ライフサイエンスコーパス: rhesus macaque

1 rgic interneurons, in human, chimpanzee, and rhesus macaque.

2 simian immunodeficiency virus (SIV)-infected rhesus macaque.

3 man primate model of MERS-CoV infection, the rhesus macaque.

4 les in SHIV.C.CH505-infected, ART-suppressed rhesus macaques.

5 egravir plasma concentration of 373 ng/ml in rhesus macaques.

6 ons with a combination of DNA and protein in rhesus macaques.

7 atory syndrome coronavirus 2 (SARS-CoV-2) in rhesus macaques.

8 inst SIVmac251 challenges in naive recipient rhesus macaques.

9 vaccinia virus Ankara (MVA)-SHIV vaccines in rhesus macaques.

10 thsin (Q-GRFT) in rectal tissue samples from rhesus macaques.

11 lateral or medial subdivisions of the OFC in rhesus macaques.

12 rain regions across humans, chimpanzees, and rhesus macaques.

13 ynamics and immunopathology of SHIV.CH505 in rhesus macaques.

14 essure flow studies in 16 male and 22 female rhesus macaques.

15 ol of simian immunodeficiency virus (SIV) in rhesus macaques.

16 arly AIDS virus replication and pathology in rhesus macaques.

17 olonged in vivo half-life in huFcRn mice and rhesus macaques.

18 ate, and one MHC class II DRB allele-matched rhesus macaques.

19 s an indicator of acute stress in laboratory rhesus macaques.

20 e model of pathogenic SIVmac251 infection of rhesus macaques.

21 tic repopulating cells in humanized mice and rhesus macaques.

22 n, and those that are unique, to rabbits and rhesus macaques.

23 l of HCMV is rhesus CMV (RhCMV) infection of rhesus macaques.

24 o the sublingual and buccal (SL/B) tissue of rhesus macaques.

25 iated with the clearance of SIV infection in rhesus macaques.

26 o a CD4-mimetic miniprotein (gp140-M64U1) in rhesus macaques.

27 V1 neutralizing sera from immunized mice and rhesus macaques.

28 cy virus (SIV) infection of adult humans and rhesus macaques.

29 rtial protection against viral challenges in rhesus macaques.

30 alue per implant, N = 41) of cabotegravir in rhesus macaques.

31 ku-Mayinga infection during acute disease in rhesus macaques.

32 tered prophylactically or therapeutically in rhesus macaques.

33 enhance protection against SIV infection in rhesus macaques.

34 ponse of type-1 and type-2 T helper cells in rhesus macaques.

35 produce robust HIV-1-specific antibodies in rhesus macaques.

36 eractions, transmission, and pathogenesis in rhesus macaques.

37 re observed in the prostate of ZIKV-infected rhesus macaques.

38 2 spike (S) protein and evaluated them in 35 rhesus macaques.

39 ce imaging and neurocognitive assessments in rhesus macaques.

40 arts, and lungs, in humans, chimpanzees, and rhesus macaques.

41 We report rhesus macaque A3G structures that show different inter-

42 Recently, crystal structures of full-length rhesus macaque A3G variants were solved which suggested

43 d choice between risky options in humans and rhesus macaques across three tasks with different levels

44 rected CD8 T cells to the small intestine in rhesus macaque ACT experiments.

45 lome of the nucleus accumbens core (NAcc) of rhesus macaques after chronic alcohol use.

46 tudy T-cell-mediated immunity in vivo In the rhesus macaque AIDS virus model, infusing simian immunod

47 human immunodeficiency virus (SHIV)-infected rhesus macaques, an earlier and sharper decline in viral

48 orm a comparative editome study in human and rhesus macaque and uncover a substantial proportion of m

49 40 along with HIV envelope (Env) vaccines to rhesus macaques and bnAb immunoglobulin knock-in (KI) mi

50 ected from experimental iBCI measurements in rhesus macaques and from a clinical-trial participant wi

51 k skin or scrotal skin of castrated pubertal rhesus macaques and matured to produce functional sperm.

