ライフサイエンスコーパス: house dust mite

1 at the baseline and after sensitization with house dust mite.

2 asthma via regulation of immune response to house dust mite.

3 t of a commonly studied airway allergen, the house dust mite.

4 ivate GPCRs such as Alternaria alternata and house dust mite.

5 and respiratory challenge with an extract of house dust mite.

6 zation with two different allergens, OVA and house dust mite.

7 hallenge relative to the common aeroallergen house dust mite.

8 and asymptomatic sensitization to pollen and house dust mite.

9 eatment for local allergic rhinitis (LAR) to house dust mites.

10 with allergic rhinitis and sensitization to house dust mites.

11 otective high dose of LPS before exposure to house dust mites.

12 allergic airway inflammation in response to house dust mites.

13 irected against staple food antigens but not house dust mites.

14 tradermal SIT in children/adults allergic to house dust mite (10 trials), grass pollen or other inhal

15 The prevalence of sensitization to house dust mite (-4.3%; 95% CI, -6.0% to -2.6%) and cat

16 rse, (2) timothy grass/birch, (3) molds, (4) house dust mites, (5) peanut/wheat flour/mugwort, (6) pe

17 firmed in a chronic model of asthma by using house dust mite, a human allergen.

18 -specific B-cell responses during 2 years of house dust mite AIT were compared between responder and

19 Skin prick test (SPT) sensitivity to house dust mite allergen (HDM) and current wheeze were a

20 ild-type mice with Aspergillus fumigatus and house dust mite allergen and compared the effects on air

21 NC/Nga mice were sensitized with house dust mite allergen and treated topically with HOCl

22 The major house dust mite allergen Der p 2 is a structural and fun

23 otects against epicutaneous sensitization to house dust mite allergen Der p 2.

24 In addition, we discuss of house dust mite allergen extracts as a prototypical comp

25 ing repeated exposures of 3 hours per day to house dust mite allergen in an allergen challenge chambe

26 lized a mechanistic IL-13-driven model and a house dust mite allergen mucosal sensitization model of

27 Diverse factors contribute to house dust mite allergenicity through the activation of

28 d late airway responses after challenge with house dust mite allergens in 15 patients with mild aller

29 levels of IgE specific for staple foods and house dust mite allergens in DOCK8-deficient patients an

30 junction downregulation in a mouse model of house dust mite allergic airway inflammation.

31 NA networks operate to regulate Th2 cells in house dust mite-allergic or helminth-infected animals an

32 ybridoma technology using human B cells from house dust mite-allergic patients was used to identify f

33 ll tolerated and reduces the CPT reaction in house dust mite-allergic patients.

34 nd IgA2 contribute to the clinical status of house dust mite-allergic patients.

35 ing and IL-3-secreting Th cells were high in house dust mite-allergic patients.

36 House dust mite allergics showed IgE reactivity only to

37 Since 2015, for patients with house dust mite allergies, we used a standardized house

38 Specifically, for patients with house dust mite allergies, which are often underestimate

39 th tablets containing carbamylated monomeric house dust mite allergoids was to determine the most eff

40 (TSSs) were recorded by 21 participants with house dust mite allergy (M+) in the natural setting and

41 of common airborne allergens, including the house dust mite, Alternaria, and Aspergillus, for up to

42 Chronic exposure to house dust mite and A alternata were compared in a neona

43 Age-specific prevalence of sensitization to house dust mite and cat did not differ between year-of-b

44 lower levels of sensitization, especially to house dust mite and cat, after the age of 20 years.

45 of ImmunoCAP-identified IgE directed against house dust mite and cockroach, but not against timothy g

46 ta allergen, Aspergillus fumigatus antigens, house dust mite and endotoxin antigens increase the risk

47 sthma and rhinitis, focusing on responses to house dust mite and grass.

48 ysteine protease and major allergen from the house dust mite and is associated with allergic rhinitis

49 xt of acute allergic lung inflammation using house dust mite and OVA murine models.

50 al allergens including insect allergens from house dust mites and cockroaches contribute to allergic

51 and fruits, certain inhalant allergens from house dust mites and cockroaches, and lipocalins.

52 We assess whether exposure to fungi, house dust mites and endotoxin increases the risk of ecz

53 nalyses for a reduction in SPT reactivity to house dust mites and perennial allergens.

54 d with lower odds of sensitization to grass, house dust mite, and cat allergens, but rodent ownership

55 y to the age of 7 with asthma, atopy (grass, house dust mite, and cat skin prick test) and atopic vs.

