ライフサイエンスコーパス: monocyte-derived dendritic cell

1 mulated KG1 cells (phenotypically similar to monocyte-derived dendritic cells).

2 cytic cell line (THP-1) and in human primary monocyte-derived dendritic cells.

3 he differentiation and the function of human monocyte-derived dendritic cells.

4 by LRP-expressing U87-MG cells and by human monocyte-derived dendritic cells.

5 d upregulation strategy was applied in human monocyte-derived dendritic cells.

6 rnalization was observed in freshly isolated monocyte-derived dendritic cells.

7 LT-induced activation of human monocytes and monocyte-derived dendritic cells.

8 Migration assays were performed using human monocyte-derived dendritic cells.

9 g-fusion protein of BTN2A1 bound to immature monocyte-derived dendritic cells.

10 governing recognition by DC-SIGN on immature monocyte-derived dendritic cells.

11 N-gamma in response to self-CD1 expressed on monocyte-derived dendritic cells.

12 lls, NK cells, and mature, but not immature, monocyte-derived dendritic cells.

13 against infected monocytes, macrophages, and monocyte-derived dendritic cells.

14 essing Mtb39 (adenoMtb39) was used to infect monocyte-derived dendritic cells.

15 ass II-depleted cell cultures by adding back monocyte-derived dendritic cells.

16 stimulation with autologous, ZIKV-infected, monocyte-derived dendritic cells.

17 argeting twenty-one candidate genes in human monocyte-derived dendritic cells.

18 e rise to a subset of monocytes that yielded monocyte-derived dendritic cells.

19 5aR2 expression in pulmonary eosinophils and monocyte-derived dendritic cells.

20 of CD11b(+) conventional dendritic cells and monocyte-derived dendritic cells.

21 ced expression of nitric oxide synthase 2 in monocyte-derived dendritic cells.

22 n TLR stimulation compared with donor-paired monocyte-derived dendritic cells.

23 ction of the interleukin-12 (IL-12) in human monocyte-derived dendritic cells.

24 were CCR2-bearing monocytes/macrophages and monocyte-derived dendritic cells.

25 to be required for the infection of immature monocyte-derived dendritic cells.

26 ticles and fusion to primary CD4 T cells and monocyte-derived dendritic cells.

27 m this method using peripheral cells such as monocytes derived dendritic cells.

28 BK virus peptide libraries loaded or not on monocytes-derived dendritic cells.

29 TF viruses were also captured by monocyte-derived dendritic cells 1.7-fold more efficient

30 Monocyte-derived dendritic cells acquired from male dono

31 oinflammatory cytokine production by MDM and monocyte-derived dendritic cells activated by NOD1 or TL

32 We use our methodology to study how human monocyte-derived dendritic cells alert neighboring cells

33 Transient deletion of monocyte-derived dendritic cells also reduces Th1 and bo

34 om transcriptomic data measuring response of monocyte derived dendritic cells and A549 epithelial cel

35 mpletely inhibited FVIII endocytosis by both monocyte-derived dendritic cells and bone marrow-derived

36 In this study, the interaction between human monocyte-derived dendritic cells and C. jejuni was studi

37 rophages (MDMs), which differed from that in monocyte-derived dendritic cells and CD4 T cells, withou

38 re system of AIRE-expressing primary patient monocyte-derived dendritic cells and demonstrated that c

39 dent type I IFN responses in healthy primary monocyte-derived dendritic cells and fibroblasts.

