Matsumoto T, Harada Y, Yamaguchi K, Matsuzaki H, Sanada I, Yoshimura T, Honda M, Tanaka R
Acta Haematol. 1984;72(4):264-73. doi: 10.1159/000206399.
A cytogenetic study was undertaken in 15 cases of Pelger-Huët (P-H) anomaly in 3 families. An enlarged short arm of chromosome 22 (22p+) was found in 14 cases, but in these families 4 cases without P-H anomaly did not show 22p+ in the karyotype. In P-H anomaly, delayed skin hypersensitivity reactions, levels of serum IgG, IgM and IgA, lymphocyte subpopulations, and natural killer and antibody-dependent, cell-mediated cytotoxicity activities were within normal range. The level of serum IgE, mitogen responses in peripheral blood lymphocyte and plaque-forming cell counts were also within normal range with the exception of a case with atopic eczema. Enzymatic activities, nitroblue tetrazolium reduction and phagocytic capacities of neutrophils appeared normal. Abnormalities of neutrophils in cases of P-H anomaly, as compared with normal subjects, were also negative in examinations for chemotaxis and spontaneous migration under agarose and in a membrane filter.
对3个家族中的15例Pelger-Huët(P-H)异常病例进行了细胞遗传学研究。14例患者发现22号染色体短臂增大(22p+),但在这些家族中,4例无P-H异常的患者核型中未显示22p+。在P-H异常中,迟发性皮肤超敏反应、血清IgG、IgM和IgA水平、淋巴细胞亚群以及自然杀伤细胞和抗体依赖性细胞介导的细胞毒性活性均在正常范围内。血清IgE水平、外周血淋巴细胞的丝裂原反应和空斑形成细胞计数除1例特应性皮炎患者外也在正常范围内。中性粒细胞的酶活性、硝基蓝四氮唑还原能力和吞噬能力似乎正常。与正常受试者相比,P-H异常病例中性粒细胞在趋化性以及琼脂糖和膜滤器下的自发迁移检查中也呈阴性。