ライフサイエンスコーパス: cross-reactivity

1 tigenic seniority and exposure-type specific cross reactivity.

2 We aimed to assess this possible cross reactivity.

3 d it with the receptor, and confirmed murine cross-reactivity.

4 S albumins may account for observed clinical cross-reactivity.

5 o Catcher/Tag systems, which did not express cross-reactivity.

6 s the molecular basis for their IgE antibody cross-reactivity.

7 Daratumumab up to 370 kBq due to the lack of cross-reactivity.

8 cks related to sensitivity, specificity, and cross-reactivity.

9 detection sensitivity, reproducibility, and cross-reactivity.

10 damage and platelet dysfunction by antigenic cross-reactivity.

11 persistent trigger in human autoimmunity via cross-reactivity.

12 F protein that could guide the emergence of cross-reactivity.

13 abling both enhanced sensitivity and reduced cross-reactivity.

14 minated with OTA, and were used to model OTA cross-reactivity.

15 d classic predictions about the scope of TCR cross-reactivity.

16 hibition tests with both allergens confirmed cross-reactivity.

17 s or Epstein-Barr virus, indicating possible cross-reactivity.

18 y is often hampered by clinically irrelevant cross-reactivity.

19 daratumumab up to 370 kBq because of lack of cross-reactivity.

20 ly conserved pan-allergens showing extensive cross-reactivity.

21 otype, which is associated with self-antigen cross-reactivity.

22 lexing capacity, are costly, and can exhibit cross-reactivity.

23 dentified as crucial for IgE-recognition and cross-reactivity.

24 d Ani s 3, indicating lack of T-cell epitope cross-reactivity.

25 r, less is known about the underlying T-cell cross-reactivity.

26 mer to elucidate the structural basis of its cross-reactivity.

27 Serologic cross-reactivity, a hallmark of orthopoxvirus (OPXV) inf

28 Due to cross-reactivity, a positive first-line serology test re

29 whereby CD8(+) T cells confer unprecedented cross-reactivity across all influenza viruses, a key fin

30 nition and provide evidence of CD8(+) T cell cross-reactivity across IAV, IBV and ICV.

31 xpected outcomes in antibody specificity and cross-reactivity after influenza vaccination in individu

32 Our results suggest that differences in cross-reactivity after influenza vaccination should be e

33 f MP at picomolar concentrations without any cross-reactivity against chlorpyriphos and fenthion.

34 esent in DERAA(-/-) individuals and can have cross-reactivity against joint antigens.

35 Three mAbs showed cross-reactivity against multiple strains of RV A viruse

36 diversity affect T cell responses and their cross-reactivity against multiple variants of the virus

37 mplexity of competing cleavages and antibody cross reactivities all illustrate limitations in our und

38 ifferent plants, they are prone to extensive cross-reactivity among allergen pollen extracts.

39 ibodies suffer from low sensitivity and high cross-reactivity among different flaviviruses.

40 Recent reports have reported considerable cross-reactivity among different M types, suggesting the

41 The high level of cross-reactivity among flaviviruses and their cocirculat

42 We estimated the levels of serologic cross-reactivity among humans primed with seasonal influ

43 However, the potential cross-reactivity among porcine coronaviruses is a major

44 ogues in mice-yet we anticipate broad immune cross-reactivity among the AAV serotypes.

45 sequence identity alone was insufficient for cross-reactivity among the M peptides.

46 No cross-reactivity among two drugs was observed according

47 ing should be considered to detect potential cross-reactivity amongst glycopeptides.

48 Cross reactivity analysis showed the selectivity of dete

49 on serologic testing that are complicated by cross reactivity and therefore unable to distinguish Zik

50 me the individual limitations of antibodies' cross-reactivity and aptamers' slow binding kinetics.

51 ntial for interleukin-17 A (IL-17A)-mediated cross-reactivity and associated with cross protection.

52 Cross-reactivity and cross-neutralization between this c

53 ncluding sensitivity, specificity, potential cross-reactivity and cross-protectivity, the diagnostic

54 to ZIKV-induced B-cell responses and humoral cross-reactivity and discuss relevant considerations for

55 istent antibodies predominantly demonstrated cross-reactivity and potent neutralization toward a phyl

56 ation, which imposes challenges in balancing cross-reactivity and selectivity.