56 Alternaria alternata, Aspergillus fumigatus, house dust mite, and ovalbumin) for 4 wk.

57 acute challenge with Alternaria alternata or house dust mite, and secretion of IL-33 and activation o

58 otein D (rfhSP-D) has been shown to suppress house dust mite- and Aspergillus fumigatus-induced aller

59 enuated allergic airway responses to fungi-, house dust mite-, and cockroach-associated allergens in

60 After exposure to house dust mite antigen, Zbtb46-negative CD64(+) inflamm

61 oup of mice was also intranasally exposed to house dust mite antigen.

62 ecent publications were identified by using "house dust mite" as a key search term to evaluate the cu

63 Cell culture and ovalbumin (OVA)- or house dust mite-based murine asthma models were used in

64 xtracellular traps potentiated the uptake of house dust mites by CD11b(+)Ly-6C(+) dendritic cells and

65 that lacked the IL-33 receptor given inhaled house dust mite, cat dander, or Alternaria, and the effe

66 serum specific IgE to common aeroallergens (house dust mite, cat, and grass) and total IgE levels we

67 articipants underwent skin prick testing for house dust mite, cat, grasses and moulds.

68 eriostin were also decreased in the lungs of house dust mite-challenged ERp57-deleted mice.

69 hyperreactivity and mucus hypersecretion in house dust mite-challenged mice.

70 duced by 6.2-fold in pulmonary epithelium of house dust mite-challenged mice.

71 House dust mite concentrations varied across cohorts.

72 he airways upon intranasal immunization with house dust mite, confirming the ability of IL-9-producin

73 House dust mite-derived proteases contribute to allergic

74 zing intranasal doses of an extract from the house dust mite Dermatophagoides farinae (Df) sharply in

75 tion of Th2 and Th17 immune responses to the house dust mite Dermatophagoides farinae through the gen

76 one of the most important allergens from the house dust mite Dermatophagoides pteronyssinus Identific

77 Der p 1 is a major allergen from the house dust mite, Dermatophagoides pteronyssinus, that be

78 fungal driven and proinflammatory, the other house dust mite driven and chemokine dominant, with the

79 Likewise, in house dust mite-driven asthma, CD2-Gata3 Tg mice were si

80 -specific Notch deficiency in mice prevented house dust mite-driven eosinophilic airway inflammation

81 velopment and TH2 polarization, as seen in a house dust mite exposure model.

82 In the tropics, house dust mite exposure, a known risk factor for asthma

83 sponsiveness (AHR) compared with those after house dust mite exposure.

84 roup, dust samples were collected to measure house dust mite exposure.

85 hyperoxia promoted allergic TH responses to house dust mite exposure.

86 This study hypothesizes that standardized house dust mite extract (HDM group) was superior to non-

87 ukin 13 (IL-13) when stimulated by papain or house dust mite extract (HDM) and induce eosinophilic in

88 ing dimaprit in both the ovalbumin (OVA) and house dust mite extract (HDM) murine models of respirato

89 s over 3-weeks to either saline, DEP, and/or house dust mite extract (HDM).

90 lveolar lavage fluid of mice challenged with house dust mite extract after oral administration (50 mg

91 Mice were chronically exposed to house dust mite extract and then infected with influenza

92 dust mite allergies, we used a standardized house dust mite extract for subcutaneous immunotherapy,

93 patients), the initial dose of standardized house dust mite extract was 1 JAU or less.

94 Standardized house dust mite extract was more effective than non-stan

95 model was exposed to allergens (ovalbumin or house dust mite extract) to decipher in vivo the implica

96 House dust mite extract, Alternaria alternata extract, o

97 In rSCIT using standardized house dust mite extract, lowering the target dose at the

98 -type and RAGE knockout mice by using IL-33, house dust mite extract, or Alternaria alternata extract

99 ation in mice following acute challenge with house dust mite extract.

100 a decrease in skin prick test reactivity to house dust mite from 7.0 +/- 1.3 to 2.7 +/- 0.5 mm (P =

101 ere sensitized and challenged with high-dose house dust mite (>10 mug) or with low-dose house dust mi

102 House dust mites have been implicated in the etiology an

103 Some allergens such as derived from house dust mites have proteolytic activity which can ind

104 Balb/c mice were challenged with PBS or house dust mite (HDM) (Days 0, 7, 14-18) and exposed to

105 House dust mite (HDM) acts on the airway epithelium to i

106 The house dust mite (HDM) allergen Der p 13 could be a lipid

107 in crystallographic studies suggest that the house dust mite (HDM) allergen Der p 5 potentially inter

108 a natural field study, sublingual tablets of house dust mite (HDM) allergen extracts (STG320) were ef

109 how endogenous CD4(+) T cells specific for a house dust mite (HDM) allergen form and function.

