ライフサイエンスコーパス: intraepithelial lymphocyte

1 fic CD8 T cells in comparison to gut mucosal intraepithelial lymphocytes.

2 uired a surface phenotype resembling that of intraepithelial lymphocytes.

3 e of gammadelta T cells and TCRgammadelta(+) intraepithelial lymphocytes.

4 ransforming growth factor beta production by intraepithelial lymphocytes.

5 imilar to that observed for mouse regulatory intraepithelial lymphocytes.

6 d subepithelial collagen plate and increased intraepithelial lymphocytes.

7 -expressing cells, including most intestinal intraepithelial lymphocytes.

8 ymphoid tissues tested, including intestinal intraepithelial lymphocytes.

9 nction as a homing or retention molecule for intraepithelial lymphocytes.

10 lls including gammadelta TCR-positive (TCR+) intraepithelial lymphocytes.

11 cells, CD8+ T lymphocytes, and TCRgammadelta intraepithelial lymphocytes.

12 e in intimate contact with subepithelial and intraepithelial lymphocytes.

13 nducing proliferation of cultured intestinal intraepithelial lymphocytes.

14 unity, including reduced type 1 alarmins and intraepithelial lymphocytes.

15 elta T cells, innate lymphoid cells, and gut intraepithelial lymphocytes.

16 is spatially matched by Nkrp1g on subsets of intraepithelial lymphocytes.

17 FD promoted a decreased in the proportion of intraepithelial lymphocytes.

18 ected statistically significant elevation in intraepithelial lymphocytes (49%; 95% CI: 9%, 105%) and

19 Like adaptive TCR alphabeta+ T cells, intraepithelial lymphocytes, a subset enriched in TCR ga

20 to function in the regulation of intestinal intraepithelial lymphocyte activity.

21 mmune response in the small intestine and by intraepithelial lymphocytes after a single intraperitone

22 T cells, NKT cells, regulatory T cells, and intraepithelial lymphocytes all develop in the thymus an

23 olecules involved in pathogen elimination by intraepithelial lymphocytes and changed the intestinal m

24 ions and artifacts, including distinguishing intraepithelial lymphocytes and differentiating villous

25 beta(7)(+) DC (alphaE-DC) were distinct from intraepithelial lymphocytes and distinguishable from CD1

26 eraction between integrin alpha(E)beta(7) on intraepithelial lymphocytes and E-cadherin on epithelial

27 al tissues and cells, including increases in intraepithelial lymphocytes and fluid extravasation thro

28 In the ileum, the proportion of intraepithelial lymphocytes and goblet cells reduced, an

29 lpha E beta 7 is highly expressed on colonic intraepithelial lymphocytes and has been suggested to fu

30 found predominantly within the intestine as intraepithelial lymphocytes and have been shown to be in

31 EATL derives from a clonal proliferation of intraepithelial lymphocytes and is often disseminated at

32 Here we show that small intestinal intraepithelial lymphocytes and lamina propria lymphocyt

33 opulations of anatomically distinct T cells, intraepithelial lymphocytes and lamina propria lymphocyt

34 D8alpha(+) T and natural killer cells in the intraepithelial lymphocytes and lamina propria lymphocyt

35 Aberrant intraepithelial lymphocytes and lymphoma cells are intra

36 d with excess interferon-gamma production by intraepithelial lymphocytes and Myd88 activity.

37 on most small intestinal lamina propria and intraepithelial lymphocytes and on a small subset of per

38 Immunohistochemical studies of the intraepithelial lymphocytes and PCR amplification reveal

39 ratio [Vh:Cd]), and frequency of intestinal intraepithelial lymphocytes and peripheral gut-homing T

40 illus blunting, increased lamina propria and intraepithelial lymphocytes, and epithelial apoptosis, l

41 neutrophils with occasional crypt abscesses, intraepithelial lymphocytes, and goblet cells in the int

42 , CD8alphaalphaTCRalphabeta small intestinal intraepithelial lymphocytes, and innate memory phenotype

43 , CD8alphaalphaTCRalphabeta small intestinal intraepithelial lymphocytes, and innate memory phenotype

44 Intraepithelial lymphocytes are decreased following smal

45 as the immunoscore (IS) or quantification of intraepithelial lymphocytes are only slowly being adopte

46 Gamma delta intraepithelial lymphocytes are thought to coordinate re

47 while cell numbers in the lamina propria and intraepithelial lymphocytes are unaffected.

