Quantification of human immunodeficiency virus type 1 (HIV-1) is useful in
obtaining information about the prognosis of patients and monitoring of ant
iviral therapy. Today, commercial assays based on reverse transcription-pol
ymerase chain reaction (RT-PCR), the branched DNA (bDNA) technology and on
nucleic acid sequence-based amplification (NASBA) are available. Clinical r
elevance of those assays is limited because of relatively poor reproducibil
ity, especially for low copy numbers and unequal amplification dynamics for
different genotypes. Better standardisation is most important in order to
improve the reliability of quantitative molecular assays. (C) 2001 Elsevier
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