ライフサイエンスコーパス: uninfected

1 n infant will be infected with RSV or remain uninfected.

2 infants and children who are HIV-exposed but uninfected.

3 ty and higher beta-diversity compared to HIV-uninfected.

4 One-hundred and forty-five HIV-uninfected (68 IIV3 and 77 placebo-recipients) and 140 H

5 ss was 41% higher in HIV-infected versus HIV-uninfected (adjusted hazard ratio [aHR], 1.41; P < 0.001

6 seroprevalence between HIV-infected and HIV-uninfected adolescents and adults, and the low response

7 T-6, and Rv2660c, for M.tb-infected and M.tb-uninfected adults.

8 ay 21, followed by exposure to feeding by an uninfected Aedes aegypti mosquito at day 42 to assess su

9 raft loss was 41% higher in HIV-infected vs. uninfected (aHR,1.41; P<0.001).

10 Uninfected AMs were isolated from bronchoalveolar lavage

11 Long term follow-up occurred for 173 uninfected and 106 infected infants at age 4 years (rang

12 Long term follow-up occurred for 173 uninfected and 106 infected infants at age 4 years (rang

13 articipants (aged 18-65 years), who were HIV-uninfected and at low-risk for HIV, were randomly assign

14 samples showed a clear discrimination among uninfected and early-stage (1 and 2 months) and cancerou

15 acterized blood plasma-derived EVs from both uninfected and HIV-infected individuals, little is known

16 ed from 0.82 to 0.92 and 0.81 to 0.85 in HIV-uninfected and HIV-infected individuals, respectively.

17 Uninfected and HIV-infected macrophages and T cells trea

18 HIV-uninfected and HIV-infected Malawian adults initiating a

19 aracterization of SP and SP-derived EVs from uninfected and HIV-infected men.

20 sing subclinical and clinical disease in HIV-uninfected and HIV-infected persons, assessed by area un

21 l translocation, compared to HIV-exposed but uninfected and HIV-unexposed children, which may play a

22 Determinants of transitions between uninfected and infected states were assessed by hrHPV ty

23 temporal dynamics of the URT microbiomes of uninfected and influenza virus-infected humans and ferre

24 e (SP) in human immunodeficiency virus (HIV)-uninfected and to IPTp-placebo in HIV-infected women.

25 infection, which was significantly lower in uninfected animals and SIV-infected animals receiving AR

26 negative tissue and respiratory samples from uninfected animals tested negative on the Ultra.

27 he DRG of SIV-infected animals compared with uninfected animals.

28 In uninfected asthmatic subjects, higher numbers of circula

29 dividuals infected with SARS-CoV-2 and those uninfected at a hospital in Sweden.

30 on infected blood, ticks were transferred to uninfected blood to stimulate bacterial replication with

31 infection in vitro, both virus-infected and uninfected bystander cells resist STAT1 phosphorylation

32 ting TRAILshort causes more HIV-infected and uninfected bystander cells to die.

33 stines and feces, leading to transmission to uninfected cage-mate mice.

34 ring BoHV-1 latency than in reactivation and uninfected calves.

35 protein (NAB1) to induce myelosuppression of uninfected CD34(+) hematopoietic progenitor cells (HPCs)

36 both vaccines were protective compared to an uninfected cell lysate.

37 basolateral export of HSV-1 from infected to uninfected cells by direct cell-to-cell contact.

38 HSV-1 may spread from infected to uninfected cells by two main routes: by cell-free virus

39 y in HSV-1-infected cells and only rarely in uninfected cells or infected cells exposed to antivirals

40 Confocal imaging of uninfected cells shows endogenous Mov10 localized at P-b

41 e EV pathway to transfer proviral signals to uninfected cells that prime the cellular environment for

42 litate local inflammation and recruitment of uninfected cells to activation sites, causing latently i

43 ion, we characterized exosomes released from uninfected cells, and demonstrated that over 99% of the

44 infected bat cells were higher, relative to uninfected cells, and disrupting the interferon response

45 In uninfected cells, GBF1 activates small GTPases of the Ar

46 Compared with uninfected cells, significant upregulation of over 4,000

47 When compared to uninfected cells, the TCR repertoire of reservoir cells

48 moglobin from the suspension of infected and uninfected cells, which significantly increased the sens

49 re than 4,700 proteins in prion infected and uninfected cells.

