ライフサイエンスコーパス: titer

1 roconversion or a >/=4-fold rise in antibody titer.

2 donors was investigated as a means to boost titers.

3 symptomatic dengue disease at high antibody titers.

4 .1% agreement with the traditional ZIKV PRNT titers.

5 M survival niches and sustained long-term Ab titers.

6 rrow range of preexisting anti-DENV antibody titers.

7 D4(+) T-cell responses, and low Env antibody titers.

8 s whereas the Western diet plus DHA improved titers.

9 s of larval worker infection on hemolymph Vg titers.

10 -inhibition (HAI) titers, and neutralization titers.

11 s used to measure patient and donor antibody titers.

12 detectable despite high postvaccination HAI titers.

13 and glutamic acid decarboxylase autoantibody titers.

14 n, which was associated with increased viral titers.

15 oocysts in control mosquitoes) and antibody titers.

16 ker gp120 binding and lower plasma total IgG titers.

17 ith targeted therapy and decreasing CrAg LFA titers.

18 erarchical clustering of bnAb neutralization titers.

19 ant and inversely correlated with viral load titers.

20 des and bone marrow, correlating with low Ab titers.

21 presence of high serum neutralizing antibody titers.

22 despite the lack of appreciable Env antibody titers.

23 st results and infectious Ebola virus (EBOV) titers.

24 78% female; median age 58 years; median AMA titer 1:160; extrahepatic autoimmune disorders 46%; norm

25 exaggerated syncytium formation, reduced VZV titers (-1.5 log10), and smaller plaques than with the p

26 015 showed a high prevalence of IDV antibody titers (11.7%), while archive sera from 2009 showed stat

27 ing strains-namely, A. niger H915-1 (citrate titer: 157 g L(-1)), A1 (117 g L(-1)), and L2 (76 g L(-1

28 We measured antibody titers (50% plaque reduction neutralization test) using

29 The peak titers achieved after infection were approximately 10-fo

30 media that led to a 50% increase in product titer after 96 h of fermentation.

31 associated with increased ZIKV neutralizing titers after exposure.

32 A NAb titer against the donor's strain <4 log10 before transpl

33 2x10(10) particle-unit dose (geometric mean titer against the Zaire antigen at week 4, 2037 vs. 331;

34 lope-pseudotyped viruses with neutralization titers against 16 broadly neutralizing antibodies and 30

35 IgG titers against glycoprotein (gp) 70V1V2 92TH023 increase

36 Individuals with low titers against group 3 pneumococcal surface protein C (P

37 teins, and correlated strongly with ADCC-Abs titers against H7N9 virus-infected cells.

38 Post-2vHPV NAb titers against HPV-16 and -18 were not statistically dif

39 Natural antibody titers against M2FA are elevated in atherosclerosis-pron

40 igens used, all animals developed protective titers against rabies virus, illustrating that a bivalen

41 postvaccination hemagglutination inhibition titers against representative H3 variants circulating du

42 failure to establish long-term protective Ab titers against S. aureus was not a consequence of dimini

43 At any time, patients with high NAb titers against the replicating strain had a lower risk o

44 a decrease in average measles virus antibody titers among plasma donors, which is reflected in intrav

45 e exhibited a significant reduction in virus titer and improvement in survival that is associated wit

46 CD4 T-cell count, RPR titer and syphilis stage did not affect treatment result

47 g 2-bromopalmitate (2-BP) affected the virus titer and the interaction of UL20 and gK but did not aff

48 d with CX4C viruses also had higher antibody titers and a Th1-biased T cell memory response at 75 day

49 an inhibitor of palmitoylation reduced HSV-1 titers and altered the localization of UL20 and glycopro

50 veloped chronic hepatitis with 10-fold lower titers and antigen-specific IgGs, (anti-HBs, anti-HBc),

51 The constructs grew to high titers and efficiently and stably expressed GP.

52 mals, exhibiting increased intestinal tissue titers and enhanced reovirus fecal shedding.

53 , PCV13 elicits significant increases in OPA titers and IgG concentrations that persist 2 years postv

54 ype-specific opsonophagocytic activity (OPA) titers and immunoglobulin G (IgG) concentrations were de

55 (-/-) mice of higher intestinal tissue viral titers and increased viral shedding in the stool.

