Nurmi T, Uhari M, Linna S L, Silvennoinen-Kassinen S, Koskela M, Kiuttu J, Tiilikainen A
Clin Exp Immunol. 1982 Apr;48(1):179-85.
Non-specific, cell-mediated and humoral immunity were evaluated in six patients with different autosomal deletions, and in two patients with X-chromosome deletions. Six had an increased number of bacterial, viral, and mycotic infections. Mild disturbances were found in the immunological functions of almost every patient. Granulocyte phagocytosis and killing of bacteria were normal in all patients. The chemotactic response was increased in two, and normal in the others. The responses to phytohaemagglutinin and pokeweed mitogen were normal in all patients and the response to concanavalin A was decreased in one patient. The lymphocyte response to purified protein derivative was decreased in the patients as a group when compared to the controls (P less than 0 . 005), but normal to oidiomycin. The number of acid-alpha-naphthyl acetate esterase positive cells was low in four patients. One had a high titre of antinuclear and antithyroid antibodies. One had a low concentration of serum IgA, C3 and C4. One had a high concentration of IgM. Two had elevated levels of C3 and C4. Our results show that several different chromosomal deletions are associated with immunological abnormality.
对6例患有不同常染色体缺失的患者以及2例患有X染色体缺失的患者进行了非特异性免疫、细胞介导免疫和体液免疫评估。其中6例患者的细菌、病毒和真菌感染次数增多。几乎每位患者的免疫功能均存在轻度紊乱。所有患者的粒细胞吞噬和杀菌功能均正常。趋化反应在2例患者中增强,其余患者正常。所有患者对植物血凝素和商陆有丝分裂原的反应均正常,1例患者对刀豆球蛋白A的反应降低。与对照组相比,患者组对纯化蛋白衍生物的淋巴细胞反应降低(P<0.005),但对曲古霉素的反应正常。4例患者的酸性α-萘乙酸酯酶阳性细胞数量较低。1例患者的抗核抗体和抗甲状腺抗体滴度较高。1例患者的血清IgA、C3和C4浓度较低。1例患者的IgM浓度较高。2例患者的C3和C4水平升高。我们的结果表明,几种不同的染色体缺失与免疫异常有关。