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1 re positive (allergic) and 29 were negative (nonallergic).
2 less frequently non-IgE-mediated allergy or nonallergic.
3 d hay fever, suggesting that pathways may be nonallergic.
4 se label of drug allergic and false label of nonallergic.
5 sponses at 24 h were similar in both groups (nonallergic, 110 +/- 24 eosinophils/mm2; allergic, 113 +
6 for asthma among adolescents, especially for nonallergic adolescents and those exposed to maternal sm
7 d IL-4 synthesis both in T cells from normal nonallergic adult subjects as well as in naive T cells f
8 f this resistance is preserved in nonatopic, nonallergic adults and is unmasked during exposure to an
9 of resistance to HDM challenge in nonatopic, nonallergic adults was muted T-cell activation in the pe
12 eq) of the nasal epithelium was performed on nonallergic and house dust mite-allergic AR patients to
14 sophagitis, with a more pronounced effect in nonallergic and younger individuals, especially in the p
15 in RV strain 1B-infected naive BALB/c mice (nonallergic) and identified CCL7 and IFN regulatory fact
16 is classified into allergic asthma (AA) and nonallergic asthma (NA), yet both are treated identicall
18 : eosinophilic allergic asthma, eosinophilic nonallergic asthma and noneosinophilic nonallergic asthm
22 Our goal was to understand the mechanism of nonallergic asthma that leads to airway hyperreactivity
23 er, the association of maternal obesity with nonallergic asthma was observed in boys (2.39, 1.40-4.09
34 e major bee venom allergen PLA isolated from nonallergic beekeepers show increased expression of IL-1
35 0.1 kUa/L discriminated between allergic and nonallergic best (AUC, 0.96; sensitivity, 94%; specifici
36 No eosinophil infiltrate was observed in nonallergic biopsies at 30 min and 6 h, whereas signific
37 py, as well as their increased expression in nonallergic but high-dose allergen-exposed beekeepers.
39 et al. establish a clear association between nonallergic childhood asthma, lower whole-blood sphingol
40 8) from 52 highly characterized allergic and nonallergic children (0.5-17 years) with severe treatmen
41 ase had more epilepsy in their lifetime than nonallergic children (logistic regression, adjusted odds
44 he effect of being overweight was greater in nonallergic children (RR = 1.77, 95% CI: 1.26, 2.49) tha
46 children with atopic dermatitis and healthy nonallergic children in rural and urban settings from th
53 n to compare demographics and seasonality of nonallergic conjunctivitis with allergic conjunctivitis.
54 Weekly total clinical diagnoses at UCSF of nonallergic conjunctivitis, allergic conjunctivitis, gla
55 different in allergic subjects from that in nonallergic control subjects (deltaPD20 = -0.40 versus -
58 tal IgE, 133-4692 IU/mL; n = 28) and healthy nonallergic controls (n = 12) using peptide/MHCII tetram
60 ically reactive) to milk, egg, or peanut and nonallergic controls for stimulation with endotoxin and
62 ith immediate allergic reactions compared to nonallergic controls, allergic patients produced functio
63 moderate, persistent asthma and 10 matched, nonallergic controls, and then incubated with concentrat
64 in serum were similar to levels measured in nonallergic controls, but HDM-specific levels of IgA2 in
65 cells from nickel-allergic patients, but not nonallergic controls, show significant IL-9 production i
69 er psychosocial outcomes compared with their nonallergic counterparts; however, few studies have pros
72 an important cytokine in the pathogenesis of nonallergic diseases, especially in diseases that includ
74 ed higher proliferation to grass pollen than nonallergic donors (P = 0.002, and 0.010, respectively),
76 OD1-primed dendritic cells from allergic and nonallergic donors were characterized in vitro on their
81 been limited by a poor understanding of how nonallergic environmental exposures, such as air polluti
82 e-to-severe remodeled asthma, (3) late-onset nonallergic eosinophilic asthma, and (4) late-onset nona
83 nflammation in response to both allergic and nonallergic exposures and suggest that airway inflammato
84 s might regulate asthma, particularly in its nonallergic forms, such as asthma associated with air po
85 nary stent implantation were compared with a nonallergic group (n=250) matched for demographics and a
87 pheral blood and nasal biopsy specimens from nonallergic healthy control subjects (n = 3) and patient
88 ute anaphylaxis with several control groups (nonallergic, history of allergen-triggered anaphylaxis,
89 d, including those that rely on allergic and nonallergic humoral and antibody-dependent cellular resp
90 mmatory conditions, such as the psoriasis, a nonallergic hyperproliferative skin inflammatory disorde
94 hil levels, with a more pronounced effect in nonallergic individuals (65.9 +/- 25.3 vs 1.4 +/- 1.1 eo
95 cates that allergen-specific CD4+ T cells in nonallergic individuals are distinct from those in aller
97 e addition of alpha-gal-specific IgG Ab from nonallergic individuals changed the IgE recognition of B
100 cytokine pattern to allergic donors, whereas nonallergic individuals were essentially nonreactive.
