ライフサイエンスコーパス: dendritic cell

1 hose with abundant IRF7 protein levels (e.g. dendritic cells).

2 ted in its membrane-bound form by follicular dendritic cells.

3 esses CD11C, a marker typically expressed on dendritic cells.

4 mediated interactions between Treg cells and dendritic cells.

5 important role of SWAP-70 in Cer dynamics in dendritic cells.

6 t of monocytes that yielded monocyte-derived dendritic cells.

7 en exposure or in vitro by using tolerogenic dendritic cells.

8 of Th17 differentiation cytokines in splenic dendritic cells.

9 g by depleting cross-presenting conventional dendritic cells.

10 ered to direct the HIV-1 coat protein Env to dendritic cells.

11 ell type-specific deletion of Prdm1 in T and dendritic cells.

12 ntiate into monocyte-derived macrophages and dendritic cells.

13 n pulmonary eosinophils and monocyte-derived dendritic cells.

14 ection by LECs was similar to that of dermal dendritic cells.

15 LR4-mediated activation of lung conventional dendritic cells.

16 fibroblastic reticular cells and follicular dendritic cells.

17 and instead primarily target hepatocytes and dendritic cells.

18 mphoid organs and sustain Ag presentation on dendritic cells.

19 tein 70 (SWAP-70) in lipid raft formation of dendritic cells.

20 rget antigen-presenting-cells (APCs) such as dendritic cells.

21 ion and required the presence of CD8alpha(+) dendritic cells.

22 timulatory molecules of LPS-stimulated human dendritic cells.

23 dent on type I IFNs produced by plasmacytoid dendritic cells.

24 on different subsets of T cells and CD11b(-) dendritic cells.

25 migration of various cancer cells as well as dendritic cells.

26 r 4-mediated proallergic properties of human dendritic cells.

27 endothelial cells, T cells, macrophages and dendritic cells.

28 nterleukin-6 (IL-6) from human blood-derived dendritic cells.

29 tion, with ZIKV replication detected in some dendritic cells.

30 ssive TNF-alpha secretion predominantly from dendritic cells.

31 n the interaction between Chlamydia and host dendritic cells.

32 from WAS patients and in WAS-knockout mouse dendritic cells.

33 40 interaction for the function of T, B, and dendritic cells.

34 libraries loaded or not on monocytes-derived dendritic cells.

35 s, Langerhans cells, and interstitial dermal dendritic cells.

36 gely due to the recruitment of monocytes and dendritic cells.

37 in antigen cross-presentation by Igfbp7(-/-) dendritic cells.

38 ubsets were markedly distinct from PBMos and dendritic cells.

39 exosomes, which are taken up by and activate dendritic cells.

40 ar STING has been studied in macrophages and dendritic cells.

41 uption (i.e., in T cells, myeloid cells, and dendritic cells) achieved only partial or no improvement

42 ast, early signatures of innate immunity and dendritic cell activation were highly associated with pr

43 associated cytokine synthesis, and pulmonary dendritic cell activity was assessed.

44 diated efferocytosis, negative regulation of dendritic cell activity, and dysregulated production of

45 ntestinal epithelial cells, macrophages, and dendritic cells all bridge the innate and adaptive immun

46 transcript 3 (ILT3), a marker of tolerogenic dendritic cells, also known as LILRB4/LIR5/CD85k, and it

47 We tested the role of Stat5 in dendritic cell and alveolar macrophage (AM) homeostasis

48 data measuring response of monocyte derived dendritic cells and A549 epithelial cells to influenza i

49 nd CCL20, resulting in reduced chemotaxis of dendritic cells and CD4(+) T cells.

50 atumorally, including infusion of autologous dendritic cells and even tumor-reactive T lymphocytes.

51 stantiate a critical role for skin migratory dendritic cells and in particular Langerhans cells at go

52 nimals revealed increased numbers of CD1d(+) dendritic cells and increased numbers of iNKT cells.