48 d 8), expressed predominantly by innate-like intraepithelial lymphocytes, as the ligand engaging epit

49 of CD8 alpha alpha homodimers in some of the intraepithelial lymphocytes, as well as low expression o

50 s, natural killer (NK) cells, and intestinal intraepithelial lymphocytes, as well as normalization of

51 significantly increased in cecal tonsil and intraepithelial lymphocytes at days 6 and 8, respectivel

52 ed IFN-gamma transcript levels in intestinal intraepithelial lymphocytes at this time.

53 These data demonstrate that gamma delta intraepithelial lymphocytes can protect the host from pa

54 y and follicular helper-like CD4(+) T cells, intraepithelial lymphocytes, CD8(+) and gammadelta T cel

55 is accompanied by a dramatic decrease in the intraepithelial lymphocyte CD8alpha(+)TCRgammadelta(+)/C

56 eta(+)CD4(-)CD8alpha(+)CD8beta(-) intestinal intraepithelial lymphocytes (CD8alphaalpha IELs) are an

57 f villous atrophy were numbers of gammadelta intraepithelial lymphocyte cells followed by age and hom

58 2.0 afterward; P = .0007; density of CD3(+) intraepithelial lymphocytes changed from 61 to 91 cells/

59 ncreased epithelial integrity, and decreased intraepithelial lymphocytes compared with controls.

60 ound in intestinal tissues, primarily in the intraepithelial lymphocyte compartment and lamina propri

61 secrete IL-4 and IFN-gamma is present in the intraepithelial lymphocyte compartment of the rat.

62 cells, which are abundant in the intestinal intraepithelial lymphocyte compartment.

63 n of CD8 T cells into the lamina propria and intraepithelial lymphocyte compartments.

64 Intraepithelial lymphocytes constitute a group of T cell

65 , a population of wild-type CD8alphaalpha(+) intraepithelial lymphocytes constitutively expressed gra

66 ion of the integrin CD103alpha(E)/beta(7) by intraepithelial lymphocytes controls the retention of ly

67 0.66); and the difference in change in total intraepithelial lymphocyte count was -12.73% (95% CI -77

68 umed oats, 0.24; 95% CI, 0.01-4.8; P = .35), intraepithelial lymphocyte counts (standardized mean dif

69 tween groups, morphologic changes and CD3(+) intraepithelial lymphocyte counts differed significantly

70 (villous height-to-crypt depth ratio; VHCD); intraepithelial lymphocyte counts; Marsh score; and pati

71 ased intraepithelial lymphocytes, markers of intraepithelial lymphocyte cytotoxicity, gliadin-specifi

72 Effects on intraepithelial lymphocyte density and symptoms suggest

73 Secondary end points included intraepithelial lymphocyte density, the Celiac Symptom I

74 Secondary endpoints were CD3-positive intraepithelial lymphocyte density; clinical symptoms me

75 Intestinal intraepithelial lymphocyte-derived interferon-gamma prot

76 C(lo) supports TCRalphabeta(+) CD8alphaalpha intraepithelial lymphocyte development; meanwhile, mTEC(

77 e dendritic epidermal T cells are prototypic intraepithelial lymphocytes, displaying an almost monocl

78 tains CD4(+)CD8alphaalpha(+) double-positive intraepithelial lymphocytes (DP IELs), which originate f

79 chronic inflammation, lymphocyte aggregates, intraepithelial lymphocytes, eosinophils, and villous bl

80 In contrast, most CD8 intraepithelial lymphocytes exhibited 2B4 but not NKG2A.

81 ale scRNA-seq, FACS, organoid generation and intraepithelial lymphocyte expansion.

82 at CD8+ T-cell receptor alphabeta intestinal intraepithelial lymphocytes express and secrete this cyt

83 addition, all intestinal lamina propria and intraepithelial lymphocytes express GPR-9-6.

