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2 2287 significantly decreased esophageal and bronchoalveolar eosinophilia but only when given as a th
4 d anti-inflammatory cytokines (IL-10) in the bronchoalveolar fluid, and IL-2 and IFN-gamma cytokines
7 tegrated study of human small airway tissue, bronchoalveolar lavage (BAL) and an experimental murine
9 bit AHR, increased numbers of eosinophils in bronchoalveolar lavage (BAL) and increased collagen cont
10 a methacholine test, airway inflammation in bronchoalveolar lavage (BAL) and lung tissue, and total
11 e expression and activity were determined in bronchoalveolar lavage (BAL) and lungs of human donors a
12 Conventional methods to identify HBEC in bronchoalveolar lavage (BAL) and wash (BW) have throughp
14 cDNA library derived from mRNA isolated from bronchoalveolar lavage (BAL) cells and leukocytes of sar
15 was to investigate the expression of iNOS in bronchoalveolar lavage (BAL) cells and tissue from centr
16 ring healthy aging, the proportions of blood bronchoalveolar lavage (BAL) classical monocytes peak in
17 increased eosinophilia and interleukin-5 in bronchoalveolar lavage (BAL) compared to sham-OVA mice.
18 We sought to determine the relationship of bronchoalveolar lavage (BAL) cytokine/chemokine expressi
19 perimental model of allergic asthma, matched bronchoalveolar lavage (BAL) fluid and plasma were colle
20 igatus Its performance has been validated on bronchoalveolar lavage (BAL) fluid and serum specimens,
23 ecommendation was made in favor of obtaining bronchoalveolar lavage (BAL) fluid for lymphocyte cellul
24 (log(10) mean value, 4.2), secretory IgA in bronchoalveolar lavage (BAL) fluid from immunized mice,
27 70 have been found in the sputum, serum, and bronchoalveolar lavage (BAL) fluid of asthma patients an
29 rometry based proteome analysis of acellular bronchoalveolar lavage (BAL) fluid samples on an observa
33 red CD4+ T cells in whole blood, spleen, and bronchoalveolar lavage (BAL) fluid, but not in the lung
36 ics and function in rhesus macaque blood and bronchoalveolar lavage (BAL) following mucosal adenoviru
38 igated M. tuberculosis-specific responses in bronchoalveolar lavage (BAL) from persons with latent M.
40 ollowing alveolar airspace infiltration, the bronchoalveolar lavage (BAL) neutrophil proteome is furt
42 xpression in airway immune cells obtained by bronchoalveolar lavage (BAL) of individuals with latent
43 phenotype of NKG2C NK cells in the blood and bronchoalveolar lavage (BAL) of lung transplant recipien
44 We collected endobronchial brush (EB) and bronchoalveolar lavage (BAL) samples from 39 asthmatic p
45 ng injury in CIP, we prospectively collected bronchoalveolar lavage (BAL) samples in ICI-treated pati
47 nd increased CD4+ T cell counts in blood and bronchoalveolar lavage (BAL) samples, it did not reduce
49 ng flow cytometry and a multiplex assay with bronchoalveolar lavage (BAL) specimens (n = 68) from 52
50 eporting for 259 adult inpatients submitting bronchoalveolar lavage (BAL) specimens for laboratory an
55 ergic patients underwent SAC, and cells from bronchoalveolar lavage (BAL) were collected after 24 hou
57 ased age, a low percentage of lymphocytes in bronchoalveolar lavage (BAL), a decreased transfer facto
58 flux of neutrophils and macrophages into the bronchoalveolar lavage (BAL), and human CD45(+) cells in
60 linically indicated fiberoptic bronchoscopy, bronchoalveolar lavage (BAL), endobronchial brushings, a
61 mation as proven by increased cellularity in bronchoalveolar lavage (BAL), pulmonary transcriptomic p
66 aeruginosa, P. aeruginosa) were analyzed in bronchoalveolar lavage (BAL); and alveolar SGLT1 was ana
67 oneal (p = 0.037), systemic (p = 0.019), and bronchoalveolar lavage (p = 0.011) quantitative bacteria
70 oxic amyloids that can be recovered from the bronchoalveolar lavage and cerebrospinal fluids of criti
72 ion model, IL-10-producing CD4(+) T cells in bronchoalveolar lavage and lung were significantly decre
73 log(10) reductions in median viral loads in bronchoalveolar lavage and nasal mucosa compared with af
74 log(10) reductions in median viral loads in bronchoalveolar lavage and nasal mucosa, respectively, a
75 ided complete or near-complete protection in bronchoalveolar lavage and nasal swabs after SARS-CoV-2
77 ues, we performed transcriptomic analyses of bronchoalveolar lavage and peripheral blood and proteomi
78 ition of ADAM10 reduces sEphrin-B2 levels in bronchoalveolar lavage and prevents lung fibrosis in mic
79 MIF decreases neutrophil infiltration to the bronchoalveolar lavage and tissue and simultaneously dec
82 ophils in bone marrow (BM), blood, lung, and bronchoalveolar lavage as well as airway hyperresponsive
83 subjects had symptom scores, spirometry, and bronchoalveolar lavage before and after rhinovirus-induc
85 ere analyzed based on serum antibody levels, bronchoalveolar lavage cell counts, lung histology, lung
88 T-cell recruitment and activation within bronchoalveolar lavage cells of ACE2-high subjects was r
89 anscriptional profiling of cells isolated by bronchoalveolar lavage confirmed that influenza infectio
90 .RESULTSActivated CD4+ T cell frequencies in bronchoalveolar lavage correlated strongly with local C-
92 increased, and protein concentration in the bronchoalveolar lavage diminished, showing the impact of
93 GR-1) resulted in a significant decrease in bronchoalveolar lavage eosinophil counts, lung interleuk
95 niae infection was diagnosed on the basis of bronchoalveolar lavage eosinophilia and blood findings.