53 trated that trans-Ly108 interactions between dendritic cells and iNKT cells are critical for robust a

54 eptor for infection of both monocyte-derived dendritic cells and interstitial dermal dendritic cells,

55 In myeloid-derived dendritic cells and macrophages as well as resting T-cel

56 ns between host innate immune cells, such as dendritic cells and macrophages, and free, extracellular

57 cific subsets of resident and recruited lung dendritic cells and macrophages.

58 Although myeloid dendritic cells and monocytes showed superior presenting

59 D40L stimulation derived from human immature dendritic cells and naive B cells to assess the expressi

60 aled that CD40L-responsive genes in immature dendritic cells and naive B cells were significantly enr

61 This process has been defined in dendritic cells and plays a fundamental role in the indu

62 reduction of pulmonary CD11b(+) conventional dendritic cells and regulation of CD4(+) T-cell cytokine

63 is required for the sufficient migration of dendritic cells and T cells into the draining lymph node

64 ot modulated by interferon in macrophages or dendritic cells, and consequently protein levels of SAMH

65 as choroid plexus and meningeal macrophages, dendritic cells, and granulocytes.

66 on how cross-talk between epithelial cells, dendritic cells, and innate lymphoid cells translates to

67 T cells, B cells, eosinophils, neutrophils, dendritic cells, and NK cells.

68 anodal prion replication by B and follicular dendritic cells, and potential prion strain selection by

69 id cells, induce migration and activation of dendritic cells, and promote effector differentiation of

70 rly after entry into monocytes, macrophages, dendritic cells, and resting CD4 T cells, HIV encounters

71 Furthermore, dendritic cell- and IL-2/7-dependent T cell survival was

72 at chemokines produced by intratumoral Batf3 dendritic cells are critical for effector T cell recruit

73 terium tuberculosis-infected macrophages and dendritic cells are limited in their ability to present

74 (IFN-gamma), TNF-alpha, and IL-12 in myeloid dendritic cells are of importance in generating T helper

75 We show that follicular dendritic cells are stiff cells that promote strong B ce

76 s, using bone marrow-derived macrophages and dendritic cells as responders.

77 , leaving macrophages and, to a less extent, dendritic cells as the major infiltrating leukocytes.

78 terferons (IFN-alpha/beta) from plasmacytoid dendritic cells as well as the production of TLR8-depend

79 ediated tumour antigen cross-presentation by dendritic cells, as well as immunotherapeutic strategies

80 by higher mRNA expression levels of several dendritic cell-associated genes, including CD1, FLT3, CX

81 Arterial wall dendritic cells attract CD4(+) T cells and macrophages t

82 y into immunocompetent mice are macrophages, dendritic cells, B cells and T cells in the gut-associat

83 s, gammadelta T cells and NKT cells, whereas dendritic cells, B2 cells, CD4(+) T and CD8(+) T cells a

84 In the field of dendritic cell based genetic immunization, previously we

85 tic cells (moDCs), bone marrow-derived mouse dendritic cells (BMDCs), and moDC/naive CD4(+) T-cell co

86 ophage-like cells and in bone marrow-derived dendritic cells (BMDCs).

87 of Langerhans cells, macrophages, and dermal dendritic cells by 75-90% and reduced the overall number

88 We found that activation of dendritic cells by bacterial lipopolysaccharide leads to

89 innate receptor engagement on epithelial or dendritic cells by HDMs that ultimately mediates said in

90 ich prevent prions from infecting follicular dendritic cells can block their spread to the brain.

