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常见可变免疫缺陷(CVI)患者血清白细胞介素-4和白细胞介素-6水平升高与慢性免疫激活及CD4+淋巴细胞数量减少有关。

Elevated serum levels of interleukin-4 and interleukin-6 in patients with common variable immunodeficiency (CVI) are associated with chronic immune activation and low numbers of CD4+ lymphocytes.

作者信息

Aukrust P, Müller F, Frøland S S

机构信息

Medical Department A, University of Oslo, National Hospital, Rikshospitalet, Norway.

出版信息

Clin Immunol Immunopathol. 1994 Mar;70(3):217-24. doi: 10.1006/clin.1994.1032.

DOI:10.1006/clin.1994.1032
PMID:7906214
Abstract

Serum immunoreactive interleukin (IL-)1 alpha, IL-4, IL-6 and tumor necrosis factor (TNF) alpha were measured in 42 patients with primary hypogammaglobulinemia (25 common variable immunodeficiency (CVI), 10 congenital hypogammaglobulinemia (CH), 7 X-linked agammaglobulinemia (XLA), and in 21 healthy controls. The cytokine levels were correlated to other immunological parameters including serum levels of neopterin and soluble CD8 (sCD8) antigen. IL-6 was detectable in 48% and IL-4 in 36% of the CVI patients, but in none of the controls. Seventy-five percent of the CVI patients with elevated IL-4 levels had detectable IL-6. In contrast, no patients in the XLA group and only three CH patients had detectable IL-4 or IL-6 levels. TNF alpha and IL-1 alpha were detected in only a few serum samples with no significant differences between patients and controls. In the CVI group elevated IL-6 levels were significantly associated to reduced numbers of CD4+ and CD19+ lymphocytes, elevated levels of neopterin and sCD8 antigen, and occurrence of splenomegaly and bronchiectasis. The raised IL-6 levels were confirmed in longitudinal testing, probably reflecting a characteristic immunological dysregulation in these patients. Cytokine alterations may play a role in the pathogenesis of the immunodeficiency and for the clinical manifestations in CVI patients. Alternatively, elevated cytokine levels may be only a marker of chronic immune activation, particularly in monocytes, possibly delineating a distinct subgroup of patients within the heterogeneous CVI group.

摘要

对42例原发性低丙种球蛋白血症患者(25例常见变异型免疫缺陷病(CVI)、10例先天性低丙种球蛋白血症(CH)、7例X连锁无丙种球蛋白血症(XLA))及21名健康对照者检测了血清免疫反应性白细胞介素(IL)-1α、IL-4、IL-6和肿瘤坏死因子(TNF)α。细胞因子水平与其他免疫学参数相关,包括新蝶呤和可溶性CD8(sCD8)抗原的血清水平。48%的CVI患者可检测到IL-6,36%的患者可检测到IL-4,但对照组均未检测到。IL-4水平升高的CVI患者中75%可检测到IL-6。相反,XLA组无患者、CH组仅有3例患者可检测到IL-4或IL-6水平。仅在少数血清样本中检测到TNFα和IL-1α,但患者与对照组之间无显著差异。在CVI组中,IL-6水平升高与CD4 +和CD19 +淋巴细胞数量减少、新蝶呤和sCD8抗原水平升高以及脾肿大和支气管扩张的发生显著相关。纵向检测证实了IL-6水平升高,这可能反映了这些患者特有的免疫调节异常。细胞因子改变可能在免疫缺陷的发病机制及CVI患者的临床表现中起作用。或者,细胞因子水平升高可能仅是慢性免疫激活的标志物,尤其是在单核细胞中,这可能在异质性CVI组中界定出一个独特的患者亚组。

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