56 Despite similar initial viral titers and inflammatory responses between wild-type and

57 tly heightened Black Queen Cell Virus (BQCV) titers and lower expression of a Toll 7-like-receptor as

58 ndicated by the significantly lower MERS-CoV titers and MERS-CoV and mRNA levels in challenged mice t

59 wed that Fc-d E1E2 elicited anti-E2 antibody titers and neutralization of HCV pseudotype viruses simi

60 erized by high early and sustained bacterial titers and profound intestinal inflammation associated w

61 lanine or arginine substitutions had reduced titers and small plaques but differed in syncytium morph

62 etween preexisting variant-specific antibody titers and subsequent carriage of pneumococcus expressin

63 offspring, measured by neutralizing antibody titers and survival rates after virus challenge.

64 Neutralization titers and the avidity and maturation of immune response

65 particles elicited protective RABV antibody titers, and animals immunized with a combination of CDV

66 ) or anti-filamentous hemagglutinin antibody titers, and by genetic testing (polymerase chain reactio

67 for growing preparations of virus with high titers, and for isolating the virus from human samples.

68 sis, for obtaining stocks of virus with high titers, and for isolating VZV from clinical specimens.IM

69 responses, hemagglutination-inhibition (HAI) titers, and neutralization titers.

70 -fold more nuclei, a -0.5-log10 reduction in titers, and pOka-like plaques.

71 disaccharide-CRM197 constructs produced high-titer antibody responses that crossreacted with Bm-like

72 However, high-titer antidrug antibodies developed in a substantial pro

73 employ rational design and a toxin/antitoxin titering approach to produce and screen a small library

74 ther interventions to lower the autoantibody titer are effective strategies that may be considered to

75 gue virus (DENV)-neutralizing antibody (nAb) titers are associated with protection, the Ab repertoire

76 a show that clinically relevant lifelong IgE titers are not sustained by long-lived IgE(+) PCs.

77 edding rates than IHNV or where higher viral titers are required to initiate infection of naive fish.

78 e showed an increase in hIAPP-antibody serum titer as well as improvement in diabetes-associated para

79 Two doses of 4vHPV provide similar NAb titers as 3 doses for 6 years, although the clinical sig

80 enotype-specific neutralizing antibody (NAb) titers as a predictive marker for BKV replication, we me

81 g polysensitization and low food-antigen IgE titers as observed in humans with clinical food allergy.

82 d citrulline levels, anti-ADI-PEG20 antibody titer, ASS1 methylation status, and metabolic response b

83 and the proportion of those who had an hSBA titer at least as high as the lower limit of quantitatio

84 fter dose 1 significantly increased antibody titers at day 56, but the effect was diminished at 6 mon

85 eplication, we measured BKV DNA load and NAb titers at transplant and followed patients for 24 months

86 sitive methods to detect the presence of low-titer autoantibodies against glutamatergic NMDAR in sero

87 In this work, we titered bacteria and/or the proinflammatory cytokine TNF

88 there being no difference in mean lung viral titers between the groups.

89 less symptomatology and replicated to lower titers both in vivo and in vitro than those seen with wi

90 268 sera were investigated for 50% blocking titer (BT50) values of virus-like particles (VLPs) again

91 induced robust levels of HA inhibition (HI) titers, but failed to protect against five different het

92 adolescents who had an increase in the hSBA titer by a factor of 4 or more against each primary stra

93 s and were tested to quantify neutralization titers by 16 broadly neutralizing antibodies (bnAbs) and

94 annin (WM) and LY294002 (LY) increased viral titers by 3-16 folds in primary mouse macrophages, embry

95 inocula were associated with short-term, low-titer colonization whereas high-dose inocula were associ

96 e mice and reduced hypothermia and bacterial titers compared with vehicle-treated cecal ligation and

97 y such studies demonstrate improved antibody titer comparing monomeric and nano-arrayed antigen.

98 ere was also an excess of the second-highest titer component in TFI cases.

99 ting that comparison of phase I and phase II titers could be reexamined as a surveillance criterion.

100 , with increased hemagglutination-inhibition titers, CTL activity, and earlier virus clearance after

101 A CSF-TPPA titer cutoff of >/=1:640 may be useful in identifying pa

102 drug efficacy using only the observed viral titer decay rates seen in patients.

