ライフサイエンスコーパス: infiltrate

1 they appeared to be a minor component of the infiltrate.

2 cedure chest x-ray showed a right lower lobe infiltrate.

3 constituted the majority of the acute immune infiltrate.

4 ed by an eosinophil-predominant inflammatory infiltrate.

5 Seven (47%) had bilateral lung infiltrates.

6 sented with the chief complaint of pulmonary infiltrates.

7 macrophages to form prototypic granulomatous infiltrates.

8 sed tumors were scored for inflammatory cell infiltrates.

9 y AST and ALT levels, as well as immune cell infiltrates.

10 Three eyes (0.4%) developed sterile infiltrates, 1 (0.1%) had delayed epithelial healing wit

11 .00 (RAS), 4.00 (control), P = 0.62; without infiltrates, 4.5 (BOS), 0.00 (RAS), 4.56 (control), P =

12 s (median number of LVs per bronchiole: with infiltrates, 5.00 (BOS), 9.00 (RAS), 4.00 (control), P =

13 ouse model, both neutrophils and macrophages infiltrate a human Burkitt's lymphoma xenograft and inhi

14 RG-15 mice did not require preactivation but infiltrated a Burkitt's lymphoma xenograft and efficient

15 The Dry Basin infiltrated a much larger volume of water and thus had g

16 ts expression and the prominent neutrophilic infiltrate, a hallmark of the disease.

17 gulated in type 1 and type 2 diabetes and in infiltrating activated immune cells.

18 iated metastatic cervical cancer after tumor-infiltrating adoptive T cell therapy.

19 ammatory phenotype, with massive immune cell infiltrates already before birth.

20 ne levels, and reduced immature myeloid cell infiltrate and blood chemokine levels.

21 breast cancer cell lines for the ability to infiltrate and grow in CSF, a remarkably acellular, mito

22 tute a significant proportion of the initial infiltrate and have the potential to propagate secondary

23 elopment is associated with mononuclear cell infiltrate and high levels of inflammatory cytokine prod

24 fection, with a more pronounced inflammatory infiltrate and increased specific production of IFN-gamm

25 s most frequent between conclusions of other infiltrate and normal for both the reading panel and the

26 e post-trauma microenvironment in which DPCs infiltrate and resident immune cells generate cytotoxic

27 If tissue damage occurs, immune cells infiltrate and secrete cytokines, including IL-6, to rep

28 -1.09 mm; P < .001) and a 0.83-mm decreased infiltrate and/or scar size at 3 months after correcting

29 near regression revealed a 1.89-mm decreased infiltrate and/or scar size at 3 weeks (95% CI, -2.69 to

30 bers showed a significant difference between infiltrated and normal BM (P < .001).

31 Small nodal tumor infiltrates and BMM were found in a total of 21 patients

32 be size sensing resulted in large neutrophil infiltrates and clusters in response to small microbes t

33 Levels of cellular infiltrates and cytokines (IL-13, IL-22, and S100As) wer

34 on patterns with the presence of immune cell infiltrates and immune regulatory molecules, determined

35 gen exposure, with massive eosinophilic lung infiltrates and increased Th2 cytokines.

36 a reduced cardiac inflammation (less cardiac infiltrates and suppression of proinflammatory cytokines

37 ferential gene expression patterns unique to infiltrating and resident cells, suggesting unique funct

38 nate the unique composition and functions of infiltrating and resident myeloid cells in GBM, establis

39 oroid, a perivascular choroidal inflammatory infiltrate, and atrophic changes within the optic nerve

40 ssociated with CD8-dominant antitumor immune infiltrate, and together, these contribute to improved c

41 ment correlated with changes in hyperplasia, infiltrates, and differentiation markers.

42 more extensive tubular injury, inflammatory infiltrates, and fibrosis than wild-type mice.

43 itial endothelium, interstitial inflammatory infiltrates, and glomerular cells.Primary VSMCs were inf

44 wed interstitial nephritis, mononuclear cell infiltrates, and reduced size of glomeruli.

