ライフサイエンスコーパス: cell infiltration

1 cus production, tissue remodeling and immune cell infiltration.

2 tokeratin 19-positive metaplasias and immune cell infiltration.

3 e presence of cGAS, as was skin inflammatory cell infiltration.

4 of Tnfr1(-/-)/Mdr2(-/-) mice indicated TH17 cell infiltration.

5 sinophilic, neutrophilic, and ST2(+)CD4(+) T-cell infiltration.

6 priming step to improve intratumoral immune cell infiltration.

7 microenvironment by inducing intratumoral T cell infiltration.

8 toxicity associated with induction of immune cell infiltration.

9 damage response genes, and decreased immune cell infiltration.

10 ot, with increased IFNgamma content and CD8+ cell infiltration.

11 umor M1 macrophage polarization and CD8(+) T-cell infiltration.

12 scular permeability, edema, and inflammatory cell infiltration.

13 lin, MHC class I, antigen presentation and T-cell infiltration.

14 NA repair status accurately predicted immune cell infiltration.

15 s followed with much delay by reduction in T cell infiltration.

16 ed corneal edema, and decreased inflammatory cell infiltration.

17 nophilia, goblet cell hyperplasia, and T(H)2 cell infiltration.

18 alter viral load, corneal edema, and immune cell infiltration.

19 es in macrophage polarization and enhanced T cell infiltration.

20 indicating ubiquitous variability in immune cell infiltration.

21 interstitial fibrosis, and prevented immune cell infiltration.

22 sitive area, but a marked decrease in CD3(+) cell infiltration.

23 to postmortem measurements of colonic immune cell infiltration.

24 in protein repression along with decreased T-cell infiltration.

25 ion profiles associated with CD4, CD8, and B cell infiltration.

26 ppressor cells and inhibition of cytotoxic T-cell infiltration.

27 othelial cell activation, and intratumoral T-cell infiltration.

28 diffuse alveolar damage with perivascular T-cell infiltration.

29 re associated with robust (10-fold) CD8(+) T cell infiltration.

30 uction in C3b/c and C9 deposition and innate cell infiltration.

31 sence of tumor cells was required for immune cell infiltration.

32 orresponding with patterns of greater immune cell infiltration.

33 ed fibrosis, increased vascularity, and mast cell infiltration.

34 cking of these chemokines inhibited CD8(+) T-cell infiltration.

35 exhibited autoimmune phenotypes, including T cell infiltration.

36 d mice correlated with intratumoral CD8(+) T-cell infiltration.

37 ation with patient survival and tumor immune cell infiltration.

38 ion of tumor-residing cDC1s overcomes poor T-cell infiltration.

39 n the mouse cancer model boosted cytotoxic T cell infiltration.

40 itic cells, inducing immune and inflammatory cell infiltration.

41 anced disease mediated by pulmonary CD8(+) T cell infiltration.

42 val benefit and positively correlated with T cell infiltration.

43 inflammatory cytokine expression and myeloid cell infiltration.

44 as a potential physical barrier to hinder T cell infiltration.

45 ciency in mice leads to reduced lung myeloid cell infiltration, abnormal alternatively activated macr

46 elial cells forming the BBB, regulate immune cell infiltration across this barrier in the mouse.

47 perforin, positively correlates with CD8+ T cell infiltration/activity in a variety of cancers.

48 gy scores and alleviated airway inflammatory cell infiltration after adoptive transfer into mice; the

49 N via (1) enhancing renal pathogenic myeloid cell infiltration and (2) direct effects on M/M polariza

50 areas of the pancreas with respect to immune cell infiltration and a changed ratio between the number

51 ilieu with a reduction of pathogenic myeloid cell infiltration and a marked accumulation of eosinophi

52 nohistochemistry confirmed enhanced CD8(+) T cell infiltration and accumulation by R848-TSLs.

53 ells recruited in vivo) induces local immune-cell infiltration and activated dendritic cells, evoking

54 se correlation between Arf1 expression and T-cell infiltration and activation along with patient surv

55 Poor intratumoral T cell infiltration and activation are major barriers that

56 ptional analysis were used to measure immune cell infiltration and activation in the skin of Rubcn(+/

57 titumor immune surveillance by stimulating T-cell infiltration and activation.

58 entation, interferon signalling and CD8(+) T cell infiltration and activation.