40 In microchamber migration assays, monocyte-derived dendritic cells and IL-2-activated natu

41 GN is a major receptor for infection of both monocyte-derived dendritic cells and interstitial dermal

42 mit the virus to CD4 T cells; CD14(+)CD1c(+) monocyte-derived dendritic cells and langerin-expressing

43 mbination of alpha-galactosylceramide-loaded monocyte-derived dendritic cells and low-dose lenalidomi

44 a strongly reduced internalization by human monocyte-derived dendritic cells and macrophages, as wel

45 wn to elicit inflammatory responses by human monocyte-derived dendritic cells and macrophages, includ

46 se- and ligand dose-dependent manner in both monocyte-derived dendritic cells and monocyte-derived ma

47 In in vitro assays human monocyte-derived dendritic cells and primary keratinocyt

48 They induce IL-10 secretion from human monocyte-derived dendritic cells and proved effective in

49 ne production probably via the activation of monocyte-derived dendritic cells and the TLR, TLR2, and

50 By contrast, infection of monocyte-derived dendritic cells and transfer of infecti

51 We compared monocyte-derived dendritic cells and transforming growth

52 IPSE/alpha-1 was confirmed in human primary monocyte-derived dendritic cells and was found to be a c

53 ulated these abnormal cellular phenotypes in monocytes-derived dendritic cells and primary activated

54 ing antigens in common with blood monocytes, monocyte-derived dendritic cells, and macrophages, NLCs

55 nes with correlated expression in monocytes, monocyte-derived dendritic cells, and neutrophils.

56 ivated plasmacytoid dendritic, TLR-activated monocyte-derived dendritic cells, and on B cells stimula

57 ophages, peripheral blood mononuclear cells, monocyte-derived dendritic cells, and plasmacytoid dendr

58 ease from PBMCs, LPS-triggered maturation of monocyte-derived dendritic cells, and tetanus toxoid-ind

59 Monocyte-derived dendritic cells are active participants

60 B cells, but not monocytes or monocyte-derived dendritic cells, are observed to expres

61 lso inhibited the production of IL-12 p70 by monocyte-derived dendritic cells, as well as the product

62 e expression of the above antigens occurs on monocyte-derived dendritic cells, because these molecule

63 DC is highly expressed in macrophages and in monocyte-derived dendritic cells, but not in monocytes,

64 In contrast to monocyte-derived dendritic cells, CD11b(high)Ly6C(+) cel

65 addition of TLF to human peripheral blood or monocyte-derived dendritic cell cultures resulted in cel

66 ls, have both been associated with arrest of monocyte-derived dendritic cell (DC) differentiation and

67 ation and function of cells committed to the monocyte-derived dendritic cell (DC) lineage.

68 ne receptor CCR2 was implicated in mediating monocyte-derived dendritic cell (DC) recruitment into th

69 ribe a phenotypically and functionally novel monocyte-derived dendritic cell (DC) subset, designated

70 responses, we developed an in vitro model of monocyte-derived dendritic cell (DC)-dependent, human na

71 Monocyte-derived dendritic cells (DC) also have been fou

72 FDF03 was also strongly expressed by monocyte-derived dendritic cells (DC) and preferentially

73 of CMV pp65 messenger RNA-loaded autologous monocyte-derived dendritic cells (DC) as a cellular vacc

74 ting step in the process of generating human monocyte-derived dendritic cells (DC) for clinical appli

75 s spectrometry) of microfilaria (mf)-exposed monocyte-derived dendritic cells (DC) indicated that mul

76 Monocyte-derived dendritic cells (DC) possess the unique

77 and C5a did not suppress IL-12 production by monocyte-derived dendritic cells (DC) stimulated with CD

78 Human monocyte-derived dendritic cells (DC) transduced with Ad

79 Cultured, monocyte-derived dendritic cells (DC) were transiently t

80 Stimulation of monocyte-derived dendritic cells (DC) with stress agents

81 highly enriched populations of HIV-infected monocyte-derived dendritic cells (DC).

82 ere cocultured with autologous DenV-infected monocyte-derived dendritic cells (DC).

83 ces a semimature, tolerogenic state on human monocyte-derived dendritic cells (DCs) activated by a pr

84 llergen drives the differentiation of CD209+ monocyte-derived dendritic cells (DCs) and CD23+ (FceRII

85 gonist, FP7, in vitro on human monocytes and monocyte-derived dendritic cells (DCs) and in vivo durin

86 Monocyte-derived dendritic cells (DCs) and macrophages (

87 nses via surface TLR2, which is expressed on monocyte-derived dendritic cells (DCs) and NK cells.