110 concept for oral immunotherapy to high-dose house dust mite (HDM) allergen in infancy in the prevent

111 determined early immunological responses to house dust mite (HDM) allergen in offspring challenged f

112 t the safety and efficacy of challenges with house dust mite (HDM) allergen in the Fraunhofer allerge

113 events preceding sensitization to the common house dust mite (HDM) allergen remains to be elucidated.

114 In the present study, the task force for house dust mite (HDM) allergen standardization of the Co

115 Der p 23, a new, major house dust mite (HDM) allergen that is recognized by >70

116 House dust mite (HDM) allergens are a common cause of al

117 Upon inhalation, house dust mite (HDM) allergens are deposited at the nas

118 House dust mite (HDM) allergens are responsible for the

119 Mice were sensitized with house dust mite (HDM) allergens from days 3, 15, or 60 a

120 tion was almost exclusively directed against house dust mite (HDM) allergens.

121 alyses revealed that IgE from crustaceans or House dust mite (HDM) allergic patients showed cross-rea

122 rly controlled atopic asthma associated with house dust mite (HDM) allergy, relative to non-asthmatic

123 immunotherapy (AIT) lack recommendations for house dust mite (HDM) allergy.

124 kout and wild-type mice were challenged with house dust mite (HDM) and infected with RV1B to determin

125 -mediated allergic CRS mouse model, based on house dust mite (HDM) and Staphylococcus aureus enteroto

126 or WT mice were challenged over 3 weeks with house dust mite (HDM) antigen.

127 emonstrate that Streptococcus pneumoniae and house dust mite (HDM) bear similar phosphorylcholine (PC

128 mice alleviates airway remodeling following house dust mite (HDM) challenge with decreases in mucus

129 istosoma egg antigen (SEA) immunization, and house dust mite (HDM) challenge without affecting cytoto

130 S. mansoni IgG antibodies in extracts of the house dust mite (HDM) Dermatophagoides farinae, the Aust

131 In the house dust mite (HDM) Dermatophagoides pteronyssinus, De

132 inhalation of airborne allergens such as the house dust mite (HDM) effectively activates both innate

133 protective effects of gamma-tocotrienol in a house dust mite (HDM) experimental asthma model.

134 immunized through the intranasal route with house dust mite (HDM) extract derived from Dermatophagoi

135 House dust mite (HDM) extract is a common trigger of ast

136 We used alphaT-catenin knockout mice and a house dust mite (HDM) extract model of atopic asthma, wi

137 examined constitutive and TNFalpha/IL-1beta, house dust mite (HDM) extract or lipopolysaccharide (LPS

138 ntrol mice were intranasally challenged with house dust mite (HDM) extract or PBS five days per week

139 House dust mite (HDM) extract was used to induce allergi

140 nd pulmonary Th2 inflammation in response to house dust mite (HDM) extract, as both were decreased in

141 in mice with prolonged i.n exposure to crude house dust mite (HDM) extract.

142 ced by means of intranasal administration of house dust mite (HDM) extract.

143 ession in ECs challenged with IL-4/IL-13 and house dust mite (HDM) extract.

144 gested the efficacy of sublingual tablets of house dust mite (HDM) extracts in adults with allergic r

145 16HBE cells were stimulated with house dust mite (HDM) extracts.

146 (EPIT) on further sensitization to peanut or house dust mite (HDM) in a murine model of sensitization

147 on induced by ovalbumin (OVA) in mice and by house dust mite (HDM) in guinea pigs, as well as investi

148 (ECP)] induced by bronchial instillation of house dust mite (HDM) in patients with asthma on mainten

149 A damage and DNA damage responses induced by house dust mite (HDM) in vivo and in vitro.

150 The house dust mite (HDM) is a major perennial allergen sour

151 Sensitization to house dust mite (HDM) is a risk factor for the developme

152 The initial immune response to house dust mite (HDM) is orchestrated by an interplay be

153 Using a house dust mite (HDM) model of allergic asthma and parab

154 -/-) ) mice were used in ovalbumin (OVA) and house dust mite (HDM) models of AAI.

