ライフサイエンスコーパス: thymus-derived

1 s possess the alphabeta T-cell receptor, the thymus-derived alphabeta CD8 antigen heterodimer, and si

2 Here we report the identification of thymus-derived alphabeta-T-cell receptor+ cells that exp

3 nonclassical, NK1.1+ alphabeta T cells, the thymus-derived, CD1.1-specific DN32H6 T cell hybridoma.

4 derived DCs, associated with an expansion of thymus-derived CD25(+)Foxp3(+) CD4 T cells.

5 mogeneous population of naturally occurring, thymus-derived CD4(+)CD25(+) cells (nTregs).

6 The thymus-derived CD4(+)CD25(+) T cells belong to a subset

7 Thymus-derived CD4(+)Foxp3(+) regulatory T lymphocytes (

8 ssion has been well-established and, besides thymus-derived CD4+CD25+ regulatory T (TR) cells, it bec

9 eir genetic program from naturally occurring thymus-derived CD4+CD25+ TR cells.

10 d in a relative increase of the frequency of thymus-derived CD4CD25Foxp3 Treg cells with intact suppr

11 -/- mice coexpress CD8 beta, a marker of the thymus-derived CD8+ T cells.

12 croscopy of murine PLNs to study the role of thymus-derived chemotactic agent (TCA)-4 (secondary lymp

13 d with type 1 egg-induced responses and that thymus-derived chemotactic agent 3 (TCA3), eotaxin, MIP-

14 , macrophage inflammatory protein-1beta, and thymus-derived chemotactic agent 3) do not compete for T

15 Thymus-derived chemotactic agent 4 (TCA4), a new member

16 id tissue chemokine (SLC) (6Ckine, Exodus-2, thymus-derived chemotactic agent 4 [TCA-4]).

17 e (SLC) (also known as 6Ckine, Exodus-2, and thymus-derived chemotactic agent 4), a recently describe

18 tant protein-1, T cell activation gene 3, or thymus-derived chemotactic agent 4.

19 We further show that bovine thymus-derived extracts contain antigens found in neural

20 Thymus-derived Foxp3(+) natural regulatory CD4 T cells (

21 ncer that RT enhanced spontaneous priming of thymus-derived (FOXP3+Helios+) Tregs by the tumor.

22 ripheral niches that are usually occupied by thymus-derived gammadeltaT17 cells.

23 Thymus-derived glucocorticoids antagonize T cell recepto

24 We have previously demonstrated that thymus-derived glucocorticoids antagonize TCR-mediated d

25 These results indicate that thymus-derived glucocorticoids determine where the windo

26 (ID1(tg/WT)) have a large pool of primarily thymus-derived ILC2s in the periphery that develop in th

27 al killer T cells (V(alpha)14iNKT cells) are thymus-derived innate T cells at the interface between t

28 Semi-invariant NKT cells are thymus-derived innate-like lymphocytes that modulate mic

29 Thymus-derived lung ILC2s of E protein-deficient mice sh

30 It is generally accepted that thymus-derived lymphocytes (T cells) are critically invo

31 Thymus-derived lymphocytes protect mammalian hosts again

32 Moreover, IL-6 can use TGF-beta produced by thymus-derived natural regulatory T cells (nTregs) to co

33 cells) to the effects of equivalent expanded thymus-derived natural Treg (nTreg) cells on established

34 Tregs can be divided into thymus-derived natural Tregs (tTregs) and peripherally-d

35 n-specific means can trigger the response of thymus-derived natural Tregs as well as induce Tregs.

36 ription factor Helios, which is expressed by thymus-derived natural Tregs, was increased in Tregs aft

37 Thymus-derived (natural) CD4(+) FoxP3(+) regulatory T ce

38 Thymus-derived, natural CD4(+)CD25(+) regulatory T cells

39 Thymus-derived naturally occurring regulatory T (nTreg)

40 -cells (NFAT) to control regulatory T cells: thymus-derived naturally occurring regulatory T cells (n

41 Thymus-derived, naturally occurring CD4(+)CD25(+)Foxp3(+

42 d2(-/-)E2A(-/-) mice have characteristics of thymus-derived NK cells, which develop in the absence of

43 Fetal liver- and thymus-derived NK1.1+ cells do not express known Ly-49 r

44 sion of the rearranged TCR beta-chain from a thymus-derived NK1.1+ Valpha14+ T cell hybridoma promote

45 tion is critical for the proper emergence of thymus-derived NKT cells in the mouse.

