ライフサイエンスコーパス: immunize

1 of the eight C. diphtheriae cases were fully immunized.

2 etween 2 months and 20 years of age had been immunized.

3 In 1981, we immunized a cohort of 1578 Alaska Native adults and chil

4 After immunizing a llama with human PCSK9, we selected four sd

5 In the present study we actively immunized adult zebra finches against VIP conjugated to

6 challenging a S. thermophilus strain CRISPR-immunized against a set of virulent phages, we found one

7 IgG antibodies isolated from healthy donors immunized against foreign rhesus D alloantigen or vaccin

8 sera and from mice that had been previously immunized against human influenza viruses.

9 ns, with brains of control birds, which were immunized against KLH.

10 The fractions were harvested from cows immunized against LPS derived from intestinal Escherichi

11 Neu5Gc-deficient mice immunized against Neu5Gc and fed bioavailable Neu5Gc dev

12 te performance expectations for countries to immunize all people living within their borders and main

13 Control and Treg-depleted EF4.1 mice were immunized, and the extent of the Valpha2-bearing, antige

14 m Pneumocystis pneumonia, compared with mock-immunized animals (P= .047), following immunosuppression

15 es against oral SIV acquisition, a subset of immunized animals had significantly lower peak viremia w

16 s from adoptive transfer of splenocytes from immunized animals in a Parkinson's disease mouse model i

17 iating the antibody responses of the various immunized animals that could not be obtained by conventi

18 on of binding antibodies and, in a subset of immunized animals, in the induction of detectable NAb, s

19 und to be a major myocarditogenic epitope in immunized animals.

20 esponse in both naive animals and previously immunized animals.

21 deficient mice and then challenging with the immunizing antigen, and by passive immunization with IgG

22 show that Tfr cells can be specific for the immunizing antigen, irrespective of whether it is a self

23 ock-in BCR does not functionally engage with immunizing antigen, we found that chronic immunization i

24 finity maturation through the use of complex immunizing antigens and discover an unexpected increase

25 underweight (aOR, 6.3), and too young to be immunized (aOR, 16.1) (all P </= .05).

26 K7 as neonates but not in the lungs of those immunized as adults.

27 ities (HR, 4.5; 95% CI, .7-26.0) among women immunized at >/=15 years of age who took >/=12 months (v

28 Among adolescents immunized at >/=15 years of age, a longer time to comple

29 We address this hypothesis by immunizing autoimmune-prone mice with HIV-1 Envelope (En

30 e a large number of unselected mutations, we immunized B1-8 H chain transgenic mice with nitrophenyl

31 identify novel biomarkers of senescence, we immunized BALB/c mice with senescent mouse lung fibrobla

32 responses of unimmunized and ovalbumin (OVA)-immunized BALB/c mice, and furthermore, to ascertain whe

33 5RO(+) memory T cells in unimmunized and OVA-immunized BALB/c mice.

34 e with the parental virulent virus, all pigs immunized by the intramuscular route (11/11) and all exc

35 tramuscular route (11/11) and all except one immunized by the intranasal route (5/6) survived.

36 ially enhances protective immunity, allowing immunized C57BL/6 mice to survive for up to 30 d followi

37 Using immunized C57BL/6J dams, lactational transfer to nonimmu

38 ELISPOT] assays) by splenocytes from IKEPLUS-immunized C57BL/6J mice, we identified an immunogenic pe

39 We therefore immunized cattle with purified recombinant LppQ-N' formu

40 s agents may up-regulate unimmunized and OVA-immunized CD4(+)CD44(+) memory T cells by the homeostati

41 23% to 56%, and an overall increase in fully immunized children aged 12-23 months, from 19% to 55%.

42 he prevalence and persistence of antibody in immunized children with perinatal HIV (PHIV) and their a

43 mmunity following a dose of IPV given to OPV-immunized children.

44 Conclusion: Immunizing children with LAIV does not provide better co

45 profiling of spleens from the triple peptide-immunized cohort showed substantial HD-specific differen

46 Purified IgG from immunized compared to control animals bound to the surfa

47 a in hippocampal area CA1 compared with sham-immunized controls, despite preservation of myelin and V

48 ther adjuvant at levels comparable to FI-RSV-immunized controls.

49 Passive transfer of serum from gD/AS04-immunized cotton rats conferred stronger protection agai

50 A third group of mock-immunized cows serve as challenge controls.

51 -knockout (DKO) pig (and a GGTA1-KO pig) and immunized cynomolgus monkeys with both of these cells.