59 reased immune complexity, increased CD8(+) T-cell infiltration and activity, and decreased Treg frequ

60 enhanced disease severity due to increased T cell infiltration and altered polarization and pathogeni

61 f the PD-1/PD-L1 T cell checkpoint induces T cell infiltration and anticancer responses in murine and

62 tumor microenvironment, marked by enhanced T cell infiltration and antitumor immune signatures.

63 sion of chemokine transcripts, higher immune cell infiltration and augmented TCR clonal diversity amo

64 Neutrophil and NK cell infiltration and capillary thrombosis were also sig

65 PAHSAs reduced T and B cell infiltration and CD4+ and CD8+ T cell activation, w

66 mma(High)/RXRalpha(S427F/Y) impairs CD8(+) T-cell infiltration and confers partial resistance to immu

67 e system is activated with subsequent immune cell infiltration and cytokine production.

68 NK cell infiltration and cytotoxic pathways were uniquely f

69 uced extracellular matrix remodeling, immune cell infiltration and decreased angiogenesis.

70 and anti PD-1 cooperatively induces CD8(+) T-cell infiltration and decreases levels of proteins that

71 is exacerbates the inflammatory responses, T cell infiltration and demyelination following focal spin

72 an CD141(+) DCs are associated with CD8(+) T cell infiltration and differentiation.

73 skin that functionally contributes to immune cell infiltration and epidermal hyperplasia.

74 38A) rapidly induced skin acanthosis, immune cell infiltration and expression of psoriasis-associated

75 nificant correlations between the level of T cell infiltration and fiber properties.

76 ons of Plin2 are primary mediators of immune cell infiltration and fibrotic injury in livers of obese

77 e and IDO1 inhibitor enhanced intratumoral T cell infiltration and function, but adding anti-PD-L1 an

78 rtitioning in HFD tumors, impairing CD8(+) T cell infiltration and function.

79 In the DTH model, assessment of T cell infiltration and gene expression profile at the DTH

80 ated the association of stemness with immune cell infiltration and genomic, transcriptomic, and clini

81 demonstrated the attenuation of inflammatory cell infiltration and H. pylori colonization.

82 previously been associated with poor immune cell infiltration and higher mutation numbers.

83 ified an association between decreased CD8 T cell infiltration and increased glycolysis in microsatel

84 We find that T cell infiltration and interferon-gamma (IFN-gamma) signa

85 nalysis revealed that EP favors inflammatory cell infiltration and junctional epithelium, cementum wi

86 ed by airway and adjacent parenchymal immune cell infiltration and mucus production for at least 7 wk

87 ollowing NACT, increased natural killer (NK) cell infiltration and oligoclonal expansion of T cells w

88 suggest conduit biocompatibility and Schwann cell infiltration and organization within the conduit an

89 ge, LivKO mice showed increased inflammatory cell infiltration and proinflammatory gene expression in

90 rapeutic combination partners that augment T-cell infiltration and proliferation in so-called immune

91 l inflammation via induction of inflammatory cell infiltration and prolonged cell survival.

92 Histologic analyses revealed robust T cell infiltration and prominent programmed death ligand

93 may have poor prognosis despite high CD8+ T cell infiltration and provide CD274 as a simple biomarke

94 s of artificial microenvironments to promote cell infiltration and reprogramming are discussed.

95 functional role for csMHCII in regulating T cell infiltration and sensitivity to anti-PD-1.

96 Enforced expression of CIITA increased T cell infiltration and sensitized tumors to anti-PD-1 the

97 sease burden (percentage of bone marrow mast cell infiltration and serum tryptase levels) with molecu

98 dministration also enhanced tumor-specific T-cell infiltration and spatially redistributed CD8(+) T c

99 Because the association between T cell infiltration and the EPHA2/TGF-beta/COX-2 axis is s

100 was highly correlated to the level of CD8+ T cell infiltration and the expression of CCL5.

101 panied by significant weight loss and immune cell infiltration and the expression of early inflammato

102 ealed evidence of treatment response, immune cell infiltration and the migratory path of infiltrating

103 inhibits pathways that lead to inflammatory cell infiltration and the production of inflammatory cyt

104 with talimogene laherparepvec on cytotoxic T cell infiltration and therapeutic efficacy of the anti-P

105 T cells displayed reduced cerebral CD4(+) T-cell infiltration and thrombotic activity following expe

106 intervention markedly decreases swelling, T-cell infiltration and tissue fibrosis while significantl

107 umor transcriptomes was used to infer immune cell infiltration and to categorize tumors into immune s

108 mor immune microenvironment including immune cell infiltration and upregulation of PD-L1 expression p

109 ecessary and sufficient for mediating immune cell infiltration and vascular lesions.

