ライフサイエンスコーパス: susceptibility to infection

1 cated for treatment of SAH, but can increase susceptibility to infection.

2 lammatory bowel disease, obesity, atopy, and susceptibility to infection.

3 -third of all childhood deaths via increased susceptibility to infection.

4 y is determined in part at the level of host susceptibility to infection.

5 n impaired macrophage function and increased susceptibility to infection.

6 ociated with immune deficiency and increased susceptibility to infection.

7 on the immune system, resulting in increased susceptibility to infection.

8 PMN RB defect, which may increase patients' susceptibility to infection.

9 alpha(+) dendritic cells displayed increased susceptibility to infection.

10 mutation status was predictive for enhanced susceptibility to infection.

11 t could be therapeutically targeted to alter susceptibility to infection.

12 ay increase rather than decrease performers' susceptibility to infection.

13 ity of fungal spores but did not affect host susceptibility to infection.

14 erstanding of how leptin links nutrition and susceptibility to infection.

15 ggest that rhizobia may modulate the plant's susceptibility to infection.

16 activation, expression of KLF2 and CCR5, and susceptibility to infection.

17 ncy characterized by pancytopenia and marked susceptibility to infection.

18 lly, with a subsequent increase in a child's susceptibility to infection.

19 cilitated by studying genetic differences in susceptibility to infection.

20 umbers in the spleen and resulted in greater susceptibility to infection.

21 t-BMT may be efficacious in reducing patient susceptibility to infection.

22 ich undoubtedly contribute to their enhanced susceptibility to infection.

23 stained skin peptide depletion and increased susceptibility to infection.

24 ction and that HLA-B*0801 is associated with susceptibility to infection.

25 c CD4 T cells but display markedly increased susceptibility to infection.

26 t antibodies to PVL might contribute to host susceptibility to infection.

27 and cell-mediated immunity and increases the susceptibility to infection.

28 by multiple proteoglycans, thereby determine susceptibility to infection.

29 ) plasmacytoid DC (pDC) exhibiting the least susceptibility to infection.

30 macrophage function, resulting in increased susceptibility to infection.

31 mice, but expression of mCEACAM1a increases susceptibility to infection.

32 gulate EGFR, thereby dramatically increasing susceptibility to infection.

33 pond to Ag and has the potential to increase susceptibility to infection.

34 micide, nonoxynol-9 (N-9), greatly increased susceptibility to infection.

35 fti due to maternal filariasis may influence susceptibility to infection.

36 typhimurium, but rather, leads to increased susceptibility to infection.

37 of lymphocytes is associated with increased susceptibility to infection.

38 process may alter T and B cell tolerance and susceptibility to infection.

39 an avenue for discovering genes involved in susceptibility to infection.

40 pha(2,3)-specific sialyltransferase restored susceptibility to infection.

41 i-inflammatory cytokines that play a role in susceptibility to infection.

42 -, and IL-12 p35-/- mice also show increased susceptibility to infection.

43 elper type 1 (T(H)1) responses and increased susceptibility to infection.

44 hymic atrophy, lymphopenia, and an increased susceptibility to infection.

45 ective mechanisms or factors associated with susceptibility to infection.

46 and immunosuppressive and thus may increase susceptibility to infection.

47 by acting as irritants or through increasing susceptibility to infection.

48 rains, causing humoral immune deficiency and susceptibility to infection.

49 genes are an important cause of variation in susceptibility to infection.

50 munodeficiency virus type 1 (HIV-1), affects susceptibility to infection.

51 nic lung disease (CLD), could increase their susceptibility to infection.

52 rmal, and there was no evidence of increased susceptibility to infection.

53 ich at least partially explain the increased susceptibility to infection.

54 anted consequences, most notably an enhanced susceptibility to infection.

55 lciparum, although variation exists in their susceptibility to infection.

56 g countries and is associated with increased susceptibility to infection.

57 op compromised T cell immunity and increased susceptibility to infection.

58 roduction of IL-22 by ILC3 and increases the susceptibility to infection.