91 th an increase in the number of conventional dendritic cells, CD11b(+) and CD103(+) dendritic cells,

92 ell sorting method to isolate keratinocytes, dendritic cells, CD4+ T effector cells, and CD8+ T effec

93 (CD206+) and MDSCs (Gr1+ CD11b+), increased dendritic cells (CD86+) and cytotoxic T cells (CD8+) in

94 ially expressed by the CD8alpha(+) subset of dendritic cells (CD8alpha(+) DCs) and is involved in sen

95 uggested that RelB is required for classical dendritic cell (cDC) development based on a severe reduc

96 t the heart contained two major conventional dendritic cell (cDC) subsets, CD103(+) and CD11b(+), whi

97 tage of CD103(neg) and CD103(+) conventional dendritic cells (cDC) in the intestinal lamina propria a

98 nizes inflammation by affecting conventional dendritic cells (cDC), inducing IL-10, and promoting dev

99 )-12 by tissue-resident XCR1(+) conventional dendritic cells (cDC1) promoted ILC1 production of IFN-g

100 ntal origin of conventional and plasmacytoid dendritic cells (cDCs and pDCs, respectively) resident i

101 Surprisingly, both conventional dendritic cells (cDCs) and plasmacytoid DCs (pDCs) are r

102 n of CD103(+)CD11c(hi)MHCII(hi) conventional dendritic cells (cDCs) from Flt3L-mobilized primary bone

103 The dendritic cell clade was distinct from a macrophage/mono

104 ed I-A expression on the surface of B cells, dendritic cells, cortical thymic epithelial cells, and m

105 r 2 (Th2)-like cells; (iii) interfering with dendritic cell (DC) effector function; and (iv) inhibiti

106 Here, we report that C-type lectin dendritic cell (DC) immunoreceptor (DCIR), a key compone

107 ught to be prototypic representatives of the dendritic cell (DC) lineage, they are now considered to

108 atory T cell immunity is augmented by innate dendritic cell (DC) maturation commonly initiated by TLR

109 34.5 protein, a virulence factor, stimulates dendritic cell (DC) maturation which is dependent on TAN

110 mune-modulatory functions that could enhance dendritic cell (DC) maturation.

111 Mouse strains lacking different dendritic cell (DC) populations were used, and 1-DER T c

112 Human dendritic cell (DC) response to alpha-(1,3)-glucan polys

113 ted and memory CD4 T cells, macrophages, and dendritic cell (DC) showed chemoattractantDeltadriven ve

114 que DCs.Developmental cues for the different dendritic cell (DC) subsets in the intestine are yet to

115 Dendritic cell (DC) subsets with biased capacity for CD4

116 RNA sequencing was used to characterize dendritic cell (DC) transcripts.

117 group are promising DNA vaccine carriers for dendritic cell (DC) transfection.

118 y T (Act-A-iTreg) cells on the regulation of dendritic cell (DC)-driven allergic inflammation remain

119 ction of CD169(+) cells in vivo Treatment of dendritic cell (DC)-T cell cocultures with IFN-alpha upr

120 Dendritic cells (DC) accumulate in the CNS during neuroi

121 , such as HLA-DR4 positivity, indicates that dendritic cells (DC) are of crucial importance to pathog

122 Thymic dendritic cells (DC) delete self-antigen-specific thymoc

123 Tissue-residing and ex vivo-generated dendritic cells (DC) from GCA patients were PD-L1(lo), w

124 The predominant types of dendritic cells (DC) in the skin and mucosa are Langerha

125 During infection, dendritic cells (DC) mature into antigen-presenting cell

126 Treatment of TIDC and bone marrow-derived dendritic cells (DC) with IL10 led to increased PD-1 exp

127 etermine the mechanism of MSC recruitment by Dendritic Cells (DC), hypothesising that it would be med

128 at trastuzumab facilitated uptake of HER2 by dendritic cells (DC), which was mediated by the Fc recep

129 dhesion molecule-1 for T-cell conjugation to dendritic cells (DC).

130 Dendritic cells (DCs) and monocytes play a central role

131 egulated on splenic CD8alpha(+) conventional dendritic cells (DCs) and plasmacytoid DCs upon TLR-medi

132 ressed by thymic epithelial cells and thymic dendritic cells (DCs) and, in these two stromal compartm

133 Dendritic cells (DCs) are activated by pathogens to init

134 Dendritic cells (DCs) are crucial initiators of immune r

135 involved in T helper (Th) 2 polarization by dendritic cells (DCs) are currently unclear.

