ライフサイエンスコーパス: myeloid dendritic cell

1 activated immune cells (including NK, T, and myeloid dendritic cells).

2 acrophages and subsets of neurons but not in myeloid dendritic cells.

3 body myositis and polymyositis are primarily myeloid dendritic cells.

4 accumulation of T helper 17 lymphocytes and myeloid dendritic cells.

5 activated macrophages, NK cells, and mature myeloid dendritic cells.

6 ctivator of several cell types, particularly myeloid dendritic cells.

7 lopment of mature myeloid progeny, including myeloid dendritic cells.

8 ified hemozoin on the in vitro activation of myeloid dendritic cells.

9 t for the recruitment and differentiation of myeloid dendritic cells.

10 induced by cytosolic double-stranded DNA in myeloid dendritic cells.

11 lls, NK-cells, B-cells, monocyte subsets and myeloid dendritic cells.

12 try restriction factor to HIV-1 infection in myeloid dendritic cells.

13 ext of caspase-1 activation in monocytes and myeloid dendritic cells.

14 es HagB-induced chemokine responses in human myeloid dendritic cells.

15 Therefore, we isolated dsRNA complex in myeloid dendritic cells.

16 eriod to 9 mo of age in monocytes but not in myeloid dendritic cells.

17 ndritic cells clustered together with CD11c+ myeloid dendritic cells, a distinct dendritic cell subse

18 dendritic cells, but not functionally mature myeloid dendritic cells, accumulated in tumor microenvir

19 d cells B cells, neutrophils, monocytes, and myeloid dendritic cells all efficiently bound Spike prot

20 in plasmacytoid dendritic cells, whereas in myeloid dendritic cells, all three family members were e

21 We found NET intermingling with myeloid dendritic cells also positive for neutrophil mye

22 Circulating myeloid dendritic cells also possess this costimulatory

23 on of infection, eosinophils expand IL-10(+) myeloid dendritic cells and CD4(+) IL-10(+) T lymphocyte

24 At this time point, the number of myeloid dendritic cells and expression of CD80 and CD86

25 e TSLP (29-130 + 131-159) strongly activated myeloid dendritic cells and group 2 innate lymphoid cell

26 as associated with a significant increase in myeloid dendritic cells and in vivo induction of CD4+/CD

27 sting that the antiviral cytokine sensitized myeloid dendritic cells and macrophages toward TLR4 liga

28 The number of pulmonary lymphoid and myeloid dendritic cells and macrophages was increased up

29 Although myeloid dendritic cells and monocytes showed superior pr

30 CCR7 deficiency led to an accumulation of myeloid dendritic cells and T cells in the lung in respo

31 a2 induced the recruitment and activation of myeloid dendritic cells and Th2 cells in the lung, causi

32 ET favors neutrophil proteins uploading into myeloid dendritic cells and the induction of ANCAs and a

33 gulated kinase 1/2-positive monocyte-derived myeloid dendritic cells, and increased vimentin expressi

34 macrophages, CD3+ T cells, monocyte-derived myeloid dendritic cells, and keratinocytes expressing in

35 elative dearth of MOG35-55-specific T cells, myeloid dendritic cells, and neutrophils, as well as an

36 hemokine MCP-1, which attracts monocytes and myeloid dendritic cells, and of the cytokine macrophage-

37 an monocyte-derived dendritic cells (MDDCs), myeloid dendritic cells, and plasmacytoid dendritic cell

38 acrophages, CD4+ T cells, and CD11b+ CD11c+ (myeloid) dendritic cells, and increased arginase1 and Ym

39 Because myeloid dendritic cells are a major source of IL-12 and

40 Plasma cells and myeloid dendritic cells are abundant in polymyositis and

41 In HIV-1 infection, myeloid dendritic cells are highly dysfunctional, but me

42 erferon (IFN-gamma), TNF-alpha, and IL-12 in myeloid dendritic cells are of importance in generating

43 al frequencies of intermediate monocytes and myeloid dendritic cells at baseline.

