ライフサイエンスコーパス: infect

1 evade the immune pathways of cells that they infect.

2 ic-associated harms for patients who are not infected.

3 of the share of the population that has been infected.

4 n modulating the probability of a bird being infected.

5 re HBsAg-positive, and 22/100 (22%) were HIV infected.

6 ans is an opportunistic fungal pathogen that infects ~280,000 people every year, causing >180,000 dea

7 nts with early infections, 14 shared strains infected 29 (41%) patients over five years; 16% (n=14) o

8 JC polyomavirus (JCPyV) infects 50 to 80% of the population and is the causative

9 rm that when poorly controlled, COVID-19 can infect a large proportion of the population, causing hig

10 that DksA is essential for B. burgdorferi to infect a mammalian host.

11 Toxoplasma gondii chronically infects a quarter of the world's population, and its rec

12 1N1)pdm09 viruses.IMPORTANCE Influenza virus infects a wide range of hosts, resulting in illnesses th

13 ospinal fluid (CSF) by flow cytometry in HIV-infected adults with cryptococcal (n = 31) and noncrypto

14 ian hamsters and 4 tissue samples from a NiV-infected African green monkey with viral loads as low as

15 f the bacterium Francisella tularensis, that infects alveolar macrophages.

16 were performed on stool samples from 405 HIV-infected and 111 uninfected participants of the Copenhag

17 a is subjected to ubiquitination in both EBV-infected and EBV-negative cells.

18 Thousands of health workers have been infected and outbreaks have occurred in hospitals, aged

19 ntiation was achieved between specimens from infected and uninfected subjects, and a wide range of se

20 ID-19, to not believe that they would become infected, and to feel less prepared for an outbreak.

21 ive, with unclear pathogenicity in naturally infected animals and only one experimental study demonst

22 SIV-infected animals showed decreased diversity of gut micro

23 In chronically infected animals with viremia initially controlled by co

24 ed by using histopathology images from these infected animals.

25 ntrol, randomized, open-label study in HIV-1-infected antiretroviral therapy-naive adults (CD4+ >=50

26 d increases colorectal tumorigenesis in 11G5-infected Apc(Min/+) mice.

27 by Mycobacterium tuberculosis (Mtb) latently infects approximately one-fourth of the world's populati

28 However, actively infected astrocytes were inducible, leading to increased

29 ds, and parts of South America, often become infected at birth and account for up to 95% of newly rep

30 EBV protein EBNA3A is expressed in latently infected B cells and is important for efficient EBV-indu

31 s associated with in vivo susceptibility, we infected BALB/c mice with recombinant AIVs with R292K (m

32 e whole genome of MERS-CoV from persistently infected bat cells, we identified that bat cells repeate

33 BEC and LEC, respectively) to show that KSHV-infected BECs progressively lose viral genome as they pr

34 y of paraffin-embedded sections of naturally infected biopsies indicated that CD20(+) B lymphocytes,

35 Airway sensitization of naive mice with RSV-infected BMDCs exacerbate a live challenge with RSV infe

36 ment downregulated CCR7 on Y. enterocolitica-infected bone marrow-derived DCs and purified MLN DCs, w

37 the probability of an individual host being infected by a haemosporidian parasite.

38 Single plant cells infected by bacteria were selected and sampled directly

39 agocytophilum from mice that were previously infected by feeding with DC-microinjected nymphal ticks.

40 diarrheal disease cholera, Vibrio cholerae, infected by ICP1, a phage ubiquitous in clinical samples

41 e laboratory strains of mice are not readily infected by SARS-CoV-2 because of species-specific diffe

42 nst fatal malaria in Plasmodium berghei ANKA-infected C57BL/6J mice, an experimental CM model.

43 T-treated HIV subjects occur in vitro in HIV-infected CD4 T cells remains unknown.

44 ll require the elimination of a reservoir of infected CD4+ T cells that persists despite HIV-specific

45 een groups following stimulation with an EBV-infected cell lysate.

46 imed to investigate the interactions between infected cell protein (ICP)0 and key elements of the IFN

47 n unit 1 (IEtu1) promoter that drives bovine infected cell protein 0 (bICP0) and bICP4 expression.

48 Infected cell protein 0 (ICP0), an E3 ubiquitin ligase o

49 On the basis of immunofluorescence, infected cell types included CD68(+) type A (macrophage-

50 tion of Env on the surface of a virion or an infected cell.

