ライフサイエンスコーパス: lamina propria

1 3(-) intestinal macrophages (MPs) within the lamina propria.

2 conserved receptors on CD4(+) T cells in the lamina propria.

3 municate with immune cells of the underlying lamina propria.

4 Fibrosis essentially was exclusive to the lamina propria.

5 s, the most abundant immune cell type in the lamina propria.

6 roducing macrophages in the inflamed colonic lamina propria.

7 d in vivo at the site of inflammation in the lamina propria.

8 on of T cells into the small intestinal (SI) lamina propria.

9 ability to rapidly deplete CD4(+) T cells in lamina propria.

10 crophages, neutrophils, and monocytes in the lamina propria.

11 ducing innate lymphoid cells (ILCs) in colon lamina propria.

12 toward TH1-dominant immune responses in the lamina propria.

13 EoE, in addition to select cells within the lamina propria.

14 ed in loss of NKp46+ ILC22 in the intestinal lamina propria.

15 ng the RALDH-3 expressing fibroblasts of the lamina propria.

16 increased in the epithelium, but not in the lamina propria.

17 in response to detection of flagellin in the lamina propria.

18 live GI eosinophils isolated from the murine lamina propria.

19 h a diminution in CD103(+) DC numbers in the lamina propria.

20 variables and connective tissue loss in the lamina propria.

21 the intraepithelial compartment and into the lamina propria.

22 R/IL-17 double-positive MCs within bronchial lamina propria.

23 ithelial cells and inflammatory cells in the lamina propria.

24 APC subsets in the small and large intestine lamina propria.

25 eased leukocyte recruitment into the colonic lamina propria.

26 bone marrow or isolated from small intestine lamina propria.

27 epithelium, as well as in fibroblasts in the lamina propria.

28 ar system for exocytosis into the intestinal lamina propria.

29 as observed in cells of the small intestinal lamina propria.

30 al epithelial barrier and gain access to the lamina propria.

31 loss of Th17 cells from the small intestinal lamina propria.

32 t inside epithelial cells and within colonic lamina propria.

33 -stabilizing cytokines within the intestinal lamina propria.

34 )CD64(+)CX3CR1(+) macrophages in the gastric lamina propria.

35 ing the basal epithelium from the underlying lamina propria.

36 tory population highly enriched in the colon lamina propria.

37 etwork of phagocytes in the small intestinal lamina propria.

38 ers of DCs in the mesenteric lymph nodes and lamina propria.

39 01b(+) antigen-presenting cells (APC) in the lamina propria.

40 ose tissue, skeletal muscle, and the colonic lamina propria.

41 e-resident memory T cells (TRM cells) in the lamina propria.

42 n colon adenocarcinomas and unaffected colon lamina propria.

43 Experiment 1: PN significantly reduced lamina propria (1) CD4CD25 (activated) and (2) CD4CD25LP

44 PN significantly reduced lamina propria (1) IgD (naive), (2) IgDLPAM (antigen-act

45 PN reduces lamina propria activated and T regulatory cells and also

46 s with increased IL-13 immunostaining in the lamina propria also had increased IL-4 and TSLP expressi

47 mphoid organs including the gastrointestinal lamina propria, alveolar macrophages in lung, and epithe

48 atomic distribution of virus with sparing of lamina propria and a lack of microbial translocation.

49 d numbers of CD4(+) alphabeta T cells in the lamina propria and activation of T cell receptor gammade

50 fibrocytes of the tunica adventitia and the lamina propria and an inner epithelial lining composed o

51 eak of viremia but only transiently infected lamina propria and caused little or no acute depletion o

52 development of T helper 2 (Th2) cells in the lamina propria and eosinophilic enteritis and fibrosis i

53 is highly expressed both in the cells of the lamina propria and epithelium.

54 ndothelial apoptosis in the small intestinal lamina propria and facilitated recovery of crypt SCCs, p

55 an attempt to combat escaped microbes in the lamina propria and in distal tissues.

56 s identified within lymphatic vessels of the lamina propria and in spaces of >5 mum between a small n

57 opy studies revealed a lack of lipids in the lamina propria and intercellular space in Gpat3(-/-) mic

58 d the expression of TREM-2 in the intestinal lamina propria and its role in the development of coloni

59 ler T (iNKT) cells accumulate in the colonic lamina propria and lung, resulting in increased morbidit

60 4-HNE-protein adducts were found in the lamina propria and macrophages in areas of colorectal in

61 ially in the neuronal fibers innervating the lamina propria and mechanoreceptors.