88 affect trafficking of monocytes/macrophages, monocyte-derived dendritic cells (DCs) and T-helper cell

89 Human monocyte-derived dendritic cells (DCs) are capable of ex

90 Importantly, when purified matured monocyte-derived dendritic cells (DCs) are used as stimu

91 s were used to test protein binding to human monocyte-derived dendritic cells (DCs) by flow cytometry

92 f cytokine regulation were observed in human monocyte-derived dendritic cells (DCs) costimulated with

93 er the immunostimulatory properties of human monocyte-derived dendritic cells (DCs) could be enhanced

94 We investigated whether human monocyte-derived dendritic cells (DCs) differed from ton

95 Autologous monocyte-derived dendritic cells (DCs) electroporated wi

96 igate whether iNKT cells can be activated by monocyte-derived dendritic cells (DCs) exposed to lipid

97 Generation of human monocyte-derived dendritic cells (DCs) for cancer vaccin

98 induce caspase-dependent apoptosis in human monocyte-derived dendritic cells (DCs) in vitro.

99 r associated with DAP12/KARAP that activates monocyte-derived dendritic cells (DCs) in vitro.

100 e expression patterns were measured in human monocyte-derived dendritic cells (DCs) infected in vitro

101 Autologous monocyte-derived dendritic cells (DCs) pulsed with this

102 However, the infected inflammatory monocyte-derived dendritic cells (DCs) that transport M.

103 Exposure of human monocyte-derived dendritic cells (DCs) to cell culture-g

104 ergens and nonallergenic homologues on human monocyte-derived dendritic cells (DCs) to investigate ho

105 wn to promote chemotactic migration of human monocyte-derived dendritic cells (DCs) toward the chemok

106 Monocyte-derived dendritic cells (DCs) transfected with

107 Human monocytes and monocyte-derived dendritic cells (DCs) were exposed to Y

108 Monocyte-derived dendritic cells (DCs) were stimulated w

109 The infection of cultured monocyte-derived dendritic cells (DCs) with HIV-1 involv

110 o systems of nasal epithelial cells (HNECs), monocyte-derived dendritic cells (DCs), and HNEC-DC co-c

111 roducing Ly6C(hi) inflammatory monocytes and monocyte-derived dendritic cells (DCs), suggesting that

112 aureus In coculture with S. aureus-infected monocyte-derived dendritic cells (DCs), Vdelta2(+) cells

113 investigated the effect of ICOS-Fc on human monocyte-derived dendritic cells (DCs).

114 GN for invasion and persistence within human monocyte-derived dendritic cells (DCs).

115 individuals, and stimulated with autologous monocyte-derived dendritic cells (DCs).

116 nt (Seppic Inc, Fairfield, NJ), or pulsed on monocyte-derived dendritic cells (DCs).

117 nd were directly inhibitory toward activated monocyte-derived dendritic cells (DCs).

118 ritic-like cells (KG-1 and MUTZ-3) and human monocyte-derived dendritic cells (DCs).

119 Additional studies using immature monocyte-derived dendritic cells demonstrated that altho

120 so expressed on circulating dendritic cells, monocyte-derived dendritic cells, dendritic cells in lym

121 , mannose receptor, or DC-SIGN expression in monocyte-derived dendritic cells did not prevent FVIII u

122 fection from relapsers and observed impaired monocyte-derived dendritic cell differentiation, a reduc

123 nocyte CD11b and CD86 expression, and induce monocyte-derived dendritic cell differentiation.

124 ial challenge assays using keratinocytes and monocyte-derived dendritic cells established distinct IL

125 cyte-derived human macrophages (MDM) but not monocyte-derived dendritic cells express basal levels of

126 When pulsed with targeted liposomes, human monocyte-derived dendritic cells expressing CD169/Sn act

127 gB-recombinant glycoprotein interaction with monocyte-derived dendritic cells expressing DC-SIGN.