52 ved cells, we show that foster nursing by an immunized dam results in development of CD8(+) T cells i

53 , particularly IgG, in the milk of mucosally immunized dams.

54 nd effect on hapten/carrier immunization, we immunized DBA/2 mice (whose IEbetad chain is similar to

55 A71 and CV-A16 serotypes provide a temporary immunizing effect against each other.

56 dge of mammary gland immune protection, cows immunized either intramuscularly or intramammarily with

57 Monkeys immunized either once or twice with rPA plus DV230-Ficol

58 ccine coverage with the last 9 birth cohorts immunized exclusively with inactivated polio vaccine (IP

59 To test this theory, we immunized female C3H/HeOuJ mice subcutaneously with a ge

60 This MVA-H7-Sh2 viral vector was used to immunize ferrets and proved to be immunogenic, even afte

61 n MLC effector cells derived from a G14D-CCV-immunized fish were preincubated with CC41 mAb, killing

62 Here, to test this hypothesis, we immunized four cows with BG505 SOSIP.

63 de-enriched Ag preparations were analyzed in immunized guinea pigs.

64 ERG E-pore region induce QTc prolongation in immunized guinea-pigs by targeting the HERG channel inde

65 Children who were older when first immunized had higher antibody responses to priming doses

66 Novel immunizing haptens were synthesized by derivatizing at t

67 gical data showed no evidence of fibrosis in immunized hearts.

68 Moreover, the minimum interval from an immunizing heparin exposure to the development of HIT is

69 th Goodpasture disease and, in alpha3135-145-immunized HLA-DR15 transgenic mice, alpha3135-145-specif

70 e of other studies in infected or previously immunized hosts.

71 Furthermore, plasma CXCL13 levels in immunized humans correlated with the magnitude of Ab res

72 er, lymphoid tissue is rarely available from immunized humans, making the monitoring of GC activity b

73 proximately 2 billion tOPV doses per year to immunize hundreds of millions of children.

74 imulatory receptor FcgammaRIII), by actively immunizing IgE-deficient mice and then challenging with

75 We immunized IgH- and Igkappa-humanized mice with the AE.A2

76 eflect a systemic immune deficiency, because immunized IL-1R1(-/-) mice survived subsequent lethal VA

77 In contrast, Th17 response was absent in immunized IL-23R(-/-) mice that failed to induce protect

78 us vaccines present a unique problem in that immunized individuals when infected by virus can develop

79 will reduce morbidity and mortality rates in immunized individuals, with the potential to contribute

80 Immunizing individuals through direct vaccination or the

81 isease risk in Bacille Calmette-Guerin (BCG) immunized infants from the MVA85A efficacy trial.

82 rm with rhesus cytomegalovirus by repeatedly immunizing infected animals with nonfunctional versions

83 ty; (2) a decrease in the incidence of cross-immunizing infection with Salmonella Enteritidis; (3) an

84 e with inactivated influenza virus, and then immunized into BALB/c mouse to determine the immunogenic

85 e THP1.In vivo, adult CB6F1 female mice were immunized intramuscularly with H1N1 influenza vaccine an

86 gen and mucosal adjuvant, respectively, when immunized intranasally in mice.

87 Mice immunized intranasally with Ty21a-AR-Ss produced antibod

88 hat binds to VRC01-class bnAb precursors and immunized knock-in mice expressing germline-reverted VRC

89 avy chain-only antibodies, JM2 and JM4, from immunized llamas.

90 Analysis of memory B cells from the immunized macaque suggests that elicitation of broadly n

91 Ag-specific GC Tfh cells in HIV Env protein-immunized macaques (BG505 SOSIP).

92 in protection of 55% of pentavalent-vaccine-immunized macaques from simian-human immunodeficiency vi

93 KEX1-immunized macaques were protected from Pneumocystis pneu

94 y in draining lymph nodes of immunized mice, immunized macaques, and HIV-infected humans.

95 sion in mammalian cells or purification from immunized mammals.

96 ceptors (TCRs), there is growing emphasis on immunizing melanoma patients with altered peptide ligand

97 fied vaccinia virus Ankara (MVA) and used to immunize mice in a prime-boost regimen.

98 /68 viruses and protection for a majority of immunized mice against a heterologous A/California/07/20

99 The immunized mice also developed a robust T cell response.

100 polyclonal anti-AAV1 neutralizing sera from immunized mice and rhesus macaques.