62 we define four DC subsets present within the lamina propria and mesenteric lymph node compartments ba

63 D45RA(-) ) were isolated from the intestinal lamina propria and mesenteric lymph nodes (MLNs), and th

64 onal dendritic cells (cDC) in the intestinal lamina propria and mesenteric lymph nodes were GFP(+) Ho

65 f Ly6C(+)CD11b(+)MHCII(+) macrophages in the lamina propria and mesenteric lymph nodes.

66 CD8(+)/CD103(+) Tregs within the intestinal lamina propria and mesenteric lymph nodes.

67 sient infection of CD4(+) T cells in the gut lamina propria and no microbial translocation.

68 to pathogenesis of diabetes (small intestine lamina propria and pancreatic lymph node).

69 in inflammatory microenvironments within the lamina propria and suggest that this subset has a critic

70 is not clear how the immune responses in the lamina propria and the epithelium, separated by a baseme

71 eview the immune processes that occur in the lamina propria and their potential effects on epithelial

72 rosis via TLR2 signaling on monocytes in the lamina propria and TNFRI signaling on intestinal epithel

73 ss of CD11b(+)CD103(+) DCs in the intestinal lamina propria and to a corresponding decrease of IL-17-

74 sically activated macrophages in the colonic lamina propria and worsened the severity of inflammation

75 plasma cells, and lymphocytes located in the lamina propria and, to a lesser extent, lymphocytes in t

76 (2) IgDLPAM (antigen-activated homed to the lamina propria) and CD44 memory B cells, whereas PN-BBS

77 en, mesenteric lymph nodes, small intestinal lamina propria, and colonic lamina propria was determine

78 ion, T cell infiltration into the intestinal lamina propria, and IFN-gamma production by colitogenic

79 ove and interact with bacteria in the lumen, lamina propria, and lymphoid tissue of the colon.

80 enterocytes, diffusive distribution over the lamina propria, and subsequent transport through lacteal

81 sustentacular cells, deep fibroblasts of the lamina propria, and the superficial fibroblasts, respect

82 Lamina propria APCs could be subdivided into CD11c(+)CD1

83 h muscle populations in the adult intestinal lamina propria are highly sensitive to the level of Hh l

84 f CD39(+)CD161(+) CD4(+) T cells in blood or lamina propria are noted in patients with CD, and levels

85 with the amount of connective tissue in the lamina propria as determined by image analysis.

86 on prevented increases in B220+ cells in the lamina propria as well as mucosal Il4 and Il5 mRNA in re

87 howed increased numbers of Th17 cells in the lamina propria at steady state, in lymph nodes after imm

88 ophilic degranulation in both epithelium and lamina propria, basal zone hyperplasia, and the presence

89 ritic) cells were frequently observed in the lamina propria below epithelial infectious centers.

90 ) regulatory T cells specifically within the lamina propria but not other secondary lymphoid tissues.

91 expansion and proteolytic remodeling of the lamina propria, but few studies have examined these chan

92 perforin expression was downregulated in the lamina propria, but not in the epithelium.

93 under normal conditions colonization of the lamina propria by glial cells commences during early pos

94 Infiltration of the lamina propria by peripherally expanded CD8(+) T cells w

95 opulation was distinguished from that of the lamina propria by the absence of CD4+CD11c+ cells and an

96 emonstrate that dendritic cells (DCs) of the lamina propria can sample and process both circulatory a

97 l steady-state migration of small intestinal lamina propria CD103(+) DCs into the MLN.

98 rcentages of IFN-gamma- and IL-17A-producing lamina propria CD3+D4+ T cells compared with Rag1(-/-) r

99 ls of interleukin 17 (IL-17) expression from lamina propria CD4(+) cells than from cells from animals

100 Experiment 2: PN significantly reduced lamina propria CD4CD25Foxp3 T regulatory cells compared

101 indings demonstrate that intraepithelial and lamina propria CD8(+) T cells exhibit different dynamics

102 h muscle precursors further diversified into lamina propria cells directly adjacent to the ureteric e

103 eins, WARS and S100A8, were more abundant in lamina propria cells during the acute stage of cholera.