96 b induced a rise in circulating eosinophils, bronchoalveolar lavage eosinophilia, and eosinophil pero
97 sham at day 13 showed an increased number of bronchoalveolar lavage eosinophils and increased express
98 l7r(cre) mice showed complete suppression of bronchoalveolar lavage eosinophils and mucous metaplasia
100 im of this study was to analyze cytokines in bronchoalveolar lavage fluid (BALF) and explore predicti
101 infected with Streptococcus pneumoniae, and bronchoalveolar lavage fluid (BALF) and lung CFU values
102 d temporal kinetics of GT and bmGT in serum, bronchoalveolar lavage fluid (BALF) and lungs of A. fumi
103 s the overlap in metabolites between matched bronchoalveolar lavage fluid (BALF) and plasma, identifi
104 tinfection and included cellular profiles in bronchoalveolar lavage fluid (BALF) and serum IgG and Ig
106 understanding of the proinflammatory role of bronchoalveolar lavage fluid (BALF) exosomes in patients
108 alysis on gene expression data from cells in bronchoalveolar lavage fluid (BALF) from COVID-19 patien
109 us 6B (HHV-6B) DNA is frequently detected in bronchoalveolar lavage fluid (BALF) from immunocompromis
110 with human MSCs when stimulated with LPS or bronchoalveolar lavage fluid (BALF) from patients with A
111 by using mass spectrometry) were measured in bronchoalveolar lavage fluid (BALF) from patients with N
113 cytomegalovirus (HCMV) DNA detection in the bronchoalveolar lavage fluid (BALF) indicates HCMV repli
115 emic stroke caused a significant increase in bronchoalveolar lavage fluid (BALF) macrophages and neut
116 induce apolipoprotein E (APOE) expression by bronchoalveolar lavage fluid (BALF) macrophages from ast
118 We measured iron and ferritin levels in the bronchoalveolar lavage fluid (BALF) of participants enro
119 a diffuse lung injury marked by increases in bronchoalveolar lavage fluid (BALF) protein and histoche
120 rformed a retrospective multicenter study on bronchoalveolar lavage fluid (BALF) samples obtained fro
126 2 ligands was significantly increased in the bronchoalveolar lavage fluid 48 hours after segmental al
127 o DC subsets (DC2/3 and DC5) are expanded in bronchoalveolar lavage fluid 8 h after lipopolysaccharid
128 urbiprofen augmented the release of IL-33 in bronchoalveolar lavage fluid after Alternaria challenge,
129 ased airway hyperreactivity to methacholine, bronchoalveolar lavage fluid albumin, and serum IgE leve
130 healthy volunteers and examine the impact on bronchoalveolar lavage fluid and blood MP repertoire.