44 tage of CD1c(+)CD19(-)CD14(-)CD303(-) type 1 myeloid dendritic cells at disease onset had a significa

45 g have been demonstrated in plasmacytoid and myeloid dendritic cells, B cells, and T cells.

46 ignificant separation between species, while myeloid dendritic cells best associated macaque populati

47 Immature bone marrow-derived myeloid dendritic cells (BMDCs) are induced to undergo p

48 pha) in wild-type murine bone marrow-derived myeloid dendritic cells (BMDCs) but did not stimulate in

49 Moreover, myeloid dendritic cells both activated Valpha24JalphaQ T

50 S-induced signalling pathways selectively in myeloid dendritic cells but not in macrophages.

51 s gave rise to granulocyte, monocyte, and/or myeloid dendritic cells, but not MegE lineage cells in t

52 psoriasis pathogenesis, termed inflammatory myeloid dendritic cells (CD11c(+)/blood dendritic cell (

53 r stroma showed enrichment of two subsets of myeloid dendritic cells (cDC), cDC1 and cDC2, that secre

54 so seen in other subsets, including CD11c(+) myeloid dendritic cells, classical monocytes, two subset

55 Accordingly, myeloid dendritic cells co-cultured with esophageal aden

56 in contrast to plasmacytoid dendritic cells, myeloid dendritic cells, co-cultured with Barrett's esop

57 nofluorescence staining, CD11c+, a marker of myeloid dendritic cells, colocalized with PD-L1 and PD-L

58 the effect of intracellular mammalian DNA on myeloid dendritic cell (DC) activation.

59 the study of signaling pathways involved in myeloid dendritic cell (DC) differentiation, we have dev

60 phase of acute infection, Tetherin enhanced myeloid dendritic cell (DC) function.

61 mammalian target of rapamycin (mTOR), during myeloid dendritic cell (DC) generation confers resistanc

62 The misguided myeloid dendritic cell (DC) model proposes that high-ris

63 oviral delivery of human TGF-beta1 to murine myeloid dendritic cell (DC) progenitors on (i) their in

64 unctional differences between the human skin myeloid dendritic cell (DC) subsets, epidermal CD207(+)

65 mice resulted in the reduced accumulation of myeloid dendritic cells (DC) and activated CD4(+) T cell

66 Monocytes are the common precursors for myeloid dendritic cells (DC) and macrophages.

67 toid cells (PC) and CD1c(+) peripheral blood myeloid dendritic cells (DC) are two human DC precursors

68 e by modulating the functional properties of myeloid dendritic cells (DC) during the acute immune res

69 red the maturation of human monocyte-derived myeloid dendritic cells (DC) following inoculation with

70 In this study, we propagated myeloid dendritic cells (DC) from BALB/c (H2(d)) mouse b

71 In small animals and humans, conventional myeloid dendritic cells (DC) have been shown to select o

72 d vigorous primary T-cell immune response by myeloid dendritic cells (DC) in blood and tissues could

73 sulted in the accumulation of iNKT cells and myeloid dendritic cells (DC) in pancreatic lymph nodes (

74 c and functional differences between classic myeloid dendritic cells (DC), and DC that reportedly dev

75 uclear leukocytes, macrophages, T cells, and myeloid dendritic cells (DC).