59 immunodeficiency (CID), leading to increased susceptibility to infections.

60 spiratory immunity is linked to the enhanced susceptibility to infections.

61 n and cellular entry may explain a decreased susceptibility to infections.

62 have deficits in wound healing and increased susceptibility to infections.

63 ptive immune systems that may influence host susceptibility to infections.

64 sorders that involve chronic neutropenia and susceptibility to infections.

65 as silencing of GhSWEET10 compromises cotton susceptibility to infections.

66 n certain populations and leads to increased susceptibility to infections.

67 al block in T and B cells, resulting in high susceptibility to infections.

68 of whites and are associated with increased susceptibility to infections.

69 Aged skin heals wounds poorly, increasing susceptibility to infections.

70 ults in interstitial pneumonia and increased susceptibility to infections.

71 inal microbiota and, paradoxically, increase susceptibility to infections.

72 ed with impaired host response and increased susceptibility to infections.

73 nsequence of this functional program is high susceptibility to infections.

74 delta and alphabeta T cells and an increased susceptibility to infections.

75 s associated with a considerable increase in susceptibility to infections.

76 to elucidate the role obesity plays in host susceptibility to infections.

77 T-cell and macrophage populations and their susceptibilities to infection.

78 ine may inhibit T-cell function and increase susceptibility to infection after injury.

79 The clinical phenotype of WAS includes susceptibility to infection, allergy, autoimmunity, and

80 Immune system impairment and increased susceptibility to infection among alcohol abusers is a s

81 Early life is characterized by a high susceptibility to infection and a TH2-biased CD4 T-cell

82 8-deficient mice, which correlates with high susceptibility to infection and a very low number of IL-

83 munity and inflammation as well as determine susceptibility to infection and autoimmunity and respons

84 -induced urticaria, antibody deficiency, and susceptibility to infection and autoimmunity.

85 The elderly face significant risk for susceptibility to infection and cancer because of declin

86 ive agents may confer risks of both enhanced susceptibility to infection and decreased responsiveness

87 eals important immune factors that influence susceptibility to infection and demonstrates for the fir

88 ased immunity with a concomitant increase in susceptibility to infection and diminished efficacy of v

89 ate that host AIC regulatory networks confer susceptibility to infection and establish a proteomic re

90 Type 1 diabetes enhances susceptibility to infection and favors the sepsis develo

91 ts in the microbiota composition change host susceptibility to infection and how dietary changes or m

92 the host environment, skin barrier defects, susceptibility to infection and immunological factors.

93 r sometimes concomitantly, lead to increased susceptibility to infection and loss of self-tolerance.

94 microbes could improve our understanding of susceptibility to infection and may indicate new strateg

95 and exhaustion that contributes to increased susceptibility to infection and mortality.

96 han offset by other effects, such as reduced susceptibility to infection and reduced infectiousness.

97 distinct immune responses that contribute to susceptibility to infection and reduced vaccine response

98 ccount for the previously reported increased susceptibility to infection and reinfection with S. mans

99 okine receptors or certain HLA types, affect susceptibility to infection and subsequent clinical cour

100 Taken together, these results suggest that susceptibility to infection and subsequent disease after

101 SIV/HIV infection likely is limited by their susceptibility to infection and subsequent inactivation

102 lly causal link among inborn errors in SETX, susceptibility to infection and the development of neuro

103 t risk factors for asthma are the underlying susceptibility to infection and the exaggerated reaction

104 increased infection by increasing both their susceptibility to infection and the length of time they

105 anding human genetic markers associated with susceptibility to infection and the use of molecular dia

106 which can induce changes in an individual's susceptibility to infection and transmission, as well as

107 bacterium tuberculosis infection and enhance susceptibility to infection and/or disease.

108 vaccinations can have nontargeted effects on susceptibility to infections and allergic disease.

109 IgA Abs, which could contribute to a higher susceptibility to infections and altered responses to va

110 The elderly are known to have enhanced susceptibility to infections and an impaired capacity to

111 receptor (VDR) gene have been implicated in susceptibility to infections and bone-related diseases.