104 g of isolated intestinal intraepithelial and lamina propria cells eliminated type II refractory celia

105 olone or 2,4,6-trinitrobenzenesulfonic acid; lamina propria cells from these mice expressed lower lev

106 Lamina propria cells in colon tissues of patients with I

107 Macrophages were isolated from lamina propria cells of mice, IL1beta production was mea

108 Immunomonitoring of lamina propria cells revealed loss of virtually all IL-2

109 NOD2), or dextran sodium sulfate; intestinal lamina propria cells were collected and analyzed.

110 Epithelial and lamina propria cells were isolated and analyzed by immun

111 icile induces tryptophan catabolism in cecal lamina propria cells, which restricts C. difficile-assoc

112 ying connective tissue to surround a core of lamina propria cells.

113 Ly6C(hi) monocyte recruitment to the colonic lamina propria (cLP) during infection, which prevent dis

114 NF-kappaB activity in the crypt-denuded lamina propria (CLP) increased within 24 h postinfection

115 17F and IL-17A expression in nasal/bronchial lamina propria compared to MA and controls, and a higher

116 -17(+)CD4(+) T cells in the large intestinal lamina propria compared with littermate controls.

117 of CD8 T cells in the intraepithelial versus lamina propria compartment.

118 e intraepithelial compared with the adjacent lamina propria compartment.

119 CX3CR1(+) macrophages in the intestinal lamina propria contribute to gut homeostasis through the

120 cialized taste buds, the basal lamina, and a lamina propria core with matrix molecules, fibroblasts,

121 We conclude that lamina propria CX3CR1(+) DCs facilitate the surveillance

122 Finally, overall apoptosis of lamina propria DC subsets was increased during infection

123 VentX expression was elevated in intestinal lamina propria DCs (LPDCs) of inflamed mucosa from infla

124 Lamina propria DCs containing parasites were negative fo

125 remodelling after 12 weeks, both within the lamina propria (decreased thickness, p = 0.005) and with

126 By using conditional depletion of lamina propria dendritic cell (LPDC) subsets, we demonst

127 Lamina propria dendritic cell phenotype and cytokine pro

128 e steady-state migration of small intestinal lamina propria dendritic cells (DCs) into draining mesen

129 Although both TLR5 and CD172alpha(+) lamina propria dendritic cells (LPDC) have been shown to

130 Activation of lamina propria dendritic cells and T cells was analyzed

131 appear to play a role in antigen capture by lamina propria dendritic cells in the steady state.

132 axonal damage via long-lasting imprinting on lamina-propria-derived Treg cells.

133 T lymphocytes residing in the human colonic lamina propria, encountered by Shigella upon its crossin

134 nd dilated intercellular spaces; P < .0001), lamina propria eosinophilia (P < .0001), and fibrosis (P

135 -10, CD4(+)CD44(+) T cells isolated from the lamina propria exhibited lower levels of the repressive

136 D2 mutant CX3CR1(+) myeloid cells within the lamina propria fail to exhibit the characteristic morpho

137 red eighty-six biopsy specimens had adequate lamina propria for evaluation of subepithelial remodelin

138 rtant role in positioning these cells in the lamina propria for proper IgA production to maintain int

139 studying the function of both peripheral and lamina propria FOXP3+ lymphocytes in patients with the h

140 The GI lamina propria from CD22 gene-targeted mice harbored mor

141 n pre-diabetic male PAT mice, the intestinal lamina propria had lower Th17 and Treg proportions and i

142 5 to sustain ILC2 homeostasis in the resting lamina propria in mice.

143 in epithelium and glands but not within the lamina propria in NPs.

144 ls was not observed in ileum, and the entire lamina propria in sections of duodenum, jejunum, and ile

145 n the dermis of the skin but not the mucosal lamina propria, in the absence of a connective tissue in

146 lium, often accompanied by loosely organized lamina propria infiltrates.

147 was increased in airway epithelial cells and lamina propria inflammatory cells in severe asthma compa

148 cancer, particularly for patients with deep lamina propria invasion combined with other risk factors

149 gnostic factors in HGT1 bladder cancer, deep lamina propria invasion had the largest negative impact,

150 Fibrosis of the esophageal lamina propria is a known complication of eosinophilic e

151 II flow cytometer analyzed Peyer patches and lamina propria isolated lymphocytes for homing phenotype

152 gh expression of PLZF and their absence from lamina propria; iTh17 cells are found therein.

153 nificant upregulation in both epithelial and lamina propria leukocyte (LPL) compartments.

154 creased MAPK (p-P38 and p-JNK) activation in lamina propria leukocytes as well as decreased NFkappaB

155 amples were collected from patients with CD; lamina propria leukocytes were isolated and expression o

156 Incubation of intestinal lamina propria leukocytes with granulocyte-macrophage co

157 of CD4(+) T cell depletion predominantly in lamina propria leukocytes.