76 M-CSF + IL-4 stimulated, bone marrow-derived myeloid dendritic cells (DC).

77 Crosslinking CD28 by agonistic antibodies or myeloid dendritic cells (DC; these express the CD28 liga

78 ough there is evidence for distinct roles of myeloid dendritic cells (DCs [mDCs]) and plasmacytoid pr

79 ial, whether expansion of inflammatory blood myeloid dendritic cells (DCs) and conversion of Tregs to

80 lope 2 proteins (E2), activate monocytes and myeloid dendritic cells (DCs) and partially reproduce ab

81 virtually all blood immune cells, including myeloid dendritic cells (DCs) and plasmacytoid DCs (pDCs

82 We characterized lesional myeloid dendritic cells (DCs) and T cells and their infl

83 CD11c(+) myeloid dendritic cells (DCs) and the serum epidermal gr

84 tural killer (NK) cells and plasmacytoid and myeloid dendritic cells (DCs) are depleted, and their fu

85 Myeloid dendritic cells (DCs) are potent APCs and play a

86 We find that human myeloid dendritic cells (DCs) are superior to other anti

87 Myeloid dendritic cells (DCs) are the first professional

88 Myeloid dendritic cells (DCs) coordinate innate immune r

89 Immature myeloid dendritic cells (DCs) express only low levels of

90 To determine the phenotype and function of myeloid dendritic cells (DCs) from human cutaneous squam

91 circulating osteoclast precursors (OCPs) and myeloid dendritic cells (DCs) in blood.

92 In this review, we discuss the role of myeloid dendritic cells (DCs) in cell-associated HIV-1 t

93 nocytes, nonclassical monocytes, and CD1c(+) myeloid dendritic cells (DCs) in the blood, and mutation

94 In response to locally produced calcitriol, myeloid dendritic cells (DCs) migrated from cutaneous va

95 Myeloid dendritic cells (DCs) were characterized by usin

96 CD207+ Langerhans cells (LCs) and CD11c+ myeloid dendritic cells (DCs) were found in both the epi

97 ells are activated by lipid Ags presented by myeloid dendritic cells (DCs), after which they generate

98 ating B lymphocytes, monocytes, neutrophils, myeloid dendritic cells (DCs), and at very low levels on

99 ession of the costimulatory molecule CD86 on myeloid dendritic cells (DCs), and reduced the number of

100 s and a mixed population of plasmacytoid and myeloid dendritic cells (DCs), including cells expressin

101 s-derived eVLPs elicited maturation of human myeloid dendritic cells (DCs), indicating their immunoge

102 fect of IFNbeta in mature, but not immature, myeloid dendritic cells (DCs).

103 ation, including monocytes, macrophages, and myeloid dendritic cells (DCs).

104 efficiently infects and replicates in human myeloid dendritic cells (DCs).

105 ion of human embryonic stem (hES) cells into myeloid dendritic cells (DCs).

106 mulatory molecule CD40 on neonatal and adult myeloid dendritic cells (DCs).

107 examined in the context of the maturation of myeloid dendritic cells (DCs).

108 is characterized by the liver enrichment of myeloid dendritic cells (DCs).

109 Additionally, chompB mice have decreases in myeloid dendritic cells (DCs).

110 the contrary, adoptive transfer of wild-type myeloid dendritic cells did not have such effects.

111 inflamed tissue, and supports the concept of myeloid dendritic cell differentiation from trafficking

112 Moreover, CNS pDCs suppressed CNS myeloid dendritic cell-driven production of IL-17, IFN-g

113 igen-presenting cells (mostly Langerhans and myeloid dendritic cells) exhibit a tolerogenic phenotype

114 -55)), microglial cells and CNS-infiltrating myeloid dendritic cells expressed CMKLR1, as determined

115 Additionally, a large frequency of colonic myeloid dendritic cells expressed IL-15Ra, implicating m

116 Myeloid dendritic cells expressed phosphorylated peroxis

117 migration, activation, and Ag-processing of myeloid dendritic cells from the lung to the draining ly

118 tal autoimmune encephalomyelitis but, unlike myeloid dendritic cells, have a minor role in T cell act

119 cules CD80, CD86, and CD40, on monocytes and myeloid dendritic cells in a TLR-dependent manner.

120 e been shown to increase suppressor immature myeloid dendritic cells in cancer patients.

