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IgG4 在单纯性和合并性膜性狼疮性肾炎中的沉积。

IgG4 deposits in pure and combined membranous lupus nephritis.

作者信息

Herrera van Oostdam David, Martínez Martínez Marco U, Oros-Ovalle Cuauhtémoc, Martínez-Gala David, Jaimes Piñón Gerardo T, Abud Mendoza Carlos

机构信息

Departamento de Reumatología y Patología, Hospital Central "Dr. Ignacio Morones Prieto", Universidad Autónoma de San Luis Potosí, Venustiano Carranza 2395, Zona Universitaria, San Luis, Mexico.

出版信息

Clin Rheumatol. 2016 Jun;35(6):1619-23. doi: 10.1007/s10067-016-3276-z. Epub 2016 May 2.

Abstract

The aim of this study is to determine the frequency and prognosis of IgG4 deposits in renal biopsy of patients with membranous lupus nephritis (MLN). This is a retrospective cohort study in which we included patients with class V alone or combined (III/V or IV/V) of lupus nephritis according to the 2004 ISN/RPS. All the patients included must have availability of renal tissue for immunohistochemistry analyses. We excluded other classes of lupus nephritis. The renal tissue was examined by a nephro-pathologist. We included 65 patients with MLN; of these, 24 (37 %) were class V, and the other had proliferative concomitant with membranous patterns. Seven renal specimens had IgG4 deposits (10 %). Patients with IgG4 deposits had higher levels of eosinophils in serum. All of the patients with IgG4 had renal involvement as first manifestations of systemic lupus erythematosus. The rate of renal failure was 42 and 43 % in IgG4 positive and negative, respectively, 28 % of IgG4 required renal replacement therapy. From a histological view, 42 % of IgG4 had evidence of arteriolar vasculitis in renal biopsies. Lupus patients with IgG4 deposits were more likely to have renal involvement as a first manifestation of systemic lupus erythematosus, and they course with a worse prognosis since they required more dialysis. Also, they have more probability of vascular inflammation on the renal biopsy.

摘要

本研究的目的是确定膜性狼疮性肾炎(MLN)患者肾活检中IgG4沉积的频率和预后。这是一项回顾性队列研究,我们纳入了根据2004年国际肾脏病学会/肾脏病理学会(ISN/RPS)标准诊断为单纯V级或合并(III/V或IV/V)级狼疮性肾炎的患者。所有纳入的患者必须有可用于免疫组织化学分析的肾组织。我们排除了其他类型的狼疮性肾炎。肾组织由肾病理学家进行检查。我们纳入了65例MLN患者;其中,24例(37%)为V级,其他患者伴有增殖性膜性病变。7份肾标本有IgG4沉积(10%)。有IgG4沉积的患者血清嗜酸性粒细胞水平较高。所有有IgG4沉积的患者均以肾脏受累作为系统性红斑狼疮的首发表现。IgG4阳性和阴性患者的肾衰竭发生率分别为42%和43%,28%的IgG4阳性患者需要肾脏替代治疗。从组织学角度看,42%的IgG4阳性患者肾活检有小动脉血管炎的证据。有IgG4沉积的狼疮患者更有可能以肾脏受累作为系统性红斑狼疮的首发表现,并且由于需要更多透析,其病程预后较差。此外,他们在肾活检时发生血管炎症的可能性更大。

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