Wood G S, Bourguin A, Crooks C F, Sklar J
Department of Dermatology, Case Western Reserve, University School of Medicine, Cleveland, Ohio.
Am J Pathol. 1991 Jun;138(6):1503-9.
A method is described that allows the quantitation of T-cell DNA within a tissue biopsy specimen. This method is based on the densitometric evaluation of the multiband pattern of TCR-gamma gene rearrangements detectable in Southern blot analyses of polyclonal T-cell DNA digested with HindIII. These rearrangements can be detected down to a limit of approximately 5% T-cell DNA. The information derived from this type of analysis can be used to roughly assess the total T-cell content of lesional tissue specimens expressed as a percentage of total tissue DNA, and can be correlated with the pattern of T-cell infiltration visualized by immunohistology. This assessment can be used also to determine the threshold, expressed as a percentage of total lesional T-cell DNA instead of total tissue DNA, required for the detection of a monoclonal T-cell population by Southern blot analysis. These quantitative relationships may prove useful for studying cutaneous T-cell lymphoma and associated precursor conditions.
本文描述了一种能够对组织活检标本中的T细胞DNA进行定量分析的方法。该方法基于对经HindIII消化的多克隆T细胞DNA进行Southern印迹分析时可检测到的TCR-γ基因重排多带模式的光密度评估。这些重排可检测到低至约5%的T细胞DNA。从这类分析中获得的信息可用于大致评估病变组织标本中T细胞的总含量,以占总组织DNA的百分比表示,并可与免疫组织学观察到的T细胞浸润模式相关联。该评估还可用于确定通过Southern印迹分析检测单克隆T细胞群体所需的阈值,该阈值以病变T细胞DNA总量的百分比而非总组织DNA的百分比表示。这些定量关系可能对研究皮肤T细胞淋巴瘤及相关前驱病症有用。