50 lular environment to promote virus spread to uninfected cells.

51 o increase the efficiency of virus spread to uninfected cells.

52 nd altered vesicle size compared to EVs from uninfected cells.

53 cromolar range while showing no toxicity for uninfected cells.

54 duced senescence, promoting proliferation of uninfected cells.

55 event spread of virus to neighboring, as yet uninfected, cells.

56 ly enriched in viral genomic RNA relative to uninfected cellular mRNAs, and we mapped at single-nucle

57 y human immunodeficiency virus (HIV)-exposed uninfected children (HEU), with elevated rates of all-ca

58 impaired immunity in perinatally HIV-exposed uninfected children (HEU), with elevated rates of all-ca

59 2 years of life among HEU and HIV-unexposed uninfected children (HUU) in the United States.

60 infected children, and 56 HIV-unexposed and -uninfected children aged 2-10 years old in Uganda.

61 ition of gut microbiota in HIV-infected and -uninfected children and assessed associations between gu

62 or positive anti-HCV at age >=24 months; 2) uninfected children lacked these criteria and had negati

63 ically significant") was detected in 5.8% of uninfected children, 14.7% of HIV-infected participants

64 tional study in 57 PHIVs, 59 HIV-exposed but uninfected children, and 56 HIV-unexposed and -uninfecte

65 e an infected sibling contact (p=0.001) than uninfected children.

66 ness of the microbiota closer to that of HIV-uninfected children.

67 ces between HIV-infected and HIV-exposed but uninfected children.

68 Infected and uninfected chub exhibited no significant differences in

69 of D. citri nymphs and adults into healthy (uninfected) citron leaves when both vector stages were r

70 moniae carrier mice were able to transmit to uninfected cohabitating mice.

71 colons was 5- to 10-fold higher than that in uninfected colons.

72 smoking (P < .001) and comorbid illness than uninfected comparators.

73 Under uninfected condition, Apc(Min/+)/Atg16l1(DeltaIEC) mice

74 ubstantially differentially methylated under uninfected conditions.

75 luenza A(H1N1) infection and 10 age-matched, uninfected control lungs.

76 stpartum HM exosomes from HIV-1 infected and uninfected control mothers (n = 36).

77 in infected subjects than responses seen in uninfected control subjects.

78 trachomatis (CT) infection and asymptomatic, uninfected control women from an urban sexually transmit

79 ad a higher prevalence of elevated FeNO than uninfected controls (27.5% vs 12.3%; P < .001).

80 lence of M-HS was lower in PWH compared with uninfected controls (8.6% vs 14.2%, P < .01).

81 PLWH had higher FeNO than uninfected controls (median, 17.0 [interquartile range {

82 itial chest CT findings in PWH (n = 754) and uninfected controls (n = 470).

83 viral respiratory infection (n = 138) and in uninfected controls (n = 74).

84 18 in HIV-1-infected individuals compared to uninfected controls (p < 0.001) and a significant correl

85 PWH with human immunodeficiency virus (HIV)-uninfected controls and determined risk factors for M-HS

86 We assessed FeNO levels in PLWH and matched uninfected controls and investigated whether human immun

87 ction Study and in 1618 age- and sex-matched uninfected controls from the Copenhagen General Populati

88 stinguish HIV-infected patients from healthy uninfected controls in a total of 120 blood plasma sampl

89 ts, area hospitals during April-June 2020 vs uninfected controls matched on gestational age.

90 drial transcripts were similar to those from uninfected controls or increased slightly during vesicle

91 ), and 30 human immunodeficiency virus (HIV)-uninfected controls were assessed.

92 d between 3 and 8 days post-infection, and 3 uninfected controls were enrolled in this study.

93 Eight hundred sixty-four PWH and 75 uninfected controls were included.

94 IV infection and 125 demographically-matched uninfected controls who completed MRI and neuropsycholog

95 in NT-proBNP levels between PHIV with HF and uninfected controls with HF.

96 ral pathogens were quantified by ELISA in 68 uninfected controls, 62 individuals with latent TB infec

97 b responses or no neutralization breadth and uninfected controls, identifying consistent features of

98 with human immunodeficiency virus (PWH) and uninfected controls, IL-10 was measured in serum samples

99 tochondrial genes were similar to those from uninfected controls, whereas others increased slightly d

100 microcephaly, asymptomatic ZKV infection, or uninfected controls.