128 Methods to "polarize" human monocyte-derived dendritic cells for the preferential in

129 pregulation of CD40, CD80, CD83, and CD86 on monocyte-derived dendritic cells from allergic patients

130 Monocyte-derived dendritic cells from healthy volunteers

131 reduced costimulatory molecule expression on monocyte-derived dendritic cells from healthy volunteers

132 Finally, human monocyte-derived dendritic cells from IRF5 disease-assoc

133 emokine and cytokine secretion compared with monocyte-derived dendritic cells from low-expressing IRF

134 An MD-2-like activity is also released by monocyte-derived dendritic cells from normal donors.

135 s also have an effect on monocyte and moDCs (monocyte-derived dendritic cells) function, driving thei

136 We investigated the ability of monocyte-derived dendritic cells generated in the presen

137 fied myeloid dendritic cells, monocytes, and monocyte-derived dendritic cells (GM-CSF/IL-4/TGF-beta).

138 e- and genome-wide analyses in primary human monocyte-derived dendritic cells here showed that TLR8 s

139 The capacity of human monocyte-derived dendritic cells (hmoDCs) to capture foo

140 e found on endothelial cells, human immature monocyte-derived dendritic cells (iDCs) bound rBRAK with

141 moted tumour-directed maturation of immature monocyte-derived dendritic cells (iDCs).

142 SP-D enhanced the binding of HIV to immature monocyte derived dendritic cells (iMDDCs) and was also f

143 ons were demonstrated in LGTV-infected human monocyte-derived dendritic cells, important target cells

144 We have used monocyte-derived dendritic cells in a limiting dilution

145 This work redefines the role of monocyte-derived dendritic cells in melanoma and provide

146 e HCV-specific CD8(+) T cells and autologous monocyte-derived dendritic cells in the absence or prese

147 contained significantly more macrophages and monocyte-derived dendritic cells in the dermis after VAC

148 ses, it stimulated strong IL-12 responses by monocyte-derived dendritic cells in the presence of IFN-

149 Expression of CD1d was found on monocyte-derived dendritic cells in vitro, and immunohis

150 chain B molecules expressed by ZIKV-infected monocyte-derived dendritic cells, in synergy with IL-12

151 rleukin-18 (IL-18)-dependent manner, whereas monocyte-derived dendritic cells induced NK activation t

152 ounters between human T cells and allogeneic monocyte-derived dendritic cells induces durable, profou

153 antiviral landscape in a population of human monocyte-derived dendritic cells infected with ZIKV at t

154 s maintained or induced during dermal DC and monocyte-derived dendritic cell/inflammatory dendritic e

155 overexpression in cell lines and in primary monocyte-derived dendritic cells inhibits the replicatio

156 tes, conventional dendritic cells (DCs), and monocyte-derived dendritic cells internalized and proces

157 flammatory cytokine expressing monocytes and monocyte-derived dendritic cells involved in innate immu

158 ether proinflammatory cytokine expression by monocyte-derived dendritic cells is affected by the indu

159 oma, infects three types of dendritic cells: monocyte-derived dendritic cells, Langerhans cells, and

160 This study shows that human blood monocyte-derived dendritic cells loaded with liposome-co

161 N-gamma to neutrophil-depleted mice restores monocyte-derived dendritic cell maturation and reactive

162 this antiviral activity were cocultured with monocyte-derived dendritic cells matured with CD40 ligan

163 fect the in vitro maturation and function of monocyte-derived dendritic cells (MDC).

164 IFN-alpha) and inducible chemokines by human monocyte-derived dendritic cells (mDCs) and plasmacytoid

165 gamma interferon (IFN-gamma) dependent, and monocyte-derived dendritic cells (mDCs) promote IgG2 pro

166 l miRNA-protein networks that regulate human monocyte-derived dendritic cell (MDDC) differentiation.