158 tory T cells (Tregs), to the large intestine lamina propria (LILP).

159 of hematopoietic elements in the small bowel lamina propria, liver, and spleen was present for greate

160 on, CD11b(-) CD8(+) DC were activated in the lamina propria (LP) and acquired the ability to process

161 These cells originate in the lamina propria (LP) and migrate to the mesenteric lymph

162 Dendritic cells (DCs) in the intestinal lamina propria (LP) are composed of two CD103(+) subsets

163 istinct APC populations exist in the mucosal lamina propria (LP) below the intestinal epithelium, but

164 associated bacteria and isolated small-bowel lamina propria (LP) cells.

165 tially expressed by small intestine CD103(+) lamina propria (LP) DCs.

166 Abnormal handling of E. coli by lamina propria (LP) macrophages may contribute to Crohn'

167 diately after scar ablation, we transplanted lamina propria (LP) of the olfactory mucosa alone or in

168 sion in cells residing in the lung, airways, lamina propria (LP) of the small intestine, brain, visce

169 xhibit inflammatory cell infiltration in the lamina propria (LP) of their small intestine, they do no

170 Lamina propria (LP) T helper 17 (Th17) cells participate

171 The lamina propria (LP) underlies the expansive single-cell

172 on Ag encounter and subsequently home to the lamina propria (LP) where they mediate effector function

173 ment also occurs within the mouse intestinal lamina propria (LP), where the associated V(D)J recombin

174 he epithelium and the papillary layer of the Lamina propria (LP), whereas CD68+ macrophages, CD117+ m

175 cular basement membrane (Rbm) and underlying lamina propria (LP).

176 h1 and Th17 cells in normal human intestinal lamina propria (LP).

177 translocation of commensal bacteria into the lamina propria (LP).

178 nduction among lymphocytes in the intestinal lamina propria (LPL) and cervical lymph nodes (CLN).

179 Using colonic lamina propria lymphocytes (LPL) and peripheral blood ly

180 Normal human lamina propria lymphocytes (LPLs) induce differentiation

181 nflammatory cytokine levels were elevated in lamina propria lymphocytes (LPLs).

182 IL-17(+) FoxP3(+) cell population in CD4(+) lamina propria lymphocytes derived from patients with UC

183 port that the major population of intestinal lamina propria lymphocytes expressing IL-1 receptor 1 (I

184 Fusing intestinal lamina propria lymphocytes from mice monocolonized with

185 generate Ts cell lines from freshly isolated lamina propria lymphocytes from patients with ulcerative

186 ions between intestinal epithelial cells and lamina propria lymphocytes give rise to a population of

187 ions between intestinal epithelial cells and lamina propria lymphocytes give rise to a population of

188 and IL-17 production were assessed in CD4(+) lamina propria lymphocytes isolated from IBD patients an

189 cosal tissues, including intraepithelial and lamina propria lymphocytes of the small intestine, Peyer

190 piratory tract (RT) and GALT Peyer patch and lamina propria lymphocytes, lowers gut and RT immunoglob

191 d within the intestinal epithelium and among lamina propria lymphocytes.

192 +) IEL but not in CD8alphaalpha(+) IEL or in lamina propria lymphocytes.

193 Whether IL10R regulates lamina propria macrophage function during infant develop

194 Lamina propria macrophages (LpMs) preferentially express

195 erance to intestinal microbiota by rendering lamina propria macrophages hyporesponsive to commensal b

196 intestinal tissues, LRRK2 is detected in the lamina propria macrophages, B-lymphocytes, and CD103-pos

197 o increased survival of epithelial cells and lamina propria macrophages, higher IL-6 expression owing

198 ers of live S typhimurium recovered from the lamina propria, mesenteric lymph nodes, spleen, and live

199 3(-)) cells account for 80% of mouse colonic lamina propria MHC-II(hi) cells.

200 f bacteria, proliferation in colonic crypts, lamina propria mononuclear cell function, and T-cell act

201 , IL-1beta, and TNF-alpha or supernatants of lamina propria mononuclear cells (LPMC) and evaluated fo

202 polygyrus bakeri-infected Rag mice added to lamina propria mononuclear cells (LPMC) isolated from co

203 Mainly the transcriptome of lamina propria mononuclear cells (LPMC) was affected by

204 Isolated lamina propria mononuclear cells (LPMCs) and mucosal tis

205 We also analyzed TIMP-3 levels in lamina propria mononuclear cells (LPMCs) collected from

206 ate tumor-infiltrating leukocytes (TILs) and lamina propria mononuclear cells (LPMCs) from the tumor

207 Lamina propria mononuclear cells and T cells were isolat

208 expression of NFIL3 was observed in CD14(+) lamina propria mononuclear cells from Crohn's disease an

209 Furthermore, colonic CD11b(+) lamina propria mononuclear cells from Nfil3(-/-) mice sp

210 We measured levels of TREM-2 in lamina propria mononuclear cells from surgical specimens

211 13, and decreased production of IFN-gamma in lamina propria mononuclear cells in vivo.