51 that H(2)S/RSS impacts bacterial survival in infected cells and animals.

52 trate co-transport of Rab11A and IAV vRNA in infected cells and provide direct evidence that vRNA-ass

53 ately supports the inflammatory breakdown of infected cells at later time points.

54 Furthermore, HVT blocks apoptosis in infected cells but activates apoptosis in noninfected by

55 ional RNA/DNA hybrids (R-loops) that form in infected cells during S-phase as a consequence of beta-A

56 otein redirects T cells to specifically lyse infected cells expressing the target virus-derived pepti

57 is used as a mechanism to remove bacterially infected cells from the body.

58 the JCI, Chaillon and coworkers assessed HIV-infected cells from various anatomic compartments obtain

59 re efficiently and produces higher yields in infected cells than T3D.

60 the potential locations of reservoirs of HIV-infected cells that persist during therapy.

61 Superresolution microscopy revealed in infected cells the vertical displacement of paxillin and

62 nowledge regarding mechanisms that allow HIV-infected cells to persist in individuals during combinat

63 sed ion-beam scanning electron microscopy of infected cells validated numerous membranous structures

64 smaller reduction in the proportion of HIV-1-infected cells within LNs per year on therapy that was s

65 luding the lifespans of short and long-lived infected cells, and the time to reach viral suppression

66 Within infected cells, EBOV downregulates STAT1 mRNA and interf

67 In infected cells, NucC activation leads to complete destru

68 virus particles from the plasma membranes of infected cells.

69 rol were rapidly trafficked to ehrlichiae in infected cells.

70 stence of a long-lived reservoir of latently infected cells.

71 l destruction and limited drug delivery into infected cells.

72 ere evaluated for the ability to detect FFPE infected cells.

73 pseudokinase (MLKL)-dependent necroptosis in infected cells.

74 l replication compartments in the cytosol of infected cells.

75 dding of viral particles from the surface of infected cells.

76 y early formation of a reservoir of latently infected cells.

77 N RNA in the cytoplasm compared to wild-type-infected cells.

78 s and promotes accelerated cell death in HSV-infected cells.

79 important immunomodulatory complexes within infected cells.IMPORTANCE Many viruses replicate almost

80 eplicate almost entirely in the cytoplasm of infected cells; however, how these pathogens are able to

81 Our results suggest that timing of TI in HIV-infected children has a long-term and measurable impact

82 Of 927 STEC-infected children, 41 (4.4%) had HUS at presentation; of

83 Interestingly, infected chub exhibited lower oxidative damage compared

84 on with CD4 count or HAND status for the HIV-infected cohort.

85 ever, the percentage of IFN-gamma(+) ILCs in infected colons was 5- to 10-fold higher than that in un

86 clear, as is the potential for this virus to infect companion animals, livestock, and wildlife that c

87 We found that, compared with isotype-treated infected control mice, anti-PD-1-treated mice had improv

88 tibiotarsal joints that were not observed in infected control mice.

89 h severe clinical disease compared with mock-infected controls.

90 ify the specific clinical characteristics of infected critically ill patients that mediate the associ

91 te with viral loads in recipients who became infected, cross-reactivity did appear to influence early

92 We showed that Mtb-infected CSE(-/-) mice survive longer than WT mice, and

93 We hypothesized that Chlamydia-infected DCs and epithelial cells present overlapping se

94 ding survival of cardiac allografts from CMV-infected donors.

95 and underlying mechanisms of HIV Tat in KSHV-infected endothelial cells undergoing viral lytic reacti

96 ster virus (VZV) is a skin-tropic virus that infects epidermal keratinocytes and causes chickenpox.

97 The virus naturally infects epithelial cells of the feather follicle epithel

98 thod for separating all stages of Plasmodium-infected erythrocytes through lysis and removal of uninf

99 By killing trophozoite-infected erythrocytes, PfGARP could synergize with other

100 especially in classical bacteriophages that infect Escherichia coli or Salmonella, yet, less is know

101 Specifically, small, infected females produced fewer offspring of poorer cond

102 te to protecting the host through killing of infected, foreign, stressed or transformed cells.

103 ronal apoptosis and microglial activation in infected ganglia.