101 nfected controls, and 7.1% of monocytes from uninfected controls.

102 , showed increased MUC16 binding compared to uninfected controls.

103 collected from 177 HIV-infected and 103 HIV-uninfected controls.

104 OMO) Study and matched 1:1 on age and sex to uninfected controls.

105 ncytial virus and measles virus, compared to uninfected controls.

106 PWH compared with demographically comparable uninfected controls.

107 trollers; 30 viremic controllers; and 30 HIV-uninfected controls.

108 blood CD8 T cells in ART-treated HIV(+) and uninfected controls.

109 mong patients with TB disease and latent and uninfected controls.

110 a7-defined subsets at acute infection and in uninfected controls.

111 ter praziquantel treatment and compared with uninfected controls.

112 d lab raised beagles to varying densities of uninfected copepods in 2 liters of water to evaluate the

113 endothelial cells in culture, but not their uninfected counterparts.

114 lity than children who are HIV-unexposed and uninfected despite safer breastfeeding and improved mate

115 Studies of outliers-individuals remaining uninfected despite viral exposure and healthy young pati

116 SARS-CoV-2-uninfected donor sera exhibited specific neutralizing ac

117 The priority is to select uninfected donors to transplant uninfected recipients wh

118 3 in atherosclerotic plaque tissues from HIV-uninfected donors.

119 at most of the population of Geneva remained uninfected during this wave of the pandemic, despite the

120 contacts who were either infected (LTBI) or uninfected (EMI-TB Discovery Cohort, Pontevedra Region,

121 in KSHV-infected cells was recapitulated in uninfected endothelial cells by the exogenous expression

122 n infected erythrocyte (IRBC) is attached to uninfected erythrocytes (URBC).

123 ce, these antibodies induce the clearance of uninfected erythrocytes after binding to PS exposed in t

124 The loss of uninfected erythrocytes is an important contributor to m

125 ed erythrocytes through lysis and removal of uninfected erythrocytes.

126 esis of malaria by inducing the clearance of uninfected erythrocytes.

127 2017 among Thai and Vietnamese PHIV and HIV-uninfected females 12-24 years, matched by age group and

128 We enrolled 93 PHIV and 99 HIV-uninfected females.

129 in fields with high disease pressure than in uninfected fields, and microbiome succession over time w

130 exhibited lower oxidative damage compared to uninfected fish, irrespective of their pollutant load.

131 e consumption of pathogen-laden carcasses by uninfected fish.

132 ated to an increase in the somatic growth of uninfected fish.

133 otent protection; 10 of 12 macaques remained uninfected following 15 SIV challenges.

134 hat the array is readily able to distinguish uninfected from convalescent COVID-19 subjects, and prov

135 ; complete repair occurred within ~10 min in uninfected gastroids.

136 combined HIV-positive groups but not in the uninfected group.

137 formed in active S. stercoralis infected and uninfected groups.

138 hich did not cross-react in vaccinated or in uninfected guinea pigs.

139 Sera from O. viverrini-infected and uninfected hamsters were analyzed using multivariate ana

140 hearts transplanted/donors recovered) of HCV-uninfected (HCV-) to those of HCV+ nonviremic (HCV-NV) a

141 tely distinguished between convalescents and uninfected healthy blood donors with a predominantly CD4

142 ere adults aged 18 to 50 years, who were HIV-uninfected, healthy at screening based on their medical

143 (iii) In uninfected HEp-2 cells, hnRNPA2B1 is localized in the nu

144 IV-unexposed (HU) (n = 212) and HIV-exposed, uninfected (HEU) (n = 71) children received measles vacc

145 obiota of HI and perinatally HIV-exposed-but-uninfected (HEU) children will significantly differ from

146 e anthropometric outcomes in HIV-exposed but uninfected (HEU) children with those in children not exp

147 MPAACT] P1060); 183 age-matched, exposed but uninfected (HEU) children; and 182 unexposed and uninfec

148 Children who are HIV-exposed uninfected (HEU) have higher morbidity and mortality tha

149 found and lasting impacts on the HIV-exposed uninfected (HEU) infant, including increased mortality a

150 HIV-exposed but uninfected (HEU) infants are at an increased risk of man

151 hospitalization for infection in HIV-exposed uninfected (HEU) infants as compared to HIV-unexposed (H

152 Human immunodeficiency virus (HIV)-exposed, uninfected (HEU) infants experience high rates of infect

153 human immunodeficiency virus (HIV)-exposed, uninfected (HEU) infants, but the effects of this treatm

154 n born to HIV-positive mothers (HIV exposed, uninfected [HEU]) are more susceptible to severe infecti

155 ce compared to both IAV-infected LF mice and uninfected HF mice.