84 A subpopulation of isolated human intestinal intraepithelial lymphocytes expressed the fractalkine re

85 rveillance behavior, we investigated whether intraepithelial lymphocytes expressing the gammadelta T

86 rveillance behavior, we investigated whether intraepithelial lymphocytes expressing the yd T cell rec

87 In addition, analysis of intestinal intraepithelial lymphocytes following feeding of OVA did

88 The change in the proportion of aberrant intraepithelial lymphocytes from baseline to week 12 wit

89 pha) and gamma interferon (IFN-gamma), while intraepithelial lymphocytes from calves with cryptospori

90 x vivo reverse transcriptase PCR of RNA from intraepithelial lymphocytes from control calves showed a

91 ce within the intestine through retention of intraepithelial lymphocytes, functional redistribution o

92 Here we show that gammadelta intraepithelial lymphocytes (gammadelta IEL) of the smal

93 Gammadelta intraepithelial lymphocytes (gammadelta IEL) reside at t

94 ists of both resident populations-gammadelta intraepithelial lymphocytes (gammadelta IELs)-and transi

95 Although intestinal intraepithelial lymphocytes have a distinct localization

96 ables were addressed in the small intestine: intraepithelial lymphocyte (IEL) and lamina propria lymp

97 In the gut, the Thy-1(+)TCRalphabeta(+) intraepithelial lymphocyte (IEL) compartment is surprisi

98 he proper development and composition of the intraepithelial lymphocyte (IEL) compartment.

99 tinal mucosa was significantly lower and the intraepithelial lymphocyte (IEL) count (x 100 enterocyte

100 both exhibit abnormal thymic and intestinal intraepithelial lymphocyte (IEL) development, but the de

101 ion, results in marked changes in intestinal intraepithelial lymphocyte (IEL) function and phenotype.

102 (CD103)beta 7 is thought to be important for intraepithelial lymphocyte (IEL) localization or functio

103 The function of the intraepithelial lymphocyte (IEL) network of T cell recep

104 The intraepithelial lymphocyte (IEL) network possibly compos

105 is study, we investigate how obesity impacts intraepithelial lymphocyte (IEL) persistence and functio

106 An early and rapid increase of the intraepithelial lymphocyte (IEL) population of orally in

107 specifically promotes a distinct CD8aa+CD4+ intraepithelial lymphocyte (IEL) population that acquire

108 mice appear normal, we demonstrated that the intraepithelial lymphocyte (IEL) populations of small (S

109 st selection of TCRalphabeta(+)CD8alphaalpha intraepithelial lymphocyte (IEL) progenitors (IELps), ev

110 D4(+) T helper functions and induction of an intraepithelial lymphocyte (IEL) program that included e

111 e reported that the pathogens induce a rapid intraepithelial lymphocyte (IEL) response important for

112 Peyer's patch (PP), lamina propria (LP), and intraepithelial lymphocyte (IEL) T cell populations were

113 To understand the relevance of intraepithelial lymphocyte (IEL)-derived KGF expression

114 We reveal a local intestinal intraepithelial lymphocyte (IEL)-GLP-1 receptor (GLP-1R)

115 is crucial for the development of intestinal intraepithelial lymphocytes (IEL) and delivery is mediat

116 aracterize the phenotype of large intestinal intraepithelial lymphocytes (IEL) and lamina propria leu

117 Intraepithelial lymphocytes (IEL) are a critical effecto

118 Intestinal intraepithelial lymphocytes (IEL) are an abundant popula

119 ro studies have demonstrated that intestinal intraepithelial lymphocytes (IEL) are constitutively cyt

120 Intestinal intraepithelial lymphocytes (IEL) are mostly CD8 single

121 Intestinal intraepithelial lymphocytes (IEL) bear a partially activ

122 TCR alpha beta+ intestinal intraepithelial lymphocytes (IEL) can express either the

123 In this context, intestinal intraepithelial lymphocytes (IEL) compose a large, highl

124 Intestinal intraepithelial lymphocytes (IEL) comprise a diverse pop

125 Previous studies have found that intraepithelial lymphocytes (IEL) contain virus-specific

126 Cytotoxic CD8alphabeta(+) intraepithelial lymphocytes (IEL) contribute to the deve

127 ntrol mice, TCR gammadelta and TCR alphabeta intraepithelial lymphocytes (IEL) developed efficiently