57 The cross-reactivity and sequential pollen seasons within th

58 munopathogenesis, 4) antigenic diversity and cross-reactivity, and 5) population seroprevalence.

59 ) and 38 Flucelvax-induced MAbs for avidity, cross-reactivity, and any selectivity toward the head ve

60 od plasma, without having any matrix effect, cross-reactivity, and false-positives.

61 ngmL(-1) (S/N=3), without any matrix effect, cross-reactivity, and false-positives.

62 We evaluated the magnitude, cross-reactivity, and functionality of NS1-specific IgG

63 successfully applied to tests for recovery, cross-reactivity, and real samples.

64 ce in the same geographic regions, serologic cross-reactivity, and similar but often less severe clin

65 n testing, "oral challenge or provocation," "cross-reactivity," and "antimicrobial stewardship".

66 ted, we identified several ways in which CD8 cross-reactivity appeared to influence HIV-1 viral evolu

67 The molecular rules driving TCR cross-reactivity are poorly understood and, consequently

68 r interest for allergenic proteins with high cross-reactivity as observed in the lipid transfer prote

69 cating that neuraminidase-based vaccines and cross-reactivity assays should be employed to monitor an

70 Efficiency, specificity and cross-reactivity assays showed statistically significant

71 Here, we demonstrate that cross-reactivity at the level of T cell responses among

72 rtant arthropod-related proteins involved in cross-reactivity between A. aegypti and other allergenic

73 erstanding of the underlying pathogenesis of cross-reactivity between animal albumins and meat albumi

74 those with severe disease, and (c) there was cross-reactivity between antibodies to SARS-CoV-1 and SA

75 were performed to determine the existence of cross-reactivity between both nsLTPs.

76 Our findings support possible cross-reactivity between dengue virus and SARS-CoV-2, wh

77 gen in biological fluids, as well as reduced cross-reactivity between different serotypes of dengue a

78 evidence has led to the hypothesis of immune cross-reactivity between emm types.

79 ays where the antibody response must resolve cross-reactivity between foreign and self-proteins beari

80 Cross-reactivity between grass pollen protein and fresh

81 explanation for the absence of inter-species cross-reactivity between human and mouse 4-1BB and 4-1BB

82 ell epitopes with potential antigen-specific cross-reactivity between influenza and allergens.

83 n subsets, there is a considerable degree of cross-reactivity between many species.

84 No cross-reactivity between metronidazole and ornidazole in

85 id syndrome (APS) as a model, we demonstrate cross-reactivity between non-orthologous mimotopes expre

86 ted in Europe and appear mainly to rely upon cross-reactivity between nonspecific lipid transfer prot

87 driven by the knowledge on patterns of DHR, cross-reactivity between NSAID and pharmacological effec

88 itization process would occur because of the cross-reactivity between Ole e 7 and Pru p 3 observed in

89 Despite low cross-reactivity between PCN and later-generation cephal

90 tent with previous reports of a low allergic cross-reactivity between PCN and later-generation cephal

91 Cross-reactivity between penicillin and cephalosporin dr

92 Ferret antisera detected no or little cross-reactivity between the 2 A(H3N2)v clusters or betw

93 Low levels of cross-reactivity between the H3N2v and sH3N2 viruses fro

94 We also show cross-reactivity between the SARS-CoV-1 S-directed VHH a

95 Ferret antisera detected no or little cross-reactivity between the two A(H3N2)v clusters, or b

96 bat sera, we assess the level of serological cross-reactivity between the virus-specific antisera and

97 f surface-exposed residues, suggests limited cross-reactivity between these allergens and Blo t 1.

98 Cross-reactivity between these two proteins was confirme

99 In vespid venom allergy, cross-reactivity between venoms of different species can

100 veral groups have demonstrated immunological cross-reactivity between ZIKV and other flaviviruses and

101 from mugwort, is frequently involved in this cross-reactivity, but no antibody-binding epitopes have

102 The ZIKV-NS1 IgG cross-reactivity by samples from secondary DENV infectio

103 t human antibodies to N1 NA with exceptional cross-reactivity can be recalled by vaccination and high

104 for other infectious agents in parallel, as cross-reactivity can occur.

