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1 n healing, pain resolution, and cessation of viral shedding).
2 ntly declined among participants with no/low viral shedding.
3 DNAemia and limited tissue dissemination and viral shedding.
4 thus controlling both recurrent lesions and viral shedding.
5 n subjects with similar illness severity and viral shedding.
6 ce remain infected for life, with periods of viral shedding.
7 n the mid-1980s showed nearly constant fecal viral shedding.
8 because lesions are accompanied by frequent viral shedding.
9 viral titers and decreasing the duration of viral shedding.
10 duration (P = .001) and titer (P = .005) of viral shedding.
11 l reactivation by explantation or peripheral viral shedding.
12 a exist about oseltamivir's ability to alter viral shedding.
13 t seen in convalescent mice eliminated nasal viral shedding.
14 ant increase in the risk of complications or viral shedding.
15 loss of lesion pain and time to cessation of viral shedding.
16 10 animals fed intravenous TPN had continued viral shedding.
17 ques and may be useful in evaluation genital viral shedding.
18 integral features of CMV pneumonitis but not viral shedding.
19 gating asymptomatic patients, and monitoring viral shedding.
20 monitored for clinical signs of disease and viral shedding.
21 isease course, patient-specific factors, and viral shedding.
22 illness, and with lower Ct values and longer viral shedding.
23 mal signs of disease, with only intermittent viral shedding.
24 ve days reduces its efficacy in curbing peak viral shedding.
25 ing as a reservoir for recurrent disease and viral shedding.
26 follicles, suggesting a novel mechanism for viral shedding.
27 of VVC, and VVC is associated with increased viral shedding.
28 ective against symptomatic RSV infection and viral shedding.
29 resulting in pathological recurrence and/or viral shedding.
30 onsistent with the peak level of viremia and viral shedding.
31 s complicated by recrudescence of high-grade viral shedding.
32 iratory disease and/or prolonged duration of viral shedding.
33 opment of antibody did not have an impact on viral shedding.
34 5 sequential mid-turbinate swabs to measure viral shedding.
35 lted in different degrees of lung damage and viral shedding.
36 sulted in different degrees of pathology and viral shedding.
37 ection causes recurrent lesions and frequent viral shedding.
38 and lower respiratory tract and much reduced viral shedding.
39 ved survival and reduced genital lesions and viral shedding.
40 ot serum antibodies, correlated with reduced viral shedding.
41 vival but did not reduce genital lesions and viral shedding.
42 th the throat viral load and the duration of viral shedding.
43 g resistance, most probably due to prolonged viral shedding.
44 ntly declined among participants with no/low viral shedding (-0.04 +/- 0.02, P = 0.047, interaction P
46 , 15 episodes (17%) had instances of seminal viral shedding 400 copies/mL despite viral suppression i
47 train EDIM) induced complete protection from viral shedding after challenge for at least 6 weeks afte
51 indication of ISS efficacy, the magnitude of viral shedding also was significantly reduced in ISS-tre
53 ys (43.0%; 95% CI, 39.8%-46.5%) with genital viral shedding among persons with symptomatic genital HS
55 Of 37 participants challenged, 16 (43%) had viral shedding and 27 (73%) developed symptoms, with 12
59 , and HA stalk antibody levels and influenza viral shedding and disease duration using accelerated fa
60 tients face a considerable risk of prolonged viral shedding and emergence of escape mutations after e
62 es protective immunity that can reduce acute viral shedding and latent infection in a mouse genital m
63 e cohort of 128 HSV-2-infected persons whose viral shedding and lesion frequency was measured by dail
65 induced diarrhea; however, there was reduced viral shedding and mortality in the icPEDV-EnUmt-infecte
67 otracted infection was defined as persistent viral shedding and prolonged symptoms unresponsive to an
69 eneral, host immunity is sufficient to clear viral shedding and recurrences, although it is insuffici
70 avn virus-infected bats had higher levels of viral shedding and shed the virus for a longer period, p
71 gression to severe COVID-19, or cessation of viral shedding and should not be used to treat patients
77 easures were frequency of infection based on viral shedding and/or seroconversion (prophylaxis) or qu
78 a scenario with R0 = 3.0, 60% presymptomatic viral shedding, and a dialysis patient being the infecti
79 were associated with significantly shortened viral shedding, and among adults they were also associat
80 n continued protection against infection, no viral shedding, and boosting of the immune response.