128 TCR agonist-driven CD8alphaalpha intestinal intraepithelial lymphocytes (IEL) development.

129 estinal lamina propria lymphocytes (LPL) and intraepithelial lymphocytes (IEL) during primary SIV inf

130 xpress CD8 alphabeta, whereas TCR alphabeta+ intraepithelial lymphocytes (IEL) express CD8 alpha alph

131 Previous analysis of intestinal intraepithelial lymphocytes (IEL) from nude mice and a v

132 opment of signature, murine TCRgammadelta(+) intraepithelial lymphocytes (IEL) in gut and skin depend

133 The importance of intraepithelial lymphocytes (IEL) in immunoprotection ag

134 tead, there were twice as many CD8alphaalpha intraepithelial lymphocytes (IEL) in mice that were reco

135 ession of IL-10 was produced specifically by intraepithelial lymphocytes (IEL) in the small intestine

136 Although homing of intraepithelial lymphocytes (IEL) into intestinal epithe

137 aggregates in the development of intestinal intraepithelial lymphocytes (IEL) is a matter of controv

138 TCR alphabeta(+), CD8alphabeta(+) intestinal intraepithelial lymphocytes (IEL) is dependent on MHC cl

139 Intraepithelial lymphocytes (IEL) of the intestine repre

140 The differentiation of intestinal intraepithelial lymphocytes (IEL) remains controversial,

141 The intestinal intraepithelial lymphocytes (IEL) represent multi-lineag

142 Analysis of engrafted intraepithelial lymphocytes (IEL) showed that they had a

143 Mouse small intestine intraepithelial lymphocytes (IEL) that express alphabeta

144 eaks, intervillous spaces, and the number of intraepithelial lymphocytes (IEL) were measured before a

145 enriched lamina propria lymphocytes (LPL) or intraepithelial lymphocytes (IEL) were transferred into

146 both GCT and CD11c on PP lymphocytes (PPL), intraepithelial lymphocytes (IEL), and lamina propria ly

147 development of naive CD8 T cells, intestinal intraepithelial lymphocytes (IEL), and natural killer (N

148 ion of T cell receptor gammadelta-expressing intraepithelial lymphocytes (IEL), but these changes wer

149 opment occurs in the thymus, some intestinal intraepithelial lymphocytes (IEL), including TCR gamma d

150 ls and in extrathymically derived intestinal intraepithelial lymphocytes (IEL).

151 d the hypothesis that they behave like other intraepithelial lymphocytes (IEL).

152 The number of intraepithelial lymphocytes (IELs) and immune phenotypes

153 Cell-to-cell interactions between intraepithelial lymphocytes (IELs) and intestinal epithe

154 Duodenal mucosal intraepithelial lymphocytes (IELs) and lamina propria CD

155 dramatic decrease in extrathymic intestinal intraepithelial lymphocytes (IELs) and natural killer 1.

156 Intestinal intraepithelial lymphocytes (IELs) are a large and diver

157 CD8alphaalpha intraepithelial lymphocytes (IELs) are abundant T cells

158 Intestinal intraepithelial lymphocytes (IELs) are characterized by

159 Intestinal intraepithelial lymphocytes (IELs) are located at the cr

160 gammadelta intraepithelial lymphocytes (IELs) are located beneath o

161 Intraepithelial lymphocytes (IELs) are located between e

162 nt of TCRalphabeta+CD8alphaalpha+ intestinal intraepithelial lymphocytes (IELs) are not thoroughly un

163 Locally resident intraepithelial lymphocytes (IELs) are primarily T cells

164 Intraepithelial lymphocytes (IELs) are T cells important

165 Murine small intestine intraepithelial lymphocytes (IELs) bear properties of bo

166 Intraepithelial lymphocytes (IELs) bearing the gammadelt

167 amined the effects of interleukin (IL)-15 on intraepithelial lymphocytes (IELs) because they resemble

168 Intestinal intraepithelial lymphocytes (IELs) exhibit prompt innate

169 e show that, although mouse small intestinal intraepithelial lymphocytes (IELs) expressed the CD43 co