110 on of in vitro cell activities, and enhanced cell infiltration and vascularization upon in vivo impla

111 d active granuloma formation with abundant T cell infiltration and were associated with significantly

112 bited less neutrophils or polymorpho nuclear cells infiltration and had improved efferocytosis compar

113 nflammation as evidenced by increased immune cells infiltration and release of cytokines and chemokin

114 lasia, inflammatory cytokine release, immune cell infiltration, and a subsequent reduction in skin sw

115 zed by increased collagen deposition, immune cell infiltration, and alpha-smooth muscle actin (alpha-

116 ressing livers display necrotic foci, immune cell infiltration, and altered hepatocyte morphology.

117 erythema and induration, CD4(+) and CD8(+) T-cell infiltration, and attenuated global gene activation

118 ing, while histology revealed oedema, immune cell infiltration, and basal zone hyperplasia.

119 ssessed by changes in ear thickness, myeloid cell infiltration, and cytokine and chemokine secretion.

120 to oxazolone with increased ear swelling, T-cell infiltration, and expression of Ifng.

121 rentiation, increased myofibroblasts, immune cell infiltration, and increased matrix deposition.

122 by extracellular matrix remodeling, myeloid cell infiltration, and inflammation.

123 eovascularization, re-epithelization, immune cell infiltration, and mRNA levels of angiogenic and pro

124 activation of the complement system, immune cell infiltration, and phagocytosis; pathways that may d

125 on of pulmonary vascular cells, inflammatory cell infiltration, and regresses established pulmonary h

126 on measured via CT, alveolar wall thickness, cell infiltration, and surfactant protein A concentratio

127 of tissue injury that includes pain, immune cell infiltration, and swelling?

128 is, degrades versican, promotes inflammatory cell infiltration, and thus contributes to sporadic AAD

129 enhanced vascular permeability, increased T cell infiltration, and tumor growth suppression.

130 lysis predicts hematopoietic cell number and cell infiltration are modulated by CR1(long), but not CR

131 Compelling evidence points to immune cell infiltration as a critical component of successful

132 im to assess the usefulness of measures of T-cell infiltration as prognostic biomarkers in 640 stage

133 ich was correlated with increased Foxp3(+) T cells infiltration as well as CXCR-2 expression.

134 veolar bone volume and enhanced inflammatory cell infiltration, as well as an increased number of ost

135 tratumoral MYXV delivery and observed immune cell infiltration associated with tumor necrosis and gro

136 yed increased tissue damage and inflammatory cell infiltration at early time points during injury but

137 ng microenvironment to promote robust immune cell infiltration at the expense of lung function.

138 C5D+ MM murine models, which coincide with T-cell infiltration at the tumor site.

139 xpression of apelin facilitated graft immune cell infiltration, blunted vascular repair, and worsened

140 CRC patients, with high intratumoral CD8+ T cell infiltration, but poor prognosis.

141 gnificantly suppressed total leukocyte and T-cell infiltration by 50%-68%; epidermal thickness by 60%

142 loid cells to directly react to pathogenic T cell infiltration by engulfing living T cells.

143 e secreted CXCL10, in turn, stimulated the T-cell infiltration by serving as the ligand and chemoattr

144 ninvasive method by which disease and immune cell infiltration can be explored simultaneously.

145 sful wound healing, aberrant immune-mediated cell infiltration can lead to pathological inflammation

146 , alpha-smooth muscle actin, and mononuclear cell infiltration (CD11b(+) Ly-6c(hi) monocytes and CD11

147 MIP-2, RANTES, and TNF-alpha), inflammatory cell infiltration (CD3 + T cells, macrophages, and neutr

148 uates ISO-mediated increases in inflammatory cell infiltration, collagen deposition and fibrosis.

149 urrence rate and shows more anterior chamber cell infiltration compared with HLA-B27-negative patient

150 These results suggest that increased myeloid cell infiltration contributes to autoreactive CD4 T cell

151 ation, as measured by histopathology, immune cell infiltration, cytokines, and chemokines.

152 between checkpoint based fitness and tumor T-cell infiltration, cytolytic activity, and abundance (tu

153 expression, chemokine expression, and immune cell infiltration density change during progression to S

154 at a normal weight, but the degree of immune cell infiltration did not differ by BMI.