83 with lower [corrected] symptom scores, less viral shedding, and improved health, activity, and sleep
84 e incidence of reactivation and asymptomatic viral shedding, and limit morbidity and mortality from a
85 and N-antigen, burden of RNA and infectious viral shedding, and lower Spike-specific IgG levels with
86 ad more severe disease/complications, longer viral shedding, and more antiviral resistance while demo
87 d mild to moderate diarrhea, lower titers of viral shedding, and no mortality, whereas the icPC22A vi
92 CD8(+) T cells in ss7(-/-) animals prolonged viral shedding, and transfer of immune ss7(-/-) CD8(+) T
95 n high association between the CPV score and viral shedding, as long as the timing of these sessions
97 ril in decreasing the signs and symptoms and viral shedding associated with a viral respiratory infec
99 n treatment showed a significant decrease in viral shedding at day 3 relative to monotherapy, this di
101 ; however, vaccinated animals showed reduced viral shedding at multiple time points after infection.
103 seroconversion (prophylaxis) or quantitative viral shedding based on titers and duration of virus rec
107 icantly reduced IAV titers and shortened the viral shedding but did not completely block direct conta
109 buffer, compared with normal saline, reduced viral shedding by 1 log unit (10(3) vs. 10(4) 50% tissue
110 titers by 2.0 log10, the median duration of viral shedding by 3 days, and the frequency of febrile i
112 y, this data was used to demonstrate chronic viral shedding by an immunocompromised, hospital-acquire
113 on of oseltamivir treatment with duration of viral shedding by polymerase chain reaction or with the
116 the single AA331 or AA385 mutant had reduced viral shedding, comparable to cell-culture passaged CDC-
118 refed enterally for 5 days were positive for viral shedding, compared with 8 of 12 matched TPN-fed an
119 RNA throughout lactation and more-consistent viral shedding, compared with mothers who did not transm
124 o analyze jointly both symptom reporting and viral shedding data from a three-armed study of influenz
126 ion from respiratory samples, variability in viral shedding duration, lack of effective therapy, and
127 ell as in the accurate determination of live viral shedding during convalescence to inform decisions
130 yngeal and saliva samples displayed distinct viral shedding dynamics, and salivary viral burden corre
131 CE Sexual transmission of HSV-2 results from viral shedding following reactivation from latency.
132 y correlated with protection from developing viral shedding following virus challenge at day 90 and c
134 enza disease in 69% of individuals with mean viral shedding for 4-5 days and significant rises in con
135 ients with 2009 H1N1 influenza pneumonia had viral shedding for over 5 weeks despite therapy with ose
137 olling and will evaluate the effect of 4b on viral shedding from sanctuary sites in EBOV survivors.
138 or did such therapy decrease the duration of viral shedding from the nasopharynx among patients with
139 respiratory tract infection in 12 (67%), and viral shedding from the nasopharynx was prolonged for 7
143 , 15 episodes (17%) had instances of seminal viral shedding >=400 copies/mL despite viral suppression
147 luenza vaccine (LAIV) for immunogenicity and viral shedding in a randomized, placebo-controlled trial
150 contrast, there was no difference in ocular viral shedding in B6-E mice transplanted with 129 or B6
152 systemic infection and frequent, high-titer viral shedding in bodily fluids occurred following oral
153 Safety evaluations included adverse events, viral shedding in body fluids, and vector antibody respo
154 of the placenta and genital tract; increased viral shedding in breast milk from inflammation of breas
155 therapy and emergence of drug resistance on viral shedding in children infected with influenza A or
156 therapy, and emergence of drug resistance on viral shedding in children infected with influenza A or
157 s led to reduced viral loads in the lung and viral shedding in faeces, and also alleviated the inflam
158 can establish chronic infections with active viral shedding in healthy humans but whether persistence
159 therapies may lead to prolonged disease and viral shedding in individuals infected with severe acute
161 t of fever, lesion appearance, peak viremia, viral shedding in nasal and oral swabs, peak cytokine le
162 aled statistically significant reductions in viral shedding in nasal secretions (P<.001), nasal mucus
165 Time to clinical resolution and change in viral shedding in nasopharyngeal specimens were the prim
167 points were duration of clinical illness and viral shedding in patients treated less than and more th
169 The timing and intensity of respiratory viral shedding in patients with MERS closely matches tha
170 or oseltamivir to reduce patient illness and viral shedding in people with influenza, in whom treatme
171 s but that only a few of these may result in viral shedding in pigs upon infection, providing opportu
173 me polymerase chain reaction in blood and by viral shedding in saliva, in 878 people aged 3 to 89 yea
174 DNA detection by real-time PCR, in blood and viral shedding in saliva, in 878 people aged 3 to 89 yea
178 er biopsies concurrent with the detection of viral shedding in stool, and NV antigen expression was o
179 irradiation, vaccinated mice showed reduced viral shedding in tears as well as a reduction in the in
