Eighty-five percent of re-circulating lymphocyte pool cells entering the lymph system are from the blood while about 15% are from the lymph. These data are mostly derived from animal experiments [34]. They underline

the fact that an absence of resistance mutations ATR inhibitor in blood lymphocytes does not exclude the possibility that resistance is present. There is an increasing body of literature on the possible utility of assessing drug resistance mutations in the provirus. Our data are in accordance with previous observations and indicate the practical feasibility of sequencing the provirus. As reported by Bona et al. [30], we also found more drug resistance mutations, particularly key mutations, in the cell proviral DNA than in the plasma. Based on the Stanford mutation list, excluding polymorphisms and drug-selected mutations with no known significance, the proportion of mutations detected in the DNA was significantly higher than the proportion detected using standard RNA genotyping by the χ2 test. At the therapy-naïve stage, we detected seven key mutations in the RT and PR genes in different patients (10% of all included patients), and four of these (M184M/V, M184M/I, K103K/N and M46M/I) were only found in the cells. Three key mutations (K103K/N, M46L and M46M/I) were found

in different patients, for whom the follow-up was possible (4.3% of 69 patients included in the study). The K103K/N was not found in the plasma. At the time of study inclusion, 8% of patients had at least one RT mutation in the plasma, while 15% had at least one RT resistance mutation in CD4 cells. One check details therapy-naïve patient had virus with an RT resistance profile (67N, 70R and 219Q) in both CD4 cells and plasma. Before initiating treatment, PR gene sequencing showed that the percentage of patients with viruses carrying at least one PR mutation was 25% for CD4 cells and 23% for plasma. Wang et al. [31] and recently Ghosn et al. [32] reported a tight concordance of resistance profiles in paired HIV RNA and PBMC HIV DNA. Our own results demonstrate that at baseline only 55% of PR mutations and 56%

of (-)-p-Bromotetramisole Oxalate RT mutations were simultaneously present in CD4 cells and plasma, with substantial agreement between the two methods as assessed using kappa statistics. In their study, Usuku et al. [33] noted the persistence of a discrepancy between plasma and PBMCs for more than 3 years. In this study, the comparison between pretreatment amino acid sequences from CD4 cells and the plasma compartment and the comparison between pretreatment CD4 cell samples and follow-up CD4 cell samples showed a statistically significant proportion of new mutations of 22%, although the appearance of new mutations was not correlated with the time elapsed between tests. One of the 40 patients with follow-up samples had a key RT resistance mutation present in cells but not in plasma.