101 -positive cells in cultures from HLA-DR*0401 nonallergic individuals, even after expansion with IL-2.
102 her alpha-gal-specific IgG1 and IgG3 Ab than nonallergic individuals, whereas the latter showed signi
108 ly higher frequency in allergic infants than nonallergic infants (P < .004); the high fecal count of
109 Levels of human lipocalins are elevated in nonallergic inflammation and cancer, associated with inn
110 rtantly, the repeated cycles of allergic and nonallergic inflammation that comprise chronic human air
112 The (patho)physiological role of IgE in nonallergic inflammatory diseases is not well understood
113 mplicated as a mediator in both allergic and nonallergic inflammatory diseases, including allergic rh
114 tentially contributes to the pathogenesis of nonallergic (intrinsic) asthma and, accordingly, may und
115 dust mites (HDMs) (M+) and 15 nonsensitive, nonallergic (M-) participants completed 3-hour exposures
116 re associated with allergen-specific IgE and nonallergic mechanisms that may coexist in the same pati
117 y epithelium and smooth muscle compared with nonallergic mice, a finding which is replicated in sever
118 influx when infected with RSV compared with nonallergic mice, whereas viral clearance was comparable
119 es thus evokes an allergic state in normally nonallergic mice, which suggests the possibility of neur
124 nd n-6 PUFAs in breast milk of allergic- and nonallergic mothers and asthma, eczema and sensitization
125 .31-0.79), and more prevalent in children of nonallergic mothers receiving breast milk with higher le
126 gnificantly lower among children of the 8059 nonallergic mothers who consumed more P/TN in their peri
129 tolerant (n = 36) and non-peanut-sensitized nonallergic (n = 25) children underwent skin prick test
132 investigation of immune cell responses from nonallergic (NA) and peanut allergic (PA) participants c
134 ilic allergic; NEA and eight noneosinophilic nonallergic; NN) and nine healthy controls in high altit
135 IFN-alpha, P= .004; IFN-lambda1, P= .02) and nonallergic nonasthmatic children (IFN-alpha, P= .002; I
138 teen allergic asthmatic (AA) patients and 18 nonallergic nonasthmatic subjects (healthy volunteers [H
141 SPINK5, and TSLP in asthmatic, allergic, and nonallergic nonasthmatic white and black children partic
144 frequent, but the effect of PPD exposure in nonallergic occupationally exposed subjects is unknown.