103 ADCC-Abs titers directed against H7N9 HA or NA proteins.

104 As a confirmatory assay, the ZIKV RVNT titers displayed 93.1% agreement with the traditional ZI

105 ere used to identify the number of component titer distributions and the proportion of serum samples

106 Four titer distributions were identified.

107 For other antigens, variant-specific IgG titers do not predict colonization.

108 aive pretransplant, but showed high antibody titers during the neurological symptoms, with the IgM de

109 TITER extracts the sequence features of translation init

110 stributions, we show that 2009 H1N1 antibody titers fall into four titer subgroups and that H3N2 tite

111 fall into four titer subgroups and that H3N2 titers fall into three subgroups.

112 ntation to realize sufficiently high ethanol titers favorable for more economical ethanol recovery.

113 Ab titers peaked early, with no increase in titer following a second vaccine dose.

114 rticipants who had an increase in their hSBA titer for each of 4 primary strains by a factor of 4 or

115 eroconversion rates and 3D/2D geometric mean titers for anti-HPV-16 and anti-HPV-18.

116 loped a deep learning-based framework, named TITER, for accurately predicting TISs on a genome-wide s

117 in paired hemagglutinin antibody inhibition titers from 1 month postvaccination until end-of-study p

118 Even after excluding TPO-Ab and low-titer GAD65-Ab, Abs strongly suggesting an autoimmune ca

119 d lower hemagglutination-inhibition antibody titer geometric mean fold increase against influenza B a

120 Significantly higher serum blocking titers (geometric mean titer [GMT], 1,704) were found am

121 higher serum blocking titers (geometric mean titer [GMT], 1,704) were found among IgA-deficient indiv

122 ection (hemagglutination-inhibition antibody titer >/=1:40 on day 28 after vaccination).

123 91.5%) subjects had JE neutralizing antibody titers >/=10 (reciprocal serum dilution) against the hom

124 ortion of immunized students with protective titers >/=1:4 against an isolate from the campus outbrea

125 s, the proportion of immunized students with titers >/=1:4 was 86% (95% CI, 71%-95%) against the isol

126 Plasma CRAG titers >1:160 predict meningitis, requiring more intensi

127 Of participants with plasma CRAG titers >1:640, 96% (27 of 28) had cryptococcal meningiti

128 rditis had phase I immunoglobulin G antibody titers >800 but did not meet the CSTE case definition fo

129 tive) whereas 50% (7 of 14) with 1:160-1:320 titers had meningitis.

130 to 4 (DENV1-4), a specific range of antibody titer has been shown to enhance viral replication in vit

131 Although persistent IgE titers have been attributed conventionally to long-lived

132 donors with high ZIKV neutralizing antibody titers have expanded clones of memory B cells that expre

133 discovered in Norway rats can establish high-titer hepatotropic infections in laboratory mice with im

134 f C57BL/6 mice with CPS-CRM197 produced high-titer IgG and opsonizing antibody responses against the

135 mmunization with Hcp1 and TssM produced high-titer IgG and robust gamma interferon-secreting T cell r

136 milar sensitivity as the corresponding viral titer in phosphate buffer despite the presence of growth

137 CX4C had a 0.7 to 1.2 log10-fold lower virus titer in the lung at 5 days postinfection (p.i.) and had

138 infection decreased total hemolymph protein titers in 1 and 7-day old adult bees (-50% in the 10 K a

139 genome replication, protein expression, and titers in a concentration-dependent fashion and also blo

140 inversely associated with pre-challenge HAI titers in a dose-dependent manner.

141 could also boost RSV neutralization antibody titers in African green monkeys that had been infected p

142 Mount Elgon bat virus, and was found at high titers in bat flies but not in blood or on mucosal surfa

143 High ZIKV-specific antibody titers in cases were unrelated to prior dengue virus inf

144 Since H7 vaccines typically induce low titers in HI and MN assays, they have been considered to

145 We show that NiV-B replicated to high titers in human lung grafts and caused similar cytopathi

146 reviously showed that NiV replicates to high titers in human lung grafts in NOD-SCID/gamma mice, resu

147 We show that VZV grows to much higher titers in human neurons than in other cell types in vitr

148 tigate the decline in measles virus antibody titers in IVIGs and to ensure consistent product release

149 S-Cav1 F) induces high neutralizing antibody titers in naive animals, but it remains unknown to what

150 The observed increases in viral titers in NLRC5-deficient mice correlated with impaired

151 results in higher birth anti-pertussis toxin titers in preterm neonates.

152 IV5/G were also able to boost neutralization titers in RSV-preexposed African green monkeys.

153 ection for 20 patients (52.6%), and CrAg LFA titers in serum and CSF samples ranged from 1:5 to >/=1:

154 The virus replicates to high titers in the liver of these animals after intravenous i

155 TRIM29 (-/-) mice have lower adenovirus titers in the lung, and are resistant to lethal herpes s

156 ction and regulates fecal shedding and viral titers in tissue.