155 ole of Sema3E in airway angiogenesis using a house dust mite (HDM) murine model of allergic asthma.

156 ty were evaluated in the ovalbumin (OVA) and house dust mite (HDM) murine models.

157 siologically relevant aeroallergens, such as house dust mite (HDM) or Alternaria alternata, to induce

158 Mice were sensitized to house dust mite (HDM) or cockroach at day 0, treated wit

159 ) mice were challenged with saline, DEPs, or house dust mite (HDM) or DEP+HDM.

160 d profiles during type 2 immune responses to house dust mite (HDM) or helminth infection and to ident

161 cells (PBECs) in response to RSV, poly(I:C), house dust mite (HDM) or IL-33 using RT-qPCR, Luminex an

162 n D-replete diet, and exposure to intranasal house dust mite (HDM) or saline was commenced from day 3

163 Atopic status remained stable; however, house dust mite (HDM) sensitisation decreased by 5.6% (1

164 We employed acute ovalbumin (OVA) and house dust mite (HDM) sensitization and challenge models

165 As house dust mite (HDM) sensitization is dependent on TLR4

166 airway inflammation was induced following a house dust mite (HDM) sensitization protocol.

167 acy, safety and immunological response of SQ house dust mite (HDM) SLIT-tablet treatment in relation

168 nd during the last 8 weeks of treatment in 2 house dust mite (HDM) SLIT-tablet trials (n = 1768).

169 acebo-controlled, randomized clinical trial, house dust mite (HDM) sublingual AIT was found to be eff

170 The house dust mite (HDM) sublingual allergen immunotherapy

171 The house dust mite (HDM) sublingual immunotherapy (SLIT) ta

172 Mice were exposed to house dust mite (HDM) to provoke Th2-mediated immune res

173 ent mice, challenged with ovalbumin (OVA) or house dust mite (HDM), and accessed for TH2 inflammation

174 l exposure to common human allergens such as house dust mite (HDM), in the absence of additional adju

175 Exposure to environmental antigens, such as house dust mite (HDM), often leads to T helper 2 (Th2) c

176 Exposure to allergens, such as house dust mite (HDM), through the skin often precedes a

177 ng 24 (Trim24) was predicted to be active in house dust mite (HDM)- and helminth-elicited Il4(gfp+)al

178 r D. farinae were assessed in sera from 1302 house dust mite (HDM)-allergic patients living in variou

179 aim was to analyze the role of B cells in a house dust mite (HDM)-based murine asthma model.

180 House dust mite (HDM)-challenged Apoe(-/-) mice display

181 tch signaling induced by DCs is critical for house dust mite (HDM)-driven allergic airway inflammatio

182 igate the therapeutic efficacy of SAHM1 in a house dust mite (HDM)-driven asthma model.

183 ing the Cd11c promotor) to acute and chronic house dust mite (HDM)-driven asthma models.

184 e sought to address the role of B cells in a house dust mite (HDM)-driven TH2-high asthma mouse model

185 e) control mice were evaluated in a model of house dust mite (HDM)-induced AAI.

186 expansion and cytokine production to prevent house dust mite (HDM)-induced airway inflammation and re

187 important role for the VLDLR in attenuating house dust mite (HDM)-induced airway inflammation in exp

188 s adaptive immune responses in patients with house dust mite (HDM)-induced airways disease.

189 sure to DEPs and in response to DEP-enhanced house dust mite (HDM)-induced allergic airway inflammati

190 in patients with AR and in a mouse model of house dust mite (HDM)-induced allergic asthma and whethe

191 de of effect of sublingual immunotherapy for house dust mite (HDM)-induced allergic rhinitis with or

192 evaluating several dosages in patients with house dust mite (HDM)-induced allergic rhinoconjunctivit

193 role of PAG1 in a preclinical mouse model of house dust mite (HDM)-induced allergic sensitization and

194 TJs in the nasal epithelium of patients with house dust mite (HDM)-induced AR and in an HDM-induced m

195 leukocyte infiltration, protecting mice from house dust mite (HDM)-induced asthma or Leishmania major

196 s, an induced psoriasis-like inflammation, a house dust mite (HDM)-induced asthma-like allergic lung

197 ptotic cells by lung phagocytes might dampen house dust mite (HDM)-induced lung inflammation has not

198 current study, we employed a mouse model of house dust mite (HDM)-induced lung inflammation to explo