155 r, melanocyte proliferation, or inflammatory cell infiltration, did not explain melanoma susceptibili

156 sition through LOXL2 suppression increases T cell infiltration, diminishes exhausted T cells, and abr

157 ed groups showed virtually no sign of immune cell infiltration, except minimal infiltration in white

158 with DNA repair gene variants but without T cell infiltration exhibited upregulation of TGF-beta and

159 41BB agonistic Abs led to increases in CD8 T cell infiltration followed by tumor regression in murine

160 were analyzed for vascularity, inflammatory cell infiltration, growth pattern, and tumor expression

161 uppressive function, (ii) increased CD8(+) T-cell infiltration, (iii) enhanced M1/M2 macrophage ratio

162 Based on the positive prognostic value of T cell infiltration, Immunoscore has been developed and va

163 found to be significantly associated with T cell infiltration in ADC samples.

164 y somatic mutations and the extent of immune cell infiltration in adenomatous premalignancy and assoc

165 roinflammatory cytokines and restrict immune cell infiltration in ADPKD.

166 ysical disability and cleared the brain of T-cell infiltration in an EAE mouse model of multiple scle

167 growth regulatory kinase Erk5 can increase T-cell infiltration in an established Pten-deficient mouse

168 gene expression profile and decreased immune cell infiltration in an intradermal model of infection y

169 Despite adaptive immune cell infiltration in claudin-low tumors, treatment with

170 ells in particulate form and improved immune cell infiltration in draining lymph nodes.

171 The investigation of myeloid cell infiltration in HCC, NET and intrahepatic CCA tumor

172 in peritumoral area; and (4) reduces glioma cell infiltration in healthy parenchyma.

173 tment with FOLR1-TCB induced strong CD8(+) T-cell infiltration in HeLa tumors, where (89)Zr-Df-IAB22M

174 ral pathways, IFN signaling, and cytotoxic T cell infiltration in human cancers, while a FBXO44-immun

175 derived from human cells) do not stimulate T-cell infiltration in immuno-competent mice.

176 by myeloid cells is key for orchestrating T cell infiltration in immunoreactive and immunoresponsive

177 between disease outcomes and high levels of cell infiltration in lungs including CD11b(+)CD16(hi) ma

178 ascular perfusion and increases inflammatory cell infiltration in mouse MI/R.

179 This coincides with viral replication or T cell infiltration in primary tumors.

180 ha/NFkappaB signaling, which promotes immune cell infiltration in regressing and residual tumors.

181 overexpression was associated with CD8(+) T cell infiltration in solid tumors.

182 The HFD induced prominent immune cell infiltration in the adipose tissue, an important SI

183 of WNV by affecting viral replication and T-cell infiltration in the brain.

184 ion resulted in a reduction of myeloid and T cell infiltration in the central nervous system and a si

185 rrier (BBB) disruption and peripheral immune cell infiltration in the cerebellum following blast expo

186 ssociated with decreased inflammatory immune cell infiltration in the CNS and increased Treg cells in

187 in stem, and on axon degeneration and immune cell infiltration in the distal portion of the facial ne

188 Recently, we reported increased T cell infiltration in the fibrotic myocardium of nonische

189 The mechanisms mediating immune cell infiltration in the kidney are not well understood

190 tractant protein 1]), increases inflammatory cell infiltration in the kidney, reduces telomerase expr

191 sed MRL.Fas(lpr) mouse survival, decreased T cell infiltration in the kidneys, and reduced T cell cyt

192 Immune cell infiltration in the myocardium can have adverse eff

193 T-cell, macrophage, and dendritic cell infiltration in the periapical lesion was dramatica

194 gG4 level, abundance of IgG4 enhanced plasma cell infiltration in the portal region of the liver, and

195 nterface hepatitis with IgG4 positive plasma cell infiltration in the portal region, without evidence

196 is an autoimmune disease characterized by T-cell infiltration in the skin that leads to fibrosis, wh

197 t decreases epidermal thickness as well as T cell infiltration in the skin.

198 mmatory phenotype, and impairs FOXP3(+)/Treg cell infiltration in the spinal cord of hSOD1(G93A) mice

199 t the SA-IL-4 fusion protein prevents immune-cell infiltration in the spinal cord, decreases integrin

200 and function, and decreased CD11b(+) myeloid cell infiltration in the tumor.

201 ssues showed significantly more inflammatory cell infiltration in the WT ligated but not in the TLR9(

202 alone or combined with anti-PD-1 augmented T cell infiltration in tumor-draining lymph nodes.

203 dels, and a decrease in local cardiac immune cell infiltration in wild-type NMRI mice.