121 lic surface ligand-coated AuNP that targeted myeloid dendritic cells in lymph nodes as a peptide anti

122 Macrophages and myeloid dendritic cells in the kidney were detected as C

123 ndritic cells expressed IL-15Ra, implicating myeloid dendritic cells in trans presentation of IL-15 t

124 t IL-4 induces recruitment and maturation of myeloid dendritic cells in vivo and increases T cell rec

125 Finally, chemerin stimulation of myeloid dendritic cells induced the high-affinity bindin

126 LC2 were similar to monocytes or myeloid dendritic cells, involving in immune responses a

127 urthermore, Ly49Q expression on pDC, but not myeloid dendritic cells, is necessary for optimal IL-12

128 Myeloid dendritic cells isolated from lung-draining lymp

129 od mononuclear cells identified migration of myeloid/dendritic cell lineage cells one day after vacci

130 We demonstrate that CNS-infiltrating myeloid dendritic cells, macrophages, and resident micro

131 Using primary culture HBEC and human myeloid dendritic cell (mDC) cocultures, we show in this

132 ndritic cell release of IFN-B, and assessing myeloid dendritic cell (mDC) contribution to hydroxychlo

133 Current immunological opinion holds that myeloid dendritic cell (mDC) precursors migrate from the

134 LACV infection indicated that differences in myeloid dendritic cell (mDC) responses between weanling

135 The mechanism of myeloid dendritic cell (mDC)-mediated impaired T-cell fu

136 Myeloid dendritic cells (mDC) activated with a B7-DC-spe

137 When individual populations were isolated, myeloid dendritic cells (mDC) and macrophages but not pl

138 receptor (TLR) responses of peripheral blood myeloid dendritic cells (mDC) and monocytes were tempora

139 Freshly purified myeloid dendritic cells (MDC) and plasmacytoid DC (PDC)

140 Whereas many studies have assessed myeloid dendritic cells (mDC) in the induction of antitu

141 In mice, CD8alpha(+) myeloid dendritic cells (mDC) optimally cross-present Ag

142 Blood monocytes, myeloid dendritic cells (mDC), and monocyte-derived DC (

143 n iNKT cells and CD1d-expressing circulating myeloid dendritic cells (mDC), as mDC of patients with a

144 particularly macrophages, granulocytes, and myeloid dendritic cells (mDC).

145 In vitro, myeloid dendritic cells (mDCs) (GM-CSF bone marrow-deriv

146 of the activating FcgammaRIIa on circulating myeloid dendritic cells (mDCs) after high-dose, but not

147 fect and induce maturation of human CD11c(+) myeloid dendritic cells (MDCs) and CD123(+) plasmacytoid

148 he main activities of TSLP are activation of myeloid dendritic cells (mDCs) and modulation of cytokin

149 d the cytokine responses of peripheral blood myeloid dendritic cells (mDCs) and monocytes to in vitro

150 -induced changes in gene expression in human myeloid dendritic cells (mDCs) and monocytes, identify s

151 ly TLR7/8-L and TLR9-L induced activation of myeloid dendritic cells (mDCs) and plasmacytoid DCs (pDC

152 rus and RSV mobilize immune cells, including myeloid dendritic cells (mDCs) and plasmacytoid dendriti

153 Airway myeloid dendritic cells (mDCs) and plasmacytoid dendriti

154 that is characterized by reduced numbers of myeloid dendritic cells (mDCs) and Th17 cells in the CNS

155 Monocytes and myeloid dendritic cells (mDCs) are important orchestrato

156 Phenotypically immature myeloid dendritic cells (mDCs) are preferentially infect

157 improves the functional capacity of classic myeloid dendritic cells (mDCs) by altering expression of

158 VEE) exhibited enhanced infection of primary myeloid dendritic cells (mDCs) compared to mammalian-cel

159 Type 1 myeloid dendritic cells (mDCs) contribute to inception o

160 Lung myeloid dendritic cells (mDCs) derived from cigarette sm

161 To directly assess the role of C5L2 on myeloid dendritic cells (mDCs) during allergen sensitiza

162 ow that a fraction of blood monocyte-derived myeloid dendritic cells (MDCs) express B7-H1, a member o

163 oncoding RNA (lncRNA) MIR4435-2HG in primary myeloid dendritic cells (mDCs) from ECs.