104 xpression of Wnt3a and Dvl3 in P. gingivalis-infected gingival tissues, and increases disease severit

105 return-to-work considerations for exposed or infected health care workers, risk stratification and ma

106 strated that ATM expression is higher in HCV-infected hepatocytes and chronic HCV-infected liver biop

107 Kidney transplant (KT) outcomes for HIV-infected (HIV+) persons are excellent, yet acute rejecti

108 g the same HSV-1 epitope-specificities, from infected HLA-A*0201 positive symptomatic (SYMP) vs. asym

109 virus, increases the surface temperature of infected host plants (by an average of 2 degrees C), whi

110 he 993 infections, 260 were acquired from an infected household contact.

111 x tuberculosis (TB) cases and their latently infected household contacts who developed active TB up t

112 ey step during HCMV reactivation in latently infected HPCs is reexpression of viral major immediate e

113 ORF8b was abundantly expressed in MERS-CoV-infected Huh-7 cells.

114 HPVs infect human keratinocytes, and we previously reported t

115 tibody profile to HA and NA in two naturally infected human cohorts in Auckland, New Zealand: (i) a s

116 During pregnancy, the Zika flavivirus (ZIKV) infects human placentas, inducing defects in the develop

117 and 589,800 (95% PI, 578,800-595,600) people infected in 12 months, respectively.

118 se of neurodevelopmental sequelae in infants infected in utero.

119 CDRH2 that was isolated from the chronically-infected individual from whom the bent CDRH3 bNAbs were

120 with increased pvdbp copy number are able to infect individuals with naturally acquired antibodies hi

121 ses are often associated with high number of infected individuals (prevalence) and high pathogen load

122 (TAF) improves renal tubular markers in HIV-infected individuals but the impact on estimated glomeru

123 nfection rates, only a fraction of H. pylori-infected individuals develop gastric cancer.

124 f population-wide restrictions, isolation of infected individuals is key to curtailing transmission.

125 The unhealthy ecostates of infected individuals progress towards the healthy ecosta

126 Viral sequences from infected individuals were grouped into 3 distinct cluste

127 h the fecal-oral route, shed in the stool of infected individuals, and spread either by direct contac

128 ntaining CDRH3 is specific to particular HCV-infected individuals, we solved a crystal structure of t

129 nt of coronavirus disease 2019 (COVID-19) in infected individuals, who can either exhibit mild sympto

130 iagnostic testing capability for identifying infected individuals.

131 nsity dependence and the role of chronically infected individuals.

132 ent an opportunity to improve care for HIV-2-infected individuals.

133 ecting probably no more than 1 in 1,000 such infected individuals.

134 ections and providing the best treatment for infected individuals.

135 -B alleles, HLA-B*52:01, present in 22.5% of infected individuals.

136 evelopment of an adaptive immune response in infected individuals.METHODSWe studied 509 patients conf

137 ructural and functional MRI showed that ZIKV-infected infant rhesus macaques had persistent enlargeme

138 Human tracheal aspirates from RSV-infected infants showed elevated pro-IL-1beta mRNA and p

139 pe I, II, or III IFN receptors or STAT1 were infected intracerebrally with MuPyV.

140 t (KO) mice and wild-type (WT) controls were infected intranasally with S pneumoniae.

141 e and inhibited amastigote multiplication in infected J774 macrophages and BALB/c mice, respectively.

142 In sharp contrast, KSHV-infected LECs predominantly entered lytic replication, u

143 in Swiss mice using Porphyromonas gingivalis infected ligatures.

144 in HCV-infected hepatocytes and chronic HCV-infected liver biopsy specimens.

145 Graft and patient survival among HIV-infected LT recipients have shown improvement over time.

146 STAT-1 and STAT-4 phosphorylation in 29 HCV-infected LTx-recipients and 17 HCV-infected patients dur

147 paired hypoxic pulmonary vasoconstriction in infected lung regions, no studies have determined whethe

148 ication, both in vitro and in vivo in SIVmac-infected macaques, by upregulating antioxidant pathways

149 e and defines an adaptive homeostasis in the infected macrophage.

150 lar proliferation of T. cruzi amastigotes in infected macrophages in a concentration-dependent manner

151 Nevertheless, Legionella-infected macrophages induce an interleukin-1 (IL-1)-depe

152 In contrast, co-culture of LVS-infected macrophages with LVS-immune lymphocytes halted

153 FN-gamma binds to its receptor on Leishmania-infected macrophages, resulting in their activation, pro

154 elevated in Mycobacterium tuberculosis (Mtb)-infected macrophages.