112 response and by creating increased risk and susceptibility to infections and cancer.

113 t mucosa, processes that ultimately increase susceptibility to infections and contribute to negative

114 ribed for measles vaccine (MV), or increased susceptibility to infections and death, as described fol

115 mune deteriorization that leads to increased susceptibility to infections and decreased responses to

116 se data suggest that Th2 conditions increase susceptibility to infections and identify pharmacologica

117 ld be linked to differing responsiveness and susceptibility to infections and immune/inflammatory-rel

118 humoral immunity, as manifested by increased susceptibility to infections and impaired vaccine respon

119 mined diseases that typically have increased susceptibility to infections and in many cases also have

120 Pregnancy is associated with changes in host susceptibility to infections and inflammatory disease.

121 Idiosyncratic susceptibility to infections and malignancy is noted.

122 e results support the concept that increased susceptibility to infections and poor adaptive immune re

123 dely used in consumer products, might affect susceptibility to infections and the development of alle

124 severe infection, increasing the children's susceptibility to infection, and increasing infectiousne

125 An individual's immune function, susceptibility to infection, and response to immunosuppr

126 terplay between inflammatory responses, host susceptibility to infection, and the development of prot

127 identification of the factors that modulate susceptibility to infection, and the impact of enteric p

128 sociated with suppressed immunity, increased susceptibility to infections, and diminished antitumor r

129 nuclear leucocytes (PMNs), increased patient susceptibility to infections, and hepatocellular carcino

130 eficiency, cell-mediated immune dysfunction, susceptibility to infections, and increased oxidative st

131 e characterized by neutropenia, lymphopenia, susceptibility to infections, and myelokathexis, which d

132 iabetes, despite evidence suggesting greater susceptibility to infections, and worse outcomes.

133 duces this susceptibility, and if changes in susceptibility to infection are accompanied by parallel

134 Systemic inflammation and susceptibility to infection are characteristic pathophys

135 and the compounds associated with increased susceptibility to infection are highlighted.

136 e that heterogeneous biting or heterogeneous susceptibility to infection are important and pervasive

137 Susceptibility to infection as well as response to vacci

138 BALB/c and A/J strains demonstrated greater susceptibility to infection, as evidenced by significant

139 years to study the role of host genetics in susceptibility to infection, as well as the community im

140 ect results in a less profound yet prominent susceptibility to infections, as well as multiorgan atop

141 pact and mechanism of benzodiazepine-induced susceptibility to infection at anxiolytic doses in mice.

142 exposure impairs host defense and increases susceptibility to infection because of compromised innat

143 ed how RRV VP4 protein governs cholangiocyte susceptibility to infection both in vitro and in vivo in

144 mune disorder that not only causes increased susceptibility to infection, but also to inflammatory co

145 ifferent host cells showed various levels of susceptibility to infection, but no differences in infec

146 Vitamin D level is linked to susceptibility to infections, but its relevance in candi

147 injury, and it completely protected against susceptibility to infection by a cytotoxic strain in a m

148 on intestinal epithelium and measured their susceptibility to infection by a DAF-binding CVB3 isolat

149 nes during ageing, as shown by the increased susceptibility to infection by both previously encounter

150 s, six related arithmetic parameters and the susceptibility to infection by Chrysomyxa rhododendri in

151 /-) mice with G-CSF reversed their increased susceptibility to infection by enhancing both circulatin

152 ater failed to gain weight, showed increased susceptibility to infection by fecal and commensal bacte

153 receptor 2 (TLR2) deficiency enhances murine susceptibility to infection by Francisella tularensis as

154 as administration of SECM to mice decreased susceptibility to infection by GAS.

155 es, when expressed in HepG2 cells, conferred susceptibility to infection by HCVpp and cell culture-gr

156 infection while MARCO(-/-) mice have reduced susceptibility to infection by herpes simplex virus type

157 emonstrate that ablation of AXL enhances the susceptibility to infection by influenza A virus and Wes

158 endocytic proteases can determine host cell susceptibility to infection by intracellular pathogens.