45 This delay correlated with increased infiltrating antitumor macrophages.

46 Inflammatory infiltrates are common but are small and of doubtful pat

47 lecular signatures of macrophages and T cell infiltrates are relatively high within distinct subsets

48 P3(+) regulatory T cells within the cellular infiltrates around the islet isografts.

49 e growth factor FGF-2, which activates tumor-infiltrating B cells to produce the growth factor IGF-1.

50 e tumor types on both cancer cells and tumor-infiltrating blood vessels, making it a potentially idea

51 We characterized T cells infiltrating both breast cancer tumors and the surroundi

52 Size of the overall T-cell infiltrate, but not the level of clonality, correlated w

53 intestinal experimental liver metastases are infiltrated by neutrophils.

54 esenchymal glioblastoma TPC suppressed their infiltrating capability.

55 a and the proliferation marker Ki67 in tumor-infiltrating CAR T cells when combined with alpha-4-1BB.

56 Tumor-infiltrating CCR5(+) MDSCs displayed higher immunosuppre

57 L2 or MIF expression and the number of tumor-infiltrating CD33(+) MDSCs (P<0.01).

58 rway inflammation, approximately 30% of lung-infiltrating CD4 T cells express Foxp3, indicative of Tr

59 Tumor-infiltrating CD4(+) and CD8(+) T cells in patients with

60 were also expressed on human PD1(hi) tumour-infiltrating CD8 T cells.

61 ironment, increasing the proportion of tumor-infiltrating CD8(+) T cells and sensitizing tumors to su

62 d with PD-L1 suppression, increases in tumor-infiltrating CD8(+) T cells and tumor cell killing.

63 The percentage of tumor-infiltrating CD8(+) T cells coexpressing PD-1 and Tim-3

64 Remarkably, infiltrating CD8(+) T cells do not cause tissue damage i

65 Here we describe a subset of tumor-infiltrating CD8(+) T cells marked by high expression of

66 Brain-infiltrating CD8(+) T cells represent an activated subse

67 Tumor-infiltrating CD8(+) T cells with high CD39 expression ex

68 Consequently, our data indicated infiltrating CD8+ T cells could promote the proliferatio

69 otein expression (immunohistochemistry), and infiltrating cell populations (flow cytometry).

70 ltiple tumor clones and assorted stromal and infiltrating cell populations to pooled genomic data.

71 oth muscle cell proliferation, and had fewer infiltrating cells but retained endothelialization.

72 s in GBM, establishing a rationale to target infiltrating cells in this neoplasm.

73 -positive endothelium and underlying SMC and infiltrating cells such as macrophages and leukocytes.

74 ive fibers, with a reduction in inflammatory infiltrates, compared with those in vehicle-treated mice

75 sequelae, possessed a significant leukocytic infiltrate composed primarily of CD4(+) T cells and macr

76 performed transcriptomic profiling of tumor-infiltrating CTLs from treatment-naive patients with lun

77 ll of origin, as APRIL-producing neutrophils infiltrated CXCL-8(+) DLBCL from both germinal center (G

78 notherapeutic regimen caused homing of tumor-infiltrating DC to draining lymph nodes and increased in

79 with placebo after controlling for baseline infiltrate depth (95% CI, 0.22-fold to 0.84-fold; P = .0

80 detecting consolidation, but poor for other infiltrates despite attempts at a rigorous standardizati

81 A 0.6 x 0.5 cm Nottingham grade 1 infiltrating ductal carcinoma was removed from the right

82 vels of IL-33 have been associated with deep infiltrating endometriosis, its contribution to the dise

83 About 8.8% +/- 4.8% of the infiltrating eosinophils exhibited EETs in patients' nas

84 No cytogenetic anomalies were found in the infiltrate except in 1 case in which neoplastic cells of

85 striking subepithelial lichenoid lymphocytic infiltrate extending into the muscularis mucosae.

