Bredius R G, de Vries C E, Troelstra A, van Alphen L, Weening R S, van de Winkel J G, Out T A
Clinical Immunology Laboratory, Academic Medical Center, Amsterdam, The Netherlands.
J Immunol. 1993 Aug 1;151(3):1463-72.
To assess the function of IgG subclass antibodies we studied the opsonization of Staphylococcus aureus (STAW) and Haemophilus influenzae type b (Hib) by natural IgG1 and IgG2 antibodies from five healthy individuals. Phagocytosis by polymorphonuclear leukocytes (PMN) was analyzed using FITC-labeled bacteria and flow cytometry. All PMN donors were typed for the High- and Low-Responder phenotype of the human Fc gamma receptor (hFc gamma) type IIa (CD32) and the NA1/NA2 allotype of the hFc gamma RIIIb (CD16). When PMN were used that were heterozygous for hFc gamma RIIa and hFc gamma RIIIb, phagocytosis of STAW opsonized with IgG1 antibodies was similar to that with IgG2, both in the presence and absence of a source of complement (agammaglobulinemic serum). Phagocytosis of Hib opsonized with IgG2 anti-Hib proved significantly lower (p < 0.05) than with IgG1 anti-Hib using preparations from 4 of the 5 individuals tested. IgG2 anti-Hib from one donor, however, proved more effective than IgG1 anti-Hib. The properties of PMN with hFc gamma RIIaLR,LR and hFc gamma RIIaHR,HR were compared, using hFc gamma RIIIb NA1/NA2-matched PMN. hFc gamma RIIaHR,HR PMN were virtually incapable of phagocytosing STAW and Hib opsonized with IgG2 anti-bodies without complement, in contrast to hFc gamma RIIaLR,LR PMN. Phagocytosis of IgG2-oposonized bacteria by hFc gamma RIIaLR,LR PMN was effectively inhibited by mAb against hFc gamma RIIa (IV.3). IgG1-mediated phagocytosis was blocked by mAb against hFc gamma RIIIb (CLB/FcRGran 1) to a greater extent than by anti-hFc gamma RIIa mAb. Inhibition studies with mAb against CR3 (B2.12) and hFc gamma RIIa showed that both receptors cooperated in phagocytosis. We conclude that PMN phagocytosis can be effectively mediated by antibacterial IgG2 anti-STAW and anti-Hib. Thus, IgG2 may have a critical role in the immune defense against these bacteria. However, the role of antibacterial IgG2 in opsonization and phagocytosis may be limited in individuals homozygous for hFc gamma RIIaHR.
为评估IgG亚类抗体的功能,我们研究了来自五名健康个体的天然IgG1和IgG2抗体对金黄色葡萄球菌(STAW)和b型流感嗜血杆菌(Hib)的调理作用。使用异硫氰酸荧光素标记的细菌和流式细胞术分析多形核白细胞(PMN)的吞噬作用。所有PMN供体均针对人Fcγ受体(hFcγ)IIa型(CD32)的高反应者和低反应者表型以及hFcγRIIIb(CD16)的NA1/NA2同种异型进行分型。当使用对hFcγRIIa和hFcγRIIIb杂合的PMN时,无论有无补体来源(无丙种球蛋白血症血清),用IgG1抗体调理的STAW的吞噬作用与用IgG2抗体调理的相似。在测试的5名个体中的4名个体的样本中,用IgG2抗Hib调理的Hib的吞噬作用明显低于(p < 0.05)用IgG1抗Hib调理的。然而,来自一名供体的IgG2抗Hib比IgG1抗Hib更有效。使用hFcγRIIIb NA1/NA2匹配的PMN比较了具有hFcγRIIaLR,LR和hFcγRIIaHR,HR的PMN的特性。与hFcγRIIaLR,LR PMN相比,hFcγRIIaHR,HR PMN几乎无法吞噬未添加补体的用IgG2抗体调理的STAW和Hib。hFcγRIIaLR,LR PMN对IgG2调理的细菌的吞噬作用被抗hFcγRIIa单克隆抗体(IV.3)有效抑制。IgG1介导的吞噬作用被抗hFcγRIIIb单克隆抗体(CLB/FcRGran 1)阻断的程度大于抗hFcγRIIa单克隆抗体。用抗CR3(B2.12)和hFcγRIIa单克隆抗体进行的抑制研究表明,这两种受体在吞噬作用中协同作用。我们得出结论,PMN吞噬作用可由抗STAW和抗Hib的抗菌IgG2有效介导。因此,IgG2在针对这些细菌的免疫防御中可能起关键作用。然而,抗菌IgG2在调理作用和吞噬作用中的作用在hFcγRIIaHR纯合个体中可能有限。