiveness to gamma-interferon in vitro indicates that patients with SCID will not respond to treatment with this lymphokine. Our data also increase understanding of the normal mechanisms regulating the genes for the HLA Class II cell-surface glycoproteins.
HLA II类阴性重症联合免疫缺陷(SCID)是由一种先天性缺陷引起的,其特征是缺乏HLA II类抗原。患有该疾病的患者外周血淋巴细胞中没有HLA - DR、DQ或DP抗原或mRNA。受影响的基因是一个隐性的反式作用调节基因,它控制II类基因的表达。我们使用来自一组SCID患者的已建立的爱泼斯坦 - 巴尔病毒转化的B细胞系和皮肤成纤维细胞系研究了HLA II类基因表达的调控。患者的淋巴母细胞样B细胞系中没有HLA - DR、DQ和DPα及β多肽的mRNA,但确实表达了与HLA相关的恒定链的mRNA,该恒定链通常与HLA II类抗原共同调节。在一名患者的B细胞系中,可以检测到极少量的DR mRNA,这表明SCID存在一些异质性。细胞因子γ干扰素是多种正常细胞中II类基因的强诱导剂,但在任何SCID B细胞系中都不能恢复II类基因的表达。更重要的是,与在正常成纤维细胞中观察到的有效诱导相反,γ干扰素无法在SCID患者的成纤维细胞系中诱导任何II类mRNA。然而,恒定链基因在SCID成纤维细胞中被诱导,证实了恒定链和II类基因调控中的独特解偶联。因此,SCID患者的遗传缺陷不仅影响B细胞谱系而且还影响通常在II类阴性细胞如成纤维细胞中观察到的HLA II类基因的可诱导表达。这种体外对γ干扰素的无反应表明SCID患者对这种细胞因子治疗无反应。我们的数据也增加了对调节HLA II类细胞表面糖蛋白基因的正常机制的理解。