86 assing both cancer cells and multiple immune infiltrates following localized exposure to different ch

87 The dermal infiltrate from the 33 study patients (20 female; median

88 Spatial profiling of the iron-laden infiltrates further demonstrated that higher numbers of

89 cancer, we reinforced the concept that tumor-infiltrating gammadeltaT17 cells are endowed with protum

90 The nature of the histiocytoid infiltrate has generated considerable controversy in the

91 rize molecular features of immune cells that infiltrate hepatocellular carcinomas (HCCs) to determine

92 iated microglia and macrophages (GAM), which infiltrate high-grade gilomas, constitute a major cellul

93 that appear to perform similar functions in infiltrating host cells.

94 that both H03-IPSE and H06-IPSE proteins can infiltrate HTB-9 bladder cells when added exogenously to

95 OPD is driven by a Th1 response activated by infiltrating ILC1, NK, and LTi cells.

96 Second, infiltrating immune cell populations were decreased in v

97 rize a tumor's neoantigen load, its cadre of infiltrating immune cell types, the T or B cell receptor

98 infiltrating immune cells vs >/=5% of tumour-infiltrating immune cells [IC2/3]), chemotherapy type (v

99 ed tumor onset and increased levels of tumor-infiltrating immune cells comprised of CD11b(+) cells, m

100 , such as keratinocytes and fibroblasts, and infiltrating immune cells expressed CXCL10 at lesional s

101 ancer-promoting cytokine that is secreted by infiltrating immune cells in several cancer models.

102 on on <1% [IC0] or 1% to <5% [IC1] of tumour-infiltrating immune cells vs >/=5% of tumour-infiltratin

103 1/2/3 (>/=1% PD-L1 on tumour cells or tumour-infiltrating immune cells).

104 w reduced expression of markers of cytotoxic infiltrating immune cells, especially CD8(+) T cells, an

105 Among tumor-infiltrating immune cells, tumor-associated macrophages

106 e immunological response by interacting with infiltrating immune cells.

107 n colonic epithelium potentially assisted by infiltrating immune components.

108 has demonstrated essential roles for several infiltrating immune populations in the metaplastic progr

109 of the immunohistochemical phenotype of the infiltrate in histiocytoid Sweet syndrome.

110 is elevated selectively in the inflammatory infiltrate in human and murine colitis.

111 e original study observed sparse lymphocytic infiltrate in IgG-treated tumors and increased inflammat

112 Macrophages are the predominant infiltrate in the corneas of mice that have been ocularl

113 subsets of myeloid-derived suppressor cells infiltrate in the primary tumour and distant organs with

114 ve increase in a predominantly CD4(+) T-cell infiltrate in the prostate epithelial and stroma of tumo

115 beta and IL-18, reduced myeloid inflammatory infiltrate in the skin and spleen, and substantial decre

116 ly driven by CD8(+) T cells, and immune cell infiltrate in the tumor could be reprogrammed toward a h

117 nduced by beta2GPI in activated T cells that infiltrate in vivo atherosclerotic lesions of primary AP

118 %), with characteristic multifocal choroidal infiltrates in 29 eyes (39%).

119 eated tumors and increased inflammatory cell infiltrates in anti-CD47 treated tumors.

120 In WT-infected mice, infiltrates in gastric tissues were predominantly compos

121 fects of checkpoint blockade on tumor immune infiltrates in human melanoma and murine tumor models.

122 s in many cancer types, these reduced immune infiltrates in muIDH1 glioma tumors may contribute in pa

123 ncept for ERK5 as a target to enhance T-cell infiltrates in prostate cancer, with possible implicatio

124 Monoclonality was observed in a few infiltrates in the presence of lymphoepithelial lesions.

125 still contained variably elevated leukocytic infiltrates in their islets when examined at 20-40 wk of

126 ents have shown the presence of inflammatory infiltrates, in some cases with features of B cell-rich

127 ontrol subjects, and islet inflammatory cell infiltrates, independently of the severity of the exocri

128 mposed mainly of macrophages and neutrophils infiltrate infected DRGs and account for the development

129 mposed mainly of macrophages and neutrophils infiltrate infected sensory ganglia and are responsible

130 the RAGE antagonist FPS-ZM1 in mice, and the infiltrated inflammatory cells and cytokines were assess

131 ase 9 (MMP-9), IL-17, and IL-23 release from infiltrated inflammatory cells.