136 Mast cells (MCs) and dendritic cells (DCs) are essential innate sentinels pop

137 CD4(+) and CD8(+) T cells, Tregs, and dendritic cells (DCs) are highly mobile, going along mic

138 Dendritic cells (DCs) are the main target cells of DENV,

139 Dendritic cells (DCs) are thought to form a dendritic ne

140 Although dendritic cells (DCs) are vital for the induction of T-c

141 RPalpha with CD47 preferentially occurred in dendritic cells (DCs) but not in macrophages.

142 ARgamma plays a key role in both T cells and dendritic cells (DCs) for development of type-2 immune r

143 cells normally depend on signals from CD8(+) dendritic cells (DCs) for their activation, we used the

144 y susceptibility to TB, we infected with MTB dendritic cells (DCs) from putatively resistant individu

145 Dendritic cells (DCs) have a unique capacity to promote

146 Tolerogenic dendritic cells (DCs) have emerged as relevant clinical

147 The origin and specification of human dendritic cells (DCs) have not been investigated at the

148 cal role for splenic langerin(+) CD8alpha(+) dendritic cells (DCs) in exosomal Ag cross-presentation.

149 n-dependent antigen presentation by CD11c(+) dendritic cells (DCs) in offspring was required for oral

150 0, which we found to be produced by CD103(+) dendritic cells (DCs) in T cell-inflamed tumors.

151 ltiphoton microscopy was used to image renal dendritic cells (DCs) in vivo using CD11c reporter mice.

152 Dendritic cells (DCs) initiate immune responses to commo

153 Enhanced TLR7 signaling in Vsir (-/-) dendritic cells (DCs) led to the hyper-activation of Erk

154 Dendritic cells (DCs) play critical roles in developing

155 Dendritic cells (DCs) promote either tolerogenic or immu

156 The mechanism of dendritic cells (DCs) recruitment across the blood brain

157 e T cells; however, the function of Smad7 in dendritic cells (DCs) remains elusive.

158 ting the frequency and makeup of intrathymic dendritic cells (DCs) required for effective thymocyte n

159 Cross-presentation is a critical function of dendritic cells (DCs) required for induction of antitumo

160 that control the presentation of antigens by dendritic cells (DCs) to naive T lymphocytes.

161 emonstrated for the haptotactic migration of dendritic cells (DCs) toward higher concentrations of im

162 Trafficking of tissue dendritic cells (DCs) via lymph is critical for the gene

163 ous lesions containing pathological CD207(+) dendritic cells (DCs) with constitutively activated mito

164 We hypothesized that loss of SOCS1 in dendritic cells (DCs) would improve T cell responses by

165 wide variety of cell types, including mature dendritic cells (DCs), and is required for optimal T-cel

166 infiltrated MAC387(+) macrophages, T cells, dendritic cells (DCs), and residential macrophages near

167 e show a contrasting function for glucose in dendritic cells (DCs), as glucose represses the proinfla

168 er CD40 or LOX-1, two endocytic receptors on dendritic cells (DCs), in rhesus macaques primed with a

169 esenting cell (APC) populations, B cells and dendritic cells (DCs), in the presence of B7- and CD40-d

170 HIV-1 infection of noncycling cells, such as dendritic cells (DCs), is impaired due to limited availa

171 BM-derived dendritic cells (DCs), lung-resident cluster of differen

172 e of immune reactions with a high density of dendritic cells (DCs), macrophages and T cells.

173 Dendritic cells (DCs), the essential immunoregulatory an

174 The skin hosts a variety of dendritic cells (DCs), which act as professional APC to

175 ssential autophagy protein ATG5 in classical dendritic cells (DCs), which are present at low frequenc

176 Targeting newborn dendritic cells (DCs), which integrate vaccine signals i

177 taining IgG immune complexes (Ig-ICs) by gut dendritic cells (DCs).

