ライフサイエンスコーパス: lamina propria

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

2 ing the basal epithelium from the underlying lamina propria.

3 tory population highly enriched in the colon lamina propria.

4 etwork of phagocytes in the small intestinal lamina propria.

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

6 01b(+) antigen-presenting cells (APC) in the lamina propria.

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

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

9 n colon adenocarcinomas and unaffected colon lamina propria.

10 nodes and Peyer's patches, as well as in the lamina propria.

11 3(-) intestinal macrophages (MPs) within the lamina propria.

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

13 municate with immune cells of the underlying lamina propria.

14 Fibrosis essentially was exclusive to the lamina propria.

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

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

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

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

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

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

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

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

23 nal lumen and the sterile environment of the lamina propria.

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

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

26 live GI eosinophils isolated from the murine lamina propria.

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

28 loss of Type 2 ILC (ILC2) in the intestinal lamina propria.

29 of IL17A and other inflammatory cytokines in lamina propria.

30 of other T helper fates or migration to the lamina propria.

31 erentiation, respectively, in the intestinal lamina propria.

32 lived, were observed to localize only in the lamina propria.

33 biologically active IL-10 to the intestinal lamina propria.

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

35 n type 3 innate lymphoid cells (ILC3) in the lamina propria.

36 roducing macrophages in the inflamed colonic lamina propria.

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

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

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

40 is associated with bacterial invasion of the lamina propria, accompanied by induction of inflammation

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

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

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

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

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

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

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

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

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

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

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

52 of Peyer's Patches while cell numbers in the lamina propria and intraepithelial lymphocytes are unaff

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

54 eal B1b cells, which culminates in increased lamina propria and luminal IgA.

55 4-HNE-protein adducts were found in the lamina propria and macrophages in areas of colorectal in

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

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

58 tion, and 16S ribosomal RNA gene sequencing; lamina propria and mesenteric lymph node tissues were an

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

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

61 ts in a larger influx of immune cells in the lamina propria and mice with high parasitemia display sp

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

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

64 cells expressing all tested cytokines in the lamina propria and the epithelium was higher in CD patie

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

66 and gene expression profiles in both the gut lamina propria and the tumor microenvironment.

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

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

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

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

71 the carcinomas were tiny and confined to the lamina propria, and 1 was transmural.

72 nodes, IgG(+) and IgA(+) plasmablasts in the lamina propria, and Abs in intestinal fluid.

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

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

75 pulations of CD103-expressing DCs in the gut lamina propria are enhanced by the activation of NOD2, i

76 -producing neurons (VIPergic neurons) in the lamina propria are in close proximity to clusters of ILC

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

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

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

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

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

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

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

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

85 ncreased the exposure of the bacteria to the lamina propria by injecting HBUS mice with diphtheria to

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

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

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

89 the intraepithelial CD3(+) T-lymphocyte and lamina propria CD138(+) plasma cell densities simultaneo

90 Lamina propria CD20 cells were persistently elevated in

91 th microscopic inflammation showed increased lamina propria CD20 levels.

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

93 cosal intraepithelial lymphocytes (IELs) and lamina propria CD3, CD4, CD8, and CD20 lymphocytes were

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

95 d changes in gene and cytokine expression by lamina propria CD4(+) T cells, many of which were BHLHE4

96 omplex 1 (MTORC1) nutrient responsiveness in lamina propria CD4+ lymphocytes.

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

98 Intraepithelial and lamina propria CD8 Trm cells showed a high clonal overla

99 Functionally, lamina propria CD8 Trm cells were potent cytokine produc

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

101 l epithelial death and significantly reduced lamina propria cell apoptosis.

102 4%; 1% Q-GRFT: median 7%) and of the CD4(+) lamina propria cells (placebo: median 30%; 0.1-1% Q-GRFT

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

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

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

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

116 e intraepithelial compared with the adjacent lamina propria compartment.

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

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

119 Duodenal lamina propria crypt CD4 T cells were decreased in CG, a

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

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

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

123 Lamina propria DCs containing parasites were negative fo

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

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

126 Lamina propria dendritic cell phenotype and cytokine pro

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

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

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

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

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

132 rophages in the submucosa, which differ from lamina propria DP macrophages, may be missed from pinch

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 ial height in proportion to thickness of the lamina propria (epithelium-lamina propria ratio).

136 cretion from T helper 17 (Th17) cells of the lamina propria, followed by the expansion of the circula

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

138 ells and IL27(+) DCs were increased in colon lamina propria from Ffar2(fl/fl)CD11c-Cre mice with coli

139 The colonic lamina propria from patients with CD was infiltrated by

140 Colon lamina propria from Ptpn2-LysMCre mice had significant i

141 3 promotes XCL1 secretion by small intestine lamina propria gammadelta T cells that, in turn, induces

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

143 atory gene expression in duodenal tissue and lamina propria immune cells by flow cytometry analysis.