132 alignant cells increased the number of tumor-infiltrating interferon gamma-producing natural killer (

133 Here we demonstrate that T cells infiltrate into the kidney of salt-sensitive hypertensiv

134 Mesenchymal stromal cells (MSCs) tend to infiltrate into tumors and form a major component of the

135 They infiltrate into tumors and modulate the tumor microenvir

136 both wild type and CCR7-/- CD11c-eYFP cells infiltrated into the CNS but cells that lacked CCR7 were

137 Results Myeloid cells infiltrated into the injured cord at 6 and 24 hours afte

138 ater (up to several mg L(-1) biocides) being infiltrated into the soil surrounding houses.

139 ddition, it was found that the released MK2i infiltrated into the tissue with a cumulative manner in

140 l is upregulated in CD8(+) T cells that have infiltrated into transplanted lymphoma tumours, and Grai

141 s and longer PFS with increased T-lymphocyte infiltrates, irrespective of PD-1 expression.

142 al findings (n=7) revealed atypical lymphoid infiltrates, Kupffer cell hyperplasia with erythrophagoc

143 urified glomeruli have identified glomerulus-infiltrating leukocyte populations in NZM2328 (NZM) lupu

144 muscle injury, being expressed mostly in the infiltrating leukocytes (CD45(+) cells), including macro

145 p53 activation in TME comprising overt tumor-infiltrating leukocytes (TILeus) induces systemic antitu

146 Infiltrating leukocytes are responsible for driving the

147 Immunophenotyping of skin-infiltrating leukocytes confirmed substantial infiltrati

148 inhibition did not reduce the proportion of infiltrating leukocytes in the tumor microenvironment bu

149 -pathogenic CD8(+) T cells relative to other infiltrating leukocytes, perhaps preventing further tiss

150 eribronchial regions, which were enriched in infiltrating leukocytes.

151 seases by reducing the recruitment of tissue-infiltrating leukocytes.

152 t occurring in response to stimuli by tissue-infiltrating leukocytes.

153 a less extent, dendritic cells as the major infiltrating leukocytes.

154 We demonstrated here that FL-infiltrating LN and BM stromal cells overexpressed CXCL1

155 Infiltrating low grade gliomas (LGGs) are heterogeneous

156 follicular dendritic cells of the metastasis-infiltrated lymph node.

157 We isolated tumor-infiltrating lymphocytes (TIL) and intra-hepatic lymphoc

158 CD4 mRNAs and their relationship with tumor-infiltrating lymphocytes (TIL) and PD-L1 IHC expression.

159 Recent studies have found that tumor-infiltrating lymphocytes (TIL) expressing PD-1 can recog

160 The presence of tumor-infiltrating lymphocytes (TIL) is a favorable prognostic

161 Accumulating evidence indicates that tumor-infiltrating lymphocytes (TILs) are associated with clin

162 It is well known that CD8(+) tumor-infiltrating lymphocytes (TILs) are correlated with posi

163 however, the antigen specificities of tumor-infiltrating lymphocytes (TILs) are not well understood.

164 Although the presence of tumor-infiltrating lymphocytes (TILs) indicates an endogenous

165 However, the evaluation of tumor-infiltrating lymphocytes (TILs) relies on histopathologi

166 and chromatin accessibility in CD8(+) tumor-infiltrating lymphocytes (TILs) that recognize a model t

167 Percentage of tumor cells and tumor-infiltrating lymphocytes (TILs) with PD-L1 expression, i

168 t cancer is associated with increased tumour infiltrating lymphocytes (TILs), however, MAPK activity

169 int inhibitors increases the number of tumor-infiltrating lymphocytes and overall survival after DNA

170 mmuno-PET) can visualize tumors by detecting infiltrating lymphocytes and, through longitudinal obser

