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1 a detectable viral load (local prevalence of viraemia).
2 T cells and the rapid reappearance of plasma viraemia.
3 wed by a slower second-phase decay of plasma viraemia.
4 ion of HIV-positive partners with detectable viraemia.
5 ties with an at least 5% local prevalence of viraemia.
6 th-care providers 6 weeks after clearance of viraemia.
7 h higher ranges and persistence of low-level viraemia.
8 o ART strongly predict time to the return of viraemia.
9 Two patients receiving ART had transient HIV viraemia.
10 ection of rhesus monkeys and before systemic viraemia.
11 g the 'eclipse' phase, and before detectable viraemia.
12 seroconversion and extended the duration of viraemia.
13 IV dissemination and strongly reduced plasma viraemia.
14 lated significantly with reduced acute phase viraemia.
15 y has a role in reduction of cytomegalovirus viraemia.
16 t HCMV serostatus was also a risk factor for viraemia.
17 dren, resulting in antigenaemia and possible viraemia.
18 infected were half as likely to develop new viraemia (12% [12/98]), even after accounting for risk b
19 -week 24 was spent with persistent low-level viraemia (80-5,000 copies/ml) and 10% with VL rebound >/
21 -1 gag/pol/nef vaccine did not reduce plasma viraemia after infection, and HIV-1 incidence was higher
25 tential HIV transmission risk and detectable viraemia among serodiscordant couples warrant intensifie
28 combination antiretroviral therapy (ART) on viraemia and immune responses, sexual risk behaviour, an
29 occurrence and recurrence of cytomegalovirus viraemia and improved the time-to-event for viraemia epi
30 d that identify protection as the absence of viraemia and the absence of an anamnestic antibody respo
31 rol coincides with a final escalation of the viraemia and the terminal failure of the immune system.
32 A more than 150 copies per mL (prevalence of viraemia); and the proportion of participants with HIV w
34 C117 is safe and effective in reducing HIV-1 viraemia, and that immunotherapy should be explored as a
35 lonal antibodies have been shown to suppress viraemia, but the therapeutic potential of these monoclo
38 proximately tenfold lower vaccine-associated viraemia compared to the first-generation vaccine and bo
39 al immunity by vaccination might achieve CMV viraemia control without the need for antiviral agents.
40 eles of the B58 supertype associate with low viraemia, delayed onset of AIDS and, possibly, cytotoxic
41 nst all four dengue virus serotypes, and the viraemia due to each of the four vaccine components afte
42 time to viral rebound correlated with total viraemia during acute infection and with proviral DNA at
43 We investigated the occurrence of detectable viraemia during ART below this threshold and its effect
45 a single treatment rapidly suppressed plasma viraemia for 3-5 weeks in some long-term chronically SHI
46 er half-life of antibodies led to control of viraemia for an average of 60 days after cessation of th
50 the community programme, shorter duration of viraemia, higher CD4 count and transfers into programme
51 workplace patients had a longer duration of viraemia, higher VL, lower CD4 count, and higher reporte
52 e failure of ART with a lenient threshold of viraemia (HIV RNA viral load >/=1000 copies per mL).
55 ntibodies can prevent infection and suppress viraemia in humanized mice and nonhuman primates, but th
56 heir ability to block infection and suppress viraemia in macaques infected with the R5 tropic simian-
57 viral load-the approximately stable value of viraemia in the first years of chronic infection-is a st
59 ompared the incidence and persistence of HCV viraemia in these two groups over four consecutive 6-mon
65 e we show that sudden breakthrough of plasma viraemia occurred after prolonged immune containment in
66 ERPRETATION: In this large cohort, low-level viraemia occurred frequently and increased the risk of v
69 gical failure--which we defined as confirmed viraemia of more than 1000 copies per mL--in the switch
70 mpromised local viral retention, exacerbated viraemia of the host, and impaired local B-cell activati
72 nset delayed, reflecting significantly lower viraemia (p<0.0001) and blood monocyte-activation patter
74 ts with seropositive donors, the duration of viraemia (p=0.0480) and number of days of ganciclovir tr
76 oss-reactive antibodies prolonged YF vaccine viraemia, provoked greater pro-inflammatory responses, a
77 -1-infected individuals by 0.8-2.5 log10 and viraemia remained significantly reduced for 28 days.
79 We have investigated whether cytomegalovirus viraemia remains a significant risk factor for progressi
81 he occurrence rate of clinically significant viraemia resulting in initiation of cytomegalovirus-spec
83 BTV infection of ruminants results in a high viraemia, suggesting that repeated sharing of needles be
84 on, and tight correlation of PET signal with viraemia suggests target-cell activation determines stea
85 fections are characterized by early peaks of viraemia that decline as strong cellular immune response
86 characterized by: occasional blips of plasma viraemia that ultimately waned; predominantly undetectab
87 on dynamics showed that the duration of HCMV viraemia, the peak viral load, and the growth rate of HC
88 gh the Zika virus (ZIKV) rapidly establishes viraemia, the target cells and immune responses, particu
89 in a rapid and precipitous decline of plasma viraemia to undetectable levels in rhesus monkeys chroni
95 g resting CD4(+) T cells of patients in whom viraemia was fully suppressed by antiretroviral therapy,
100 ssociated with very low levels of persistent viraemia, which leads to the establishment of T-cell imm
101 s in epitopes associated with suppression of viraemia will accumulate as the epidemic progresses, and
105 uick and accurate approach for assessing HIV viraemia, with excellent concordance with validated labo
106 rcentage point in a community, prevalence of viraemia would need to be reduced by 4.34%, and ART use
107 NA and are rapidly eliminated at the peak of viraemia, yet the mechanism by which HIV-1 induces helpe
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