105 vely, we believe these results show that CD8 cross-reactivity could be an important consideration in

106 in both dog and human groups, as well as no cross-reactivity could be detected among sera with other

107 vergence of hemagglutinin variants with poor cross-reactivity could potentially lead to circulation o

108 display differences in their specificity and cross-reactivity dependent on pre-existing immunity.

109 ral loads in recipients who became infected, cross-reactivity did appear to influence early viral evo

110 ies revealed that the primary determinant of cross-reactivity did indeed appear to be a preference fo

111 Although this cross-reactivity did not seem to affect viral control in

112 ferent m(1)A antibody that lacks cap-binding cross-reactivity does not show enriched binding in 5'UTR

113 We show how the TCR specificity/cross-reactivity duality can be rationalized from struct

114 ologous H5 viruses with different degrees of cross-reactivity; Egy/09 ca vaccine antisera were more s

115 T cell cross-reactivity ensures that diverse pathogen-derived e

116 vine serum albumin), resulting in negligible cross-reactivity except for sucrose.

117 igeria or Sierra Leone exhibited substantial cross-reactivity for binding to LASV nucleoprotein and t

118 Overall, our data suggest limited cross-reactivity for both CD4 and CD8 T cell responses b

119 n B2, was observed, together with negligible cross-reactivity for other mycotoxins produced by the sa

120 osen depending on their virtual affinity and cross-reactivity for the experimental step.

121 There was less cross-reactivity for the Zinc protein.

122 No interference/cross-reactivity from Salmonella enteritidis, Enterobact

123 T-cell cross-reactivity generally correlated with allergen sequ

124 wever, Wnt lipidation and Wnt-Frizzled (Fzd) cross-reactivity have hindered translational Wnt applica

125 mer exhibiting a combination of broad target cross-reactivity, high affinity and remarkable specifici

126 lavivirus strain can result in immunological cross-reactivity; however, the consequences to infection

127 In contrast to IgM cross-reactivity, IgG and IgA antibodies against ZIKV no

128 bility and immunological and pharmacological cross-reactivities in DHR.

129 cific patterns of allergen isoform and group cross-reactivities in the repertoires were observed, pat

130 nd subsequent peptide generation, and T-cell cross-reactivity in a BALB/c murine model.

131 ntigenically related flaviviruses that share cross-reactivity in antibody and T cell responses, and c

132 ole and ornidazole and to determine possible cross-reactivity in between.

133 Our data demonstrate that the lack of cross-reactivity in glycan hole antibodies is due to ami

134 All antigens 5 showed extensive cross-reactivity in sIgE analyses, inhibition assays, an

135 or stx subtypes, respectively and showed low cross-reactivity in spiked urine, serum and milk samples

136 V-1 infection, but little is known about CD8 cross-reactivity in the context of HIV-1 vaccination.

137 rt a role for non-orthologous commensal-host cross-reactivity in the development and persistence of a

138 s reveal mechanisms of specificity and a K11 cross-reactivity in the K33 affimer.

139 Finally, ZIKV induces greater cross-reactivity in the MBC pool than in serum antibodie

140 Here, we evaluated vaccine-induced CD8 cross-reactivity in two preventative HIV-1 vaccine effic

141 ngue virus (DENV), the role of immunological cross-reactivity in ZIKV and DENV infections has become

142 es after vaccination as well as the level of cross-reactivity induced by the vaccine.

143 analysis in real world samples, without any cross reactivity, interferences, and false-positives.

144 T-cell cross-reactivity is essential for effective immune surve

145 This cross-reactivity is explained by the sequence similarity

146 Cross-reactivity is limited between the tested genotypes

147 a1 have been identified in P. jirovecii Such cross-reactivity is rare, and our findings suggest that

148 pomyosin T-cell cross-reactivity, unlike IgE cross-reactivity, is dependent on structural stability r

149 residues, this technique may be hindered by cross-reactivity issues, or by matrix-molecule interfere

150 y but carries the risk of creating undesired cross-reactivity leading to potential serious adverse ef

151 We determined the MAb cross-reactivities, localized the epitopes, and measured

152 plains their high target specificity and low cross-reactivity, making them promising candidates for t

153 NO2 and EBNA1 peptides demonstrated antibody cross-reactivity, mapping to ANO2 [aa 140 to 149] and EB

154 ing to 2019-nCoV S, suggesting that antibody cross-reactivity may be limited between the two RBDs.