171 The mechanisms through which infiltrating lymphocytes cause disease remain unknown.

172 Tumor-infiltrating lymphocytes coexpressed PD-1 with the inhib

173 FACS-based enumeration of intracranial tumor-infiltrating lymphocytes directly correlated with quanti

174 for melanoma, Runx3-deficient CD8(+) tumour-infiltrating lymphocytes failed to accumulate in tumours

175 d PD-L1 levels and reduced numbers of tumour-infiltrating lymphocytes in mouse tumours and in primary

176 Patients with increased numbers of tumor-infiltrating lymphocytes in primary colon tumors and liv

177 The presence of tumor-infiltrating lymphocytes in triple-negative breast cance

178 ted with significantly lower levels of tumor-infiltrating lymphocytes in triple-negative breast cance

179 Systematic interrogation of tumor-infiltrating lymphocytes is key to the development of im

180 found in the draining lymph nodes and tumor-infiltrating lymphocytes of OSCC patients with early or

181 In conclusion, we show that pituitary-infiltrating lymphocytes proliferate in situ during AH,

182 hermore, we show that human and mouse tumour-infiltrating lymphocytes share a core tissue-residency g

183 engineering reinstated Th1 function in tumor-infiltrating lymphocytes that had been functionally disa

184 inhibition can promote recruitment of tumor-infiltrating lymphocytes to the tumor, here we show that

185 l, GSK-3i inhibited PD-1 expression on tumor-infiltrating lymphocytes, while increasing Tbx21 (T-bet)

186 SLOs occurred with a massive accumulation of infiltrated MAC387(+) macrophages, T cells, dendritic ce

187 further demonstrated that higher numbers of infiltrating macrophage iron deposits was associated wit

188 concurrent double depletion of microglia and infiltrated macrophages slightly, but significantly, com

189 ar endothelial growth factor expression, and infiltrating macrophages (Ly6C(+)CD45(high)CD11b(+)).

190 optotic cells and exhibited lower numbers of infiltrating macrophages and neutrophilic granulocytes.

191 the cells of the tumor mass, including both infiltrating macrophages and resident brain microglia.

192 and suppresses tumor development, suggesting infiltrating macrophages as a key source for steatosis-i

193 the innate immune response of microglia and infiltrating macrophages clears up cellular debris and p

194 f CD11b(+)F4/80(-)I-A(-) M2b-like glomerulus-infiltrating macrophages in LN and reinforce macrophages

195 t/beta-catenin as a novel signal produced by infiltrating macrophages induced by steatosis that promo

196 Although infiltrating macrophages influence many pathological pro

197 mitate-stimulated CD11b(+)F4/80(low) hepatic infiltrating macrophages, but not CD11b(+)F4/80(high) Ku

198 age in the liver, inflammatory cells such as infiltrating macrophages, T lymphocytes, neutrophils, an

199 Infiltrating macrophages/monocytes constituted approxima

200 Immunohistochemical characterization of infiltrating MCs and the effects of gliadin peptides on

201 Infiltrating MCs were associated with the severity of mu

202 Importantly, premetastatic liver-infiltrating MDSCs induced tumor cell survival without i

203 was not associated with regions of cellular infiltrates (median number of LVs per bronchiole: with i

204 cs (TPC) in defining the character of highly infiltrating mesenchymal glioblastoma cells (Wnt5a(High)

205 d with poor prognosis and also discriminated infiltrating mesenchymal glioblastoma from poorly motile

206 several derepressed miR-155 targets in tumor-infiltrating, miR-155-deficient CD8(+) T cells, suggesti

207 ouse models, we provide evidence that tumour-infiltrated mMDSCs facilitate tumour cell dissemination

208 l cells and the local resident microglia and infiltrating mo-MPhi within the lesion area, as a mechan

209 lesional macrophages in general and Ly6c(hi) infiltrating monocyte-macrophages in particular, accompa

210 ty was greater on sandier soils, where water infiltrates more readily, and in areas where the maximum

211 on and thereby impair the functions of tumor-infiltrating murine and human myeloid dendritic cells (T

212 lates apoptosis and the numbers of activated infiltrating murine neutrophils but not neutrophil cellu

213 Moreover, we identified changes in tumor-infiltrating myeloid cell (TIM) subsets that likely comp

214 the regulation of PD-L1 expression in tumor-infiltrating myeloid cells and, therefore, reprogramming

215 rs responsible for the protumoral effects of infiltrating myeloid cells can be used to target establi

216 ) reverts the immunosuppressive phenotype of infiltrating myeloid cells, by modulating inflammatory g

217 Glomerular damage mediated by glomerulus-infiltrating myeloid-derived cells is a key pathogenic e

218 complement C5a receptor 1 expressed on tumor infiltrating myeloid-derived suppressor cells.