167 We used monocyte-derived dendritic cells (MDDC) and CD4 T cells

168 Although macrophages (Mphi) and monocyte-derived dendritic cells (MDDC) come from a comm

169 Monocytes and monocyte-derived dendritic cells (mdDC) from allergic pa

170 d cytokine secretion was diminished in human monocyte-derived dendritic cells (MDDC) from rs7282490 I

171 ed to monocyte-derived macrophages (MDM) and monocyte-derived dendritic cells (MDDC) in virus-like pa

172 ycoproteins on virus uptake by primary human monocyte-derived dendritic cells (MDDC) in vitro and on

173 we investigated the effects of PMT on human monocyte-derived dendritic cells (MDDC) in vitro and sho

174 We have previously shown that HHV-8 enters monocyte-derived dendritic cells (MDDC) through DC-SIGN,

175 es and cells with the morphology of immature monocyte-derived dendritic cells (MDDC) were observed.

176 de more TNF, IL-6, and pro-IL-1beta than did monocyte-derived dendritic cells (MDDC), despite similar

177 either human monocyte-derived macrophages or monocyte-derived dendritic cells (MDDC).

178 SHAS-OVA were taken up by human monocyte-derived dendritic cells (mdDCs) and murine DCs

179 profile of gene expression of human immature monocyte-derived dendritic cells (MDDCs) and peripheral

180 ously showed that galectin-1 activates human monocyte-derived dendritic cells (MDDCs) and triggers a

181 NAg), but not deglycosylated PNAg, activated monocyte-derived dendritic cells (MDDCs) as measured by

182 Monocyte-derived dendritic cells (MDDCs) can efficiently

183 Human monocyte-derived dendritic cells (MDDCs) infected with T

184 a hypothesis that mature rhesus monkey (Rh) monocyte-derived dendritic cells (MDDCs) modified by gen

185 ediates the binding and transfer of HIV from monocyte-derived dendritic cells (MDDCs) to permissive T

186 , leaving the immune system and specifically monocyte-derived dendritic cells (MDDCs) understudied.

187 on of adenosine receptors expressed by human monocyte-derived dendritic cells (MDDCs) was performed w

188 alpha, upregulate costimulatory molecules in monocyte-derived dendritic cells (MDDCs), enabling effec

189 Human monocyte-derived dendritic cells (MDDCs), myeloid dendri

190 t of Vpr for facilitating HIV-1 infection of monocyte-derived dendritic cells (MDDCs), one of the fir

191 nd CD4(+) T-cells and compared it to that of monocyte-derived dendritic cells (MDDCs), which are less

192 nduced maturation and migration processes of monocyte-derived dendritic cells (MDDCs).

193 oluble E2 bound to immature and mature human monocyte-derived dendritic cells (MDDCs).

194 e and membrane trafficking in immature human monocyte-derived dendritic cells (MDDCs).

195 AL008 also promoted human monocyte-derived dendritic cell-mediated T cell prolifer

196 ation of Vy9Vd2 T cells by Lm-infected human monocyte-derived dendritic cells (Mo-DC) we engineered L

197 oid cells, including monocytes, macrophages, monocyte-derived dendritic cells (mo-DC), and dendritic

198 wledge, we cultured live B. burgdorferi with monocyte-derived dendritic cells (mo-DCs) from healthy d

199 ic inflammatory monocytes differentiate into monocyte-derived dendritic cells (MO-DCs), which are CD1

200 relies on lung-infiltrating neutrophils and monocyte-derived dendritic cells (Mo-DCs).

201 hose for ex vivo human primary monocytes and monocyte-derived dendritic cells (Mo-mDC).