159 vivo, Myo1f-deficient mice showed increased susceptibility to infection by Listeria monocytogenes an

160 st mechanistic link between PS and increased susceptibility to infection by microbial pathogens.

161 ked N288D and K313I polymorphisms may affect susceptibility to infection by microorganisms.

162 nized mice, a mutation causing both profound susceptibility to infection by mouse cytomegalovirus and

163 ermine whether antibiotic exposure increases susceptibility to infection by opportunistic pathogens.

164 en linked to strain-dependent differences in susceptibility to infection by poxviruses.

165 terminant of species-specific differences in susceptibility to infection by retroviruses bearing part

166 of intestinal fucosylation led to increased susceptibility to infection by Salmonella typhimurium.

167 ride (PS), resulting in a markedly increased susceptibility to infection by Streptococcus pneumoniae.

168 oth from immunocompetent mice and determined susceptibility to infection by the 43816 strain and 4 ne

169 ) in Eif2ak4, encoding GCN2, which increased susceptibility to infection by the double-stranded DNA v

170 of transgenic plants also displayed enhanced susceptibility to infection by the fungal pathogen Botry

171 followed by lifelong homotypic immunity, but susceptibility to infection by the other three DENVs rem

172 e T helper (Th) type 2 cells correlates with susceptibility to infection by the protozoal parasite Le

173 receptor-type sialic acid on cells and their susceptibility to infection by the virus.

174 patterns and, therefore, may influence host susceptibility to infection by these viruses.

175 of different species and tissue origins for susceptibility to infection by three N-acetyl-neuraminic

176 increased the Spm level, leading to enhanced susceptibility to infection by V. dahliae, and the level

177 orld primate species were screened for their susceptibility to infection by vesicular stomatitis viru

178 and the impact of a genetic deletion on the susceptibility to infection can be accurately assessed b

179 n that leads to organ ischemia and increased susceptibility to infection caused by functional aspleni

180 wn as mannose-binding lectin) show increased susceptibility to infections caused by a wide range of p

181 Consistent with their lower susceptibility to infection, CD4(+) TCM cells of SIV-inf

182 ated with TB patient infectiousness, contact susceptibility to infection, contact risk of progression

183 SOCS proteins can define host susceptibility to infection, contribute to peripheral di

184 ities to be infected by MMTV and showed that susceptibility to infection correlated with the presence

185 In vivo susceptibility to infection cosegregated with the inheri

186 o important aspects of tuberculosis, such as susceptibility to infection, disease reactivation, morta

187 ower genetic diversity and subsequent higher susceptibility to infection, enabling microsporidia to i

188 reduced apoptosis, did not confer increased susceptibility to infection, even when the phagocytes we

189 Susceptibility to infection following sepsis has been at

190 in natural history, response to treatments, susceptibility to infections, genetic risk factors, and

191 Susceptibility to infections had been documented in 2/6

192 identification of host factors that control susceptibility to infection has been hampered by a lack

193 l transplantation (HCT) results in increased susceptibility to infection; however, transplantation of

194 ly important problems, such as chronic pain, susceptibility to infection, hypothermia, and some cance

195 ective was to determine if HS increases host susceptibility to infection, if IL-6 administration at r

196 nt of innate and adaptive immunity, relative susceptibilities to infections, immune tolerance, bioava

197 cute-on-chronic liver failure (ACLF) include susceptibility to infection, immuneparesis, and monocyte

198 udy the molecular pathophysiology leading to susceptibility to infection in 3 siblings with severe G6

199 ctive dose of Crry-Ig significantly enhanced susceptibility to infection in a mouse model of acute se

200 TLR2/9(-/-) mice displayed markedly enhanced susceptibility to infection in association with combined

201 ts identify previously unknown mechanisms of susceptibility to infection in asthma and suggest new ap

202 o identify chromosomal sites associated with susceptibility to infection in C3H/HeJ mice.

203 rylated form of SAMHD1 that corresponds with susceptibility to infection in cell culture.