219 Moreover, PD-1 precisely identified marrow-infiltrating, myeloma-specific T cells in a mouse model

220 wo miRNAs are prominently expressed in wound-infiltrated neutrophils and macrophages and play central

221 ing that the immune response is dominated by infiltrating neutrophils and elicits a mixed TH17/TH1 re

222 Tumor-infiltrating neutrophils have been implicated in maligna

223 n is the production of oxidized compounds by infiltrating neutrophils.

224 n individuals with rheumatoid arthritis (RA) infiltrate non-lymphoid tissue sites, maneuver through e

225 ized as abnormal (consolidation and/or other infiltrate), normal, or uninterpretable.

226 The dermal infiltrate of cutaneous lesions of histiocytoid Sweet sy

227 kidney injury includes a robust inflammatory infiltrate of PMNs and macrophages.

228 Both T and B cells were common infiltrates of spinal cords in diseased mice.

229 e examined the sexual dimorphism in cellular infiltrates of the salivary glands by using functional s

230 clinical and laboratory signs and absence of infiltrate on chest radiograph).

231 The same effect of macrophage infiltrate on EGFR activation was also seen in a colorec

232 best spectacle-corrected visual acuity, and infiltrate or scar size at 3 months.

233 itis; however, it did not reduce immune cell infiltrates, or the deposits of IgG and complement in th

234 ced proinflammatory signaling in macrophages infiltrating pancreatic islets.

235 of skin inflammation and reductions in skin-infiltrating pathogenic effector Th2 cells and TSLP.

236 -methylation programs were acquired in tumor-infiltrating PD-1hi CD8 T cells, and approaches to rever

237 Tumor-infiltrating PD-L1(+) cells isolated from tumor-bearing

238 ic GN and severe proteinuria, few glomerulus-infiltrating PMN were found, leaving macrophages and, to

239 ne-derived microparticles released by tissue infiltrating PMNs (PMN-MPs) serve as shuttles to protect

240 ript, is expressed by mononuclear phagocytes infiltrating primary melanoma and is induced by IFNgamma

241 Infiltrating river water becomes anoxic in the uppermost

242 cle-corrected visual acuity (BSCVA), 3-month infiltrate/scar size, corneal perforation, and re-epithe

243 This infiltrate should not be interpreted as leukemia cutis.

244 emotely supplying a distinct subset of tumor-infiltrating SiglecF(high) neutrophils, which exhibit ca

245 or fabricating WCu alloys using spark plasma infiltrating sintering of copper-coated graphene (Cu@Gr)

246 These analyses reveal a spectrum of tumor-infiltrating T cell populations that are highly similar

247 ckade targets only specific subsets of tumor-infiltrating T cell populations.

248 tion) revealed that a discrete proportion of infiltrating T cells and B cells underwent proliferation

249 hich was accompanied by activation of kidney-infiltrating T cells and cytokine production.

250 filing reveals that antigen-specific, tumour-infiltrating T cells are highly heterogeneous.

251 Infiltrating T cells co-localized with dendritic cells i

252 s study, we tested the hypothesis that tumor-infiltrating T cells could be more effectively activated

253 ed the persistence and accumulation of tumor-infiltrating T cells in vivo, compared with the parental

254 Tumor-infiltrating T cells play an important role in many canc

255 Dysregulation of this pathway in tumor-infiltrating T cells results in diminished anti-tumor im

256 ating CD45RO(+) memory T cells and most skin-infiltrating T cells.