178 during pregnancy boosted OVA uptake by fetal dendritic cells (DCs).

179 cific interactions between T lymphocytes and dendritic cells (DCs).

180 R4 on the tolerogenic function of intestinal dendritic cells (DCs).

181 e-sensitivity and inefficient translation in dendritic cells (DCs).

182 SLP in Th2 responses include CD4 T cells and dendritic cells (DCs).

183 ts for the early steps of TLR9 activation in dendritic cells (DCs).

184 from both fungal species with MUTZ-3-derived dendritic cells (DCs).

185 ergy: (i) a self-vaccinal effect mediated by dendritic cells (DCs); and (ii) an inflammatory repolari

186 and induction was suppressed by plasmacytoid dendritic cell depletion.

187 e absence of gammadelta T cells, CD8alpha(+) dendritic cells did not accumulate in the livers of vacc

188 ls prior to committed monocyte/macrophage or dendritic cell differentiation and provide the first exa

189 tory factor (IRF)-8, which promotes monocyte/dendritic cell differentiation while limiting granulocyt

190 CD300f-deficient dendritic cells displayed hyperactive phagocytosis of ap

191 membrane protein (LAMP) family includes the dendritic cell endocytic receptors DC-LAMP and CD68, as

192 Here we have found that dendritic cells expressing the apoptotic cell-recognizin

193 strains upon stromal cell-derived follicular dendritic cells (FDC) in the Peyer's patches in the smal

194 tic stem cells or bone marrow-derived MSC or dendritic cells) for optimization of appropriate conditi

195 40, CD80, CD83, and CD86 on monocyte-derived dendritic cells from allergic patients was analyzed by u

196 o be essential for the ability of intestinal dendritic cells from DNFB-fed mice to inhibit ACD on ado

197 We also show that small intestine dendritic cells from pregnant, but not from non-pregnant

198 lonic inflammation as a result of defects in dendritic cell function that were associated with abnorm

199 co-cultured with GM-CSF derived bone marrow dendritic cells (G-BMDCs).

200 D25(+)) lymphocytes, tissue macrophages, and dendritic cells (Iba-1(+) and CD83(+)), with a small num

201 cted maturation of immature monocyte-derived dendritic cells (iDCs).

202 In bone marrow-derived dendritic cells, IL-33 induces the production of IL-6, I

203 Using antigen-loaded dendritic cells improved T cell expansion and favored ce

204 ene silencing in a mouse asthma model, human dendritic cell in vitro stimulation assays, and surface

205 ollowing enzymatic cleavage, activates human dendritic cells in an NKT-cell dependent manner, and gen

206 ace ligand-coated AuNP that targeted myeloid dendritic cells in lymph nodes as a peptide antigen carr

207 pression in the jejunum; numbers of CD103(+) dendritic cells in MLNs were significantly increased.

208 Further, the severe loss of dendritic cells in the draining lymph node had no impact

209 hat Dll4 was expressed on CD11b(+) pulmonary dendritic cells in the lung and draining lymph nodes in

210 Infiltrating T cells co-localized with dendritic cells in the pituitary and produced increased

211 turation and cytokine release of bone marrow dendritic cells in vitro.

212 IVM had no major impact on the functions of dendritic cells in vivo and in vitro, IVM impaired T-cel

213 ional dendritic cells, CD11b(+) and CD103(+) dendritic cells, in the lung-draining lymph node, as wel

214 tion and abrogated monocyte, macrophage, and dendritic cell increase in the affected kidneys, whereas

215 APT lesions showed higher T cell and dendritic cell infiltrates vs. CONTROLS: Seven hundred a

216 nduced during dermal DC and monocyte-derived dendritic cell/inflammatory dendritic epidermal cell dif

217 amatically affected the outcome of Chlamydia-dendritic cell interactions for both the bacterium and t

218 d: (i) the early entrance of CD4 T cells and dendritic cells into pancreatic islets was reduced, (ii)

219 e types of dendritic cells: monocyte-derived dendritic cells, Langerhans cells, and interstitial derm

220 B cell morphology, having in general a more dendritic cell-like appearance.

221 nized mice immunized with long-lived induced-dendritic cells loaded with the pp65 viral antigen (iDCp

222 , TSLPR(+) mono express higher levels of the dendritic cell marker CD1c.