204 ith reduced Ki-67 level and augmented CD8+ T cell infiltration in xenograft tumors.

205 ere higher proportions of anti-cancer immune cells infiltration, including activated memory CD4+ T ce

206 h lower levels of Th1 cytokines, decreased T cell infiltration, increased B cell numbers, and decreas

207 h were characterized by increased effector T-cell infiltration, increased effector T-cell function, a

208 rged retroperitoneal lymph nodes, and immune cells infiltration, indicating that blocking VEGF-C sign

209 ckout (I-SGPL(-/-)) augmented massive immune cell infiltration initiating colitis with lesions and ca

210 neous hyperplasia in this model, decreased T cell infiltration, interleukin (IL)-22 transcription, an

211 locked BBB disruption and prevented CD4(+) T-cell infiltration into cerebellum.

212 tion, a hallmark of obesity, involves immune cell infiltration into expanding adipose tissue.

213 lso inhibited CD3(+) T-cell and gammadelta T-cell infiltration into skin regions.

214 tumor-associated macrophage (TAM) and CD8 T cell infiltration into subcutaneously implanted murine l

215 (PDAC), we observed early and robust myeloid cell infiltration into the brain.

216 uding fatal cerebral edema associated with T cell infiltration into the brain.

217 -17, IL-22, and KC, and showed severe immune cell infiltration into the bronchioles.

218 ed skin is required to direct effector CD8 T cell infiltration into the challenge site to elicit CHS,

219 In mice, TFH cells accordingly promote B cell infiltration into the CNS and the severity of MS an

220 result of reduced demyelination and myeloid cell infiltration into the CNS tissue.

221 s functional BBB integrity and limits immune cell infiltration into the CNS.

222 ed CD11b-positive CD3-negative innate immune cell infiltration into the colon.

223 T-cell infiltration into the ileum was increased; epitheli

224 autoimmune process initiates first with a T cell infiltration into the islets, where they have restr

225 CCL7 blockade in mice reduced myeloid cell infiltration into the kidney and ameliorated AKI.

226 Immune cell infiltration into the lung in the rat OVA model of

227 ardiomyopathy, characterized by inflammatory cell infiltration into the myocardium and a high risk of

228 y microvascular leakage, fibrosis and immune cell infiltration into the myocardium.

229 st cell activation and markedly reduced mast cell infiltration into the small intestine.

230 ce with chronic EAE, SA-IL-4 inhibits immune-cell infiltration into the spinal cord and completely ab

231 that NSD1 inactivation results in reduced T cell infiltration into the tumor microenvironment, impli

232 e inflamed tumor environment with enhanced T-cell infiltration into tumors and T-cell-mediated cytoto

233 elevated pulmonary congestion, inflammatory cell infiltration, iron overload, and secretion of IL-6

234 tract integrity is degraded in areas where T-cell infiltration is highest, providing a noninvasive me

235 and dysfunctional and, thus, immune effector cell infiltration is impaired.

236 distribution of desmoplastic elements and T-cell infiltration is necessary to delineate their roles.

237 Immune cell-infiltration is controlled by activated PPARgamma/R

238 that Gal1 blockade increases intratumoral T cell infiltration, leading to a better response to anti-

239 spond to immune checkpoint therapies where T-cell infiltration may be a key limiting factor.

240 and host cells, and baseline intratumoral T cell infiltration may improve response likelihood to ant

241 rs, since the potential adverse effect on NK cell infiltration might limit the antitumor activity of

242 Fibrosis follows UUO, but inflammatory cell infiltration mostly depends upon Notch3 expression

243 reduced weight loss, pulmonary inflammatory cell infiltration, mucus production, and airway resistan

244 cardiomyopathy characterized by inflammatory cell infiltration, necrosis, and cardiac fibrosis.

245 ce burn) and determined the degree of immune cell infiltration, NETosis, and the cytokine levels in t

246 c analysis was used to evaluate inflammatory cell infiltration, numbers of osteoblasts and osteoclast

247 that deletion of TSP-1 reduced inflammatory cell infiltration of muscle fibers, but only early in di

248 T-cell infiltration of solid tumors is associated with imp

249 vealed significant loss of BMAT with myeloma cell infiltration of the marrow, whereas BMAT was restor

250 However, although there is considerable T cell infiltration of the maternal decidua, the functiona

251 p120-catenin further prevents diffuse glioma cell infiltration of the mouse brain with marginalized m

252 FGR and pre-eclampsia are associated with T-cell infiltration of the placenta and placental patholog

253 T cell infiltration of tumors plays an important role in d

254 ociated with T cells, suggesting increased T cell infiltration of tumors.