257 nown about human antigenic targets for islet-infiltrating T cells.

258 h DCB displayed a higher proportion of tumor-infiltrating T lymphocytes (TIL) (n = 24, Mann-Whitney p

259 How tumor-infiltrating T lymphocytes (TILs) adapt to the metabolic

260 de increases IFNgamma-producing CD8(+) tumor-infiltrating T lymphocytes and results in a profound ext

261 We report a heterogeneous population of infiltrating T lymphocytes.

262 -target suppression of the activity of tumor-infiltrating T lymphocytes.

263 4/6 inhibition significantly increased tumor-infiltrating T-cell activation and cytotoxicity and decr

264 n of glomerulonephritis and diminished renal-infiltrating Tfh and Th1 cells, and improved overall sur

265 glioma development and had higher microglial infiltrate than mice with wild-type GAMs.

266 of the oral lesions revealed a subepithelial infiltrate that was primarily composed of CD3- and CD4-p

267 T cells infiltrate the CNS in multiple sclerosis, yet little is

268 c peripherally activated CD4(+) T cells that infiltrate the retina.

269 t a later time point, inflammatory monocytes infiltrate the spleen parenchyma but remain mainly intra

270 M-MDSCs infiltrated the vaccine injection site, but not vaccine-

271 der to limit the number of activated T cells infiltrating the CNS.

272 atrix protein synthesis, and the macrophages infiltrating the dystrophic muscles were the source of m

273 METHODS AND Leukocytes infiltrating the failing heart were analyzed by a multis

274 T cells infiltrating the injured heart significantly upregulated

275 nterstitial macrophages (IMs) from monocytes infiltrating the lung or mobilized from the spleen.

276 flammatory monocytic cells were not observed infiltrating the skin of DSS cases on whole-mount histol

277 cMy-mOVA-OT-II mice, yet more CD3(+) T cells infiltrated their myocardium when compared with TAC-oper

278 dies that were based on genotypes from tumor-infiltrated tissue to examine whether genotyping errors

279 infiltration of macrophages, and skewed this infiltrate toward M1 polarization.

280 Acute hypoxemic patients with bilateral infiltrates treated with high-flow nasal cannula present

281 25 expression is largely restricted to tumor-infiltrating Treg cells in mice and humans.

282 cgammaRs led to effective depletion of tumor-infiltrating Treg cells, increased effector to Treg cell

283 comparable with that of mouse GITR in tumor-infiltrating Tregs despite being drastically lower in ot

284 4166 downregulated FOXP3 mRNA in human tumor infiltrating Tregs, suggesting that, in addition to enha

285 The low apoptosis rate of infiltrating TTP-deficient neutrophils was comparable to

286 s with specificity for common pathogens also infiltrate tumors.

287 ultiple myeloid cell subsets that frequently infiltrate tumors.

288 Cytotoxic T cells infiltrating tumors are thought to utilize HIF transcrip

289 ions showed higher T cell and dendritic cell infiltrates vs. CONTROLS: Seven hundred and forty-three

290 On lesional biopsy, a lichenoid infiltrate was observed in the underlying dermis, predom

291 ome cases, cytogenetic studies of the dermal infiltrate were also performed.

292 While greater T-cell infiltrates were observed in lesional vs nonlesional AD,

293 nto CL group; 1 eye (8%) had sterile corneal infiltrates, which did not affect the final visual acuit

294 resulted in minimal to moderate lymphocytic infiltrate, while the original study observed sparse lym

295 d single-walled carbon nanotube (SWCNT) film infiltrated with 2,2,7,-7-tetrakis(N,N-di-p-methoxypheny

296 All pulmonary structures become infiltrated with benign-appearing spindle and epithelioi

297 In the clinic, breast tumors poorly infiltrated with immune cells are more resistant to tras

298 These tumors were more heavily infiltrated with tumor-associated neutrophils (TAN) and

299 e, mild B-lymphocyte and moderate macrophage infiltrates, with perivascular predominance as well as d

300 ysis showed absent to low-grade inflammatory infiltrates without cardiomyocyte necrosis.