157 ed in our experiments, demonstrating that EV titers in VPS52 and VPS54 knockout (KO) cells were compa

158 EBOV GP and RABV GP-specific antibody titers increased exponentially during the trial, with ra

159 caused up to a 10(4)-fold boost in antibody titers, increased Th1-associated responses, and expanded

160 However, revaccination-induced titer increases were only about 2-fold and short-lived.

161 However, the antibody titers induced by H7 viruses were significantly lower wh

162 For high-titer inhibitors, the incidence rate had an almost three

163 aptamers, we transduce extracellular product titer into fluorescence, allowing ultrahigh-throughput s

164 determinants and adjuvants in promoting high-titer, long-lived antibody responses against Pfs25.

165 e available for H3N2, but right-censoring of titers makes these interpretations difficult to validate

166 BKV genotype-specific NAb titers may be a meaningful predictive marker that allows

167 orkers with earlier sIgG responses of higher titer (mean value 42.25 mug/mL) compared to delayed resp

168 mpared to delayed responders with lower sIgG titers (mean value 14.79 mug/mL) more frequently develop

169 uses, protection is correlated with antibody titers measured by hemagglutination inhibition (HI) and

170 fluenza virus HA1 protein using a continuous titer measurement from a protein microarray assay.

171 levels and hemagglutination inhibition (HAI) titers, more than 8-month post-vaccination compared to i

172 ntibodies but high flu-specific IgG-antibody titers mounted rapid functional antibodies after infecti

173 ergo lysis within 48 h after exposure to low titers (multiplicity of infection > 0.07) of an African

174 emically inactivated BNSP333-S1 induced high-titer neutralizing antibodies.

175 Differences in titer observed between intradermal jet injected and need

176 a pallidum hemagglutination assay (CSF-TPHA) titer of >/=1:640 is specific for neurosyphilis diagnosi

177 et, the diagnostic specificity of a CSF-TPPA titer of >/=1:640 was high and did not differ significan

178 If a CSF-TPPA titer of >/=1:640 was used in addition to a reactive CSF

179 tion of total PCBs was observed using a cell titer of 5 x 10(5) Dehalobium chlorocoercia and Paraburk

180 tralizing antibody responses with an average titer of about 115 against a panel of heterologous Tier

181 hus far it has been difficult to measure the titer of Ag-specific Abs or the expansion of Ag-specific

182 ence presented suggests that a high cellular titer of phosphorylated SaeR is required for biofilm for

183 A low titer of rAAV2/5 alpha-syn results in progressive foreli

184 reductase (HMGCR) antibodies (Abs), and the titer of these Abs is correlated with disease activity.

185 er agroinfiltration, thus maintaining a high titer of virus in this intermediate host used to produce

186 Moreover, paired sera showed that blocking titers of >/=160 were maintained over a 6-year period ag

187 ent success was defined as a decrease in RPR titers of >/=2 dilutions (4-fold) during a 12-month foll

188 Patients with pretransplant titers of 1 or more in 8 received rituximab 1 month befo

189 The remaining 13 patients had CrAg LFA titers of 1:2 (n = 11) or 1:5 (n = 2) and were ultimatel

190 r patients with first-time positive CrAg LFA titers of 1:2.

191 d corn stover achieved unprecedented ethanol titers of 79.2, 81.3, and 85.6 gL(-1) in batch shake fla

192 High titers of ADCC-Abs against H7N9 virus-infected cells wer

193 Both patients had high serum titers of anti-Trichosporon asahii antibody.

194 ody response in individuals who develop high titers of anti-ZIKV antibodies, we screened cohorts in B

195 e 1 diabetes have been reported to have high titers of antibodies against cow's milk proteins.

196 At day 28, geometric mean titers of antibodies against ZEBOV glycoprotein were hig

197 Mice produced equivalent titers of antibodies to all viruses as measured by enzym

198 mice with an anti-IL-21 blocking Ab reduced titers of autoantibodies, delayed progression of glomeru

199 Guinea pigs developed high titers of broadly cross-reactive antibodies; mice and fe

200 we show that WT-HCMV produces extremely low titers of cell-free virus but can efficiently infect fib

201 n who developed celiac disease had increased titers of cow's milk antibodies before the appearance of

202 Increased titers of cow's milk antibody before anti-TG2A and celia

203 Infectious titers of EBOV or herpes simplex virus type 1 (HSV-1) in

204 iters of myo-inositol increased 5.5-fold and titers of glucaric acid increased from unmeasurable to >

205 ng GP from the pre-N position developed high titers of GP neutralizing serum antibodies.