46 -expression is required for both spleen- and thymus-derived nTreg-mediated suppression, but is not re

47 n were found in normal bone marrow cells and thymus-derived or fetal liver-derived normal lymphocyte

48 In addition to thymus-derived or natural T regulatory (nT(reg)) cells,

49 specific subset of CD4(+) T cells, known as thymus-derived or natural T(reg) (nT(reg)) cells, in res

50 overy of thymopoiesis and development of new thymus-derived peripheral T cells.

51 IL-7 and enhanced proliferation of both the thymus-derived progenitor cells and the bone marrow-deri

52 (CD4CD45ROCD25-CD127) cells, Th1 cells, and thymus-derived regulatory (Treg) (CD4CD45ROCD25CD127) ce

53 cription factor critical for the function of thymus-derived regulatory T (Treg) cells (ie, FOXP3), re

54 Thymus-derived regulatory T (tTreg) cells are key to pre

55 in a substantial reduction in the number of thymus-derived regulatory T cells (T reg cells) in mice.

56 sion of self antigen in a peripheral tissue, thymus-derived regulatory T cells (T(reg) cells) become

57 cells can be generated in the thymus, termed thymus-derived regulatory T cells (tTregs), but their de

58 y T cells induced ex vivo are the progeny of thymus-derived regulatory T cells bearing a similar phen

59 Nrp1 also helps migrate thymus-derived regulatory T cells to vascular endothelia

60 esting that Th1/Th17 cells are not converted thymus-derived regulatory T cells.

61 Specifically, the loss of the perinatal thymus-derived resident dermal population resulted in de

62 SDF-1 mRNA was previously detected in human thymus-derived stromal cells, but its role in thymopoies

63 and CD4+CD25+ regulatory T (Treg) cells are thymus-derived subsets of regulatory T cells that have a

64 y T cells were shown to represent a distinct thymus-derived T cell subset, also suggest the role of a

65 These results demonstrate that mature, thymus-derived T cells can migrate to the intestine and

66 In 73 of the infants, thymus-derived T cells expressing CD45RA and T-cell anti

67 that the homing and/or expansion of typical, thymus-derived T cells in the intestine may be driven by

68 ect expression of the human CD8 beta gene on thymus-derived T cells in transgenic animals.

69 phaalpha IELs) are an abundant population of thymus-derived T cells that protect the gut barrier surf

70 Since CD8 expression on thymus-derived T cells was normal, other enhancers regul

71 can be compensated for by the production of thymus-derived T cells, although the new naive T cells m

72 at 6F/6F mice generated increased numbers of thymus-derived T reg cells.

73 suggesting that FOXP3(+) cells in NP are not thymus-derived T-reg.

74 blood cell rosettes were used as markers for thymus-derived (T) lymphocytes and one of its subpopulat

75 cytes with either bone marrow-derived (B) or thymus-derived (T) surface markers.

76 events through modification of the primary, thymus-derived TCR repertoire.

77 IL-7(+/-) mice had similar numbers of fetal thymus-derived TCRgammadelta cells in their skin.

78 Together, these results show that thymus-derived, Thy1+alphabetaTCR+ donor cells generated

79 We show that thymus-derived Treg cells constitute most Treg cells in

80 s how self-antigens define the repertoire of thymus-derived Treg cells to subsequently endow this cel

81 Thymus-derived Treg cells were selected by self-antigens

82 , either pre- or post-PTCy ablation of donor thymus-derived Tregs (tTregs) abolished PTCy protection

83 The Treg compartment is composed of thymus-derived Tregs (tTregs) and peripheral Tregs (pTre

84 Thymus-derived Tregs (tTregs) and their peripherally ind

85 t and function of the two main Treg subsets, thymus-derived Tregs and induced Tregs (iTregs).

86 e selection of autoreactive B cells required thymus-derived Tregs and MHC class II-restricted self-an

87 nduced in the absence of naturally occurring thymus-derived Tregs.

88 rity of gingival gammadeltaT cells are fetal thymus-derived Vgamma6(+) cells, and to a lesser extent