52 d oxytocin intranasally and intravenously to rhesus macaques and measure, with mass spectrometry, con

53 ere, in simian immunodeficiency virus (SIV)+ rhesus macaques and patients diagnosed with HIV, brain r

54 ntical HIV-1 vaccine regimens to rabbits and rhesus macaques and performed detailed comparisons of va

55 ch (dMNP) delivery of hepatitis B vaccine in rhesus macaques and provides evidence that dMNP delivery

56 of natural textures across the fingertips of rhesus macaques and recorded the responses evoked in Bro

57 these vectors into the cerebellar cortex of rhesus macaques and tested vector efficacy in three ways

58 different vaccines that were administered to rhesus macaques and that delivered the same envelope pro

59 enomes in experimentally inoculated pregnant rhesus macaques and their fetuses.

60 bidity and mortality affecting the supply of rhesus macaques and, potentially, their responses to exp

61 rLCV-infected lymphomas from an SIV-infected rhesus macaque, and we report latent and lytic circRNAs

62 During training, 60 humans, 7 rhesus macaques, and 22 capuchin monkeys learned to sele

63 The tracer was also studied in rhesus macaques, and PET images were analyzed with an ar

64 arily, hepatocytes from cynomolgus macaques, rhesus macaques, and pigs became fully susceptible to HB

65 ficient for protection against SARS-CoV-2 in rhesus macaques, and that cellular immune responses may

66 This virus was used to infect 120 rhesus macaques, and we report here the analysis of the

67 15, researchers capitalized on the fact that rhesus macaques are commonly used to model viral immunit

68 The establishment of the rhesus macaque as a model of COVID-19 will increase our

69 vity in the amygdala and ventral striatum of rhesus macaques as they solved a task that required them

70 Pregnant rhesus macaques at 127 days of gestation (80% of term) w

71 us 2 (SARS-CoV-2) infection in young and old rhesus macaques, baboons and old marmosets.

72 In study 3, at a 0.1-mg/kg dose, 2 rhesus macaques became infected, consistent with a 7.2-f

73 estigated MAIT cell dynamics and function in rhesus macaque blood and bronchoalveolar lavage (BAL) fo

74 In rhesus macaques, BMS-529 complexed to CD4 bs-targeting c

75 e addressed the susceptibility of two infant rhesus macaques born healthy to dams infected with Zika

76 port a vaccine-induced sex bias, with female rhesus macaques but not males displaying significantly r

77 in 3 species and found that the response in rhesus macaques, but not in mice, closely resembled that

78 against hard-to-neutralize SHIV challenge in rhesus macaques by inducing tier 2 nAbs, provided approp

79 Here, we show that male rhesus macaques can learn categories by a transitive inf

80 Our results demonstrate that rhesus macaques can learn to use a middle concept for a

81 urally occurring model of the disease in the rhesus macaque caused by homozygous mutations in the pho

82 ity of this molecule to induce signaling via rhesus macaque CD200R, as well as the potential function

83 Here, we recorded from the BLA of two male rhesus macaques choosing between different juices.

84 mononuclear cells (PBMC) collected from male rhesus macaques classified as CMD or CHD after 12 months

85 Fortunately, two such animal models-the rhesus macaque CMV and guinea pig CMV-are characterized

86 dendritic cells (pDCs) and CD141(+) DCs from rhesus macaques, compared to the induction of apoptosis

87 Rhesus macaques conditioned to associate particular colo

88 and polyfunctional V2-focused Ab response in rhesus macaques, described herein.

89 that PFC cells recorded from male and female rhesus macaques during a complex task show a moderate le

90 A single immunization of rhesus macaques elicited a rapid and robust antibody res

91 by simian-human immunodeficiency viruses in rhesus macaques-elicited patterns of Env-antibody coevol

92 n developed an isolation technique to purify rhesus macaque eosinophils from peripheral blood and per

93 Tamarins and rhesus macaques exhibited loss of zonal occludens-1 (ZO-

94 Here we show that rhesus macaques experimentally coinfected simultaneously

95 by the emergence of a novel KIR allele in a rhesus macaque family.