206 munogenicity included induction of increased titers of high-quality complement-independent antibodies

207 of IgG2a(a) 3F7.A10 to BALB/c mice with high titers of IgG1 anti-3F7.A10 led to glomerular deposits o

208 most ten- and fivefold increases in specific titers of myo-inositol and glucaric acid, respectively.

209 d pathways in Escherichia coli, resulting in titers of myo-inositol increased 5.5-fold and titers of

210 infection, progestin treatment increased the titers of neutralizing and IgG antibodies against both c

211 Although these vaccines have generated high titers of neutralizing antibodies (NAbs), their inductio

212 tigen-specific CD8 T cell responses and high titers of neutralizing antibodies, demonstrating its sup

213 ovalbumin (OVA) in Was(-/-) mice induced low titers of OVA-specific IgE compared to the WT-OVA/alum m

214 F, with or without packaging, induced higher titers of pre-F specific antibodies in hamsters, and imp

215 n vitro In BALB/c mice, 5C4 reduced the peak titers of RSV 1,000-fold more than 1129 did in both the

216 ous formation of germinal centers, increased titers of serum autoantibodies and excessive accumulatio

217 aromatic amino acid biosynthesis to increase titers of shikimate in E. coli from unmeasurable to >100

218 stant S. aureus (MRSA) strains, despite high titers of specific antibodies and circulating T cells, i

219 d heterologous protein expression and higher titers of terpenoid production.

220 lytic effects required significantly higher titers of the presumed more virulent FSS13025 Cambodia (

221 The results revealed that the titers of the total IgG and subtype IgG1 anti-SjHSP60 an

222 been favored for SSF, can produce ethanol at titers of up to 86 gL(-1) Then, optimizing SSF of CELF-p

223 irus caused mild to moderate diarrhea, lower titers of viral shedding, and no mortality, whereas the

224 igens in the presence of GLA-SE induced high titers of virus-neutralizing antibodies and conferred co

225 Antibody titers often increased across pediatric groups before de

226 to the AAV capsid without compromising viral titer or infectivity.

227 nd monophosphoryl lipid A (MPL), blockade Ab titers peaked early, with no increase in titer following

228 sIgG and sIgE titers plotted against exposure duration were compared b

229 To investigate the accuracy of low-titer positive CrAg LFA results, we performed chart revi

230 and mouse models of PDAC, we found that LIF titers positively correlated with intratumoral nerve den

231 Re-emergence of or increase in antibody titers precedes a clinical relapse.

232 umsporozoite protein (CSP)-specific antibody titers, prechallenge, were associated with protection in

233 Furthermore, the TITER prediction score can be related to the strength of

234 idered true-positive results for 5 patients (titer range, 1:10 to >/=1:2,560), due to clinical improv

235 ion rates and postvaccination geometric mean titer ratios for each antigen using US regulatory criter

236 e to viral infection, morbidity, viral organ titers, recovery time, or mortality with these diets, in

237 compared and determine the minimal antibody titers required to halt transmission in different settin

238 Another patient had a titer rise of 2 dilutions treated with 1 immunoadsorptio

239 BNSP333-S1 grew to titers similar to those of the parental vaccine vector B

240 estingly, those four animals shed virus with titers similar to those of the pH1N1, which readily tran

241 high-quality RSV-neutralizing antibodies at titers similar to those of wild-type RSV and provided pr

242 e HSV-1 infection, with kinetics and overall titers similar to those seen in undifferentiated SH-SY5Y

243 ination with inactive SpeA, resulted in high-titer SpeA-specific antibodies in vivo.

244 hat 2009 H1N1 antibody titers fall into four titer subgroups and that H3N2 titers fall into three sub

245 , our interpretation is that the two highest-titer subgroups correspond to recent and historical infe

246 is directly correlated with insulin antibody titers, suggesting insulin-specific T- and B-cell intera

247 -dose recipients had significantly lower NAb titers than 2-/3-dose recipients, their NAb titers were

248 autologous titers versus tier 1 V3-sensitive titers than BG505 SOSIP.664.

