ライフサイエンスコーパス: conventional dendritic cell

1 s-presented Ag by depleting cross-presenting conventional dendritic cells.

2 impaired for viral entry in comparison with conventional dendritic cells.

3 immune cells was limited to a subset of CD8+ conventional dendritic cells.

4 okines and chemokines by bone marrow-derived conventional dendritic cells.

5 issue distribution that differs from that of conventional dendritic cells.

6 persistent TLR4-mediated activation of lung conventional dendritic cells.

7 guishes them from other cell types including conventional dendritic cells.

8 Colon gamma/delta T cells in mice that lack conventional dendritic cells 2 produced increased amount

9 ours after local allergen challenge, whereas conventional dendritic cells accumulated after several d

10 tion with Th2 polarization in the absence of conventional dendritic cell activation.

11 able for their ability to differentiate into conventional dendritic cells after appropriate stimulati

12 a consistently sparse population of resident conventional dendritic cells, among the last cells to in

13 was due to type I IFN-dependent depletion of conventional dendritic cells and could be reproduced by

14 in a paracrine manner, incited activation of conventional dendritic cells and lymphocytes in Cre(LysM

15 on their role in the modulation of CD11b(+) conventional dendritic cells and monocyte-derived dendri

16 iated with a reduction of pulmonary CD11b(+) conventional dendritic cells and regulation of CD4(+) T-

17 enerate pDCs, MPs were polarized to generate conventional dendritic cells and the kinetics of pDC gen

18 the development of NK cells and CD8alpha(+) conventional dendritic cells, and is also involved in ma

19 ected in South African children's monocytes, conventional dendritic cells, and plasmacytoid dendritic

20 molecules produced mainly by macrophages and conventional dendritic cells, as well as type I interfer

21 0 is transiently expressed on the surface of conventional dendritic cells, but is constitutively expr

22 Targeting Ags to conventional dendritic cells can enhance Ag-specific imm

23 associated with an increase in the number of conventional dendritic cells, CD11b(+) and CD103(+) dend

24 odes (LNs) constitutes a central paradigm in conventional dendritic cell (cDC) biology but remains po

25 Here, we used two conventional dendritic cell (cDC) depletion systems to i

26 onstrated that the heart contained two major conventional dendritic cell (cDC) subsets, CD103(+) and

27 function, location, and migratory pattern of conventional dendritic cells (cDC) and plasmacytoid DCs

28 Conventional dendritic cells (cDC) are necessary and suf

29 Conventional dendritic cells (cDC) are professional anti

30 small percentage of CD103(neg) and CD103(+) conventional dendritic cells (cDC) in the intestinal lam

31 APCs, antagonizes inflammation by affecting conventional dendritic cells (cDC), inducing IL-10, and

32 terleukin (IL)-12 by tissue-resident XCR1(+) conventional dendritic cells (cDC1) promoted ILC1 produc

33 show that the human chemokines bound type 1 conventional dendritic cells (cDC1), and that immunizati

34 Here, we report that type 1 conventional dendritic cells (cDC1s), which are defined

35 , one of the most important alkylphenols, on conventional dendritic cells (cDCs) and adaptive T-cell

36 Surprisingly, both conventional dendritic cells (cDCs) and plasmacytoid DCs

37 high-level expression of type 1 IFNs by both conventional dendritic cells (cDCs) and plasmacytoid den

38 Conventional dendritic cells (cDCs) are critical APCs fo

39 Conventional dendritic cells (cDCs) are critical for pro

40 In humans, conventional dendritic cells (cDCs) exist as two unique

41 immature, a small population of CD11c(high) conventional dendritic cells (cDCs) exists that expresse

42 the generation of CD103(+)CD11c(hi)MHCII(hi) conventional dendritic cells (cDCs) from Flt3L-mobilized

43 The existence of conventional dendritic cells (cDCs) has not yet been dem

44 We explored the physiological role of conventional dendritic cells (cDCs) in acute colitis ind

45 I IFN-driven upregulation of FcepsilonRI on conventional dendritic cells (cDCs) in the lung.

46 TLR-stimulated cross-presentation by conventional dendritic cells (cDCs) is important in host

47 Conventional dendritic cells (cDCs) play an essential ro

48 9G2(+) NK cells stabilized and then enhanced conventional dendritic cells (cDCs) recovery after infec

49 t of plasmacytoid dendritic cells (pDCs) and conventional dendritic cells (cDCs) requires the ligand

50 unexpectedly induces IL-1beta production in conventional dendritic cells (cDCs) via a STAT3-dependen

51 Here we show that IL-21 induced apoptosis of conventional dendritic cells (cDCs) via STAT3 and Bim, a

52 Two subsets of conventional dendritic cells (cDCs) with distinct cell s

53 hat localized proximal to IL-1beta-producing conventional dendritic cells (cDCs) within SLT.

