Parrillo J E, Lawley T J, Frank M M, Kaplan A P, Fauci A S
J Allergy Clin Immunol. 1979 Aug;64(2):113-21. doi: 10.1016/0091-6749(79)90044-7.
Because previous studies have suggested an important link between eosinophilia and immunologic reactivity, we investigated various components of the immune system in a large number of patients with the idiopathic hypereosinophilic syndrome (HES) to elucidate a possible role for immunologic phenomena in the etiology and pathogenesis of this disease. Immunoglobulin G, A, or M levels were only rarely abnormal. However, in 8 of 21 (38%) patients with HES, IgE levels were markedly elevated suggesting an association of an IgE-mediated mechanism with eosinophilia in this subgroup. Severe dermatographism was present in three fourths of patients, and 2 patients with intermittently elevated histamine levels manifested an unusual form of immediate-pressure urticaria. Serum complement determinations showed elevated C4 and C3 levels in 27% and 77% of patients, respectively. Antigen-antibody complexlike material measured by C1q binding was elevated in the serum of 7 of 22 (32%) patients; this finding may relate to the known ability of eosinophils to avidly phagocytose antigen-antibody complexes. When compared with normals, lymphocytes from patients with HES showed a variety of abnormalities of lymphocyte surface receptors and lymphocyte function. Thus, patients with HES demonstrate a variety of immunologic abnormalities which may be related primarily or secondarily to the pathogenesis of this syndrome.
由于先前的研究表明嗜酸性粒细胞增多与免疫反应性之间存在重要联系,我们对大量特发性高嗜酸性粒细胞综合征(HES)患者的免疫系统各组成部分进行了研究,以阐明免疫现象在该疾病病因和发病机制中可能发挥的作用。免疫球蛋白G、A或M水平仅偶尔出现异常。然而,在21例HES患者中有8例(38%),IgE水平显著升高,提示在该亚组中IgE介导的机制与嗜酸性粒细胞增多有关。四分之三的患者存在严重皮肤划痕症,2例组胺水平间歇性升高的患者表现出一种不寻常的速发型压迫性荨麻疹。血清补体测定显示,分别有27%和77%的患者C4和C3水平升高。通过C1q结合测定的抗原-抗体复合物样物质在22例患者中的7例(32%)血清中升高;这一发现可能与嗜酸性粒细胞 avidly吞噬抗原-抗体复合物的已知能力有关。与正常人相比,HES患者的淋巴细胞表现出淋巴细胞表面受体和淋巴细胞功能的多种异常。因此,HES患者表现出多种免疫异常,这些异常可能主要或次要地与该综合征的发病机制有关。