Montefiori David C
Duke University Medical Center, Durham, North Carolina.
Curr Protoc Immunol. 2005 Jan;Chapter 12:12.11.1-12.11.17. doi: 10.1002/0471142735.im1211s64.
Neutralizing antibody assays are powerful tools for assessing humoral immunity in AIDS virus infection and vaccine development. Although many different assays have been described, all are based on the same principle, measuring reductions in virus infectivity. This unit describes two assays utilizing a genetically engineered cell lines that are susceptible to infection by most strains of HIV-1, SIV, and SHIV. One assay is designed for optimal performance with uncloned viruses produced in either PBMC or CD4+ T cell lines. A second assay is designed for single-cycle infection with molecularly cloned pseudoviruses produced by transfection in 293T cells. Both assays are performed in a 96-well format and use tat-responsive luciferase reporter gene expression as readout.
中和抗体检测是评估艾滋病病毒感染中的体液免疫和疫苗开发的有力工具。尽管已经描述了许多不同的检测方法,但所有方法都基于相同的原理,即测量病毒感染性的降低。本单元介绍了两种利用基因工程细胞系的检测方法,这些细胞系易受大多数HIV-1、SIV和SHIV毒株感染。一种检测方法专为在PBMC或CD4+ T细胞系中产生的未克隆病毒实现最佳性能而设计。第二种检测方法专为用在293T细胞中通过转染产生的分子克隆假病毒进行单循环感染而设计。两种检测均以96孔板形式进行,并使用tat反应性荧光素酶报告基因表达作为读数。