170 Intraepithelial lymphocytes (IELs) expressing the TCRgam

171 Intraepithelial lymphocytes (IELs) from human intestinal

172 D134) in the activation of CD8(+) intestinal intraepithelial lymphocytes (IELs) has been studied usin

173 Intestinal intraepithelial lymphocytes (IELs) in mice include two m

174 Furthermore, gut intraepithelial lymphocytes (IELs) interact with neutrop

175 e of an enlarged clonal population of innate intraepithelial lymphocytes (IELs) lacking classical B-,

176 selection of CD8alphaalpha and CD8alphabeta intraepithelial lymphocytes (IELs) of the intestine, whi

177 Intraepithelial lymphocytes (IELs) play an important rol

178 Because intraepithelial lymphocytes (IELs) produce a number of c

179 Intraepithelial lymphocytes (IELs) represent a significa

180 The development of intestinal intraepithelial lymphocytes (IELs) requires the movement

181 Intestinal intraepithelial lymphocytes (IELs) reside in the gut epi

182 his model of intestinal inflammation, CD8(+) intraepithelial lymphocytes (IELs) secrete transforming

183 urn modulate a distinct population of CD4(+) intraepithelial lymphocytes (IELs) that express CD8alpha

184 lial cells (ECs) is a population of resident intraepithelial lymphocytes (IELs) that provide host-pro

185 termine the contribution Vgamma1+ intestinal intraepithelial lymphocytes (IELs) vs systemic Vgamma1+

186 , no expansion of CD8 alpha alpha intestinal intraepithelial lymphocytes (IELs) was observed, despite

187 estine tissues were collected and intestinal intraepithelial lymphocytes (IELs) were measured; we als

188 elta T cells isolated from murine intestinal intraepithelial lymphocytes (IELs) were separated into g

189 of naturally occurring Vgamma4(+)/Vdelta1(+) intraepithelial lymphocytes (IELs) with innate cytolytic

190 The gut epithelium is populated by intraepithelial lymphocytes (IELs), a heterogeneous T ce

191 , CD8alphaalpha(+)TCRalphabeta(+) intestinal intraepithelial lymphocytes (IELs), arose from a unique

192 uding natural killer (NK) cells, NK T cells, intraepithelial lymphocytes (IELs), CD8 T cells, and gam

193 sical lymphoid cells, broadly referred to as intraepithelial lymphocytes (IELs), intercalate the inte

194 such as TCRalphabeta((+))CD8alphaalpha((+)) intraepithelial lymphocytes (IELs), require full-agonist

195 isolation and purification of rat intestinal intraepithelial lymphocytes (IELs), we previously identi

196 ion requirements of TCR-alphabeta intestinal intraepithelial lymphocytes (IELs), we utilized the 2C t

197 mall intestine, the types of T(RM) cells are intraepithelial lymphocytes (IELs), which contain high l

198 pulated by CD8(+) alpha beta and gamma delta intraepithelial lymphocytes (IELs), which monitor the in

199 Specialized intraepithelial lymphocytes (IELs), which reside at thes

200 rface of T lymphocytes, including intestinal intraepithelial lymphocytes (IELs).

201 s, and distinct subpopulations of intestinal intraepithelial lymphocytes (IELs).

202 cularly for T cell receptor (TCR)-gammadelta intraepithelial lymphocytes (IELs).

203 n is different in colon and small intestinal intraepithelial lymphocytes (IELs).

204 re T cells, and subpopulations of intestinal intraepithelial lymphocytes (IELs).

205 eal immune cells commonly defined as DCs are intraepithelial lymphocytes (IELs).

206 that AHRR is vital to sustaining intestinal intraepithelial lymphocytes (IELs).

207 antigen-driven expansion of CD8alphabeta(+) intraepithelial lymphocytes (IELs).

208 l (CD8alphabeta and CD4) T cells, designated intraepithelial lymphocytes (IELs).

209 pha and were sequestered as CD8alphaalpha(+) intraepithelial lymphocytes (IELs).