204 tion but possibly also provide clues for the susceptibility to infection in different regions of the

205 innate immune system tolerance and increased susceptibility to infection in humans.

206 functional Th17 cells resulted in increased susceptibility to infection in immunized mice.

207 NE adducts in human muscle are indicative of susceptibility to infection in individuals with severely

208 part, a molecular explanation for increased susceptibility to infection in lung diseases associated

209 ation-associated chronic disease and greater susceptibility to infection in obese people represents a

210 e that regulate virulence in the pathogen or susceptibility to infection in the host.

211 Increased susceptibility to infection in the neonate is attributed

212 The mechanisms that underlie susceptibility to infection in these patients are unclea

213 Loss of IRF8 or IRF1 function causes severe susceptibility to infections in mice and in humans.

214 tion results in severe myeloid cytopenia and susceptibility to infections in the lag period before he

215 cells expressing CCR5 in the mucosa and the susceptibility to infection, in terms of both the viral

216 Ethanol is known to increase susceptibility to infections, in part, by suppressing ma

217 ns and has previously been implicated in the susceptibility to infections, including Rotavirus and No

218 This greater susceptibility to infection is associated with impaired

219 Systematic identification of genetic susceptibility to infection is being undertaken through

220 Host susceptibility to infection is controlled in large measu

221 However, CD71(+) cell-mediated susceptibility to infection is counterbalanced by CD71(+

222 Susceptibility to infection is determined by restricted

223 Dermatophytes initiate dermatophytosis, but susceptibility to infection is dictated by host genetic

224 Susceptibility to infection is in part genetically drive

225 tumorigenic signaling pathways and cellular susceptibility to infection is not well defined.

226 f polymorphisms in this gene family on human susceptibility to infection is poorly understood.

227 th intrarectal and intravaginal routes, (ii) susceptibility to infection is proportional to the numbe

228 ion equally and determining how individuals' susceptibility to infection is related to other componen

229 od cell function manifesting as an increased susceptibility to infection is well established.

230 ven the critical role of mucosal surfaces in susceptibility to infection, it is imperative that effec

231 ompatibility complex (MHC) haplotype affects susceptibility to infection, it remains unclear whether

232 epresent a human health concern due to their susceptibility to infection, large global population, an

233 Taken together, silica's ability to alter susceptibility to infection may be due to impaired infla

234 that factors--such as divergence in genetic susceptibility to infection--may influence infection in

235 Reduced CD4 cell susceptibility to infection, neutralizing antibody, sing

236 We recovered 18 mutants with increased susceptibility to infection, none of which were previous

237 system and may contribute to the increase in susceptibility to infections observed in smokers.

238 ges in vitro does not correlate with in vivo susceptibility to infection of Bacillus anthracis.

239 may be an important factor in the increased susceptibility to infections of patients with active sys

240 cies (PID) are characterized by an increased susceptibility to infections, often associated with aber

241 Greater susceptibility to infection on exposure in women is beli

242 -GvHD therapies that do not adversely affect susceptibility to infection or graft-vs.-tumor immunity

243 increased transmission (by either increasing susceptibility to infection or increasing infectiousness

244 beta(low) or TNFbeta(high) alleles predicted susceptibility to infection or rejection after renal tra

245 represent a mechanistic link to variation in susceptibility to infection or response to vaccination.

246 and inhibitory signals results in increased susceptibility to infection or the induction of autoimmu

247 munosuppression during active disease causes susceptibility to infections, possibly complicated by se

248 ions of reduced numbers of CD4+T cells, with susceptibility to infection potentially associated with

249 odeficiency, quite distinct from the limited susceptibilities to infection previously reported for he

250 Eczema and susceptibility to infections resolved in all 6 patients.

251 Here we discuss how differences in susceptibility to infection result not out of a state of

252 lity of serum immunoglobulins with increased susceptibility to infections, resulting in significant m

253 hildbearing age, with protection against and susceptibility to infection still poorly understood.