155 Additionally, Smyd2 was induced by c-Myc in infected macrophages.

156 mpared to those of wild-type bacteria in the infected macrophages.

157 IAVs infect many avian species wherein they maintain a divers

158 Trypanosoma cruzi infects many cell types but preferentially persists in m

159 e 2 (EBV-2) strain has the unique ability to infect mature T cells.

160 Y. pestis-infected Mefv(M680I/M680I) FMF knock-in mice exhibited I

161 tical for A. phagocytophilum to productively infect mice, and immunization against their binding doma

162 f P. aeruginosa cells isolated from lungs of infected mice and examined the roles of upregulated regu

163 ile brain homogenates from symptomatic prion-infected mice are highly toxic to cultured neurons, exce

164 ) and that natural killer (NK) cells in CL13-infected mice are reduced in numbers and have an immatur

165 livery daily over 10 days to M. tuberculosis infected mice for FG2 HSA nanoparticles (0.4 mg/kg), FG

166 he wild-type virus and found that the DUBmut-infected mice had a statistically significant reduction

167 Mast cells from infected mice had lower expression of the activation mar

168 oid assay in colonic crypts isolated from CR-infected mice revealed elevated levels of LRP5/6 and FZD

169 Benznidazole treatment of infected mice significantly reduced their blood antigen

170 ulbar vacuolation in the brain parenchyma of infected mice with persistent CD11b(+) microglia/macroph

171 ast cell numbers were significantly lower in infected mice, and those that were present exhibited dec

172 examine viral population dynamics in orally infected mice, we produced over 100 CVB3 clones harborin

173 5 in the bronchoalveolar lavage fluid of RSV-infected mice, without increasing viral replication in t

174 ia is significantly decreased in Pbyop1Delta-infected mice.

175 VPA significantly augmented mortality in L.m infected mice.

176 ed inflammation, was also prevented in EW RV-infected mice.

177 Viruses that infect microorganisms dominate marine microbial communit

178 irus disease (COVID-19) pandemic has already infected millions worldwide and, with no vaccine availab

179 s and economies, with over 52 million people infected, millions of jobs and businesses lost, and more

180 Among HIV-infected, model of end-stage liver disease (aHR, 1.04; P

181 Indeed, survival of autophagy-inhibited HCMV-infected monocytes was rescued when MLKL and RIPK3 were

182 Among 12 persons who infected mosquitoes, polymerase chain reaction and ampli

183 use of antiretroviral therapy (ART) in HIV-1 infected mothers approximately 5% of new HIV-1 infection

184 is usually asymptomatic or mild, newborns of infected mothers can display severe symptoms, including

185 h phages are not motile themselves, they can infect motile bacterial hosts and spread in space via th

186 Phylogenetic analysis implies CRESS viruses infecting multicellular life have evolved independently

187 who were HIV-uninfected (n = 314) versus HIV-infected (n = 42).

188 y stricture was more likely in patients with infected necrosis or NP disease duration >=6 months.

189 eatic necrosis is indicated in patients with infected necrosis.

190 16 hai, and in olive oils containing 20% of infected olives.

191 y a key role in adaptive immunity by killing infected or cancerous cells.

192 ells of the human body to eliminate pathogen-infected or tumorigenic cells (i.e., target cells).

193 n, the ability to map its location within an infected organ or animal is needed to understand localiz

194 is the cause of an ongoing pandemic that has infected over 36 million and killed over 1 million peopl

195 of morbidity and mortality in the HBV/HIV co-infected patient population.

196 onfirmed coronavirus disease 2019 (COVID-19)-infected patients and specificity using 1,204 samples su

197 in 29 HCV-infected LTx-recipients and 17 HCV-infected patients during DAA-treatment.

198 Indonesian patients and 20% of reported H5N1-infected patients globally.

199 enerate 649 SARS-CoV-2 genome sequences from infected patients in New Zealand with samples collected

200 n of different leukocyte subsets in COVID-19-infected patients in relation to disease severity.

201 d between 20 February and 15 March 2020 from infected patients in Washington state in the United Stat

202 rigger immunopathogenic events in SARS-CoV-2-infected patients or enhance infection.