164 late carbon black (nCB) accumulates in human myeloid dendritic cells (mDCs) from emphysematous lung a

165 Myeloid dendritic cells (mDCs) have long been thought to

166 t plasmacytoid predendritic cells (pDCs) and myeloid dendritic cells (mDCs) have the functional plast

167 We found that miR-22 was upregulated in lung myeloid dendritic cells (mDCs) of smokers with emphysema

168 lood dendritic cell antigen-1(+) (BDCA-1(+)) myeloid dendritic cells (mDCs) present during BKPyVAN (o

169 - and STAT6-dependent expansion of recipient myeloid dendritic cells (MDCs) that induce contact-depen

170 intracellular double-stranded DNA (dsDNA) in myeloid dendritic cells (mDCs) that triggers a type I in

171 By contrast, myeloid dendritic cells (MDCs) were absent from malignan

172 Myeloid dendritic cells (mDCs) were differentiated from

173 of CD4 T, CD8 T, B, and NK cells, monocytes, myeloid dendritic cells (mDCs), and plasmacytoid dendrit

174 production of the chemoattractant CXCL16 by myeloid dendritic cells (mDCs), causing subsequent recru

175 Similar frequencies of myeloid dendritic cells (mDCs), plasmacytoid DCs (pDCs),

176 Peripherally derived CD11b(+) myeloid dendritic cells (mDCs), plasmacytoid DCs, CD8alp

177 el (ESM), and mouse bone marrow (BM)-derived myeloid dendritic cells (mDCs), T cells (TCs), B cells,

178 s of SHFV infection, macrophages (MPhis) and myeloid dendritic cells (mDCs), were differentiated from

179 (alpha/beta interferon [IFN-alpha/beta]) in myeloid dendritic cells (mDCs), where the mosquito cell-

180 A rare subset of myeloid dendritic cells (mDCs), which are blood DC antig

181 eceptor is selectively expressed by BDCA3(+) myeloid dendritic cells (mDCs), which have been proposed

182 istently diminished H3K27ac in monocytes and myeloid dendritic cells (mDCs), which was associated wit

183 helicases, as an intracellular DNA sensor in myeloid dendritic cells (mDCs).

184 ember, as an important viral dsRNA sensor in myeloid dendritic cells (mDCs).

185 d sequencing of poly I:C-binding proteins in myeloid dendritic cells (mDCs).

186 SLPR) when compared with levels expressed in myeloid dendritic cells (mDCs).

187 breakdown through the activation of immature myeloid dendritic cells (mDCs).

188 itis, Porphyromonas gingivalis, infect blood myeloid dendritic cells (mDCs).

189 of contaminating CD56(-), CD14(-), CD11c(+) myeloid dendritic cells (mDCs).

190 i.e., B cells, macrophages, monocyte-derived/myeloid dendritic cells (MDDCs/mDCs), and by plasmacytoi

191 8+ regulatory T cells significantly suppress myeloid dendritic cell-mediated tumor-associated antigen

192 cells were observed in most CD11c(+)CD103(+) myeloid dendritic cells migrating to mediastinal drainin

193 the innate response identified monocytes and myeloid dendritic cells (MoDC) as principal responders t

194 onRI on plasmacytoid dendritic cells (pDCs), myeloid dendritic cells, monocytes, and basophils was as

195 y, TLR8 agonists directly activated purified myeloid dendritic cells, monocytes, and monocyte-derived

196 Plasmacytoid dendritic cells (pcDC) and myeloid dendritic cells (myDC) are shown to express CD4

197 define expression of CD200R on macrophages, myeloid dendritic cells, natural killer cells, and T cel

198 allergic inflammation, through decreases in myeloid dendritic cell numbers.