155 Immunologic cross-reactivity may explain disparate outcomes of BCG v

156 This cross-reactivity may worsen symptoms of a subsequent inf

157 s was more restricted than the repertoire of cross-reactivities measured by ELISA.

158 We confirmed cross reactivity of extracts of the Japanese fireworm lu

159 Here we evaluated the cross-reactivity of a 'public', HIV-specific, CD8 T cell

160 ping is primarily based on the extensive IgE cross-reactivity of allergen homologs to the major birch

161 green turtles from Florida, we rejected the cross-reactivity of antibodies to other herpesviruses, d

162 Conformational diversity and self-cross-reactivity of antigens have been correlated with e

163 present a novel approach for controlling the cross-reactivity of biosensors by employing defined mixt

164 We examined cross-reactivity of CAR T cells toward both human and mu

165 Cross-reactivity of classical chlamydial antigens compro

166 r peptide antibody assays, suggesting severe cross-reactivity of commercial ELISAs.

167 However, despite strong cross-reactivity of convalescent antisera between relate

168 n on the presence and possible immunological cross-reactivity of different meningococcal vaccine anti

169 These results provide insights into the cross-reactivity of drugs across multiple steroidogenic

170 ons of the HLA molecule that help to explain cross-reactivity of HLA antigens.

171 nformation is crucial for the elucidation of cross-reactivity of marker allergens such as the walnut

172 The cross-reactivity of patients with IgE-mediated CHX aller

173 urs extensively in RA, permitted significant cross-reactivity of RF+ patient sera with fibrinogen in

174 The strength, prevalence and cross-reactivity of T-cell responses towards Phl p 12 ar

175 We found that both specificity and cross-reactivity of the antibodies induced by the 2009 H

176 We took advantage of the cross-reactivity of the B7-H3.CAR with murine B7-H3, and

177 h sodium metaperiodate abrogated most of the cross-reactivity of the rabbit anti-SmSEA antibodies, su

178 The breadth and cross-reactivity of these responses are important agains

179 r type B influenza may differentially affect cross-reactivity of vaccination-induced H3-specific hema

180 he affinity maturation process and potential cross-reactivity of VH3-23/VK1-5 neutralizing Abs, infor

181 The cross-reactivity of ZIKV epitopes to dengue virus (DENV)

182 To address immunological IgE cross-reactivity on molecular level, seven recombinant a

183 No cross-reactivity or interference was observed with testi

184 the enzyme assay, enabling investigation of cross-reactivity over multiple methylation sites and int

185 These difficulties often arise due to cross-reactivity, particularly in the presence of simila

186 contrast, due to their limited B- and T-cell cross-reactivity patterns, a combination of different is

187 This knowledge enables improved cross-reactivity prediction for patients suffering from

188 review topics of interest such as taxonomy, cross-reactivity, prevalence, clinical relevance, PFS, a

189 omic applications by long development times, cross-reactivity preventing multiplexing, specificity is

190 ific for foreign Ags and a moderate level of cross-reactivity primes individual cells for optimal pro

191 An alpha-Gal-associated IgE cross-reactivity profile (IgE against CTX, Bos d TG, and

192 VRC01 B cell sub-populations with distinct cross-reactivity properties were activated by each immun

193 s present at low concentrations and antibody cross-reactivity results in unspecific detection that ca

194 VID-19), healthy donor sera from 2018, and a cross-reactivity serum panel collected in early 2020.

195 Cross-reactivity should be considered when treating pati

196 inetics of EGFR phosphorylation but retained cross-reactivity similar to tSH2-WT.

197 The nonspecificity and cross-reactivity studies of the developed immunosensor w

198 Cross-reactivity studies with non-specific molecules pro

199 as well as an algorithmic approach, based on cross-reactivity studies, in patients with a suspicion o

200 A cross-reactivity study using 74 non-Bordetella bacterial

201 y, intersubclass specificity, and class-wide cross-reactivity, suggesting that some conserved epitope

202 Its cross-reactivity suggests that this nanobody may be valu

203 bolite, 6-acetylmorphine (6AM), with minimal cross reactivity to clinically used opioids.

