Lalezari P
Prog Clin Biol Res. 1977;13:209-25.
Neutrophil antigens may be classified into two major categories: antigens shared with other cells and antigens specific for neutrophils. The first category includes the ABH, I, i, 5a,b and HLA determinants. Additional antigens with special characteristics in this category are the blood-group U, Kx, JkaJkb, and Ge determinants which apparently neutrophils share only with erythrocytes. Neutrophil-specific antigens include the NA1, NA2, NB1 and 9a. These specificities are detected by the agglutination test and have been shown to be present on mature neutrophils. Independent allospecificities, detectable by the granulocytotoxicity test, may also exist. In addition, neutrophil antigens, which are species-specific, have been identified by the use of xenogeneic antibodies. The EDTA-dependent agglutination test remains a most reliable assay for the study of neutrophil-specific antigens. The lack of reproducibility known in the leukoagglutination reaction does not pertain to the modification used in the assay of neutrophil-specific antibodies. It does apply, however, to those tests that were performed in the absence of EDTA, and in connection to the study of HLA-related antigens. For every pathophysiological state involving the erythrocyte antigens a neutrophil analogue is observed, the difference being in symptomatology which is related to the structural and functional characteristics of the cells: febrile and pulmonary transfusion reactions result from incompatibility neutrophils. It is found that similarity in the HLA antigens and nonreactivity in the MLC test do not preclude immunization against neutrophil-specific antigens. Therefore, it is probable that febrile and pulmonary reactions will occur in the recipients of multiple granulocyte transfusions, even though donors and recipients may be considered "histocompatible" by the HLA assays. It has been shown that fetal-maternal incompatibility can cause neonatal neutropenia, and several forms of autoimmune neutropenia are described: in "idiopathic" neutropenia of infancy, autoantibodies have been found to have specificity against NA1 and NA2 and in one adult, autoimmune neutropenia due to anti-NA1 antibody has been observed. Neutropenia also occurs due to idiopathic, cold-reacting antileukocyte antibodies, and with cold agglutinins associated with lymphoma, infectious mononucleosis, and Mycoplasma pneumonia. Although the role of neutrophil antigens in bone marrow transplantation has not as yet been determined, these antigens are undoubtedly immunogenic and potentially play an important role in neutrophil compatibility. It is obvious that neutrophils cannot survive in the presence of antineutrophil antibodies.(ABSTRACT TRUNCATED AT 400 WORDS)
与其他细胞共有的抗原和中性粒细胞特有的抗原。第一类包括ABH、I、i、5a,b和HLA决定簇。这一类中具有特殊特征的其他抗原是血型U、Kx、JkaJkb和Ge决定簇,显然中性粒细胞仅与红细胞共有这些抗原。中性粒细胞特异性抗原包括NA1、NA2、NB1和9a。这些特异性通过凝集试验检测到,并且已证实在成熟中性粒细胞上存在。通过粒细胞毒性试验可检测到的独立同种特异性也可能存在。此外,通过使用异种抗体已鉴定出种属特异性的中性粒细胞抗原。EDTA依赖的凝集试验仍然是研究中性粒细胞特异性抗原最可靠的检测方法。白细胞凝集反应中已知的缺乏可重复性并不适用于中性粒细胞特异性抗体检测中使用的改良方法。然而,它确实适用于那些在没有EDTA的情况下进行的试验,以及与HLA相关抗原研究相关的试验。对于涉及红细胞抗原的每一种病理生理状态,都观察到了中性粒细胞类似物,不同之处在于症状与细胞的结构和功能特征有关:发热性和肺部输血反应是由中性粒细胞不相容引起的。研究发现,HLA抗原的相似性和混合淋巴细胞培养试验中的无反应性并不排除针对中性粒细胞特异性抗原的免疫。因此,即使供体和受体通过HLA检测可能被认为“组织相容性良好”,多次粒细胞输血的受者仍可能发生发热性和肺部反应。研究表明,胎儿-母亲不相容可导致新生儿中性粒细胞减少,并且描述了几种自身免疫性中性粒细胞减少的形式:在婴儿期“特发性”中性粒细胞减少症中,已发现自身抗体对NA1和NA2具有特异性,并且在一名成年人中,观察到了由于抗NA1抗体导致的自身免疫性中性粒细胞减少。中性粒细胞减少也由于特发性冷反应抗白细胞抗体以及与淋巴瘤、传染性单核细胞增多症和支原体肺炎相关的冷凝集素而发生。尽管中性粒细胞抗原在骨髓移植中的作用尚未确定,但这些抗原无疑具有免疫原性,并且可能在中性粒细胞相容性中发挥重要作用。显然,中性粒细胞在抗中性粒细胞抗体存在的情况下无法存活。(摘要截至于400字)