180 erity of genital lesions and lower levels of viral shedding in the genital tract after HSV-2 challeng
181 Seropositivity for HSV-2 is associated with viral shedding in the genital tract, even in subjects wi
182 ecreased change from baseline viral load and viral shedding in the multiple-dose group compared with
183 eral nutrition-fed animals continued to have viral shedding in the nasal passages compared to one of
189 o adrenergically induced reactivation, i.e., viral shedding in the tears, compared with rabbits infec
190 reports have describe high-level persistent viral shedding in the urine of infected patients, but th
191 ents, the proportion of participants showing viral shedding in their stools, the time to cessation of
196 oung children who acquire CMV have prolonged viral shedding into the urine and saliva, but whether th
200 e first 3 days of parotitis, suggesting that viral shedding is minimal after the first 3 days of symp
202 are common in the first 100 days after HCT, viral shedding lasts more than 3 weeks in half, and lowe
203 Bs demonstrated marked heterogeneity in RAVV viral shedding loads consistent with the Pareto Principl
204 ad significantly higher and prolonged rectal viral shedding loads, as well as significantly prolonged
205 ly prevents severe illness but also curtails viral shedding, lowering transmission risks from treated
206 h persistently infected (PI) cells extending viral shedding, maintaining inflammation, and providing
208 al and fecal samples were self-collected for viral shedding measured by reverse-transcriptase-polymer
211 neither shortened the duration of SARS-CoV-2 viral shedding nor improved symptoms in outpatients with
213 ease (3 to 4 logs) in ocular, but not nasal, viral shedding occurred during acute infection relative
216 role of variant and host in individual-level viral shedding of VOCs is essential to inform Coronaviru
218 tract (FGT) are critical for suppression of viral shedding or effective preexposure prophylaxis.
220 therapy appears to be inadequate in reducing viral shedding or mortality once pneumonia is establishe
226 comparing model accuracies across different viral shedding patterns and by parameterizing our model
231 .6%]; P = 0.93), had significantly decreased viral shedding (positive cultures compared with total cu
232 ee serotypes and intestinal immunity (faecal viral shedding post-challenge) to serotype 2, analysed i
233 pQAC-N showed reduced clinical severity and viral shedding postchallenge on par with protection obse
235 moderate disease characterized by consistent viral shedding, pulmonary infiltrates, and elevated infl
236 two tests was highest early in the course of viral shedding (r = 0.91, days 0 to 6), whereas during d
237 Our analysis suggests that the duration of viral shedding ranges from 23 to 50 days between individ
243 promised patients often experience prolonged viral shedding, resulting in an increased risk of viral
247 ess common in children than adults, although viral shedding still occurs in asymptomatic children.
248 e type I IFN receptor had minimal effects on viral shedding, suggesting that endogenous type I IFN si
249 sponses were noted during the peak period of viral shedding, suggesting that protection was due to sp
250 tion of a high Treg to Tconv ratio with high viral shedding suggests that the balance between regulat
251 with placebo, rimantadine treatment reduced viral shedding, systemic symptoms, and levels of IL-8.
252 racted SARS-CoV-2 infections with persistent viral shedding that could pose a wider public health ris
253 simplex virus 2 (HSV-2) from latency causes viral shedding that develops into recurrent genital lesi
254 n, with a prolonged period of oral and nasal viral shedding that is not accompanied by clinical signs
255 nfluenza infection, aged mice have prolonged viral shedding that is presumably due to lower anti-infl
256 ng in their stools, the time to cessation of viral shedding, the cell culture infective dose of shed
257 ngitudinal daily symptom scores, duration of viral shedding through day 10, and symptoms on day 120.
260 l performance largely depends on a monotonic viral shedding trajectory following case detection.
264 ing placebo, the median time to cessation of viral shedding was 7 days (hazard ratio [HR] = 0.81; 95%
266 measured at days 0, 7, 28, and 56, and stool viral shedding was assessed up to 28 days post-vaccinati
269 Importantly, the frequency of recurrent viral shedding was considerably reduced in GEN-003/MM-2-
271 Ten LAIV recipients shed virus; the latest viral shedding was detected 7 days after vaccination.
282 ported in the literature, but information on viral shedding was only available for 40 case-patients.
285 ly lower, and the duration of nasopharyngeal viral shedding was shorter in some vaccinated monkeys af
287 imens from HSV-2 positive women, genital HIV viral shedding was similar during symptomatic and asympt
288 ents, greater peak CMV DNAemia and increased viral shedding were associated with stronger CD8+ respon
294 Last, participants with a single day of viral shedding were three times more likely to be female
295 s, such as recurrent parotitis and prolonged viral shedding, were observed mostly in Marshallese indi
296 e of immunosuppression, leading to increased viral shedding, which could interfere with long term mis
299 p (n = 13), and the median (IQR) duration of viral shedding with therapy was reduced from 107 (83-131
300 al herpes, and we compared their patterns of viral shedding with those in a similar cohort of 90 subj