146 tantial subgroup of asthmatic patients have "nonallergic" or idiopathic asthma, which often takes a s
150 13 and IL-1B genes was found in allergic and nonallergic participants, suggesting that in vivo, epige
151 re measured in tonsil tissue of allergic and nonallergic patients and in peripheral blood of allergic
152 oducibly distinguish cefazolin-allergic from nonallergic patients using finely tuned cefazolin-hapten
156 y impulse oscillometry in female late-onset, nonallergic patients with asthma and control subjects be
157 nd, placebo-controlled study of allergic and nonallergic patients with nasal polyps and comorbid asth
158 pitope is prevalent among diverse cohorts of nonallergic peanut-consuming infants and peanut-allergic
159 st risk of asthma diagnosis, the more common nonallergic phenotypes (in 88.3% of participants) contri
161 symptoms were more frequently observed among nonallergic phenotypes as compared with allergic phenoty
163 hypersensitivity includes allergic (AR) and nonallergic reactions (NARs) influenced by genetic predi
164 ntial to differentiate proven allergies from nonallergic reactions, ensure effective treatment, and a
165 unization of mice with PM induces a shift to nonallergic responses and increases the frequency of spl
166 besity was associated with increased odds of nonallergic rhinitis (adjusted odds ratio, 1.43; 95% CI,
167 cts with chronic fatigue syndrome (CFS) with nonallergic rhinitis (n = 14), subjects with active alle
169 nd development of allergic rhinitis (AR) and nonallergic rhinitis (NAR) between the ages of 8 and 16
170 , the differential diagnosis between LAR and nonallergic rhinitis (NAR) has become a challenge for th
173 ice parameter for allergic rhinitis (AR) and nonallergic rhinitis (NAR) provides updated guidance on
174 tis (AR), the degree of impairment in QoL in nonallergic rhinitis (NAR) remained unknown for a long t
177 perennial local allergic rhinitis (LAR), six nonallergic rhinitis (NAR), and six healthy control (HC)
179 (rhinitis with sensitization to allergens), nonallergic rhinitis (rhinitis without sensitization), a
181 ntrast, first-line therapy for patients with nonallergic rhinitis consists of an intranasal antihista
182 ars, whereas the proportion of children with nonallergic rhinitis decreased slightly over the same pe
184 besity was associated with increased odds of nonallergic rhinitis in adults (adjusted odds ratio, 1.6
185 of patients previously given a diagnosis of nonallergic rhinitis or idiopathic rhinitis are now bein
186 rformed at 1-2-month interval in AR, LAR and nonallergic rhinitis patients, and in healthy controls.
190 ng 4- and 8-year-olds, allergic rhinitis and nonallergic rhinitis were associated with asthma, eczema
191 s 12 years of age and older with allergic or nonallergic rhinitis were enrolled in a noninterventiona
192 dermatitis), non-T2 diseases (T2-low asthma, nonallergic rhinitis) and assessment of T2 biomarkers (b
193 they were 8 years old; of the children with nonallergic rhinitis, 73% underwent remission during thi
196 obesity is associated with increased odds of nonallergic rhinitis, particularly in male subjects.
197 of breastfeeding were stronger predictors of nonallergic rhinitis, whereas current wheeze and eczema
203 ins unclear, and the requirement for BATF in nonallergic settings of type-2 immunity has not been exp
206 ceptor can be activated by both allergic and nonallergic stimuli, leading to several pro-inflammatory
207 ithout birch pollen allergy (group 3), and 5 nonallergic subjects (group 4) by performing skin prick
209 = 7) and mild (n = 10) allergic patients and nonallergic subjects (n = 9) to perform platelet lipidom
211 -induced histamine release from basophils in nonallergic subjects and allergen-induced histamine libe
212 RANTES intradermally into both allergic and nonallergic subjects and obtained biopsies 30 min, 6 h,
213 sent at low frequencies in both allergic and nonallergic subjects and reflect classical features of t
214 e grass allergen-specific T cells in DR*0401 nonallergic subjects are present at very low levels (e.g
215 nvolved the production of CCL17 and CCL22 in nonallergic subjects but only CCL17 in allergic patients
216 d stronger complement activation compared to nonallergic subjects following ex vivo vaccine exposure.
217 nonfall birth between (i) food allergic and nonallergic subjects in NHANES, adjusted for ethnicity,
218 DC responses between human food-allergic and nonallergic subjects is necessary to gain a better insig
221 ch allergy and tolerance to peanut; Group 4, nonallergic subjects that tolerate both peanut and peach
222 gic patients or exposure of neutrophils from nonallergic subjects to allergic donor serum in vitro im
223 from sera of 30 birch pollen-allergic and 11 nonallergic subjects to Bet v 1, 13 chimeric proteins, a
226 cells (PBMCs) from peanut-allergic (PA) and nonallergic subjects were stimulated (14-16 h) with pean
231 in 12 subjects with alder pollen allergy, 6 nonallergic subjects, and 9 allergy vaccine-treated subj
234 for walnut-reactive T cells in allergic and nonallergic subjects, particularly the relationship of p
235 ese diseases and are also present in healthy nonallergic subjects, we performed global transcriptiona
247 k histories include patients having isolated nonallergic symptoms, such as gastrointestinal symptoms,
252 ernal cohort of 71 patients (29 allergic, 42 nonallergic), with an area under the curve of 0.908 (sen
253 ice displayed the same 50% graft survival as nonallergic WT mice, that was significantly less than th