101 In glatiramer acetate-immunized mice and, moreover, in the combined treatment

102 e of Hly-immunized mice than in that of sham-immunized mice but no difference in kidney bacterial tit

103 humanized gl3BNC60 B-cell receptor (BCR), we immunized mice carrying both the heavy and light chains

104 Instead, TIV-immunized mice cleared A(H1N1)pdm09 virus and recovered

105 nes were significantly higher in LdCen(-/-) -immunized mice compared with nonimmunized mice that resu

106 Adoptive transfer of T cells from W7-791-immunized mice conferred heterologous protection, indica

107 We found that A(H1N1)pdm09 infection in TIV-immunized mice did not enhance the disease, as measured

108 lls after an established humoral response in immunized mice does not impair protection from a homolog

109 Antisera from Fc-d E1E2-immunized mice exhibited stronger competition for AR3B a

110 ens that might elicit bNAbs, we produced and immunized mice expressing the predicted germline PGT121,

111 o significant levels in the lungs of IKEPLUS-immunized mice following aerosol challenge with virulent

112 nt assays (ELISAs) showed that antisera from immunized mice inhibited monoclonal antibody binding to

113 Immunized mice lost less than 10% of their body weight a

114 mouse, we found that at least 29% of singly immunized mice produced a VRC01-class memory response, s

115 ehicle challenge, in the ankle of previously immunized mice produced time-dependent symptoms of arthr

116 d PCs after a boost with rLBNSE, rLBNSE-IL-7-immunized mice promptly produced a more potent secondary

117 Furthermore, antibodies derived from the immunized mice reduced hIAPP oligomers cytotoxicity towa

118 is assay using murine whole blood, sera from immunized mice showed functional activity.

119 Antisera from immunized mice showed that Fc-d E1E2 elicited anti-E2 an

120 L-17, heightened Th17, and Tc17 responses in immunized mice splenocytes.

121 d lower bacterial titers in the urine of Hly-immunized mice than in that of sham-immunized mice but n

122 To address this question, we immunized mice through the skin with a protein antigen,

123 inin antigen is transferable with serum from immunized mice to recipient mice in a homologous, but no

124 des conferred asthma protection, and peptide-immunized mice transferred protection through CD4(+) and

125 d that the CD4(+) T cell response in IKEPLUS-immunized mice was dominated by the recognition of multi

126 Virus titers in the lungs of KyA-immunized mice were 1,000-fold lower at 2 days post-RacL

127 Immunized mice were challenged with 10-100 MLD50 of H1N1

128 nisms of innate immune responses to KyA, KyA-immunized mice were challenged with RacL11 at various ti

129 Here, we immunized mice with Ad5 vectors encoding lymphocytic cho

130 We then immunized mice with both chaperone/alpha-synuclein combi

131 Immunized mice with Id3 expression depleted displayed a

132 e respective APCs from S. pneumoniae- or OVA-immunized mice with OVA-specific T cells, in the absence

133 To address this problem, we immunized mice with peptide Ag 2W1S coupled to PE in CFA

134 Thus, we immunized mice with recombinant NS1 from both bacteria a

135 In comparative studies, boosting of BCG-immunized mice with rLmIII/a30 induced the strongest ant

136 To test this hypothesis, we immunized mice with siderophores conjugated to an immuno

137 In this study, we immunized mice with whole inactivated reverse genetics r

138 transferred in circulation to parabionts of immunized mice, demonstrating that tissue-resident memor

139 with GC activity in draining lymph nodes of immunized mice, immunized macaques, and HIV-infected hum

140 showed similar neutralizing activity as ACT-immunized mice, indicating that this domain induced an a

141 In immunized mice, the aluminum oxyhydroxide-adsorbed formu

142 (47-58% in males and 49% in females) in the immunized mice.

143 e with development of protective immunity in immunized mice.

144 II-restricted T cell hybridomas from IKEPLUS-immunized mice.

145 V neutralizing antibody response than rLBNSE-immunized mice.

146 increased the population of plasma cells in immunized mice.

147 and two regions were identified only in NS1-immunized mice; thus, vaccination can generate Abs to re

148 dentify the ILT3 ligand, we generated mAb by immunizing mice with Jurkat acute T cell leukemia, which

149 We induced anti-MPO GN by immunizing mice with MPO and a low dose of anti-glomerul

150 Recent work shows that immunizing mice with siderophores (small molecules that

151 eveloped C8, a monoclonal antibody (mAb), by immunizing mice with sublethal inocula of a hypervirulen

152 d V3 variable regions were isolated from the immunized monkeys and humans; these monoclonal antibodie

153 es in a single visit were subsequently fully immunized, most within a 2-week period.