204 pression on BeWo EVs, but due to concern for cross reactivity to highly prevalent isoforms of intesti

205 biosensors to a set of ligands, for example, cross-reactivity to a given target family while maintain

206 Yet cross-reactivity to additional microbes is important to

207 ts supported these findings and demonstrated cross-reactivity to all other species within the birch h

208 The developed method showed low cross-reactivity to bacterial pathogens such as Salmonel

209 hat detects cmvIL-10 and LAcmvIL-10, with no cross-reactivity to cIL-10.

210 s, by measuring the prevalence, strength and cross-reactivity to clinically relevant profilins.

211 m ZIKV-infected patient sera, although lower cross-reactivity to DENV2/3-NS1 was observed.

212 bodies in cancer therapy is limited by their cross-reactivity to healthy tissue.

213 Furthermore, NSTs showed a high degree of cross-reactivity to multiple variant epitopes from clini

214 e basis for this protection, we assessed the cross-reactivity to N. gonorrhoeae of serum raised to th

215 IV-1 clade C Env proteins, with considerable cross-reactivity to other clades.

216 T-cell cross-reactivity to other profilins correlated with over

217 s, including high input RNA requirements and cross-reactivity to other RNA modifications.

218 rcial MIPs were characterized by quite broad cross-reactivity to other structurally related amphetami

219 detected all four clades of C. auris without cross-reactivity to other yeasts.

220 T-cell responses, epitope mapping and cross-reactivity to profilins (Phl p 12, Ole e 2, Bet v

221 at the anti-Ab-54149 EPS serum would exhibit cross-reactivity to Pse on other organisms.

222 ined with good developability properties and cross-reactivity to SARS-CoV-2 mutants provide a strong

223 to subdomains of S protein as well as their cross-reactivity to SARS-CoV.

224 The cross-reactivity to structurally similar PPI was also ob

225 responses to dalbavancin however two showed cross-reactivity to teicoplanin and telavancin.

226 The WV particles showed some cross-reactivity to TGEV Miller and TGEV Purdue antisera

227 due antisera, while N protein presented some cross-reactivity to TGEV Miller.

228 sted vaccines induced a similar level of CD8 cross-reactivity to that seen in acute HIV-1 infection.

229 m(1)A to 5'UTRs were the result of antibody cross-reactivity to the 5' cap.

230 Cross-reactivity to VAR2CSA was characterized by enzyme-

231 he iodinated benzothiazine probe has reduced cross-reactivity toward primary amines and is highly rea

232 demonstrate that molecular mimicry underpins cross-reactivity toward the gliadin epitopes.

233 munological perspective: A high level of IgE cross-reactivity towards allergens from the birch homolo

234 Cross-reactivity towards related ragweed species of IgE

235 anges to gluten proteins after GF treatment; cross-reactivity towards the antibodies recognizing almo

236 Tropomyosin T-cell cross-reactivity, unlike IgE cross-reactivity, is depend

237 ability of TaqMan probe qPCR assays without cross-reactivity upon probes combination.

238 Cross-reactivity was addressed in vivo using 2 different

239 No cross-reactivity was detected between DdPhyA/TgPhyA subs

240 No cross-reactivity was found with a panel of 38 food commo

241 Moreover, antibody cross-reactivity was increased when the individual's pre

242 Cross-reactivity was limited and only observed with othe

243 This cross-reactivity was more pronounced in ImmunoCAP measur

244 ross-reacted with N-acetyl DIAT; however, no cross-reactivity was observed between atabecestat and DI

245 towards their target monosaccharides, as no cross-reactivity was observed with other sugars like N-a

246 v-specific clones was dose-dependent, and no cross-reactivity was observed.

247 A feature of cross-reactivity where previous exposure to one microbe

248 However, there is no evidence of cross-reactivity, which explains this observed co-sensit

249 The aptasensor did not show cross reactivity with other commonly used pesticides suc

250 Although cross-reactivities with coagulation regulatory proteins

251 ivity was analyzed in ELISA experiments, and cross-reactivity with allergens of other poultry species

252 f (RBM) of RBD and demonstrated their strong cross-reactivity with anti-EMC-RBD antibodies.

