Morrison H L, Neal J W, Parkes A B, Jasani B
School of Biomedical Sciences, University of Wales Institute, Cardiff, UK.
Mol Pathol. 1998 Aug;51(4):227-31. doi: 10.1136/mp.51.4.227.
This paper describes the use of an autoclaving procedure followed by immunocytochemistry to enhance the detection of the human immunodeficiency virus (HIV) antigens p24, gp41, and gp120. This procedure greatly improved the detection rate of the p24 and gp41 HIV surface antigens in formalin fixed, paraffin wax embedded, HIV positive central nervous system (CNS) tissue while restricting staining to areas of the CNS showing evidence of neuropathology. However, the technique did not improve retrieval of the gp120 antigen in either HIV positive, formalin fixed CNS tissue or HIV infected T lymphoblasts. The inclusion of the high temperature autoclave step was validated using both HIV infected lymphoblasts and pre-adsorption of the specific antibodies with the appropriate recombinant HIV proteins. Using the methodology described here, formalin fixed CNS tissue from potential or known HIV positive cases can be processed reliably and safely. To ensure the reliability of this technique, it is recommended that an assessment of both the p24 and gp41 antigens is undertaken.
本文描述了一种先进行高压灭菌程序再进行免疫细胞化学的方法,以增强对人类免疫缺陷病毒(HIV)抗原p24、gp41和gp120的检测。该程序显著提高了在福尔马林固定、石蜡包埋的HIV阳性中枢神经系统(CNS)组织中p24和gp41 HIV表面抗原的检测率,同时将染色限制在显示神经病理学证据的CNS区域。然而,该技术在HIV阳性的福尔马林固定CNS组织或HIV感染的T淋巴母细胞中均未改善gp120抗原的提取。通过使用HIV感染的淋巴母细胞以及用适当的重组HIV蛋白对特异性抗体进行预吸附,验证了高温高压灭菌步骤的有效性。使用本文所述方法,可以可靠且安全地处理潜在或已知HIV阳性病例的福尔马林固定CNS组织。为确保该技术的可靠性,建议同时对p24和gp41抗原进行评估。