131 ar lavage fluid was evaluated by microscopy; bronchoalveolar lavage fluid and blood were assessed by
132 PM2.5 increased neutrophil numbers and KC in bronchoalveolar lavage fluid and caused slight peribronc
133 recruitment of monocytes and neutrophils in bronchoalveolar lavage fluid and increased neutrophils i
134 fspring had lower white blood cell counts in bronchoalveolar lavage fluid and less pronounced peribro
135 ikingly reduced numbers of leukocytes in the bronchoalveolar lavage fluid and lower expression of inf
136 ed a significantly reduced viral load in the bronchoalveolar lavage fluid and lower respiratory tract
137 ine expression in ILC2s and TH2 cells in the bronchoalveolar lavage fluid and lung tissue were assess
138 Flow cytometry and cytokine measurements in bronchoalveolar lavage fluid and lung tissue were follow
141 We detected the presence of PRELP in human bronchoalveolar lavage fluid and showed that PRELP can b
142 bronchitis, perivasculitis, and increases in bronchoalveolar lavage fluid cell numbers were detected
144 eduction of eosinophil and T cell numbers in bronchoalveolar lavage fluid compared with those in dilu
145 2 223K/K mice had persistent eosinophilia in bronchoalveolar lavage fluid compared with wild-type and
146 a, accompanied with significant reduction in bronchoalveolar lavage fluid concentration of IL-5, a cy
148 , IL-33(KO)/Tg+ mice had complete absence of bronchoalveolar lavage fluid eosinophilia, accompanied w
151 ein levels were significantly upregulated in bronchoalveolar lavage fluid from HIV-infected smokers,
153 patients with severe asthma compared with in bronchoalveolar lavage fluid from individuals without as
154 s of IL-1beta and IL-8 rapidly determined in bronchoalveolar lavage fluid from patients randomised to
155 vo, histone-C1INH complexes were detected in bronchoalveolar lavage fluid from patients with acute re
156 he protein expression patterns in plasma and bronchoalveolar lavage fluid from patients with ARDS.
158 nase activities were quantified in serum and bronchoalveolar lavage fluid from patients with CF, asth
159 anges in the miRNA composition of EVs in the bronchoalveolar lavage fluid from patients with IAV-indu
160 pulmonary eosinophilia were measured in the bronchoalveolar lavage fluid from patients with mild ast
161 r, specific ceramide species were altered in bronchoalveolar lavage fluid from patients with severe a
162 Low concentrations of IL-1beta and IL-8 in bronchoalveolar lavage fluid have been validated as effe
163 al aimed to determine whether measurement of bronchoalveolar lavage fluid IL-1beta and IL-8 could eff
164 ry inflammation, eosinophilia, and increased bronchoalveolar lavage fluid IL-4 and IL-5, whereas adop
165 eficient mice had fewer DEP exposure-induced bronchoalveolar lavage fluid immune cells and proinflamm
166 s, angiotensin-converting enzyme activity in bronchoalveolar lavage fluid increased 3.2-fold in elder
167 Following repetitive O3 exposure, higher bronchoalveolar lavage fluid inflammatory cells were obs
169 I are seen in HAECs, in association with low bronchoalveolar lavage fluid mitochondrial DNA and more
170 cells in lymph nodes, peripheral blood, and bronchoalveolar lavage fluid of AGMs and rhesus macaques
171 we report that SOCS3 protein was elevated in bronchoalveolar lavage fluid of both virus- and bacteria
172 med that leukotriene levels are increased in bronchoalveolar lavage fluid of HIV-infected patients.
174 oxidase were more frequently detected in the bronchoalveolar lavage fluid of lung transplant patients
175 f RAGE was determined in protein, serum, and bronchoalveolar lavage fluid of mice and lungs and serum
176 shown to reduce the total number of cells in bronchoalveolar lavage fluid of mice challenged with hou
178 NF-alpha, IL-9, CXCL1, CCL2, and CCL5 in the bronchoalveolar lavage fluid of RSV-infected mice, witho
179 y/severity; (2) RSV-specific CD8+ T cells in bronchoalveolar lavage fluid preinfection (subjects with
180 e exposure of vehicle-treated rats increased bronchoalveolar lavage fluid protein, albumin, neutrophi
182 ynthase similarly attenuated the increase in bronchoalveolar lavage fluid SOCS3 noted in lungs of mic
183 ption factor GATA3 and intracellular IL-4 in bronchoalveolar lavage fluid T cells, but expression of
184 ation and analysis of Aspergillus conidia in bronchoalveolar lavage fluid using the combination of tr
185 determined by whole-body plethysmography and bronchoalveolar lavage fluid was analyzed for cellular c
189 had a separate donor; however, pretransplant bronchoalveolar lavage fluid was only available from the
191 ity in lymphoid tissues and Th2 responses in bronchoalveolar lavage fluid), they also accumulate func
192 rol and PNE rat pups: 1) the 5-HT content in bronchoalveolar lavage fluid, 2) the apneic response to
193 chronic rhinosinusitis (CRS), as well as in bronchoalveolar lavage fluid, after segmental allergen c
195 concentration was also induced in the serum, bronchoalveolar lavage fluid, alveolar type II epithelia
196 d lower total cell counts and neutrophils in bronchoalveolar lavage fluid, and had earlier influx of
197 nd disaturated PC in lung tissue homogenate, bronchoalveolar lavage fluid, and lung LB was increased
198 were sensitized and challenged with OVA and bronchoalveolar lavage fluid, and the lungs were collect
199 d tumor-promoting cyto-/chemokine profile in bronchoalveolar lavage fluid, decreased TLR2/4 expressio
200 fferential cell counts were performed on the bronchoalveolar lavage fluid, followed by histological a
201 und significantly elevated total proteins in bronchoalveolar lavage fluid, higher parasitemia and tis
204 tained pulmonary or systemic health effects, bronchoalveolar lavage fluid, serum metabolic and inflam
221 ncreased ATP concentrations were reported in bronchoalveolar lavage fluids of asthmatic patients.