199 OVA- and house dust mite (HDM)-induced murine asthma models were

200 s and the stimulatory effects of IL-1beta on house dust mite (HDM)-induced release of thymic stromal

201 et (ALK) has been developed for treatment of house dust mite (HDM)-induced respiratory allergic disea

202 e sought to investigate the role of TPL-2 in house dust mite (HDM)-mediated allergic airway inflammat

203 pulmonary allergy by adoptively transferring house dust mite (HDM)-pulsed bone marrow-derived DCs (BM

204 The effect of DEPs on house dust mite (HDM)-specific memory responses was dete

205 e investigated the importance of NK cells in house dust mite (HDM)-triggered allergic pulmonary infla

206 ans of repeated intranasal administration of house dust mite (HDM).

207 exoskeleton of many organisms including the house dust mite (HDM).

208 mice exposed to local airway challenge with house dust mite (HDM).

209 helminth Schistosoma mansoni or the allergen house dust mite (HDM).

210 Allergens from house dust mites (HDM) are a common cause of asthma.

211 Group 1 allergens of house dust mites (HDM) are meaningful targets in this qu

212 the genome, transcriptome and microbiome of house dust mites (HDM) has shown that Staphylococcus aur

213 House dust mites (HDM) may serve as carriers of bacteria

214 ithelial cells, BEAS-2B, directly exposed to house dust mites (HDM) resulted in enhanced DNA damage,

215 nd compare the allergen content of different house dust mites (HDM)' sublingual treatments and to rev

216 The most frequent allergens are house dust mites (HDM), which act in vivo on the bronchi

217 (AIT) with an allergoid in the treatment of house dust mites (HDM)-induced allergic rhinitis and/or

218 irome in medically important mites including house dust mites (HDM).

219 nes were confirmed in reporter assays and in house-dust-mite (HDM) induced AAI and primary human bron

220 House dust mite/HDM atopy patch test/APT elicits positiv

221 response is dominated by a single allergen (house dust mite; HDM).

222 Twenty-three adults allergic to house dust mites (HDMs) (M+) and 15 nonsensitive, nonall

223 House dust mites (HDMs) are among the most important all

224 House dust mites (HDMs) are sources of an extensive repe

225 Allergic rhinitis induced by house dust mites (HDMs) is a highly prevalent but often

226 House dust mites (HDMs) represent one of the most import

227 2 responses triggered by allergens, such as house dust mites (HDMs).

228 uted allergens, including those derived from house dust mites (HDMs).

229 veloped countries demonstrate sensitivity to house dust mites (HDMs).

230 We show here that sensitization of mice with house-dust mites (HDMs) in the presence of low-dose lipo

231 To evaluate the use of house dust mite-impermeable bedding and its impact on se

232 to any allergen was present in 17.2% and to house dust mite in 8.7%.

233 life and as allergen levels of dog, cat, and house dust mite in bed dust samples at 1 year.

234 Using prolonged exposure to house dust mite in mice, we developed a mouse model of p

235 When challenged with house dust mite in vivo, Gimap5-deficient mice displayed

236 ical features of allergic asthma provoked by house dust mite in vivo.

237 Here we used a murine model of house dust mite-induced (HDM-induced) allergic inflammat

238 Experimental acute canine house dust mite-induced AD lesions exhibit an activation

239 During house dust mite-induced airway allergy, rEos features re

240 House dust mite-induced airway inflammation was assessed

241 TRPC1 intensifies house dust mite-induced airway remodeling by facilitatin

242 hat both DNA-HSP65 and CpG/CFP downregulated house dust mite-induced allergic airway inflammation via

243 contrast, in Th2-polarized settings such as house dust mite-induced allergic airway inflammation, th

244 ted the role of hBD2 in a steroid-sensitive, house dust mite-induced allergic airways disease (AAD) m

245 ed the impact of PKM2 on the pathogenesis of house dust mite-induced allergic airways disease in C57B

246 rresponsiveness, and mucus production during house dust mite-induced allergic asthma.

247 The house dust mite-induced allergic inflammation model was

248 ltration into the airways of mice undergoing house dust mite-induced allergic response.

249 rolled dose-finding study, 131 patients with house dust mite-induced allergic rhinoconjunctivitis wer

250 y delivery of NP-CpG could prevent and treat house dust mite-induced allergy by modulating immunity d

251 ing primary cell assays and a mouse model of house dust mite-induced asthma, we compared IL-4 vs IL-1

252 ation was assessed in a mouse model of acute house dust mite-induced asthma.

