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F (t)=E0 (0) ??For any single epitope, the probability of it fusing with the target cell it is bound to before it is disabled by a bound antibody is equal to f (?). The probability of this fusion being prevented by an antibody is pb 1{f (?) ??The probability pb of disabling a gp41 trimer in the pre-hairpin intermediate may depend on both A, the mAb concentration and on N, the number of gp41 trime

Everse transcriptase inhibitors (NNRTIs). RMP decreases the plasma concentration of protease inhibitors (PIs) to subtherapeutic levels when the PIs are given at standard doses [15?8]. Coadministration of the PI at higher doses or super-boosting the PI with higher doses of ritonavir (RTV, or r) may result in unacceptably high rates of liver toxicity [18?1]. To complicate things further, risk of tox

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Nts in clinical practice but technical optimization are needed to improve quantification. Human immunodeficiency virus (HIV) enters its host cells following the interaction between the virus envelope glycoprotein (Gp120), the cell surface CD4 receptor, and a chemokine receptor, which may be CCR5 and/ or CXCR4, acting as a coreceptor1. The HIV tropism is defined by the coreceptor(s) use and is corr

Ly 20 activation of viral transcription (see Figure 7) already precludes detection of the upstream transcription. This finding is not surprising, as we demonstrated that there is 11-fold or 38-fold more viral mRNA than *mRNA in TNF- treated cells (Figure 2D, bars 3 and 4). Predictably, our control experiments demonstrate that the ratio between the Rev- and Env-containing transcripts was 1 in untr

Es 3B and S3). We decided to use this cell line because of a smaller ratio between HIV transcripts and *mRNA in these cells compared to those in J-Lat 9.2 cells (Figure 2D, bars 3 and 4). The ratio between LTRand Rev-containing transcripts increased with the decreased levels of viral expression consistent with the rational equation (see Supplemental text 2), and revealed that the upstream transcri

Ons (mannanbinding activity) and MBL C4 cleavage activity in sera from 35 healthy adult volunteers of Caucasian, Asian, Hispanic or AfricanAmerican ancestry (females, n = 20). The sample had a 3.7 log10 range of MBL concentrations (0?,424 ng/mL) that were strongly correlated with the concordant MBL C4 cleavage values (0?7,468 U/mL; r2 = 0.91). The sample included three individuals with homozygous