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慢性同种异体疾病。I. 肾小球肾炎的发展。

Chronic allogeneic disease. I. Development of glomerulonephritis.

作者信息

Lewis R M, Armstrong M Y, André-Schwartz J, Muftuoglu A, Beldotti L, Schwartz R S

出版信息

J Exp Med. 1968 Oct 1;128(4):653-79. doi: 10.1084/jem.128.4.653.

Abstract

Glomerulonephritis, often accompanied by the nephrotic syndrome, developed in CAF(1) mice following the administration of spleen cells from normal BALB/c mice. The renal lesion was membranous glomerulonephritis. When studied with fluorescein-conjugated antisera to either mouse gamma globulin or beta(1C)-globulin, the glomeruli contained beaded and irregular deposits of these immunoproteins. The ultrastructure of the lesion was characterized by thickening of the glomerular basement membranes and the presence of electron-dense subepithelial deposits. Acid eluates of the diseased kidneys contained gamma globulin that failed to bind to sections of normal kidneys. These findings conform to the type of nephritis provoked by immune complexes. They indicate that this type of immune injury can be based on the reaction of intolerant immunocytes to normal antigens.

摘要

在给CAF(1)小鼠注射正常BALB/c小鼠的脾细胞后,这些小鼠出现了常伴有肾病综合征的肾小球肾炎。肾脏病变为膜性肾小球肾炎。当用荧光素结合的抗小鼠γ球蛋白或β(1C)球蛋白抗血清进行研究时,肾小球含有这些免疫蛋白的串珠状和不规则沉积物。病变的超微结构特征为肾小球基底膜增厚和电子致密的上皮下沉积物的存在。患病肾脏的酸洗脱液中含有不能与正常肾脏切片结合的γ球蛋白。这些发现符合免疫复合物引发的肾炎类型。它们表明这种类型的免疫损伤可能基于不耐受免疫细胞对正常抗原的反应。

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