255 pear to be associated with baseline CD8(+) T cell infiltration or baseline IFN-gamma signature.

256 re causal, either by interfering with immune cell infiltration or by enhancing melanoma cell growth.

257 ci-cellular infiltration with rare epidermal cell infiltration or necrosis, were accounted for in a p

258 ucicellular infiltration with rare epidermal cell infiltration or necrosis, were accounted for in a p

259 phenotype and promoted intratumoral CD8(+) T-cell infiltration, overcoming the exclusion effect; TGFb

260 TACE increased peri- and intratumoral immune cell infiltration (P = .002).

261 NA expression (P = 0.03), and 114% greater T-cell infiltration (P = 0.005) compared to sham-operated

262 Cationic interfaces elicit stromal cell infiltration, peripherally derived inflammation, ne

263 This hinders effector T-cell infiltration, proliferation and immune reactivity,

264 mor cytokine/chemokine signature, improved T-cell infiltration, reduced markers of T-cell exhaustion,

265 LRG1 deletion causes impaired immune cell infiltration, reepithelialization, and angiogenesis

266 ting chemokines, resulting in improved CAR-T cell infiltration, remodeling of the tumor microenvironm

267 T cell infiltration required tumor cell-derived CCL5 and w

268 ue and inversely correlated with cytotoxic T cell infiltration, suggesting that HE4 may cause deregul

269 SCLC human patients showed negligible immune cell infiltration, supporting testing MYXV as an ablativ

270 ysis revealed significantly decreased immune cell infiltration, synthesis of reactive oxygen species,

271 ity of neurons, due to cell death and immune cell infiltration that may account for the observed unde

272 ithelium (RPE) injury associated with immune cell infiltration, the nature of immune cell responses t

273 ene expression pattern that indicated immune cell infiltration; this tumor type was associated with t

274 he T-reg cell population and reducing immune cell infiltration, thus promoting longer-term infection.

275 AHR in asthma are related to a shift in mast cell infiltration to the airway epithelium, and that mas

276 Immune cell infiltration to the liver was greater and earlier i

277 eatment promoted transient polymorphonuclear cell infiltration to the vaginal cavity and protected ag

278 tumor growth in mice, increased tumor immune cell infiltration, upregulated PD-L1 on tumors, and sens

279 mals showed strikingly improved inflammatory cell infiltration versus WT.

280 Intratumoral basophils enhanced CD8(+) T-cell infiltration via production of chemokines CCL3 and

281 In stress models, inflammatory cell infiltration was initially lower in knockout mice b

282 (5.5 +/- 0.1 vs 7.8 +/- 0.2 um; p < 0.0001), cell infiltration was lower (20 +/- 2 vs 32 +/- 2 n/fiel

283 Inflammatory cell infiltration was observed in both MG and conjunctiv

284 on and pre-eclampsia, whereas CD79alpha(+) B-cell infiltration was only apparent with reduced fetal g

285 , which identifies tumors with a high immune cell infiltration, was shown to enrich for response to a

286 evels, blood-brain barrier leakage, and/or T cell infiltration, well before neurodegeneration occurs.

287 pathology, the chlamydial burden and immune cell infiltration were determined in the oviducts.

288 f epidermal hyperplasia and T-cell/dendritic cell infiltration were increased in AD tissues of all pa

289 ond infection, cytokine responses and innate cell infiltration were largely comparable to primary inf

290 neoantigen load) and the degree of CD8(+) T cell infiltration were not associated with clinical resp

291 Vascularization and immune cell infiltration were prominent in skin lesions of huma

292 at VUE is driven predominantly by maternal T cell infiltration, which is significantly different from

293 eratinocytes associated with a marked CD4+ T cell infiltration, which peaked on days 10-11 after trea

294 EP4 cKO colon stroma showed enhanced immune cell infiltration, which was accompanied by increased pr

295 ited dermal disorganization and inflammatory cell infiltration, which were improved in the 3 treated

296 ver, the reason some tumours have high CD8 T cell infiltration while others do not remains unclear.

297 associated with macrophage, CD4, CD8, and B cell infiltration with increased formation of tertiary l

298 a, have impaired parasite control and immune cell infiltration within the brain.

299 The prognostic value of immune cell infiltration within the tumor microenvironment (TME

300 ivation impairs tumor progression and immune cell infiltration without affecting cell cycle arrest in