McCall J L, Yun K, Funamoto S, Parry B R
Department of Surgery, Otago University Medical School, Dunedin, New Zealand.
Am J Pathol. 1989 Sep;135(3):421-5.
To find an alternative approach to the in vivo detection of tumor necrosis factor/cachectin (TNF alpha), an immunohistochemical method to identify TNF alpha in histologic sections was developed. This method employs the streptavidin-biotin immunoperoxidase technique, and TNF alpha-specific monoclonal and polyclonal antibodies, on cryostat sections of fresh frozen human lymphoid tissue. Staining was evident in most specimens displaying follicular hyperplasia, but was absent from histologically normal tissue. Both tingible body macrophages and follicular dendritic reticulum cells appeared from phenotype analysis in serial sections and by double staining experiments to constitute the main source of TNF alpha. This technique complements other systemically oriented assays that may fail to detect significant in vivo TNF alpha production and activity at a cellular level.
为了找到一种替代方法用于体内检测肿瘤坏死因子/恶病质素(TNFα),我们开发了一种在组织学切片中鉴定TNFα的免疫组织化学方法。该方法采用链霉亲和素-生物素免疫过氧化物酶技术以及TNFα特异性单克隆和多克隆抗体,应用于新鲜冷冻的人淋巴组织的低温恒冷切片。在大多数显示滤泡增生的标本中可见染色,但在组织学正常的组织中未观察到染色。通过连续切片的表型分析和双重染色实验表明,吞噬性巨噬细胞和滤泡树突状网状细胞均构成了TNFα的主要来源。该技术补充了其他全身性检测方法,这些方法可能无法在细胞水平检测到体内显著的TNFα产生和活性。