223 luding Langerhans cells, macrophages, dermal dendritic cells, mast cells, fibroblasts, and lymphatic

224 type I interferon responses, suppression of dendritic cell maturation and promotion of inflammatory

225 protease, inflammatory cell recruitment, and dendritic cell maturation.

226 AT6-dependent expansion of recipient myeloid dendritic cells (MDCs) that induce contact-dependent exp

227 sly shown that HHV-8 enters monocyte-derived dendritic cells (MDDC) through DC-SIGN, resulting in non

228 une system and specifically monocyte-derived dendritic cells (MDDCs) understudied.

229 litating HIV-1 infection of monocyte-derived dendritic cells (MDDCs), one of the first cell types to

230 ion and lymphocyte attraction, together with dendritic cell-mediated cross-priming, are the key eleme

231 nization with topoisomerase-I peptide-loaded dendritic cells, Mehta et al. found that early-life anti

232 of Ly6C(high) monocytes and monocyte-derived dendritic cells (moDC) and lower moDC costimulatory matu

233 7b) on the surface of human monocyte-derived dendritic cells (MoDC) and show only LAMP-2 is internali

234 ells and in CD23-expressing monocyte-derived dendritic cells (moDCs) that represent classical antigen

235 n and cytochalasin D) human monocyte-derived dendritic cells (moDCs), bone marrow-derived mouse dendr

236 es of different cell types (monocyte-derived dendritic cells [moDCs], PBMCs [peripheral blood mononuc

237 ses Kaposi's sarcoma, infects three types of dendritic cells: monocyte-derived dendritic cells, Lange

238 Dendritic cells, monocytes, and B cells in HCC tumors ex

239 -presenting cells (APCs) in the skin include dendritic cells, monocytes, and macrophages.

240 e, often coinciding with loss of circulating dendritic cells, monocytes, B cells, and natural killer

241 Clec9a (C-type lectin receptor) or DNGR-1 (dendritic cell NK lectin group receptor-1) is preferenti

242 n the metastatic cells and within follicular dendritic cells of the metastasis-infiltrated lymph node

243 promote persistent directional migration of dendritic cells or neutrophils.

244 d by infiltration of pathologic macrophage-, dendritic cell-, or monocyte-derived cells in tissues dr

245 We identified that transient plasmacytoid dendritic cell (pDC) depletion during primary Pneumoviru

246 Plasmacytoid dendritic cells (pDC) are specialized in secretion of ty

247 Plasmacytoid dendritic cells (pDCs) are important in antiviral immuni

248 nd that BCMA was transcribed in plasmacytoid dendritic cells (pDCs) in both blood and lymphoid tissue

249 Plasmacytoid dendritic cells (pDCs) were isolated from whole blood, s

250 Plasmacytoid dendritic cells (pDCs), prominent cells of antiviral imm

251 -induced IFN-alpha responses of plasmacytoid dendritic cells (pDCs), which can be deficient in patien

252 d in vitro toward macrophages, away from the dendritic cell phenotype.

253 a suggest that CXCR5-expressing conventional dendritic cells play an important role in the efficient

254 ear phagocytes such as CD11c(+) conventional dendritic cells play an important role in the initial pr

255 ion and proliferation of bone marrow-derived dendritic cells, potentiates the p65-dependent IL-6 and

256 ene expression revealed a novel plasmacytoid dendritic cell precursor preferentially mobilized by ple

257 inhibition of p38alpha in the Ag-presenting dendritic cells prevented CD8 T cell deletion.