144 -) SP macrophages, which predominated in the lamina propria in animals with SIV infection that were e

145 as increased in the airway smooth muscle and lamina propria in COPD tissue, but not asthma, when comp

146 5 to sustain ILC2 homeostasis in the resting lamina propria in mice.

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

148 tion, and submucosal edema/separation of the lamina propria in the ileocecal region and colon within

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

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

151 h increased bacterial translocation from the lamina propria into the bloodstream.

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

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

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

155 sion of IL-15 in both the epithelium and the lamina propria is required for the development of villou

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

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

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

159 Chronic ethanol consumption alters lamina propria leukocyte response to stimulation in a re

160 transcriptional and functional responses of lamina propria leukocytes (LPLs) isolated from the 4 maj

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

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

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

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

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

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

167 ed from urothelium into suburothelium (SubU)/lamina propria (LP) activate mechanisms controlling detr

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

169 d intact urothelium and suburothelium (SubU)/lamina propria (LP) and lacked the DSM and the serosa.

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

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

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

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

174 s were significantly increased in intestinal lamina propria (LP) of TCRbetaxdelta(-/-) mice after tra

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

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

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

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

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

180 ectively) as well as in GALT-free intestinal lamina propria (LP).

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

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

183 estine: intraepithelial lymphocyte (IEL) and lamina propria lymphocyte (LPL) activation status and cy

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

185 In lamina propria lymphocytes (LPLs), STAT4 activation by L

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

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

188 Fusing intestinal lamina propria lymphocytes from mice monocolonized with

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

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

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

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

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

194 and TRIF and required IFNgamma secretion by lamina propria lymphocytes.

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

196 Whether IL10R regulates lamina propria macrophage function during infant develop

197 Lamina propria macrophages (LpMs) preferentially express

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

199 S100 proteins were expressed by lamina propria macrophages in intestinal tissues from in

200 row-derived macrophages and dendritic cells, lamina propria macrophages, and mesenteric lymph node de

201 A9 in mice altered the phenotypes of colonic lamina propria macrophages, compared with wild-type mice

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

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

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

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

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

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

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

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

210 Lamina propria mononuclear cells and T cells were isolat

211 T cells and lamina propria mononuclear cells from mice were analyzed

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

213 13, and decreased production of IFN-gamma in lamina propria mononuclear cells in vivo.

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

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

216 SAPs channel food allergens to lamina propria mucosal mast cells through an IL-13-CD38-

217 In the lamina propria, noradrenergic-dependent increases in gut

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

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

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

221 17A and IL-17F expression in nasal/bronchial lamina propria of atopic mild-to-severe asthmatics and c

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

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

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

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

226 er (NK) cells was accumulated in the colonic lamina propria of Gitr(-/-) mice as compared to wild-typ

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

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

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

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

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

232 Treg cells isolated from peripheral blood or lamina propria of patients with CD and healthy individua

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

234 Lamina propria of Pggt1b(DeltaCD4) mice had increased nu

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

236 Stage T1 bladder cancers invade the lamina propria of the bladder and, despite sharing many

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

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

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

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

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

242 ction does not establish plasma cells in the lamina propria of the female reproductive tract.

243 The lamina propria of the gastrointestinal tract and other m

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

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

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

247 )CD206(+) DP macrophages predominated in the lamina propria of uninfected animals, compared with CD16

248 signals in the colon that gain access to the lamina propria once the mucosal barrier mucosa is compro

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

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

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

252 hip between microbiome and the maturation of lamina propria perivascular macrophages into a tight ana

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

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

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

258 lly, clopidogrel led to increased epithelium-lamina propria ratio while iron deposition was impaired.

259 thickness of the lamina propria (epithelium-lamina propria ratio).

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

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

265 a, structurally formed by the epithelium and lamina propria, serves as a selective barrier that separ

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

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

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

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

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

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

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

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

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

275 rleukin-15 (IL-15) in the gut epithelium and lamina propria that is characteristic of active coeliac

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

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

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

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

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

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

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

283 ated with neutrophil infiltration of the gut lamina propria, type 1 interferon activation, increased

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

285 rk intimately adherent to the entire mucosal lamina propria vasculature.

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

287 CEACAM6 in the lamina propria was localized to neutrophils predominantl

288 138(+) plasma cells from Peyer's patches and lamina propria were analyzed by flow cytometry and IgA r

289 (+)CD206(+) DP intestinal macrophages of the lamina propria were destroyed after SIV infection and re

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

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

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

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

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

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

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

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

298 ken after 7d dosing demonstrated V565 in the lamina propria with co-immunostaining on CD3(+) T-lympho

299 ntestinal mucosa and activated pSTAT3 in the lamina propria with limited systemic distribution.

300 all-sized lymphoid infiltrate, expanding the lamina propria, with a non-destructive appearance.