Membranous nephropathy in primary antiphospholipid syndrome: description of a case and induction of renal injury in SCID mice.

Human antibodies and hybridomas Pub Date : 1996-01-01
Y Levy, L Ziporen, B Gilburd, J George, S Polak-Charcon, H Amital, J Cledes, P Youinou, Y Shoenfeld
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Abstract

Primary antiphospholipid syndrome (PAPS) is a recently recognized clinical entity encompassing the combination of thromboembolic phenomena, thrombocytopenia and recurrent abortions in the presence of antiphospholipid antibodies. We present a patient with PAPS accompanied by renal involvement, manifested as membranous nephropathy, as proven by a renal biopsy. To investigate further the possible association between PAPS and the renal lesions we attempted to induce similar renal manifestations by transferring peripheral blood lymphocytes (PBL) from this patient to severe combined immunodeficiency (SCID) mice. The mice transfused with PBL from the affected patient exemplified antiphospholipid antibodies (aPL) following which a renal lesion consistent with the human membranous nephropathy lesion was precipitated. This study substantiates the role of aPL as possible inducers of renal damage.

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原发性抗磷脂综合征的膜性肾病:一例SCID小鼠肾损伤的描述和诱导。
原发性抗磷脂综合征(PAPS)是最近公认的一种临床实体,包括血栓栓塞现象、血小板减少症和存在抗磷脂抗体的复发性流产。我们报告了一位伴有肾脏受累的PAPS患者,表现为膜性肾病,经肾活检证实。为了进一步研究PAPS与肾脏病变之间的可能联系,我们试图通过将该患者的外周血淋巴细胞(PBL)转移到严重联合免疫缺陷(SCID)小鼠体内来诱导类似的肾脏表现。输注患者PBL的小鼠出现抗磷脂抗体(aPL),随后出现与人膜性肾病一致的肾脏病变。本研究证实aPL可能是肾损害的诱导剂。
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