154 Each immunized mouse had substantial immunoglobulin G targeti

155 The results from the NS1-immunized mouse sera indicated that NS1 immunization ind

156 fic for Ags against which the foster dam was immunized (Mycobacterium tuberculosis or Candida albican

157 In contrast, all immunized negative-control mice developed PcP.

158 We immunized non-lupus-prone mice with 11 allotype "a" of I

159 number of cases of meningococcal disease in immunized patients being treated with eculizumab and sug

160 addressing the weakest links, which includes immunizing populations in insecure areas and/or with dis

161 Importantly, immunized rabbits also showed neutralizing activities ag

162 mAbs derived from complex-immunized rabbits displayed footprints on gp120 more dis

163 We demonstrate that immunized rabbits generated cross-reactive neutralizing

164 eutralizing antibodies (NAbs) efficiently in immunized rabbits, we sought to improve the efficiency w

165 g synthetic resistance, reversal drives, and immunizing reversal drives.

166 to) expressed in mammalian cells was used to immunize sheep and elicited a robust immune response and

167 At 1.5-2 months, the proportion of immunized students with protective titers >/=1:4 against

168 At 7 months, the proportion of immunized students with titers >/=1:4 was 86% (95% CI, 7

169 Reduction of OBI in immunized subjects complements the well-documented unive

170 s (CFUs) per milliliter in blood from all 12 immunized subjects decreased from approximately 4000 at

171 SPR/cas9, offer the prospect intracellularly immunized T cells in HIV+ patients.

172 between the repeats of the CRISPR locus and immunize the host against the matching invader.

173 We took advantage of Gal-3 knockout mice and immunized them with a mimotope of the major mitochondria

174 In these studies, we have immunized these bovines with different VEEV immunogens a

175 ruption, being able, early in a pandemic, to immunize those who had received prepandemic vaccine with

176 Mice were immunized through the intranasal route with house dust m

177 Remarkably, P0106-125-immunized TLR2(0/0) mice exhibited a delayed recovery as

178 compared to wild-type mice, whereas Tregs in immunized TLR2(0/0) mice were only slightly increased.

179 Immunized TLR2(0/0) mice were unable to induce OX40 and

180 Immunized transgenic mice showed an increase in hIAPP-an

181 Ferrets immunized twice with a mix of recombinant rabies viruses

182 lated phages, and in another bacterial genus immunized using the heterologous SpCas9 system favoured

183 We compared the resistance of RVV-immunized wild-type, IgE-deficient, and Fcer1a-deficient

184 HSCs into the spleens of mice that had been immunized with 4-hydroxy-3-nitrophenylacetyl-Ficoll, a T

185 Guinea-pigs were immunized with a 31-amino-acid peptide corresponding to

186 protective RABV antibody titers, and animals immunized with a combination of CDV attachment protein-

187 Mice were immunized with a conformational immunogenic gp41-transfe

188 virus (RSV) infection of children previously immunized with a nonlive, formalin-inactivated (FI)-RSV

189 We show here that rabbits immunized with a novel recombinant vaccinia virus prime-

190 Mice were immunized with a pool of virus-derived T-cell epitopes.

191 Mice immunized with a purified recombinant SLTRiP protein gav

192 Mice were immunized with a recombinant fusion protein containing P

193 Splenocytes from BALB/c mice immunized with a recombinant human apoA-I, with or witho

194 G antibodies during natural infection, mice immunized with a recombinant version of the protein elic

195 Hence, BALB/c mice were immunized with a single dose of the three proteins adjuv

196 Sera from mice immunized with a single GII.17 VLP identified antigenic

197 ies, JM2 and JM4, from llamas that have been immunized with a trimeric gp140 bound to a CD4 mimic hav

198 Animals immunized with a vaccine candidate were uniformly protec

199 of antigen-specific CD4(+) T cells in cattle immunized with A. marginale outer membrane proteins or p

200 Mice were immunized with Adenovirus expressing the H1-con, H2-con,

201 and AP groups of mice when either group was immunized with adjuvanted low-dose A(H5N1) subvirion vac

202 More importantly, neither T-bet(-/-) mice immunized with an attenuated virus, nor WT mice with Th2

203 We previously reported that infants immunized with an MF59-adjuvanted rgp120 vaccine develop

204 Moreover, mice immunized with Anx-expressing ACs became refractory to a

205 We show that in hamsters immunized with Bacillus subtilis spores expressing a car

206 cted for chemical analyses, and infants were immunized with BCG.

