Boucher A, Droz D, Adafer E, Noël L H
Kidney Int. 1986 May;29(5):1043-9. doi: 10.1038/ki.1986.105.
Indirect immunoperoxidase analysis using monoclonal antibodies (Mo Ab) was performed in 33 renal biopsies with interstitial cellular infiltration obtained from non-transplanted patients. We reviewed four acute interstitial nephritis (IN), three chronic IN, four granulomatous IN, four acute tubular necrosis, four vasculitis, seven primary glomerulonephritis and seven active lupus nephritis (LN). We used Mo Ab recognizing T and B cell markers [OKT3, OKT8, T4, B1, IOT14 (IL2 receptor)], HLA-DR related antigen (I2) and monocytes/macrophages (LeuM3). In all cases the interstitial cellular infiltrates were predominantly T cells, whereas the B cell population accounted for less than 20% of the infiltrate. LeuM3+ cells were present in 28 of 32 cases, usually in a lesser proportion than T cells. IOT14+ cells were exceptional. T4+/T8+ cells were clearly greater than one in three acute IN, three granulomatous IN, two LN and two vasculitis. The T8+ cell population predominated in one case of chronic IN related to a non-steroidal anti-inflammatory drug. In all the remaining cases T4+ and T8+ cells were equally present. Aberrant strong HLA-DR expression within tubular cells was noted in nine cases (4 LN) irrespective of the presence of tubular lesions. On the basis of the phenotypic analysis, our data do not support a specific pattern of the infiltrate in regard to a given etiology and thus cannot be used as a diagnostic tool. However, such analysis may aid in understanding the mechanisms of tissue injury.
对33例非移植患者的肾活检组织进行间接免疫过氧化物酶分析,这些组织均有间质细胞浸润。我们回顾了4例急性间质性肾炎(IN)、3例慢性IN、4例肉芽肿性IN、4例急性肾小管坏死、4例血管炎、7例原发性肾小球肾炎和7例活动性狼疮性肾炎(LN)。我们使用了识别T细胞和B细胞标志物[OKT3、OKT8、T4、B1、IOT14(IL - 2受体)]、HLA - DR相关抗原(I2)以及单核细胞/巨噬细胞(LeuM3)的单克隆抗体。在所有病例中,间质细胞浸润主要为T细胞,而B细胞群体占浸润细胞的比例不到20%。32例中有28例存在LeuM3 +细胞,其比例通常低于T细胞。IOT14 +细胞罕见。在3例急性IN、3例肉芽肿性IN、2例LN和2例血管炎中,T4 + / T8 +细胞明显大于1。在1例与非甾体抗炎药相关的慢性IN中,T8 +细胞群体占主导。在所有其余病例中,T4 +和T8 +细胞数量相当。在9例(4例LN)中,无论是否存在肾小管病变,均观察到肾小管细胞内异常强的HLA - DR表达。基于表型分析,我们的数据不支持针对特定病因的浸润特定模式,因此不能用作诊断工具。然而,这种分析可能有助于理解组织损伤的机制。