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 induced by cytosolic double-stranded DNA in 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 try restriction factor to HIV-1 infection in myeloid dendritic cells.

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

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

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

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

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

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

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

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

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

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

20 Circulating myeloid dendritic cells also possess this costimulatory

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

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

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

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

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

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

27 Although myeloid dendritic cells and monocytes showed superior pr

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

43 Moreover, myeloid dendritic cells both activated Valpha24JalphaQ T

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

76 Myeloid dendritic cells (DCs) are the first professional

77 Myeloid dendritic cells (DCs) coordinate innate immune r

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

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

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

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

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

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

84 Myeloid dendritic cells (DCs) were characterized by usin

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

113 Myeloid dendritic cells isolated from lung-draining lymp

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

136 Airway myeloid dendritic cells (mDCs) and plasmacytoid dendriti

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

154 Myeloid dendritic cells (mDCs) were differentiated from

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

171 8+ regulatory T cells significantly suppress myeloid dendritic cell-mediated tumor-associated antigen

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

188 6C+ population comprised primarily of mature myeloid dendritic cells, suggesting that the underlying

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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