254 Age-dependent susceptibility to infection strongly influences epidemic

255 enge with L. monocytogenes also have reduced susceptibility to infection, suggesting that PPs are req

256 Newborns and infants present a higher susceptibility to infection than adults, a vulnerability

257 imited cell-type-related and virus-dependent susceptibility to infection; these limitations were over

258 ons suggest that TLR5392STOP increases human susceptibility to infection through an unusual dominant

259 of arginine depletion on T-cell function and susceptibility to infection was assessed through adoptiv

260 han in parental CHO cells, and the increased susceptibility to infection was blocked with anti-VLA-2

261 ritonitis, whereas the effect of CR2-Crry on susceptibility to infection was indistinguishable from t

262 This heightened susceptibility to infection was not secondary to a defec

263 Susceptibility to infection was partially restored if Ak

264 ression by macrophages and DCs vs T cells in susceptibility to infection was unclear.

265 The viral shedding and susceptibility to infection we observed in sparrows, cou

266 ifferentiate between effects on exposure vs. susceptibility to infection, we included multiple infect

267 y genetic mutations that might increase host susceptibility to infection, we performed exon sequencin

268 k between vitamin A deficiency and increased susceptibility to infections, we investigated the abilit

269 B cell(-/-) mice have enhanced susceptibility to infection when aerogenically challenge

270 as a controlling factor in the resistance or susceptibility to infection with a diverse range of intr

271 l quantitative trait loci (QTLs) influencing susceptibility to infection with Ascaris lumbricoides, t

272 iruses through reassortment because of their susceptibility to infection with both avian and human in

273 3-deficient mice also demonstrated increased susceptibility to infection with C. albicans, which is c

274 Susceptibility to infection with cell culture-adapted st

275 The ablation of DCs led to an enhanced susceptibility to infection with cell-free but not cell-

276 induced neural lineages to investigate their susceptibility to infection with HCMV strain Ad169.

277 e of biological factors such as an increased susceptibility to infection with HIV and sexually transm

278 Adult foreskin mucosa had greater susceptibility to infection with HIV(bal) than cervical

279 ther these variants are also responsible for susceptibility to infection with human T lymphotropic vi

280 nditioning of AECII is a determinant of host susceptibility to infection with IAV.

281 )) mice demonstrated comparable increases in susceptibility to infection with K. pneumoniae or E. col

282 ogenes, STK-deficient mice exhibit increased susceptibility to infection with Listeria.

283 human histo-blood group antigens (HBGAs) and susceptibility to infection with Norwalk virus (GI.1 nor

284 riod during which a host experiences a lower susceptibility to infection with other influenza viruses

285 eterm birth, low birth weight, and increased susceptibility to infection with other pathogenic sexual

286 ction is critical in determining the initial susceptibility to infection with P. carinii.

287 and that miR-126-deficient mice had greater susceptibility to infection with pseudotyped HIV.

288 Asthma is often associated with increased susceptibility to infection with rhinoviruses and with c

289 nts the results of the first genome scan for susceptibility to infection with roundworm (Ascaris lumb

290 immune deficiency characterized by increased susceptibility to infection with Staphylococcus, certain

291 y, NFAT1(-/-)x IL-4(-/-) mice show increased susceptibility to infection with the intracellular paras

292 A (IL-17A) production in the lungs increased susceptibility to infection with the invasive fungal pat

293 aptive immune responses that might influence susceptibility to infection with Vibrio cholerae, we pro

294 specifically in CD8+ T cells showed enhanced susceptibility to infection with West Nile virus.

295 is case study aimed to evaluate the familial susceptibility to infection with Wuchereria bancrofti an

296 Enhanced susceptibility to infection with X4 virus occurred durin

297 the identifiable subsets of RDC differed in susceptibility to infection, with CD11c(+) CD103(+) DC e

298 in a murine model, we demonstrated increased susceptibility to infection within 24 h.

299 e presence of asthma can influence patients' susceptibility to infections, yet research in this aspec

300 n to impaired vaccine efficacy and increased susceptibility to infections; yet, the role of dietary p