207 CD61 knockout (KO) mice were immunized with CD61(+) platelets, and T-cell-mediated IT

208 Homozygous gynogenetic catfish were immunized with channel catfish virus (CCV)-infected MHC-

209 Additionally, BALB/c mice intranasally immunized with CLH001 in a prime/boost regimen were full

210 b VLP was blocked only by antisera from mice immunized with cluster IIIb VLPs.

211 of V1/V2-specific antibodies between animals immunized with different Envs, with or without the N7 gl

212 Adoptive transfer of cells from mice immunized with DNA-HSP65 or CpG/CFP to allergic recipien

213 Recipient Lewis rats (RT1) were immunized with donor (Dark Agouti, RT1) spleen cells (da

214 molgus monkeys at 2 wk compared with animals immunized with equivalent amounts of monomeric DV230.

215 Furthermore, in vivo studies of mice immunized with FBG achieved >75% blocking efficacy of P.

216 enhanced lung pathology observed in animals immunized with formalin-inactivated RSV.

217 Mice immunized with GP+RAP/alpha-syn further rescued neurons

218 Compared with mice immunized with GP-alone or GP-alpha-syn, mice vaccinated

219 yn transgenic (tg) male and female mice were immunized with GP-alone, GP-alpha-syn (active humoral im

220 1 virus neutralization compared with animals immunized with gp120 core alone.

221 ccluded vaccine compared to those of animals immunized with gp140.

222 Sera from rabbits immunized with gp145 elicited high titer antibodies to v

223 Mice were immunized with H1N1/A/California/7/2009 subunit vaccines

224 demic and H3N2 viruses of mice that had been immunized with hemagglutinin (HA), neuraminidase (NA) an

225 ar activation in vitro, NLRP3-deficient mice immunized with HIV-1 gp120 and QS-21 showed significantl

226 er, for one reconstitution cohort, some mice immunized with iDCpp65 showed GVH-like signs on the skin

227 Here we also show that mice immunized with inactive typhoid toxins and challenged wi

228 re egg-allergic children that had never been immunized with influenza vaccine.

229 ungs of RacL11-challenged mice that had been immunized with KyA.

230 Further studies showed that mice immunized with LBNSE-CXCL13 produced more rabies virus-n

231 We previously showed that humanized mice immunized with long-lived induced-dendritic cells loaded

232 -specific CD8(+) T cells transferred to mice immunized with Lp/OVA/StII experienced a greater expansi

233 A total of 4923 students were immunized with MenB-4C in response to an outbreak at a u

234 generate anti-alpha-1,3-glucan IgA Abs were immunized with MK7 as neonates and were no longer protec

235 eting cells are present in the lungs of mice immunized with MK7 as neonates but not in the lungs of t

236 When sequentially immunized with modified gp120 glycoproteins designed to

237 WT) and Nrf2-deficient (Nrf2(-/-)) mice were immunized with myelin oligodendrocyte glycoprotein (MOG)

238 in vivo immune responses from mice that were immunized with nanoparticles-delivered OVA when compared

239 Rhesus macaques (RMs) were immunized with NPs containing TLR4 and TLR7/8 agonists m

240 in a lethal DENV vascular leak model in mice immunized with NS1 combined with aluminum and magnesium

241 in A. marginale-challenged cattle previously immunized with OMs.

242 However, animals that were immunized with only a RABV expressing the attachment pro

243 s intestinal immunity in children previously immunized with oral poliovirus vaccine (OPV).

244 ansgenic for human immunoglobulin genes were immunized with OspA from B. burgdorferi to generate huma

245 h there was a CD8(+) T cell response in mice immunized with our modified dendrimer-based RNA nanopart

246 cted with a sublethal dose of DENV2 and mice immunized with OVA (negative control).

247 C3H mice immunized with PADs developed antibodies and T cells to

248 able to escape Nab activity from mouse sera immunized with parental serotypes.