96 nes expressing common allotypes of human and rhesus macaque FcgammaR2A and FcgammaR3A were establishe

97 We sequenced Zika virus (ZIKV) from a rhesus macaque fetus that died after inoculation and ide

98 ortex is longitudinally characterized in the rhesus macaque, focusing on gestation day (G85) through

99 nd gene networks active in adipose tissue of rhesus macaques following FGF21-induced weight loss.

100 ian ZIKV clinical isolate (HS-2015-BA-01) in rhesus macaques for up to 142 d.

101 ed at five time-points in 24 male and female rhesus macaques from 6 months to adulthood at 5 years.

102 before and following SIV infection protected rhesus macaques from developing AIDS and partially from

103 -2196 or COV2-2381) as monotherapy protected rhesus macaques from SARS-CoV-2 infection.

104 The maturation of the infant rhesus macaque gut microbiome throughout the first 8 mon

105 to sites of viral reservoirs in SIV-infected rhesus macaques had no demonstrable effect on plasma vir

106 ctional MRI showed that ZIKV-infected infant rhesus macaques had persistent enlargement of lateral ve

107 y limits Mtb infection in highly susceptible rhesus macaques has important implications for vaccine d

108 l deprivation (peer-rearing, PR) in archived rhesus macaque hippocampal samples (male, n = 13).

109 Whole-genome sequencing (WGS) data from 853 rhesus macaques identified 85.7 million single-nucleotid

110 These studies reveal that rhesus macaque IgG responses during chronic SIV infectio

111 rimate model of HCMV infection, we show that rhesus macaques immunized against viral interleukin-10 (

112 the virus was first discovered in a sentinel rhesus macaque in Uganda in 1947.

113 intervention experiments with 59 adult male rhesus macaques indicated low plasma adropin concentrati

114 genic, alone and in combination, in mice and rhesus macaques, inducing IgG antibodies that mediated o

115 Rhesus macaque infants experienced on average 5% reduced

116 this synthetic swarm using samples from 120 rhesus macaques infected intravenously.

117 s the viral kinetics and immune responses in rhesus macaques infected with a clinical ZIKV Brazilian

118 control after ART discontinuation in 100% of rhesus macaques infected with an attenuated strain of si

119 marrow-liver-thymus (BLT) humanized mice and rhesus macaques infected with HIV and SIV, respectively.

120 Overall, severe anaemia in rhesus macaques infected with P. coatneyi has similar fe

121 logic sections of lungs from both humans and rhesus macaques infected with SARS-CoV-2.

122 y during infection had a clinical benefit in rhesus macaques infected with SARS-CoV-2.

123 lysates and synaptosome preparations of male rhesus macaques infected with simian immunodeficiency vi

124 on in nef We performed similar studies in 50 rhesus macaques infected with wild-type, pathogenic SIVm

125 some aspects of human infections.IMPORTANCE Rhesus macaque infection with simian immunodeficiency vi

126 tudied 4 simian/HIV-infected, ART-suppressed rhesus macaques infused with virus-specific CD4CAR T cel

127 We show that five rhesus macaques initially infected with ZIKV 22 to 28 mo

128 We found that rhesus macaques inoculated with blood-stage Plasmodium c

129 Rhesus macaques intrabronchially inoculated with simian

130 The rhesus macaque is an important animal model for AIDS and

131 The rhesus macaque is an important model species in several

132 Rhesus macaque is an Old World monkey that shared a comm

133 Canine, porcine, and rhesus macaque ISG15, such as human ISG15, stabilize USP

134 the circRNAome of the interspecies homologue rhesus macaque lymphocryptovirus (rLCV) in a naturally o