212 CD11b(+) lamina propria mononuclear cells, comprising predominant

213 agonists is recapitulated in vitro in mouse lamina propria mononuclear cells, human colonic epitheli

214 ly member IL-22 was demonstrated in CD11b(-) lamina propria mononuclear cells.

215 sed expression of HO-1 and IL-10 in CD11b(+) lamina propria mononuclear cells.

216 ared with WT and IL-10(-/-) colonic CD11b(+) lamina propria mononuclear cells.

217 y, NLRP3(R258W) functions exclusively in the lamina propria mononuclear phagocytes to directly enhanc

218 resence of human neutrophil peptide-positive lamina propria neutrophils in biopsy tissue samples.

219 BS had a significant increase in the area of lamina propria occupied by neuronal-specific enolase-pos

220 rom the mesenteric lymph nodes (MLNs) to the lamina propria occurs via gut-homing signals.

221 When E. histolytica trophozoites invade the lamina propria of a host colon, extracellular matrices a

222 e number of perforin-expressing cells in the lamina propria of acutely HIV-infected patients was posi

223 icantly increased in the aortas, spleen, and lamina propria of aged Apoe(-/-) mice compared with age-

224 ificantly increased in airway epithelium and lamina propria of asthmatic patients, particularly in pa

225 17A and IL-17F expression in nasal/bronchial lamina propria of atopic mild-to-severe asthmatics and c

226 d cytotoxic T cells was found in the gastric lamina propria of both infected groups.

227 decreased CD4 and CD8 T-cell numbers in the lamina propria of both small and large intestines under

228 In contrast, the lamina propria of Cxcr6(-/-) mice was devoid of ILC3s.

229 ltrate, and loss of connective tissue in the lamina propria of gingival biopsies (P <0.01, Spearman t

230 MPs isolated from the colon lamina propria of IFNAR1(-/-) mice produced less IL-10,

231 a significant reduction of Th17 cells in the lamina propria of ITF2357-treated animals, resulting in

232 favored Th17 responses in spleen and colonic lamina propria of mice with CDAD.

233 or small cell clusters in the subepithelial lamina propria of monkeys infected with either virus.

234 scar ablation followed by transplantation of lamina propria of olfactory mucosa and cultured olfactor

235 ied gluten peptides are also abundant in the lamina propria of patients with celiac disease.

236 Th17 and Treg cells isolated from intestinal lamina propria of patients with IBD to investigate their

237 us infection, dendritic cells (DCs) from the lamina propria of Rag mice displayed decreased expressio

238 c CD8(+) T cell activity, was evident in the lamina propria of seronegative acutely HIV-infected pati

239 ents and most nerve fibers were found in the lamina propria of the cervical region of the vagina, whe

240 Furthermore, in the lamina propria of the colitis model, most wild-type Treg

241 tissue MPhis, such as those residing in the lamina propria of the colon and the dermis, as well as i

242 f T cells, B cells, and neutrophils into the lamina propria of the distal colon in mice fed the Delta

243 ed an abundant innervation in the intestinal lamina propria of the entire gastrointestinal tract prin

244 ll as by granular amoebocytes present in the lamina propria of the gut and in circulating blood.

245 optively transferred cells isolated from the lamina propria of the large intestine from wild type or

246 ondary lymphoid organs (SLOs) and within the lamina propria of the small intestine, respectively (C.

247 dy state is their ubiquitous presence in the lamina propria of the small intestine.

248 sis factor alpha increased in the intestinal lamina propria of wild-type mice following bile duct lig

249 OEG are present only in the olfactory lamina propria, olfactory nerve, and the outer two layer

250 ith higher FGT content (P <0.01) and thinner lamina propria (P </=0.03).

251 ), deeper crypts (p = 0.0053), and a thinner lamina propria (p = 0.0004).

