Fromont P, Bettaieb A, Skouri H, Floch C, Poulet E, Duedari N, Bierling P
Centre de Transfusion, Hôpital Henri Mondor, Créteil, France.
Blood. 1992 Apr 15;79(8):2131-4.
We report the case of a healthy woman (K.M.) who, after multiple pregnancies, developed an antibody directed against a nonpolymorphic region of the polymorphonuclear neutrophil (PMN) Fc gamma receptor III (FcRIII-CD16), which caused transient neonatal alloimmune neutropenia (NAIN). The antigenic target of the antibody was determined by an immunoprecipitation procedure and by phenotyping the mother's PMN. These latter did not react with monoclonal CD16 or polyclonal and monoclonal NA1 and NA2 antibodies, demonstrating the absence of PMN-FcRIII and, consequently, the NA-null phenotype. We also determined the frequency of the NA-null phenotype in a healthy, white population. Among 3,377 random blood donors, only four (in addition to K.M.) were PMN-FcRIII-deficient. These five individuals were healthy and only one (K.M.) presented an allo-CD16 antibody. The gene frequency of the NA-null phenotype was calculated as 0.0274 +/- 0.0059. We conclude that PMN-FcRIII deficiency is a rare phenomenon that can lead to CD16 alloimmunization and thus cause NAIN.
我们报告了一名健康女性(K.M.)的病例,该女性在多次怀孕后,产生了一种针对多形核中性粒细胞(PMN)Fcγ受体III(FcRIII-CD16)非多态性区域的抗体,这导致了短暂性新生儿同种免疫性中性粒细胞减少症(NAIN)。通过免疫沉淀程序和对母亲的PMN进行表型分析来确定抗体的抗原靶点。后者与单克隆CD16或多克隆及单克隆NA1和NA2抗体均无反应,表明不存在PMN-FcRIII,因此为NA-无效表型。我们还确定了健康白人人群中NA-无效表型的频率。在3377名随机献血者中,只有四人(除K.M.外)PMN-FcRIII缺乏。这五个人均健康,只有一人(K.M.)出现了同种异体CD16抗体。NA-无效表型的基因频率计算为0.0274±0.0059。我们得出结论,PMN-FcRIII缺乏是一种罕见现象,可导致CD16同种免疫,从而引起NAIN。