135 dy mass data collected from 253 free-ranging rhesus macaque Macaca mulatta infants on Cayo Santiago,

136 key species: vervets (Chlorocebus aethiops), rhesus macaque (Macaca mulatta) and cynomolgus macaque (

137 The rhesus macaque (Macaca mulatta) is the most widely studi

138 Male rhesus macaque (Macaca mulatta) morphological traits are

139 ovo genome assembly (rheMacS) of the Chinese rhesus macaque (Macaca mulatta) using long-read sequenci

140 estimate of the de novo mutation rate in the rhesus macaque (Macaca mulatta) using whole-genome seque

141 a: cynomolgus macaque (Macaca fascicularis), rhesus macaque (Macaca mulatta), pig (Sus scrofa), and m

142 Rhesus macaques (Macaca mulatta) appear to be robustly r

143 Rhesus macaques (Macaca mulatta) are key for modeling hu

144 Infant rhesus macaques (Macaca mulatta) are susceptible to diar

145 tereotypic behaviour displayed by laboratory rhesus macaques (Macaca mulatta) is often used as an ind

146 e transfer of purified IgG from convalescent rhesus macaques (Macaca mulatta) protects naive recipien

147 Fifty-two rhesus macaques (Macaca mulatta) were immunized with Ad2

148 ns of macrophages in the intestinal tract of rhesus macaques (Macaca mulatta) with SIV/AIDS.

149 have been created for humans (Homo sapiens), rhesus macaques (Macaca mulatta), and several other nonh

150 served capacity, and tested this capacity in rhesus macaques (Macaca mulatta).

151 tly assess the binding of four common Indian rhesus macaque MHC class I molecules (Mamu-A1*001, -A1*0

152 Although the rhesus macaque model does not represent the severe disea

153 ort of an experimental coinfection using the rhesus macaque model for ZIKV and DENV infections.

154 d in many, but not all, brain regions in the rhesus macaque model is consistent with the possible exi

155 Here, a rhesus macaque model of FASD, involving oral self-admini

156 The simian immunodeficiency virus (SIV) rhesus macaque model of HIV infection can be useful to e

157 We used an infant rhesus macaque model of HIV-1 infection via breastfeedin

158 ed MK-8591 as preexposure prophylaxis in the rhesus macaque model of intrarectal challenge with simia

159 In a preterm rhesus macaque model of IUI given intra-amniotic LPS, in

160 We developed a rhesus macaque model of SARS-CoV-2 infection and observe

161 investigate the efficacy of remdesivir in a rhesus macaque model of SARS-CoV-2 infection(9).

162 c and virologic efficacy of baricitinib in a rhesus macaque model of SARS-CoV-2 infection.

163 We utilized a rhesus macaque model of SHIV infection as a tool to dist

164 In this study, using the rhesus macaque model of SIV infection and ART, we examin

165 ct of ART on the gut microbiota, we used the rhesus macaque model of SIV infection to characterize an

166 e we show that postnatal ZIKV infection in a rhesus macaque model resulted in long-term behavioral, m

167 Using the rhesus macaque model, we tested a pharmacological inhibi

168 ept will ultimately have to be tested in the rhesus macaque model, which is shown here to have MUC16-

169 /Makona-C05, and Marburg virus/Angola in the rhesus macaque model.

170 n patterns of these cells in a myeloablative rhesus macaque model.

171 e how to best utilize preclinical rabbit and rhesus macaque models to accelerate HIV vaccine candidat

172 In this rare case of a Rhesus macaque (monkey S), likely born without V1, the a

173 In two male rhesus macaque monkeys (Macaca mulatta), we found that l

174 colon cells from SIV-infected and uninfected rhesus macaque monkeys and determined the make-up of the

175 sion-weighted MRI data before and after male rhesus macaque monkeys received extensive training to le

176 We instructed male rhesus macaque monkeys to initiate saccade-free smooth p

177 the microbiome of the captive reared infant rhesus macaque more closely resembles that of human infa

178 Our results suggest that male rhesus macaque morphometric traits are either not under

179 duction and maintenance of variation in male rhesus macaque morphometric traits which may be subject

180 9,000 birth records from ~1,400 free-ranging rhesus macaque mothers, we show that short birth interva

181 early organogenesis to adulthood for human, rhesus macaque, mouse, rat, rabbit, opossum and chicken.