253 aptive immune responses were dispensable for house dust mite-induced endoplasmic reticulum stress and

254 nce recovered, subjected to an ovalbumin- or house dust mite-induced experimental asthma protocol.

255 Blockade of Runx2 inhibited the house dust mite-induced goblet cell differentiation with

256 and MCTR3 inhibited lung eosinophilia after house dust mite-induced inflammation.

257 determined in the setting of ovalbumin- and house dust mite-induced lung inflammation.

258 ema3e(-/-) mice into WT recipients increases house dust mite-induced Th2/Th17 inflammation in the air

259 ceptors, substantially reduced ovalbumin- or house-dust-mite-induced airway inflammation and bronchia

260 Here we show that house dust mite induces DNA-PK phosphorylation, which is

261 Controls were house dust mite-instilled animals receiving intravenous

262 e house dust mite (>10 mug) or with low-dose house dust mite (<3 mug).

263 Our data indicate that exposure to house dust mite markedly reduces Sema3E expression in mo

264 House dust) mite markedly increased CCL20 levels in both

265 models of experimental asthma (ovalbumin and house dust mite); miRNAs deregulated in both models were

266 he spatiotemporal dynamics of Tr1 cells in a house dust mite model of allergic airway inflammation.

267 In the house dust mite model, Tfr cells repress the production

268 es to allergic airway disease using a murine house dust mite model.

269 We used ovalbumin and house dust mite models of asthma.

270 us to interrogate the role of T(FR) cells in house dust mite models.

271 Asthma was induced in mice using intranasal house dust mite or aerosol ova-albumin challenge, and ch

272 emale BALB/c mice were repeatedly exposed to house dust mite or Alternaria alternata three times a we

273 increased after treatment with the allergen house dust mite or the bacteria Escherichia coli and bac

274 ice by repeated intranasal administration of house dust mite or the fungal allergen Alternaria altern

275 at least one of the allergens: birch, grass, house dust mite, or cat.

276 We use experimental models of house dust mite- or ovalbumin-induced airway inflammatio

277 plicate a high exposure to indoor allergens (house dust mites, pets, molds, etc), tobacco smoke, and

278 volved include seasonal or perennial such as house dusts mites, pollens, animal epithelia, moulds (al

279 Group 21 and 5 allergens are homologous house dust mite proteins known as mid-tier allergens.

280 and allergic airway inflammation induced by house dust mites, pulmonary function and cytokine profil

281 h optimal doses of grass, birch, recombinant house dust mite (rDer p2) allergen or anti-IgE (n = 10).

282 allergens from Aspergillus fumigatus and the house dust mite, resulting in an asthma-like pathology c

283 A and EAACI Asthma Guidelines (separated for house dust mite SCIT, SLIT tablets and SLIT drops; patie

284 neutrophilic asthma via different methods of house dust mite sensitization and challenge.

285 ly, depletion of alveolar macrophages during house dust mite sensitization or established disease res

286 We used a model of house dust mite sensitization to challenge wild-type, Bc

287 man atopic dermatitis skin lesions with high house dust mite sensitization.

288 l and maternal history of atopy, eczema, and house dust mite sensitization.

289 Ara h 2, tree nut, and house dust mite sensitization; coexisting food allergies

290 ting epithelial cells and dendritic cells of house dust mite-sensitized mice to dampen IFN-beta expre

291 tory allergens (ie, grass, olive/ash pollen, house dust mites), specific IgE did not show marked diff

292 cross all populations and at different ages, house dust mite-specific IgG/IgE ratios (but not IgG4/Ig

293 In vivo, loss of T(FR) cells increased house-dust-mite-specific IgE and lung inflammation.

294 nd difficult to diagnose, the efficacy of SQ house dust mite sublingual immunotherapy tablets has bee

295 Treatment with SQ (standardised quality) house dust mite sublingual tablet for 1 year resulted in

296 acerbation day (from 11% [placebo] to 5% [SQ house dust mite sublingual tablet]) and an increased pro

297 a mild AR day (from 16% [placebo] to 34% [SQ house dust mite sublingual tablet]).

298 eous application of Dermatophagoides farinae house dust mites to sensitized atopic dogs.

299 Allergic sensitization to cat, dog, and house dust mites was diagnosed longitudinally using skin

300 redominately caused by sensitization against house dust mites with a nearly complete penetrance of th