202 Human monocyte-derived dendritic cell (MoDC) have been used in

203 blocking or enhancing the Tim3-Gal9 axis on monocyte-derived dendritic cell (moDC) maturation and T-

204 ent publication, Ramalho et al. investigated monocyte-derived dendritic cell (MODC) mobilization in r

205 Here we identified a Wfdc21-dependent monocyte-derived dendritic cell (moDC) population that f

206 ired recruitment of Ly6C(high) monocytes and monocyte-derived dendritic cells (moDC) and lower moDC c

207 Cross-talk between Candida-confronted monocyte-derived dendritic cells (moDC) and NK cells res

208 and LAMP-2 (CD107b) on the surface of human monocyte-derived dendritic cells (MoDC) and show only LA

209 vivo administration of IS on the ability of monocyte-derived dendritic cells (MoDC) to differentiate

210 s can be locally activated upon injection of monocyte derived dendritic cells (moDCs) that presented

211 A class II assembly, but human monocytes and monocyte-derived dendritic cells (moDCs) also contain si

212 e-course infection of THP-1 cell line, human monocyte-derived dendritic cells (MoDCs) and macrophages

213 Human in vitro generated monocyte-derived dendritic cells (moDCs) and macrophages

214 e in a mouse food allergy model and on human monocyte-derived dendritic cells (moDCs) and PBMCs.

215 suppression of IL6R-alpha signaling in human monocyte-derived dendritic cells (moDCs) and T cells, ou

216 and adult monocytes were differentiated into monocyte-derived dendritic cells (MoDCs) and TLR agonist

217 mmunological properties of UCB monocytes and monocyte-derived dendritic cells (MoDCs) are not fully c

218 We recently showed that monocyte-derived dendritic cells (moDCs) are responsible

219 ocytes can differentiate into macrophages or monocyte-derived dendritic cells (MoDCs) but the molecul

220 ch human cytomegalovirus (HCMV) infection of monocyte-derived dendritic cells (moDCs) contribute to i

221 Monocyte-derived dendritic cells (moDCs) dramatically in

222 Monocyte-derived dendritic cells (moDCs) expressed abund

223 induced activation of neonatal monocytes and monocyte-derived dendritic cells (MoDCs) have not been r

224 here to determine the global alterations in monocyte-derived dendritic cells (moDCs) in response to

225 d that Ebola virus (EBOV) infection of human monocyte-derived dendritic cells (moDCs) inhibits dendri

226 This PD-L1 upregulation was observed in monocyte-derived dendritic cells (MoDCs) obtained from e

227 s stimulated ex vivo using either autologous monocyte-derived dendritic cells (moDCs) or HLA-A2-Ig-ba

228 P[13] replicated more extensively in porcine monocyte-derived dendritic cells (MoDCs) than did HRV Wa

229 -ICs in human B cells and in CD23-expressing monocyte-derived dendritic cells (moDCs) that represent

230 igens from more than one mTEC, and of these, monocyte-derived dendritic cells (moDCs) were determined

231 Neonatal monocyte-derived dendritic cells (moDCs) were exposed to

232 HLA-typed monocyte-derived dendritic cells (moDCs) were incubated

233 es in IFN induction and the role of DI RNAs, monocyte-derived dendritic cells (moDCs) were infected w

234 naling pathway when porcine peripheral blood monocyte-derived dendritic cells (MoDCs) were treated wi

235 uce a rapid (after 1 d) accumulation of host monocyte-derived dendritic cells (moDCs) without any inc

236 cyte-derived macrophages (MDMs), (iii) bound monocyte-derived dendritic cells (MoDCs), and (iv) trans

237 ransfected human cell lines (MelJuso), human monocyte-derived dendritic cells (moDCs), and murine bon

238 , Ly6c(hi) monocyte-derived Mphis (moMphis), monocyte-derived dendritic cells (moDCs), and myeloid-de

239 eated (bafilomycin and cytochalasin D) human monocyte-derived dendritic cells (moDCs), bone marrow-de

240 panded using HLA-mismatched immature, mature monocyte-derived dendritic cells (moDCs), or PBMCs.

241 ved accumulation of activated, antigen-laden monocyte-derived dendritic cells (moDCs), promoting long

242 granulation when cocultured with T cells and monocyte-derived dendritic cells (moDCs).

243 tudy, we examined the effects of beta(2)M on monocyte-derived dendritic cells (MoDCs).

244 py (RT) is controlled by the accumulation of monocyte-derived dendritic cells (moDCs).