252 AR was elevated in inflammatory cells in the lamina propria (P = 0.0019), bronchial epithelial (P = 0

253 , which regulate the reversible depletion of lamina propria phagocytes and inflammation in the small

254 stine via the fenestrated capillaries in the lamina propria prior to entering into the draining lymph

255 They were also less responsive to lamina proprias, producing less IL-12p40 and IL-10.

256 we demonstrate reprogramming of oral mucosal lamina propria progenitor cells from patients undergoing

257 In conclusion, oral mucosal lamina propria progenitor cells represent a source of ce

258 sk factor was depth of invasion (T1b/c) into lamina propria (progression: hazard ratio [HR], 3.34; P

259 ion of microbial molecules in the intestinal lamina propria rapidly stimulates innate immune signalin

260 nly systemic tissues but also the serosa and lamina propria region of the large intestine.

261 R1 expression in lung eosinophils, lung- and lamina propria-resident and alveolar macrophages, bone m

262 ceptor (IL-10Ralpha) mutations in intestinal lamina propria-resident chemokine receptor CX3CR1-expres

263 The mesenchymal elements of the intestinal lamina propria reviewed here are the myofibroblasts, fib

264 an increased ST2 content, restricted to the lamina propria's cellular infiltrate.

265 broblasts (IMFs) are cells in the intestinal lamina propria secreting factors that are known to modul

266 17 (Th17) population in the small-intestinal lamina propria (SI-LP) of the mouse gut.

267 sidual cells persist in the small intestinal lamina propria (siLP) of adult and neonatal Il7ra(-/-) m

268 e that the CX3CR1(+) myeloid cell within the lamina propria supports normal Paneth cell function thro

269 used intraepithelial T cell infiltration and lamina propria T cell activation.

270 Defective apoptosis of lamina propria T cells (LPTs) is involved in the pathoge

271 We observed increased expression of GATA3 by lamina propria T cells from mice with colitis compared w

272 IFN-gamma production was increased in lamina propria T cells isolated from KSR1(-/-) and KSR1(

273 oscopic inflammation, increased apoptosis of lamina propria T lymphocytes, and significantly reduced

274 Following the initial experiment 1 protocol, lamina propria T regulatory cell phenotype was evaluated

275 CD4CD25LPAM-1 (activated cells homed to the lamina propria) T cells, whereas PN-BBS assimilated chow

276 ous bacteria, into GF animals reinstated the lamina propria Th17 cell compartment and production of a

277 In addition, we found that the abundance of lamina propria Th17, but not Th1, cells is highly correl

278 nd was characterized by increased numbers of lamina propria TH2 cells, mast cells, and eosinophils, s

279 the bacterial population in the gut lumen or lamina propria that cause inflammation at this site.

280 lear apoptotic neutrophils in the intestinal lamina propria, thereby favoring a tumor-promoting envir

281 maximal high-power field, mainly in the deep lamina propria; these levels were greater than in tissue

282 Mucosal thickness, lamina propria thickness (defined as the extent of subep

283 Lamina propria thickness (P >0.21) and proportions of CT

284 +) alphabeta T cells in the small intestinal lamina propria, this increase was absent in antibiotic-t

285 s were defective in migration from the ileal lamina propria to the MLN.

286 tology showing polymorph infiltration of the lamina propria, transmural involvement, and micro absces

287 and damage of the gallbladder epithelium and lamina propria up to 2 months after Salmonella infection

288 small intestinal lamina propria, and colonic lamina propria was determined in specific pathogen-free

289 In these animals, the gastric lamina propria was infiltrated with lymphoid cells organ

290 CEACAM6 in the lamina propria was localized to neutrophils predominantl

291 metry data, neutrophils and monocytes in the lamina propria were preferentially associated with paras

292 IL-23R(+) gammadelta T cells in the colonic lamina propria were the primary producers of early, gut-

293 itro but it increases the width of the nasal lamina propria when delivered intranasally.

294 hey are most abundant in the small intestine lamina propria, where their presence requires colonizati

295 larly to Peyer's patches and small intestine lamina propria, where they upregulate LAP, downregulate

296 stine, pT(regs) are located primarily in the lamina propria, whereas intraepithelial CD4(+) T cells (

297 in SI; Mf3 formed a dense network in mucosal lamina propria, whereas Mf4 was enriched in submucosa.

298 ubsets of CD11c(+) and CD11b(+) cells of the lamina propria, which also increase after ISS-oligodeoxy

299 tive barrier between the anaerobic lumen and lamina propria, which has a high rate of metabolism.

300 thelium and in immune cells recruited in the lamina propria, which suggests that JNKBP1 contributes t