249 Infants were immunized with PCV10 or PCV13 at 2, 3, 4, and 11 months

250 We determined that mice immunized with peptide or protein Ags emulsified in IFA

251 Data from mice immunized with Phl p 12 showed that cross-reactivity to

252 of purified equine IgG obtained from horses immunized with plasmid DNA followed by boosting with Kun

253 BALB/c mice were immunized with PM, N, or P.

254 n TACI-sufficient Swedish blood donors never immunized with pneumococcal antigens.

255 Importantly, mice immunized with purified MrkA proteins also showed reduce

256 ng IgG in outbred guinea pigs which had been immunized with recombinant birch pollen allergen Bet v 1

257 Mice immunized with recombinant P. falciparum CelTOS in combi

258 rofiling in injection-site tissues from mice immunized with SAM-based vaccine revealed an early and r

259 4) Animals immunized with SERCA2a 971-990 showed Ag-specific Abs wi

260 In contrast, all 14 macaques immunized with SIV p27CE pDNA developed robust T cell re

261 effectively elicit non-NAbs when animals are immunized with SOSIP.664 trimers.

262 In this study of pregnant BALB/c mice immunized with subunit H1N1 influenza vaccine, we demons

263 gestational age, 39.3 +/- 1.3 GW) previously immunized with Tdap in the second (n = 122) or third (n

264 Mice immunized with terminal disaccharide-CRM197 constructs p

265 had chronic HCMV infection or were recently immunized with tetanus toxoid (TT) were included as cont

266 a from kidney transplant recipients (n = 60) immunized with the 2012-2013 adjuvanted or nonadjuvanted

267 s were comparable between adults and infants immunized with the alum/MNrgp120 vaccine (gp120 median f

268 Mice were immunized with the best 3 peptides and then challenged w

269 Rabbits immunized with the crosslinked complex displayed earlier

270 Mice immunized with the CTB-siderophore conjugate developed a

271 Mice were immunized with the fusion proteins in the absence and pr

272 To induce EAE, C57/BL6 mice were immunized with the Hooke lab MOG kit, sacrificed at the

273 f immunity in healthy young and older adults immunized with the live attenuated shingles vaccine Zost

274 had been previously exposed to DENV and was immunized with the live attenuated tetravalent vaccine B

275 ommunity-dwelling seniors (aged 60-75 years) immunized with the live-attenuated varicella-zoster viru

276 and 804 [adults], P = 0.50), whereas infants immunized with the MF59/SF-2 rgp120 vaccine had higher-m

277 al immunization strategy, animals previously immunized with the MVA prime/i.n. boost regimen received

278 Mice immunized with the non-flagellin OMVs produced high conc

279 ) and developed better protection than those immunized with the parent virus LBNSE or the GM-CSF-expr

280 nors with birch pollen allergy and from mice immunized with the parental allergens.

281 eceptor are protected from wild-type PV when immunized with the plant-made PV sVLPs.

282 Guinea pigs were immunized with the resulting HIV VLPs through an intramu

283 Sera from mice immunized with the RTX domain showed similar neutralizin

284 specific IgG responses in adults and infants immunized with the same MF59- and alum-adjuvanted HIV en

285 /ml) nAbs from a DENV-seropositive volunteer immunized with the tetravalent vaccine Butantan-DV, whic

286 mbination (multivalent) and compared to mice immunized with the traditional 2010-2011 FluZone and Flu

287 t any adverse effects, compared to the group immunized with the vaccine antigen alone.

288 Neonatal, but not adult, mice immunized with this alpha-1,3-glucan-bearing Enterobacte

289 Furthermore, RAGE knockout (RAGE-ko) mice immunized with TnI showed no structural or physiological

290 In contrast, animals immunized with toxoids showed no protection and remained

291 African green monkeys immunized with two doses of the vector expressing GP fro

292 immunogenicity elicited in nonhuman primates immunized with two replicating NYVAC vectors that have b

293 When B6.DR1/LAIR-1(-/-) mice were immunized with type II collagen they developed more seve

294 B6.DR1 mice were immunized with type II collagen/CFA to induce arthritis

295 on later sporozoite vaccinations, mice were immunized with uninfected salivary glands from a single

296 rom the peripheral blood of a rhesus macaque immunized with YU2gp140-F trimers in adjuvant, using JR-

297 mpts to elicit oligomannose-specific nAbs by immunizing with natural or synthetic oligomannose have s

298 rophylactic antimicrobial chemotherapies, or immunizing with oral cholera vaccines.

299 y in the spleen was reduced compared to mice immunized without the antagonist.

300 tibody reduced inflammation in hearts of TnI-immunized wt mice.