156 examine alpha-diversity measures between HIV-uninfected (HIV-) and HIV-infected (HIV+) individuals.

157 er risk for sudden arrhythmic death than HIV-uninfected (HIV-) individuals.

158 IV+) men who have sex with men (MSM) and HIV-uninfected (HIV-) MSM controls reported their difficulty

159 HAART, and a comparator group of healthy HIV-uninfected (HIV-), age-matched controls were enrolled in

160 frequencies were higher than those found in uninfected HLA-A*02:01(+) donors (~2.5 x 10(-6)), but lo

161 ol levels modulate the preferential lysis of uninfected host cells by SLO, and therefore modulate the

162 gy-dependent plastid recycling is induced in uninfected host cells.

163 ched, Mycobacterium tuberculosis-exposed but uninfected household contacts (n = 32).

164 ta secretion, which inhibits myelopoiesis in uninfected HPCs.

165 Rafts were created using uninfected human foreskin keratinocytes (HFKs) and HFKs

166 Uninfected human patients and ferret URT microbiomes hav

167 doptive transfer of treated lymphocytes into uninfected humanized mice.

168 ible to severe infection than HIV-unexposed, uninfected (HUU) children, with altered innate immunity

169 fected (HEU) children; and 182 unexposed and uninfected (HUU) children.

170 significantly differ from HIV-unexposed-and-uninfected (HUU) children.

171 POWV-infected and uninfected I. scapularis females were fed on naive mice

172 HCV coinfection displayed a higher PASP than uninfected individuals ([Formula: see text]=1.10, 95% CI

173 d higher kynurenine-to-tryptophan ratio than uninfected individuals (P < .001).

174 Eligible volunteers were HIV-uninfected individuals aged 20-40 years who were at low

175 was increased in APTB cases in comparison to uninfected individuals and the ratio of TT-specific plas

176 a flow cytometry-based method in SARS-CoV-2-uninfected individuals and were particularly prevalent i

177 e strong discriminators between infected and uninfected individuals as well as between severity stage

178 EM) or an annular, expanding skin lesion and uninfected individuals from areas of endemicity.

179 /-4 years), gender, and education with 5 HIV-uninfected individuals from the CONSTANCES cohort.

180 ight and fasting metabolic parameters in HIV-uninfected individuals randomized to cabotegravir or a p

181 sponse to infection but may carry a cost for uninfected individuals, leading to the prediction that i

182 ymphocyte activation comparable with that in uninfected individuals.

183 l DNA in their blood (P = .031), compared to uninfected individuals.

184 DNA in blood (p = 0.031) compared to malaria uninfected individuals.

185 were associated with PASP and PH compared to uninfected individuals.

186 itudes that are lower than responses seen in uninfected individuals.

187 der and more diverse profile than those from uninfected individuals.

188 re proinflammatory signature than those from uninfected individuals.

189 (COVID-19) patients, but not in plasma from uninfected individuals.IMPORTANCE In work with pathogeni

190 th pattern and morbidity of syphilis-exposed uninfected infants are less understood.

191 Human immunodeficiency virus (HIV)-exposed, uninfected infants have higher risks of respiratory sync

192 -trimoxazole guidelines for HIV-exposed, HIV-uninfected infants in areas unaffected by malaria.

193 n immunodeficiency virus (HIV)-1-exposed but uninfected infants randomly assigned at 7 days of life t

194 trimoxazole among breastfed HIV-exposed, HIV-uninfected infants whose mothers are accessing a prevent

195 res and injected into the anal pore of unfed uninfected Ixodes scapularis nymphal ticks.

196 st, IFN-kappa is constitutively expressed in uninfected keratinocytes and responds only weakly to pat

197 d 6-month post-infected hamsters compared to uninfected liver tissues.

198 ented MTB test into one of the 3 groups: MTB uninfected, LTBI, or active TB.

199 Compared to uninfected LTx-recipients, NK cells from HCV-infected LT

200 In HIV-uninfected Malawian children, treatment with amoxicillin

201 ch successive generation highly dependent on uninfected male immigrants.

