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

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

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

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

6 5aR2 expression in pulmonary eosinophils and 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 of CD11b(+) conventional dendritic cells and monocyte-derived dendritic cells.

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

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

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

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

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

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

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

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

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

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

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

28 Monocyte-derived dendritic cells acquired from male dono

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

44 We compared monocyte-derived dendritic cells and transforming growth

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

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

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

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

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

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

51 Monocyte-derived dendritic cells are active participants

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

114 Monocyte-derived dendritic cells from healthy volunteers

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

157 Monocyte-derived dendritic cells (MDDCs) can efficiently

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

181 Monocyte-derived dendritic cells (moDCs) dramatically in

182 Monocyte-derived dendritic cells (moDCs) expressed abund

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

206 Human monocyte-derived dendritic cell preparations infected wi

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

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

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

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

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

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

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

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

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

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

217 Human monocyte-derived dendritic cells up-regulate maturation

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

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

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

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

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

223 Human monocyte-derived dendritic cells were pulsed with CFP10

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

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

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

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

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