199 essed specifically on human pDCs, but not on myeloid dendritic cells or other peripheral blood leukoc

200 independently activate CB2R or PPARgamma in myeloid dendritic cells (p < 0.05).

201 d activation of primary immune cells such as myeloid dendritic cells, plasmacytoid dendritic cells, a

202 Monocytes, macrophages, myeloid dendritic cells, plasmacytoid dendritic cells, n

203 memory CD4 T cells and HLA-DR expression by myeloid dendritic cells, pointing toward defective cross

204 On immunohistochemistry, only the myeloid dendritic cell population was significantly incr

205 In conclusion, increased myeloid dendritic cell population with higher TNF-alpha

206 Targeting of myeloid-dendritic cell receptor DC-SIGN by numerous chro

207 Inflammatory myeloid dendritic cells release IL-23 and IL-12 to activ

208 es demonstrated that IFN-alpha modulated the myeloid dendritic cell response pattern by upregulating

209 ased CD11b expression on a subset of splenic myeloid dendritic cells, resulting in compromised recrui

210 results demonstrated that A(H3N2)vpM-induced myeloid dendritic cells secreted significantly lower lev

211 st to classical contact dermatitis, in which myeloid dendritic cells sense haptens, pDCs are primary

212 itic cells and our observed results in human myeloid dendritic cells, show that DEFB103 significantly

213 tions through interleukin-10; (c) repetitive myeloid dendritic cell stimulation can recover CD8+ regu

214 6C+ population comprised primarily of mature myeloid dendritic cells, suggesting that the underlying

215 ) cytokine response and expanded a subset of myeloid dendritic cells that expressed a CD11c(high)CD8a

216 SE significantly increased the proportion of myeloid dendritic cells that produced tumor necrosis fac

217 accumulation of bone marrow-derived immature myeloid dendritic cells that recruit activated lymphocyt

218 of cathepsin E message and protein in human myeloid dendritic cells, the preeminent APCs of the immu

219 ved dendritic cells (DCs) and CD23+ (FceRII) myeloid dendritic cells through the action of allergen-s

220 e the function of monocytes, macrophages and myeloid dendritic cells through the action of haemozoin

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

222 )CD8(-)CD209a(+)) and human (CD1c(+)CD19(-)) myeloid dendritic cells (TIDC), an innate immune cell ty

223 Histamine also suppressed LPS-induced myeloid dendritic cell TNF-alpha secretion and suppresse

224 thermore, imiquimod-mediated increase in the myeloid dendritic cells, TNF/inducible nitric oxide synt

225 irpin RNA efficiently reduced the ability of myeloid dendritic cells to produce IFN-beta, IL-6, and T

226 However, when bone marrow-derived myeloid dendritic cells trafficked to popliteal lymph no

227 Myeloid dendritic cells type 2 (mDC2s) are a new subtype

228 In contrast, PU.1 converted them into myeloid dendritic cells under identical culture conditio

229 sion of CCL21 were oppositely regulated, and myeloid dendritic cells upregulated CCR7 expression.

230 und that an early immune response cell type, myeloid dendritic cells, was critical for protection in

231 Although myeloid dendritic cells were able to interact with S and

232 ls, plasmacytoid dendritic cells (pDCs), and myeloid dendritic cells were characterized by flow cytom

233 more, several genes associated with immature myeloid dendritic cells were overexpressed in LCH CD207(

234 Both plasmacytoid and IgE(+)FcepsilonRI(+) myeloid dendritic cells were present in BAL fluid.

235 uman myeloid cell frequencies, specifically, myeloid dendritic cells, were elevated in the bone marro

236 found in isolated activated macrophages and myeloid dendritic cells, were widely distributed in all

237 e expression of FcepsilonRIalpha on pDCs and myeloid dendritic cells when compared with that seen in

238 th HIV-1, elite controllers have circulating myeloid dendritic cells with significantly increased ant