54 required for the development of CD8alpha(+) conventional dendritic cells (cDCs), but the basis for t

55 The THSCs--two types of conventional dendritic cells (cDCs), plasmacytoid dendri

56 numbers of Batf3- and Irf8-dependent CD103+ conventional dendritic cells (cDCs), providing new oppor

57 Two conventional dendritic cells (cDCs), the CD8alpha(+)Sirp

58 In conventional dendritic cells (cDCs), the TLR4 ligand bac

59 demonstrate that the impairment lies within conventional dendritic cells (cDCs).

60 n vitro and in vivo responses of mouse IKDC, conventional dendritic cells (DC), and natural killer (N

61 CD141 and CD161 monocytes, absence of CD11c1 conventional dendritic cells (DCs) and CD11c1/CD1231 pla

62 strongly upregulated on splenic CD8alpha(+) conventional dendritic cells (DCs) and plasmacytoid DCs

63 Conventional dendritic cells (DCs) are key APCs for T ce

64 -12 h of antigen administration, followed by conventional dendritic cells (DCs) at 12-24 h, then fina

65 nced by costimulatory molecules expressed on conventional dendritic cells (DCs) in regional lymph nod

66 )34.5 is required to block the maturation of conventional dendritic cells (DCs) that initiate adaptiv

67 recruitment and maturation of monocytes and conventional dendritic cells (DCs), resulting in TH2 pol

68 where myeloid cells, such as macrophages and conventional dendritic cells, detect infections with her

69 d B and plasmacytoid dendritic cell, but not conventional dendritic cell development.

70 with Ebola virus under the same conditions, conventional dendritic cells expressed viral proteins wh

71 ly to the MHC II self-peptidome presented by conventional dendritic cells in vivo.

72 A-aPC inhibited the inflammatory response of conventional dendritic cells independent of EPCR and sup

73 CD103(+) and CD11b(+) conventional dendritic cells interacted directly with TH

74 asmacytoid dendritic cells are necessary for conventional dendritic cell maturation in response to ga

75 that mononuclear phagocytes such as CD11c(+) conventional dendritic cells play an important role in t

76 These data suggest that CXCR5-expressing conventional dendritic cells play an important role in t

77 vity induced when these cells cocluster with conventional dendritic cells presenting Ag to naive Th c

78 c alpha1 subunit in alveolar macrophages and conventional dendritic cells produced less IL-13 and CCL

79 e used to determine whether CXCR5-expressing conventional dendritic cells propagate prions toward FDC

80 on, there was also a significant decrease in conventional dendritic cells recruitment to the lungs of

81 n this study that murine bone marrow-derived conventional dendritic cells responded to GBS by secreti

82 in the specific absence of CXCR5-expressing conventional dendritic cells the early accumulation of p

83 es demonstrate the age-dependent function of conventional dendritic cells, their role in determining

84 s promote the maturation and traffic of lung conventional dendritic cells to draining mediastinal lym

85 This suggests that prions exploit conventional dendritic cells to facilitate their initial

86 dsRNA by viral NS1 explains the inability of conventional dendritic cells to produce IFN-I on infecti

87 ted with enhanced influx of CD11b-expressing conventional dendritic cells to the lungs in response to

88 etion of bone marrow-derived macrophages and conventional dendritic cells was equally inhibited by IN

89 We show in this article that lung-resident conventional dendritic cells were direct targets of IL-2

90 Macrophages, plasmacytoid, and conventional dendritic cells were each implicated based

91 We showed that conventional dendritic cells were the major sources of e

92 We created mice in which mobile conventional dendritic cells were unable to migrate towa