202 In line with the autocrine model, uninfected males expressed IAG from the first larval sta

203 of initially uncircumcised, non-Muslim, HIV-uninfected men in the Rakai Community Cohort Study in Ug

204 ease, or primary effusion lymphoma and 8 HIV-uninfected men receiving HIV preexposure prophylaxis (Pr

205 e diverse repertoire of miRNAs than EVs from uninfected men.

206 en monitored after systemic OVA challenge in uninfected mice and in mice infected chronically with Li

207 In uninfected mice, dietary inulin stimulated the growth of

208 Both infected and uninfected microglia infiltrated into hBORGs resulting i

209 cells but had no effect on the viability of uninfected monocytes.

210 bjects received primaquine, chloroquine, and uninfected mosquito bites.

211 Infected and uninfected mosquitoes showed differential responses to c

212 (8.4; 95% CI, 5.7-12.0) compared to the HIV-uninfected mothers (3.1; 95% CI 2.3-4.0).

213 in any significant apoptosis when exposed to uninfected mouse skin.

214 us (HIV)-coinfected and more recently in HIV-uninfected MSM, especially those receiving pre-exposure

215 ctors in pregnant African women who were HIV-uninfected (n = 314) versus HIV-infected (n = 42).

216 lus, a freshwater fish, infected (n = 73) or uninfected (n = 45) by acanthocephalan parasites Pomphor

217 HL among neonates with cCMVI compared to CMV-uninfected neonates was 89.5 (95% CI, 39.7-202.0).

218 from those with ZIKV without microcephaly or uninfected neonates.

219 rol nodes, requiring fewer nodes than in the uninfected network.

220 Infected neurons, as well as uninfected neurons treated with antivirals, had a greate

221 nodules, their presence in the nuclei and in uninfected nodule cells, and, intriguingly, their expres

222 the end of cellular processes, which contact uninfected oligodendrocytes.

223 ERT2/+;R26R-YFP/+ (Lrig1/YFP) mice that were uninfected or subsequently infected with cag (+) H. pylo

224 ecently, neutrophils have been identified in uninfected organs, challenging the classical view of the

225 rmic at 30-minute post-challenge compared to uninfected OVA-challenged controls.

226 IFN-gamma)(+) MAIT cells relative to that in uninfected P2C/5-OP-RU-treated mice.

227 duced in active S. stercoralis infection vs. uninfected participants (3.8%[1/26] vs. 30.0%[33/110], r

228 We included healthy, HIV-uninfected participants (aged 18-50 years) who were cons

229 odies were maintained indefinitely among HIV-uninfected participants (half-life, infinity; 95% confid

230 stool samples from 405 HIV-infected and 111 uninfected participants of the Copenhagen Comorbidity in

231 eated participants as compared to values for uninfected participants or infected, treated participant

232 mic population, we tested a cohort of 22,239 uninfected participants over 92,877 person-years of obse

233 .9pg/mL p=0.02, respectively), compared with uninfected participants.

234 y in terms of passage from an infected to an uninfected partner.

235 eived significantly more saline flushes than uninfected patients (P < .001) during the risk period.

236 eased significantly for HIV-infected and HIV-uninfected patients (P-trends = 0.008 and <0.001).

237 both a fixed-amount subsidy and a subsidy on uninfected patients in reducing the number of HAIs in a

238 sociated with good prognosis, whereas in HIV-uninfected patients the association was heterogeneous ov

239 Compared to MTB uninfected patients, LTBI was associated with a 0.24 dec

240 In HIV-uninfected patients, nonalcoholic fatty liver disease (N

241 tic infections (OIs) in the SHCS between MTB uninfected patients, patients with LTBI, and patients wi

242 d OR = 0.67, p = 0.033) when compared to MTB uninfected patients.

243 ncreased morbidity and mortality compared to uninfected patients.

244 anced by lower than expected mortality among uninfected patients.

245 ean, 294 [264-323] vs 365 [346-385] mm Hg in uninfected patients; p = 0.0005) as in potential lung do

246 -PHIV had shorter granulocyte TL compared to uninfected peers, regardless of cART.

247 rosis and fractures in later life than their uninfected peers.

248 rosis and fractures in later life than their uninfected peers.

249 iagnosis and sex, to an equal number of HTLV-uninfected persons (controls).