210 celiac disease were villous atrophy with 40 intraepithelial lymphocytes (IELs)/100 enterocytes (ECs)

211 Human small intestinal intraepithelial lymphocytes (iIEL) are a unique populati

212 However, intestinal intraepithelial lymphocytes (iIEL) of CD3zeta eta(null)

213 ole of IL-2 in the development of intestinal intraepithelial lymphocytes (iIEL), we evaluated IL-2(-/

214 Murine intestinal intraepithelial lymphocytes (iIELs) are made up of a het

215 Hence, intestinal intraepithelial lymphocytes (iIELs) are potentially the

216 in lymphoid organs as well as in intestinal intraepithelial lymphocytes (iIELs) is dependent on the

217 T cell receptor (TCR) alpha beta intestinal intraepithelial lymphocytes (iIELs) using the 2C transge

218 o recycling into intestinal CD4(-)CD8beta(-) intraepithelial lymphocytes (iIELs).

219 We demonstrate that virus-specific intraepithelial lymphocytes in gut resemble neither cent

220 sease, can result from expansion of aberrant intraepithelial lymphocytes in refractory celiac disease

221 T cells but constitute a major proportion of intraepithelial lymphocytes in the gastrointestinal muco

222 but not in the maintenance of CD8alphaalpha intraepithelial lymphocytes in the intestine.

223 h) mice had normal numbers of TCR gammadelta intraepithelial lymphocytes in the intestines and did no

224 in spleen and intestine (lamina propria and intraepithelial lymphocytes), in suckling and juvenile m

225 nd CD8alpha(+) T cells in lamina propria and intraepithelial lymphocytes, in general, an increase of

226 se were included in the analyses of aberrant intraepithelial lymphocytes, including the primary analy

227 The density of CD3-positive intraepithelial lymphocytes increased in all groups, wit

228 ming growth factor beta(1) production by the intraepithelial lymphocytes increased, as did Smad2 expr

229 ss-linking of the T cell receptor complex on intraepithelial lymphocytes increases the avidity of alp

230 y stage NSCLC patient survival and increased intraepithelial lymphocyte infiltration.

231 ration and cytokine secretion in the spleen, intraepithelial lymphocyte inflammatory cytokines, and i

232 Intestinal intraepithelial lymphocyte interferon-gamma protein expr

233 Although an increased number of intestinal intraepithelial lymphocytes is observed at the inception

234 of NK cell subsets in the lung, tonsils and intraepithelial lymphocytes isolated from healthy indivi

235 led developmental trajectories of intestinal intraepithelial lymphocytes, lamina propria lymphocytes,

236 ively expressed granzyme B and GzmB(-/-) cre intraepithelial lymphocytes likewise expressed granzyme

237 ace proteins that are involved in intestinal intraepithelial lymphocyte localization or function, cul

238 Germ-free mice developed increased intraepithelial lymphocytes, markers of intraepithelial

239 In RCD, the immunophenotype of intraepithelial lymphocytes may be normal and polyclonal

240 Eosinophils suppress intraepithelial-lymphocyte-mediated production of interf

241 r and of abnormal morphology, and intestinal intraepithelial lymphocytes, normally containing a large

242 Intraepithelial lymphocyte numbers remained equal.

243 Subepithelial and intraepithelial lymphocytes of human adenoids and tonsil

244 Analysis of colonic intraepithelial lymphocytes of PDK1-deficient mice revea

245 The intraepithelial lymphocytes of the small intestine conta

246 Furthermore, intraepithelial lymphocytes or transfected JY' cells exp

247 organization, and regulation of the adaptive intraepithelial lymphocytes, or IEL, which are key playe

248 villous height:crypt depth ratio, numbers of intraepithelial lymphocytes, or serologic markers of cel

249 he relative change from baseline in aberrant intraepithelial lymphocyte percentage was -4.85% (90% CI

250 a homodimers, populations consistent with an intraepithelial lymphocyte phenotypic profile.

251 CD8alphaalpha TCRalphabeta(+) intestinal intraepithelial lymphocytes play a critical role in prom

252 lts indicate that changes occur in the ileal intraepithelial lymphocyte population coincidently with

253 ble-positive cells present in the intestinal intraepithelial lymphocytes population can suppress T he

254 istics of regulatory cells in the intestinal intraepithelial lymphocytes population.