203 1035 HCV-infected patients were included, 667 (64%) coinfected wi

204 ity for all patients with HF and in COVID-19-infected patients with HF.

205 ere acute respiratory syndrome coronavirus 2 infected patients, even in the absence of hypoxia.

206 ence of antibody sequences across SARS-CoV-2-infected patients, highlighting stereotyped naive respon

207 ex vivo study of circulating Tfh from HIV-2-infected patients.

208 ion was associated with lower viral loads in infected patients.

209 against HDV in 12 treatment-naive HBV/HDV co-infected patients.

210 vels were significantly elevated in COVID-19-infected patients.

211 ity among Human Immunodeficiency virus (HIV) infected patients; however no consensus exists on HIV-re

212 Depletion of TREM-1 in EV-A71-infected PBMCs with peptide LP17 resulted in decreased l

213 nocytes isolated in an acute phase from DENV-infected pediatric patients correlates with severe disea

214 ly Parvoviridae; subfamily Hamaparvovirinae) infect penaeid shrimp.

215 ity rates among human immunodeficiency virus-infected persons in Africa.

216 The proximal colon of T. suis-infected pigs exhibited general inflammation around day

217 urcation facilitates recursive processing of infected population through linear least-squares fitting

218 ecent years, H5 HPAI viruses of this lineage infecting poultry in Asia have spilled over into wild bi

219 of air travel departing from airports in the infected provinces in China and directed to Africa to es

220 -log(10) reduction), which are used to treat infected PUs clinically.

221 VZV-infected qHA-sps, but not mock-infected qHA-sps, contain

222 VZV-infected qHA-sps, but not mock-infected qHA-sps, contained intracellular amylin, APP, a

223 them at increased risk of severe COVID-19 if infected (ranging from <5% of those younger than 20 year

224 dium (CM) induced canonical Wnt signaling in infected recipient cells while simultaneously inhibiting

225 dynamics take place, e.g., as in susceptible-infected-recovered (SIR) models.

226 st to DENV, SARS and MERS CoVs predominantly infect respiratory epithelium, not macrophages.

227 Long-lasting, latently infected resting CD4(+) T cells are the greatest obstacl

228 study, we used morphine dependent SIVmac251 infected rhesus macaque (RM) model to study the impact o

229 Using SIV-infected rhesus macaques, we analyzed multiple brain reg

230 ith sustained viral control after ATI in SIV-infected RMs.IMPORTANCE While effective, antiretroviral

231 The majority of HIV infected samples for which sensitivity was low did not h

232 Herpes simplex virus 1 (HSV-1) infects several types of cells, including neurons, but h

233 th rate of malaria parasites in the blood of infected subjects is an important measure of efficacy of

234 rum/plasma antibody levels was delineated in infected subjects.

235 ulation by fitting compartmental susceptible-infected-susceptible (SIS) transmission models simultane

236 nvestigate changes in blood chemistry in NiV-infected Syrian hamsters that survived or succumbed to d

237 These data show that HTLV-1-infected T-cell clones carrying key oncogenic driver mut

238 raze toxic endophyte (Epichloe coenophialum)-infected tall fescue (E+) and are hallmark signs of fesc

239 Viruses that infect the globally abundant SAR11 bacteria (pelagiphage

240 Phage Seahorse was able to infect the host in a broad range of pH and temperatures,

241 6) A and B are ubiquitous betaherpesviruses, infecting the majority of the human population.

242 itch" to control the fungal decision between infecting the plant or proliferating out of the plant.

243 large double-stranded DNA (dsDNA) virus that infects the unicellular green alga Chlorella variabilis

244 ously described phages appear to exclusively infect this genus.

245 amplifying partial viral genomes from 6 HeV-infected tissue samples from Syrian hamsters and 4 tissu

246 nce on the mechanisms of virus spread within infected tissues.

247 ) were found in the RLN of Y. enterocolitica-infected TNFRp55(-/-) mice.

248 ent relies on early detection and removal of infected trees.

249 poorer condition, while in contrast, large, infected turtles produced greater clutch sizes and large

250 laviviruses are now globally distributed and infect up to 400 million people annually.

251 al explanation for the distribution of human-infecting viruses across the animal orders studied.

