作者: LARS E. ERIKSSON , THOMAS LEITNER , BRITTA WAHREN , ANN-CHARLOTTE BOSTROM , KERSTIN I. FALK
DOI: 10.1034/J.1600-0463.2003.1110605.X
关键词:
摘要: We have established a simple system for measuring HIV-1 DNA load in CD4+ cells. In multiplex configuration, conserved region the pol gene and section of human albumin were simultaneously amplified to estimate number copies per cellular genome. An Epstein-Barr virus (EBV) standard was used calibrate quantification. Our PCR tested on different vitro developed strains longitudinal samples from eight patients. The able amplify both vivo various genetic compositions. all patients, detected ranged between 0.17 51x10-3 cell could be monitored longitudinally, including long-term PI-ART STI. measured may select best time institution or re-institution therapy.