249 icited higher GP neutralizing serum antibody titers than the N-P viruses, and unmodified GP induced h

250 ell responses that generated higher antibody titers than the soluble trimers and liposome-bearing tri

251 that grew in lungs to over 100 times higher titers than the starting virus.

252 es, with C-prM-E VLPs giving slightly higher titers than those with prM-E VLPs.

253 VLPs generated higher neutralizing antibody titers than those with the DNA vaccines, with C-prM-E VL

254 t exhibited slower growth kinetics and lower titers than wild-type (WT) MHV68.

255 did not induce higher neutralizing antibody titers than wild-type F.

256 The mice developed a high IgG titer that was maintained at 22 months of age.

257 ation will be required to establish antibody titers that persist for several malaria transmission sea

258 should examine the effect of anti-HBs serum titers, the potential role for booster vaccinations, and

259 endent cellular cytotoxicity (ADCC), and low-titer tier 1B and tier 2 neutralizing antibody responses

260 ed sera had a >/=4-fold increase in antibody titer to cluster-related strains as well.

261 Antibody removal was performed to reduce titers to 1 or less in 8 on the day of the operation.

262 Serum immunoglobulin G (IgG) titers to 28 pneumococcal protein antigens were measured

263 opulation's natural distribution of antibody titers to an endemic infectious disease may include info

264 g ADCC antibodies in the absence of high HAI titers to circulating influenza strains.

265 ion, and most vaccines rely on HA inhibition titers to determine efficacy, despite the growing awaren

266 Antibody titers to H1N1pdm09 persisted above the protective level

267 We describe the distributions of antibody titers to subtypes 2009 H1N1 and H3N2.

268 2009 and 2013 from which we report antibody titers to the influenza virus HA1 protein using a contin

269 template can evade NAbs without compromising titer, transduction efficiency, or tissue tropism.

270 elicited a higher ratio of tier 2 autologous titers versus tier 1 V3-sensitive titers than BG505 SOSI

271 The component at the highest titer was found only in samples from women with TFI, but

272 ty of infection (MOI), though a reduction in titer was observed.

273 lly significant difference in virus-blocking titers was observed between pre- and postpandemic sera.

274 No elevation of anti-PT antibody titers was observed in the patient.

275 titers than 2-/3-dose recipients, their NAb titers were 5- to 30-fold higher than unvaccinated girls

276 Survival, weight loss, and viral titers were assessed over a 14-day study period.

277 serum immunoglobulin A and immunoglobulin G titers were associated with partial protection against r

278 Significantly lower antibody titers were detected in HIV-infected mothers and HIV-exp

279 Infectious EBOV titers were determined in SDS-treated plasma and whole b

280 bition and neuraminidase-inhibition antibody titers were determined in subjects >/=13 years.

281 all times and in all organs analyzed, virus titers were higher in CAST than in BALB/c mice.

282 Measles antibody titers were measured by enzyme-linked immunosorbent assa

283 liferation, cytokine secretion, and antibody titers were measured by using standard techniques.

284 RPR titers were monitored every 3 months.

285 the parental virus (pH1N1/NS1-wt), yet virus titers were not significantly increased in cell cultures

286 ies were induced in all 20 participants; the titers were of greater magnitude in the group that recei

287 Infectious virus titers were present in the blood and most tissues 3 days

288 or SL3261/sec, peak total serum IgG antibody titers were reached more rapidly in mice that received S

289 inclusion immunofluorescence serum antibody titers were recorded among infertile women seen at St. M

290 oneal cavity and that pathogenic natural IgM titers were reduced in the CD6(-/-) mice in association

291 40,000 (40 K) live N. ceranae spores/bee, Vg titers were significantly elevated by + 83% and + 73%, r

292 ZIKV-specific antibody titers were significantly higher in cases than in contro

293 Further analysis showed that ADCC-Abs titers were significantly higher toward H7N9 NP, as comp

294 consuming the Western diet had diminished Ab titers whereas the Western diet plus DHA improved titers

295 unity with a saturated neutralizing antibody titer, which no longer increased after challenge with an

296 n showed increased antigen-specific antibody titer with an overall balanced Th1/Th2 response, while t

297 ured increased antibody levels, ASCs and HAI titers with reduced viral load and inflammatory response

298 t least partly related to measuring antibody titers with the traditional HI and MN assays, which may

299 tration had a marked effect on reducing UPEC titers within the bladder, this treatment failed to prev

300 ricted in HUHEP mice resulting in high viral titers without pathologic effects.