253 vaccinees were associated with very limited cross-reactivity with any other flaviviruses and in five

254 y in the United Kingdom, despite a degree of cross-reactivity with Ara h 6.

255 y assess MAYV epidemiology and the extent of cross-reactivity with CHIKV from serological data collec

256 nt reacted primarily with OCT and showed IgE cross-reactivity with CHX, ALX, and PHMB.

257 aracterize pathways of T cell activation and cross-reactivity with clozapine metabolites and olanzapi

258 Despite cross-reactivity with common pathogens, pan-family assay

259 MBC responses, although ZIKV has the highest cross-reactivity with DENV3.

260 inst infection with dengue virus (DENV), yet cross-reactivity with distinct serotypes can precipitate

261 was suggested that these fruits demonstrate cross-reactivity with each other.

262 for their respective target protein and low cross-reactivity with five reference proteins.

263 for their respective target protein and low cross-reactivity with four nonspecific molecules.

264 ized with the PMD-modified HA show increased cross-reactivity with HAs from other influenza strains,

265 III domain proteins are a result of antibody cross-reactivity with human and porcine fVIII leading to

266 dies mediated ADCC efficiently and displayed cross-reactivity with IBV of both lineages.

267 the molecular mechanisms that control T-cell cross-reactivity with important implications for pathoge

268 utzneria albida (KalbTG), which exhibited no cross-reactivity with known MTG substrates or commonly u

269 Absence of cross-reactivity with mammalian species tested in the st

270 cific in vivo biotinylated nanobody of broad cross-reactivity with microcystins.

271 irch pollen extract, while displaying a weak cross-reactivity with other allergens of the PR-10 famil

272 fic antibodies and their binding avidity and cross-reactivity with other alphaviruses increased over

273 l for risk assessment but challenging due to cross-reactivity with other alphaviruses such as chikung

274 V RNA when directly used as template without cross-reactivity with other citrus pathogens.

275 ty and sensitivity but also did not show any cross-reactivity with other CoVs.

276 r associations with protective immunity, and cross-reactivity with other exposures.

277 pan-caspase inhibitor, z-VAD-FMK, and has no cross-reactivity with other known protease families.

278 ic copies/reaction) and high specificity (no cross-reactivity with other mcr variants).

279 ates and reference strains, and there was no cross-reactivity with other mollicutes, Gram-positive ba

280 revealed high specificity toward FB1 with no cross-reactivity with other mycotoxins, and it demonstra

281 Moreover, the assay showed no cross-reactivity with other nematode antigens.

282 ha- and beta-zearalenol) without significant cross-reactivity with other related mycotoxins.

283 o be highly specific for SARS-CoV-2, with no cross-reactivity with other respiratory viruses observed

284 The biosensor did not show significant cross-reactivity with other virus antigens such as influ

285 Other mAbs showed cross-reactivity with PkMSP1P-19.

286 od from the sensitization to the development cross-reactivity with pork meat is required.

287 PF cats (83%), but this was primarily due to cross-reactivity with preventive vaccine-induced anti-fe

288 ) M binding affinity for fentanyl, yet broad cross-reactivity with related fentanyl analogues.

289 Together, our data indicate that BCR cross-reactivity with self-antigen is a common feature o

290 d downstream of BCR signaling as a result of cross-reactivity with self-antigens in vivo.

291 viruses, and the virus showed a low level of cross-reactivity with serum raised against H9N2 viruses.

292 function, pathways of T-cell activation and cross-reactivity with structurally related compounds.

293 i of HCMVpp65(422-439) immunized mice showed cross-reactivity with TAF9(134-144) and dsDNA.

294 Cross-reactivity with TBRF can confound epidemiology and

295 ut suffer from poor cell permeability and/or cross-reactivity with the cysteine protease cathepsin B.

296 ased on serological testing that often shows cross-reactivity with the Dengue virus (DENV) and other

297 -fruit/vegetable syndrome', might also imply cross-reactivity with tobacco, natural latex and plant-f

298 ibition assays, rRhi o 2 exhibited extensive cross-reactivity with various other cyclophilins reporte

299 tion of serologies is confounded by antibody cross-reactivity with viruses belonging to the same sero

300 n addition, the specificity is 100%, and the cross-reactivity with West Nile and dengue viruses is mi