A team led by Dr. Chomont, had recently published an article in PLOS pathogens where they have developed a flow cytometry approach, named HIV-flow, in order to evaluate the diversity in the phenotypes of HIV-infected cells. They have based their approach on detecting positive cells. is a 24 kDa protein often referred to as the core or capsid protein of HIV-1. They have set in evidence that the double staining using two anti-p24 (Our and the KC57) gave specific, sensitive and reproducible results to detect the infected cells reservoir. They then have evaluated the expression of different other markers in the double positive cells to perform a phenotypic analysis of those infected cells. This method, well described in the article, can quantify and phenotype the producing in a simple flow cytometry-based approach.