245 ) monocytes into microbicidal macrophages or monocyte-derived dendritic cells (moDCs).

246 the PD-1/PD-L1 coinhibitory pathway on human monocyte-derived dendritic cells (MoDCs).

247 In vitro cultures of different cell types (monocyte-derived dendritic cells [moDCs], PBMCs [periphe

248 crophages and a subclass of dendritic cells (monocyte-derived dendritic cells, MoDCs), but they also

249 asize the therapeutic potential of targeting monocyte-derived dendritic cells, neutrophils, cellular

250 d IL-10 axis resulted in increased pulmonary monocyte-derived dendritic cell numbers and increased IF

251 sed type 2 innate lymphoid cells (ILC2s) and monocyte-derived dendritic cell numbers in the mediastin

252 Uptake of exosomes by monocyte-derived dendritic cells occurred silently, main

253 onocytes were up to 40-fold more potent than monocyte-derived dendritic cells or CD2- monocytes at in

254 genes are both expressed in LCs, but not in monocyte-derived dendritic cells, or in blood CD1c(+) or

255 CD4(+) T (p < 0.05), monocyte-derived dendritic cells (p = 0.06), and interme

256 aryotic sources, when transfected into human monocyte-derived dendritic cell precursors, induces high

257 In human monocytes and monocyte-derived dendritic cells preincubated with IFN-g

258 Human monocyte-derived dendritic cell preparations infected wi

259 cytes displayed limited differentiation into monocyte-derived dendritic cells, reduced formation of r

260 flammatory cytokines in PBMCs, maturation of monocyte-derived dendritic cells (rendering their profil

261 macrophages, but detection on the surface of monocyte-derived dendritic cells required stimulation wi

262 evels of mutant CARD9 protein, the patients' monocyte-derived dendritic cells responded poorly to CAR

263 s of the Ag-presenting function of CD1+CD83+ monocyte-derived dendritic cells showed that such cells

264 report that primary human CD1c(+) as well as monocyte-derived dendritic cells significantly upregulat

265 cytokine expression was scrutinized in human monocyte-derived dendritic cells stimulated with the fun

266 hemotherapy is the standard of care, a human monocyte-derived dendritic cell/T cell/carcinoma cell li

267 production by both autologous monocytes and monocyte-derived dendritic cells than either LT-IIa- or

268 In primary human monocytes and monocyte-derived dendritic cells, the RIG-I agonist bloc

269 Both fusion proteins matured monocyte-derived dendritic cells through TLR5.

270 ndritic cells and transfer of infection from monocyte-derived dendritic cells to CD4+ T cells were me

271 In a model of trans infection from monocyte-derived dendritic cells to T cells, chimeric vi

272 uptake by and maturation of peripheral blood monocyte-derived dendritic cells together with an inflam

273 21 and increases the chemotactic response of monocyte-derived dendritic cells toward higher CCL21 con

274 Human monocyte-derived dendritic cells up-regulate maturation

275 In addition, we generated monocyte-derived dendritic cells using PBMC obtained dur

276 e capacity to induce cytokines from cultured monocyte-derived dendritic cells was opposite to this ac

277 Binding capacity of N8-GP on human monocyte-derived dendritic cells was reduced compared wi

278 viruses, and the responses of infected human monocyte-derived dendritic cells were determined.

279 The monocyte-derived dendritic cells were driven toward a my

280 In vitro monocyte-derived dendritic cells were generated from hea

281 Human monocyte-derived dendritic cells were pulsed with CFP10

282 can express TL1A, fresh blood monocytes and monocyte-derived dendritic cells were stimulated with va

283 When human blood monocyte-derived dendritic cells were used, IL-38 as wel

284 itioned NK cells triggered the maturation of monocyte-derived dendritic cells, which promoted T cell

285 pendent manner, leading to the generation of monocyte-derived dendritic cells with a tolerogenic cyto

286 ignificant shift in the ratio of circulating monocyte-derived dendritic cells with significantly diff

287 Notably, we identified monocyte-derived dendritic cells within PA subendothelia