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Updated: May 26, 2026
Amplifying and Quantifying HIV-1 RNA in HIV Infected Individuals with Viral Loads Below the Limit of Detection by Standard Clinical Assays
Published on: September 26, 2011
Multicenter assessment of HIV-1 RNA quantitation in semen in the CREAThE network
Christophe Pasquier1, Corinne Andreutti, Evelyne Bertrand
1Laboratory of Virology, CHU de Toulouse, Institut Fédératif de Biologie; INSERM, U1043, Centre de Physiopathologie de Toulouse Purpan, France. pasquier.c@chu-toulouse.fr
Abstract:
Detection of HIV-1 RNA in semen is used commonly to determine the safety of semen processing procedures before assisted reproductive technology (ART). Using two panels of prepared semen samples containing HIV-1 the performances of protocols from 14 centers have been compared. No false-positive results were detected but false-negative results were frequent when the concentration was below 500 HIV-1 RNA copies/ml of seminal plasma. Frequency of HIV-1 RNA detection was higher on seminal cells than on seminal plasma. Assays (or protocols) for quantifying HIV-1 RNA in semen performed less well than standardized blood plasma assays. The HIV load in seminal plasma could be a useful marker of the risk of sexual transmission of the virus. Its use as a marker of global HAART efficiency in the HIV reservoir needs further study. Standardized assays are required for detection and measurement of HIV-1 RNA in semen samples.