258 Our results indicate that macrophages and dendritic cells produce the endocannabinoid, 2-arachidon

259 yte-monocyte progenitors (GMPs) and monocyte-dendritic cell progenitors (MDPs) produce monocytes duri

260 fect GC B cell responses, the loss of Mer in dendritic cells promotes enhanced T cell activation and

261 (CD4(+) T cells coincubated with tolerogenic dendritic cells pulsed with the main peanut allergens [p

262 Dendritic cells rapidly underwent apoptosis in response

263 Targeting of myeloid-dendritic cell receptor DC-SIGN by numerous chronic infe

264 UF1 to its cognate receptor, SIGNR1, on dendritic cells resulted in the regulation of intestinal

265 n of negative regulatory nodes is notable in dendritic cells serving to simultaneously shut down mult

266 The dendritic cell signals required for the in vivo priming

267 s Toll-like receptors 1 and 2, dectin 1, and dendritic cell-specific intercellular adhesion molecule

268 Dendritic cell-specific transmembrane protein (DC-STAMP)

269 reciprocal increase in the CD103(-)CD11b(+) dendritic cell subset.

270 reflected in differences in peripheral blood dendritic cell subsets.

271 DC-SIGN is a dendritic cell surface structure which participates in b

272 lay a higher frequency of CD11b(+) pulmonary dendritic cells than their WT controls at the baseline a

273 creased numbers of circulating monocytes and dendritic cells that produce more inflammatory cytokines

274 types, including subsets of macrophages and dendritic cells that work together to maintain steady-st

275 lamed tissue and give rise to macrophages or dendritic cells, the recruitment kinetics and functional

276 e the age-dependent function of conventional dendritic cells, their role in determining immunodominan

277 oth fusion proteins matured monocyte-derived dendritic cells through TLR5.

278 tumor-infiltrating murine and human myeloid dendritic cells (TIDC) in ovarian cancer.

279 ate their initial delivery toward follicular dendritic cells to establish host infection.

280 is suggests that prions exploit conventional dendritic cells to facilitate their initial delivery tow

281 h activated type 2 innate lymphoid cells and dendritic cells to promote differentiation of T-helper 2

282 h a reduced capacity for trophic form-loaded dendritic cells to stimulate CD4(+) T cell proliferation

283 mmatory cytokines, and recruit monocytes and dendritic cells to the site of damage through a breached

284 Dendritic cells transduced with the adjuvant, an adenovi

285 addition, in the presence of ragweed, mouse dendritic cells upregulated their activation markers, th

286 lines derived from peripheral blood-derived dendritic cells using a nonintegrating RNA virus, Sendai

287 The cellular body area of dendritic cells was about the double in MEL compared wit

288 Decreased CXCL1 production by Nlrp12(-/-) dendritic cells was not due to a difference in CXCL1 pro

289 Indeed, in cultured dendritic cells we found that high salt media potentiate

290 Tolerogenic dendritic cells were differentiated in the presence of I

291 Additionally, both CD8(+) T cells and CD8(+) dendritic cells were identified in the tumor microenviro

292 L, beyond the time of initial encounter with dendritic cells were required for the persistence of hig

293 lls and innate immune cells (macrophages and dendritic cells) where it has been shown to suppress the

294 irect virus protein antigens specifically to dendritic cells, which are now known to be the key cell

295 infection system that utilizes primary human dendritic cells, which display a robust decrease in vira

296 ncubated with antigen, or agonist to CD3 and dendritic cells, with or without antibody against CTLA4;

297 brain, they first replicate upon follicular dendritic cells within intestinal Peyer's patches.

298 ssue macrophages, prion trafficking by B and dendritic cells within the lymphoreticular system, intra

299 ived dendritic cells and interstitial dermal dendritic cells, yet the virus fully replicates only in

300 ols to generate bone marrow-derived cultured dendritic cells yield a heterogeneous mixture, including