222 ocessed 25-kDa IL-33 protein was detected in bronchoalveolar lavage fluids without any exogenous stim
227 ol for invasive pulmonary aspergillosis with bronchoalveolar lavage galactomannan and cultures perfor
228 ent in anastomotic plaques with reduction in bronchoalveolar lavage galactomannan values (7.48-2.15 n
229 L-1alpha positively correlated with elevated bronchoalveolar lavage IL-8 levels (r(2) = 0.6095, p < 0
230 were most frequently cultured from blood and bronchoalveolar lavage in humans and lungs in animals.
231 antibiotic-free days in the 7 days following bronchoalveolar lavage in the intention-to-treat analysi
233 as adjuvants resulted in elevated serum and bronchoalveolar lavage levels of anti-P6-specific IgG an
238 ll as 16S ribosomal RNA sequencing data from bronchoalveolar lavage obtained as part of the COMET-IPF
241 IV-1-infected airway macrophages obtained by bronchoalveolar lavage of HIV-1-infected individuals.
242 used to characterize macrophages from human bronchoalveolar lavage of HIV-infected and -uninfected s
243 rleukin-1 alpha (IL-1alpha) was increased in bronchoalveolar lavage of lung transplant recipients gro
244 des of the biculture and was also present in bronchoalveolar lavage of lung transplantation patients.
246 marker of PARP activation) and IL-6, in the bronchoalveolar lavage or the lung tissue, and histology
250 of interferon and interleukin-6 pathways in bronchoalveolar lavage samples and repression of natural
251 y evaluating both upper airway and acellular bronchoalveolar lavage samples from 49 subjects from thr
252 have previously demonstrated that acellular bronchoalveolar lavage samples from half of the healthy
253 rst identified two redondovirus genomes from bronchoalveolar lavage samples from human lung donors.
256 navirus testing on pooled nasopharyngeal and bronchoalveolar lavage samples taken from patients who h
257 tes for the galactomannan assay in serum and bronchoalveolar lavage samples were 61.3% and 57.1%, res
260 ubset of 61 patients, respiratory specimens (bronchoalveolar lavage specimens, tracheal aspirates, an
261 ch on-ECMO experimental step, but the lowest bronchoalveolar lavage sRAGE levels were obtained at min
267 r advanced glycation end products (sRAGE) in bronchoalveolar lavage(BAL) and plasma were performed.
268 identify cross-tissue compartment (blood and bronchoalveolar lavage) and temporal proteomic signature
269 the lung, proinflammatory cytokine levels in bronchoalveolar lavage, and alveolar capillary leakage.
270 lished prescribing practices, reluctance for bronchoalveolar lavage, and dependence on a chain of tri
280 ctive viral replication and viral genomes in bronchoalveolar-lavage (BAL) fluid and nasal swab specim
282 a higher number of lung cells obtained from bronchoalveolar lavages (BAL) than TAC pre-treatment alo
284 ignificantly higher S. maltophilia counts in bronchoalveolar lavages and lung tissue homogenates.
285 s are reticent to perform aerosol-generating bronchoalveolar lavages for galactomannan testing and mi
286 ial alarmins were measured longitudinally in bronchoalveolar lavages from lung transplant recipients
288 NA and host total RNA were isolated from 203 bronchoalveolar lavages obtained from 112 patients post-
289 NA and host total RNA were isolated from 189 bronchoalveolar lavages obtained from 116 patients post
290 s on radiographs and reduced virus titres in bronchoalveolar lavages twelve hours after the first dos
291 edding measured from nasal and throat swabs, bronchoalveolar lavages, and tissues was not reduced wit
294 throat of all of the macaques, as well as in bronchoalveolar lavages; in one macaque, we observed pro
296 cs of human DCs and monocytes recruited into bronchoalveolar space immediately following localised ac
297 mmune cells in whole lung parenchyma and the bronchoalveolar space of mice, exposed to 48 hours of hy