182 asma samples from C57BL/6J mice (n = 28) and rhesus macaques (n = 4) immunized with the same HCV E1E2

183 measured and quantified in 7 eyes of 4 male rhesus macaques (NHPs) using the Konigsberg EO system (c

184 ected from TB modelling studies performed in Rhesus macaques of Indian genotype (RM), cynomolgus maca

185 at, from 125 male and 21 female free-ranging rhesus macaques on Cayo Santiago.

186 he reproductive success of high-ranking male rhesus macaques on Cayo Santiago.

187 Here, we used infant rhesus macaques orally infected with simian/human immuno

188 Here, we report that when rhesus macaques performed a set-shifting task, lapse rat

189 ectrophysiological recordings from two adult rhesus macaques performing a perceptual task and compara

190 odes in the dorsal premotor cortex of 2 male rhesus macaques performing a visual reaction time (RT) r

191 Capuchin monkeys and especially rhesus macaques persisted to trial completion even when

192 TG and PG parameters from baboon and rhesus macaque plasma approximated that of humans.

193 und that neurons in a particular area of the rhesus macaque posterior thalamus encoded the historical

194 logic status of BM-derived CD4(+) T cells in rhesus macaques prior to SIV infection, during the early

195 Together, the rhesus macaque recapitulates the moderate disease that h

196 In study 1, 8 rhesus macaques received 3.9 mg/kg of MK-8591 orally on

197 Indian rhesus macaques received two doses of PIZV at varying co

198 lymphoid cell (ILC) dynamics and function in rhesus macaque rectal tissue and blood following mucosal

199 Compared to the current Indian rhesus macaque reference genome (rheMac8), rheMacS incre

200 of infecting and replicating efficiently in rhesus macaques, resulting in peripheral viral kinetics

201 Zika virus directly to the tonsils of three rhesus macaques results in detectable plasma viremia in

202 re, we show that depletion of CD4 T cells in rhesus macaques results in SVV reactivation, with virus

203 lls from peripheral blood and the jejunum in rhesus macaques, revealing distinct expression patterns

204 d herpesvirus (KSHV) and the closely related rhesus macaque rhadinovirus (RRV) are unique for encodin

205 herpesvirus (KSHV), and the closely related rhesus macaque rhadinovirus (RRV).

206 an immunodeficiency virus (SIV) infection of rhesus macaques (RhMs) is the best-characterized model f

207 In this study, we show that strain 68-1 rhesus macaque (RM) CMV vaccine vectors expressing HBV A

208 n toward an HIV cure by depleted Tregs in 14 rhesus macaque (RM) controllers infected with SIVsab, th

209 -renewal of SCM and CM CD4(+) T cells in the rhesus macaque (RM) model of simian immunodeficiency (SI

210 e used morphine dependent SIVmac251 infected rhesus macaque (RM) model to study the impact of opioids

211 oped a morphine dependent SIVmac251 infected Rhesus macaque (RM) model to study the impact of opioids

212 in the rabbit model can predict those in the rhesus macaque (RM) model.

213 monkey (AGM) to an AIDS susceptible species, rhesus macaque (RM).

214 odeficiency virus (SIV)/SHIV-infected infant rhesus macaques (RM) and tracked changes in frequency, t

215 Fifty percent of rhesus macaques (RM) vaccinated with a combined RhCMV-Ga

216 Here, we tested whether rhesus macaques (RM) vaccinated with viral constructs ex

217 In an effort to develop a relevant model, rhesus macaques (RM) were inoculated intravaginally with

218 man interleukin-15 (rhIL-15) in SIV-infected rhesus macaques (RM).