255 vious studies have suggested that intestinal intraepithelial lymphocytes prevent spontaneous intestin

256 ThPOK results in premature acquisition of an intraepithelial lymphocyte profile by mLN T(reg) cells,

257 of intestinal alphabeta(+) and gammadelta(+) intraepithelial lymphocytes purified from germ-free mice

258 gands for intestinal NK cell, T cell, and/or intraepithelial lymphocyte receptors.

259 in terms of the primary endpoint of aberrant intraepithelial lymphocyte reduction from baseline.

260 ma to 'educate' the natural, skin-associated intraepithelial lymphocyte repertoire to be of physiolog

261 Intraepithelial lymphocytes represent a substantial frac

262 ntramucosal Brunner's gland scores and lower intraepithelial lymphocyte scores than from the second o

263 Secondary end points included numbers of intraepithelial lymphocytes, serology test results (for

264 Intraepithelial lymphocytes, such as gammadelta T cells

265 serum, nor did it induce IL-2R expression by intraepithelial lymphocytes, suggesting that GL3 inhibit

266 An important component of the disease is the intraepithelial lymphocyte that might become clonally ex

267 receptor (TCR)alphabeta+ cells and resident intraepithelial lymphocytes that are commonly enriched i

268 The enhancer also functions in gut intraepithelial lymphocytes that express CD8alpha but no

269 Intraepithelial lymphocytes that express the gammadelta

270 is role involves cell-cell interactions with intraepithelial lymphocytes that may also play a role in

271 In the epithelium, interleukin-15 activates intraepithelial lymphocytes that promote destruction of

272 eir anatomic location within the epithelium (intraepithelial lymphocytes), the interstitium between t

273 les (one in the AMG 714 group), and atypical intraepithelial lymphocytes (three in the AMG 714 group

274 -gamma is produced by both stromal cells and intraepithelial lymphocytes through all stages of the me

275 owel transplant, the number and the ratio of intraepithelial lymphocytes to enterocytes, as well as c

276 AM-15 is involved in heterotypic adhesion of intraepithelial lymphocytes to IEC as well as in homotyp

277 In vitro exposure of colonic intraepithelial lymphocytes to IL-10 resulted in downreg

278 response and participate in the licensing of intraepithelial lymphocytes to kill intestinal epithelia

279 cell receptor alphabeta(+) CD4(-)CD8beta(-) intraepithelial lymphocytes (unconventional iIELs), a ma

280 pithelium, long-term retention of intestinal intraepithelial lymphocytes was also alphaEbeta7 indepen

281 e gamma-region gene repertoire of intestinal intraepithelial lymphocytes was regulated by interleukin

282 Extrathymic development of intestinal intraepithelial lymphocytes was studied using a reconsti

283 from baseline to week 12 with respect to all intraepithelial lymphocytes was the primary endpoint and

284 elta T cells or gammadelta TCR(+) intestinal intraepithelial lymphocytes, we hypothesized that activa

285 Tonsillar intraepithelial lymphocytes were also enriched in B cell

286 In multivariable models, intraepithelial lymphocytes were associated with CAL (ex

287 Intraepithelial lymphocytes were associated with lactulo

288 Concomitantly, intraepithelial lymphocytes were less abundant, while co

289 Although lymphocyte aggregates and intraepithelial lymphocytes were not predictive, termina

290 Numbers of intraepithelial lymphocytes were significantly higher in

291 illus height to crypt depth and densities of intraepithelial lymphocytes were the primary end points.

292 d Mucida discuss development and function of intraepithelial lymphocytes, which are found within the

293 CR alpha- and beta-chain usage by intestinal intraepithelial lymphocytes, which are predominantly CD8

294 BY55 was expressed on all intestinal intraepithelial lymphocytes, which were predominantly CD

295 Is, biopsies showed significant increases in intraepithelial lymphocytes, which were predominantly T

296 tration of a clonal population of neoplastic intraepithelial lymphocytes with an atypical immunopheno

297 n the AMG 714 and placebo groups in aberrant intraepithelial lymphocytes with respect to epithelial c

298 ondary endpoints were the change in aberrant intraepithelial lymphocytes with respect to intestinal e

299 pporting host immune function by stimulating intraepithelial lymphocytes within the epithelial barrie

300 owed by Peyer's patches, lamina propria, and intraepithelial lymphocyte yield with respiratory and in