Van Epps D E, Brown S L
Infect Immun. 1981 Dec;34(3):864-70. doi: 10.1128/iai.34.3.864-870.1981.
Immunoglobulin A (IgA) paraproteins from patients with myeloma have been shown to inhibit human neutrophil chemotaxis to C5a, casein, and chemotactic factors produced by Escherichia coli. This study demonstrates that these paraproteins also inhibit neutrophil chemotaxis in response to the synthetic peptide formylmethionyl-leucyl-phenylalanine (f-MLP). Furthermore, the neutrophil chemiluminescence response stimulated by f-MLP was markedly suppressed by the presence of IgA paraprotein. Maximal inhibition of chemiluminescence was observed when the paraprotein was present during the chemiluminescence response. The inhibitory activity was substantially reduced by removal of the Fc region of IgA or by conversion of polymeric IgA to monomeric IgA by limited reduction and alkylation. Additional experiments showed that these IgA paraproteins inhibited C5a but not phorbol myristate acetate-stimulated chemiluminescence. These observations are constant with the hypothesis that polymeric forms of IgA bind to human neutrophils and interfere with the binding of chemotactic factor to its receptor or the consequent receptor-mediated oxidative burst or both.
骨髓瘤患者的免疫球蛋白A(IgA)副蛋白已被证明可抑制人类中性粒细胞对C5a、酪蛋白以及大肠杆菌产生的趋化因子的趋化作用。本研究表明,这些副蛋白还可抑制中性粒细胞对合成肽甲酰甲硫氨酰-亮氨酰-苯丙氨酸(f-MLP)的趋化作用。此外,f-MLP刺激的中性粒细胞化学发光反应在有IgA副蛋白存在时会受到显著抑制。当化学发光反应期间存在副蛋白时,观察到化学发光的最大抑制。通过去除IgA的Fc区域或通过有限还原和烷基化将聚合IgA转化为单体IgA,抑制活性会大幅降低。额外的实验表明,这些IgA副蛋白抑制C5a刺激的化学发光,但不抑制佛波酯肉豆蔻酸酯乙酸酯刺激的化学发光。这些观察结果与以下假设一致,即聚合形式的IgA与人中性粒细胞结合,并干扰趋化因子与其受体的结合或随后的受体介导的氧化爆发,或两者兼有。