219 frequencies of T(EM) to inserted antigens in rhesus macaques (RM).

220 that enable efficient replication in Indian rhesus macaques (RM).

221 we treated two cohorts of SIVmac239-infected rhesus macaques (RM; Macaca mulatta), one with chronic i

222 Rhesus macaques (RMs) (n = 13) were infected with simian

223 Approximately 50% of rhesus macaques (RMs) expressing the major histocompatib

224 nodeficiency virus (SIV) vaccine regimens in rhesus macaques (RMs) has not been fully investigated.

225 sponses in infant (n = 6) and adult (n = 12) rhesus macaques (RMs) infected with a transmitted/founde

226 ges in the two surviving, aged AGMs and four rhesus macaques (RMs) infected with SARS-CoV-2.

227 n immunodeficiency virus (SHIV) infection in rhesus macaques (RMs) resembles human immunodeficiency v

228 eated simian immunodeficiency virus-infected rhesus macaques (RMs) undergoing CD8alpha depletion and

229 Here we show that rhesus macaques (RMs) vaccinated with Vif and Nef acquir

230 Rhesus macaques (RMs) were immunized with NPs containing

231 Here, we identified 7 SIV(mac239)-infected rhesus macaques (RMs), defined as PTCs, who started ART

232 ccine induced a similar antibody response in rhesus macaques (RMs), which are commonly used as an ani

233 CD8(+) T cells targeting non-Env epitopes in rhesus macaques (RMs).

234 T cells of African green monkeys (AGMs) and rhesus macaques (RMs).

235 orphism of detrusor function is prominent in rhesus macaques, shares many features with the human, an

236 Our results in rhesus macaques show that boosting with a specific HIV e

237 n immunized with gp150 complexed to BMS-529, rhesus macaques showed neutralization against tier 2 pse

238 Here, we used the rhesus macaque simian immunodeficiency virus model with

239 Using the rhesus macaque simian immunodeficiency virus SIVmac251 m

240 ths of combination antiretroviral therapy in rhesus macaques starting therapy within 1 year of infect

241 can elicit seroprotective anti-HBs levels in rhesus macaques that are correlated with human seroprote

242 t SARS-CoV-2 causes a respiratory disease in rhesus macaques that lasts between 8 and 16 days.

243 Here, we identified 7 SIV-infected rhesus macaques that mirrored the human posttreatment co

244 y, peripheral ganglia were collected from 12 rhesus macaques that succumbed to Ebola virus (EBOV) dis

245 Here we show in rhesus macaques that the time elapsed after ZIKV infecti

246 lower respiratory tract tissue of vaccinated rhesus macaques that were challenged with SARS-CoV-2 com

247 e or in combination with the bnAb PGT121, in rhesus macaques that were chronically infected with SHIV

248 used into viremic simian HIV (SHIV)-infected rhesus macaques, there was a 21% difference in slope of

249 sequencing, we sequenced four Indian-origin rhesus macaque tissues and obtained high-quality, full-l

250 Here, we utilize rhesus macaques to define the immunopathogenesis of the

251 knowledge gap, our laboratory studied infant rhesus macaques to evaluate how acute SIV/SHIV infection

252 rm of simian immunodeficiency virus (SIV) in rhesus macaques to investigate the generation and select

253 HIV infection, we randomly assigned newborn rhesus macaques to receive BCG vaccine or remain unvacci

254 anipulated long-term social status in female rhesus macaques to show that social subordination alters

255 us glycoprotein, which prevents mortality in rhesus macaques treated after lethal challenge with Zair

256 Previously, we reported 60-75% survival of rhesus macaques treated with rVSV vectors expressing MAR

257 were fused to the N-terminal RING domain of Rhesus macaque TRIM5alpha.