250 Unvaccinated or previously uninfected persons are susceptible to HAV infection, yet

251 tion remains higher in HIV-infected than HIV-uninfected persons.

252 ng ART but remained elevated compared to HIV-uninfected persons.

253 tabolite levels in sap from the infected and uninfected plants indicated that the transport of nitrog

254 nts infected by nitrogen-fixing bacteria and uninfected plants to investigate the effects of symbiosi

255 ver time was similar in heavily infected and uninfected plants.

256 tamate, and methylene glutamate, compared to uninfected plants.

257 icity were evaluated in HIV infected and HIV uninfected populations.

258 orty-five human immunodeficiency virus (HIV)-uninfected pregnant women (68 IIV3 and 77 placebo recipi

259 ividual participant-level data from 1617 HIV-uninfected pregnant women in Kenya (one trial; n=806) an

260 is to select uninfected donors to transplant uninfected recipients while maintaining safety for healt

261 om deceased donors with HCV viremia into HCV-uninfected recipients, followed by 8 weeks of once-daily

262 opreserved colon cells from SIV-infected and uninfected rhesus macaque monkeys and determined the mak

263 ntiating between SaLV-infected (SaLV(+)) and uninfected (SaLV(-)) saffron samples.

264 In HIV uninfected samples (n=384), the majority of RDTs had sen

265 t sensitivity was markedly lower than in HIV uninfected samples; only one RDT reached >95%.

266 Pre-exposure to uninfected sand fly bites or immunization with defined s

267 mpared the fecal microbiomes of infected and uninfected schoolchildren from the Argungu Local Governm

268 Cord blood cells from females of HIV-uninfected sex-discordant twins are more activated (p =

269 smokers (n = 11) and nonsmokers (n = 15) and uninfected smokers (n = 7) and nonsmokers (n = 10).

270 bronchoalveolar lavage of HIV-infected and -uninfected smokers and nonsmokers.

271 a cross-sectional study of 101 PLWH and HIV-uninfected South African patients with active TB and con

272 he antibody levels of COVID-19-infected and -uninfected specimens (P < .0001).

273 s no difference between HIV-infected and HIV-uninfected study participants in terms of CD4+ T-cell re

274 None of the 13 specimens from uninfected subjects displayed antibodies to either antig

275 achieved between specimens from infected and uninfected subjects, and a wide range of serum/plasma an

276 ications in children who are HIV-exposed but uninfected, such as microcephaly, warrant ongoing survei

277 d from 101 surgical patients with sepsis, 53 uninfected surgical patients, and 16 blood donors by usi

278 TG explants from latently infected, but not uninfected, TG contained significantly more GR-positive

279 ost-IIV3; with responses being higher in HIV-uninfected than HIV-infected women.

280 expression profiles of POWV-infected versus uninfected ticks.

281 vement, and subsequent unloading into distal uninfected tissues.

282 area and a higher fluid secretion rate than uninfected tubules.

283 ve similar total net extrusion per tubule to uninfected tubules.

284 had a greater accumulation of Abeta(42) than uninfected untreated neurons.

285 Among HIV-uninfected vaccinees, there was no correlation (postvacc

286 Surprisingly, we find that an uninfected, virus-immune guinea pig whose body is contam

287 ved association arises through protection of uninfected wearers (protective effect), via reduced tran

288 unger than 18 years who were HIV-exposed but uninfected with at least one head circumference measurem

289 Children who are HIV-exposed but uninfected with microcephaly had lower mean scores on ne

290 compared in children who are HIV-exposed but uninfected with or without microcephaly.

291 vaginal metabolomic profiles as compared to uninfected women both before and after adjustment for th

292 ost-IIV3, with responses being higher in HIV-uninfected women than in women living with HIV.

293 In HIV-uninfected women, the prevalence of pfcrt mutants, pfdhf

294 vaginal metabolome between CT+, CT+/MG+ and uninfected women.

295 y involving 50 pairs of HIV-infected and HIV-uninfected women.

296 robiota and metabolomes of CT+, CT+/MG+, and uninfected women.

297 lower in HIV-infected women than that in HIV-uninfected women.

298 ency virus (PHIV) may be at higher risk than uninfected youth for persistent anogenital human papillo

299 quired HIV (PHIV) may be at higher risk than uninfected youth for persistent anogenital human papillo

300 (P = .03) and persistence (P = .01) than HIV-uninfected youth over a 3-year period.