252 Bacteria-infecting viruses, called phages, can encode quorum-sens

253 esembles glycoproteins from unrelated animal-infecting viruses, suggesting a common ancestor for thes

254 ized by severe disability and high levels of infected white blood cells.

255 Notably, treatment of infected wild-type mice with apoptotic cells significant

256 severity in the ceca and colons of all mice infected with a high-virulence strain of C. difficile; h

257 f primary lymphatic endothelial cells (LECs) infected with a lytically replicating KSHV BAC16 mutant.

258 We found P. destructans was infected with a mycovirus [named Pseudogymnoascus destru

259 Neonatal rat ventricular cardiomyocytes were infected with adenoviruses expressing either wild-type C

260 Rats were orally infected with Blastocystis subtype 4 (ST4) cysts, isolat

261 ication in pregnant women who become acutely infected with Brucella melitensis is spontaneous pregnan

262 hy human feces, treated with clindamycin and infected with C difficile with the addition of human MUC

263 Twenty-eight patients infected with carbapenem-resistant P. aeruginosa isolate

264 Importantly, mice infected with Cj-P1-DCA-Anaero showed attenuation of int

265 profound immunodeficiency, mice chronically infected with CL13 could be protected by vaccination wit

266 In this paper, we show that mice chronically infected with CL13 succumb to challenge with ectromelia

267 ogical and activity data from 32 individuals infected with COVID-19, identified from a cohort of near

268 ents do not respond to therapy despite being infected with fungi that are susceptible to the drug.

269 Children infected with GII.4 had more severe symptoms requiring m

270 ople who inject drugs identified as recently infected with HIV (n = 23) were analyzed for clustering

271 mus (BLT) humanized mice and rhesus macaques infected with HIV and SIV, respectively.

272 tudy in children and adolescents perinatally infected with HIV with low LS BMD, 48 weeks of alendrona

273 nce is a hallmark of CD4(+) T cells latently infected with human immunodeficiency virus 1 (HIV-1).

274 from brain homogenates from Syrian hamsters infected with Hyper prions and WT mice infected with Roc

275 demonstrate that endothelial cells latently infected with KSHV express several neuronal and NE genes

276 oluzzii were significantly more likely to be infected with malaria, compared to those that survived i

277 erapeutic protection in mice and guinea pigs infected with MARV.

278 The wounds were infected with methicillin-resistant Staphylococcus aureu

279 ibited impaired cytolytic activity, and mice infected with mouse cytomegalovirus (MCMV) displayed ele

280 Rbeta sequences from 58 individuals latently infected with Mycobacterium tuberculosis (Mtb) and to gr

281 hly resistant to pneumococcal pneumonia when infected with other serotypes.

282 mined the global AS changes in tomato leaves infected with Phytophthora infestans, the infamous Irish

283 sters infected with Hyper prions and WT mice infected with Rocky Mountain Laboratories prions yielded

284 lungs of superinfected mice compared to mice infected with S. aureus alone.

285 identification of individuals that have been infected with SARS-CoV-2 even if the infection was asymp

286 frican ancestry and high-risk APOL1 genotype infected with SARS-CoV-2 have emerged during the COVID-1

287 ry viral loads (VL) in asymptomatic children infected with severe acute respiratory syndrome coronavi

288 of venous thromboembolism events in patients infected with severe acute respiratory syndrome coronavi

289 Rhesus macaques (RMs) (n = 13) were infected with simian/human immunodeficiency virus SHIV.C

290 ymptoms were evident in immunodeficient mice infected with T. gondii, as associated with high express

291 f the transmission bottleneck between humans infected with the influenza virus; however, the methods

292 or mouse bone marrow-derived dendritic cells infected with the protozoan parasite Toxoplasma gondii (

293 Interferon-responsive PK1 cells were infected with these viruses and produced higher levels o

294 phlebovirus, and fatality rates among those infected with this virus are high.

295 e different levels of neurovirulence in mice infected with WNV NY99 or Eg101.

296 elopmental problems in infants born to women infected with ZIKV during pregnancy(15-20), highlighting

297 iral control that occurs in some chronically infected women after childbirth.

298 induce a sustained antiviral response in WHV-infected woodchucks; the identification of a baseline in

299 Chemical complementation of infected WT and CSE(-/-) macrophages using the slow H(2)

300 humoral response to KSHV in a cohort of HIV-infected Zambian mothers without KS and identify potenti