258 ction factors in primary CD4(+) T cells from rhesus macaques under various conditions, finding dynami

259 afted with human hepatocytes (hFRG mice) and rhesus macaques using a highly pathogenic African YFV st

260 k) for immune cell gene regulation in female rhesus macaques, using paired control and GC-treated per

261 Using SIV-infected rhesus macaques, we analyzed multiple brain regions thro

262 ng-term antiretroviral therapy (ART)-treated rhesus macaques, we demonstrate that PD-1, CTLA-4 and du

263 ted functional MRI data from humans and from rhesus macaques, we first identified an asymmetrical res

264 e nonhuman primate model of SIV infection in rhesus macaques, we investigated whether KMO inhibition

265 Here, using ART-treated, SIV-infected rhesus macaques, we show that CTLA-4(+)PD-1(-) memory CD

266 aping the probability distortion patterns of rhesus macaques: we presented 2 male monkeys with binary

267 PET scans in rhesus macaques were acquired for 2 h with arterial bloo

268 (n = 4) or chronically (n = 12) SIV-infected rhesus macaques were analyzed by flow cytometry using co

269 All rhesus macaques were challenged with SHIV109CP3 on day 6

270 Three groups of rhesus macaques were each primed with the same DNA vacci

271 To test this, rhesus macaques were immunized with replicating single-c

272 Brain-dead (n = 12) and sham (n = 5) rhesus macaques were maintained for 20 hours under inten

273 Immune responses in mice and rhesus macaques were measured in a multiplex Luminex imm

274 Rhesus macaques were primed twice mucosally with replica

275 Twelve seroconverted rhesus macaques were reinoculated with homologous HEV ge

276 , provided protection from SUDV infection in rhesus macaques when administered at 50 mg/kg on days 4

277 These data were confirmed in rhesus macaques where a low dose of TMV-NPNAx5 elicited

278 ficiently utilizes human CD4 than the CD4 of rhesus macaques, whereas the closely related virus SIVma

279 ral ganglia and results in ganglionopathy in rhesus macaques, which may contribute to the neurologica

280 o efficacy of this antibody cocktail in both rhesus macaques, which may model mild disease, and golde

281 us-specific humoral responses, we vaccinated rhesus macaques with a combined mucosal prime/systemic b

282 We vaccinated 30 rhesus macaques with Ad26-SIV Env/Gag/Pol and SIV Env gp

283 The authors found that treating rhesus macaques with ART restored CD4+ T cells in whole

284 Vaccination of rhesus macaques with bivalent VLPs generated strong humo

285 mune responses in pathogenicity, we infected rhesus macaques with Borrelia turicatae (a new world RF

286 To accomplish this, we prime-boosted rhesus macaques with clade C NFL trimers and identified

287 o target plasma cells, we treated sensitized rhesus macaques with daratumumab (anti-CD38 mAb).

288 Here, we selected groups of 6 rhesus macaques with either high or low serum nAb titers

289 ple anatomical sites in chronically infected rhesus macaques with high (>10,000 copies/mL plasma) or

290 es in the mesenteric lymph nodes relative to rhesus macaques with high VLs.

291 Rhesus macaques with low viral loads (VLs) harbored high

292 ent and function of CCR5(+)CD8(+) T cells in rhesus macaques with or without Simian immunodeficiency

293 is or immune dysfunction, we treated healthy rhesus macaques with protease, integrase, or reverse tra

294 Immunization of mice, rabbits and rhesus macaques with RC1 elicited serological responses

295 Treatment of SIV-infected rhesus macaques with short-term antiretroviral therapy (

296 We propose that infections of rhesus macaques with SIVmac239 G382R/H442Y might better

297 In total, the synovium of 28 of 30 rhesus macaques with terminal filovirus disease had evid

298 rrent study, we evaluated the performance of rhesus macaques with ventral striatum (VS) lesions on a

299 In this study, we rechallenged five rhesus macaques with ZIKV 22 to 28 months after a primar

300 eukocytes and alveolar epithelial cells, and rhesus macaques, without noticeable toxicity.