Jenis E H, Valeski J E, Calcagno P L
Clin Nephrol. 1981 Mar;15(3):111-4.
Anti-GBM staining by indirect immunofluorescence microscopy was performed on renal biopsies from 64 patients with a variety of diseases in which no in vivo bound immunoglobulin or complement components were identified by direct immunofluorescence microscopy. The glomeruli of all of the entities examined bound anti-GBM antibodies except for four of nine cases of hereditary nephritis of the Alport-type. The absence of anti-GBM staining was found to correlate with the severity of GBM splitting identified by electron microscopy.
对64例患有各种疾病的患者的肾活检组织进行间接免疫荧光显微镜抗肾小球基底膜（GBM）染色，这些患者通过直接免疫荧光显微镜未发现体内结合的免疫球蛋白或补体成分。除9例Alport型遗传性肾炎中的4例之外，所有检查实体的肾小球均结合抗GBM抗体。发现抗GBM染色缺失与电子显微镜鉴定的GBM分裂严重程度相关。
