ライフサイエンスコーパス: natural regulatory T-cell

1 while enhancing accumulation of pre-existing natural regulatory T cells.

2 phenotype cells, memory phenotype cells, and natural regulatory T cells.

3 ells (TMTregs) arose both from precommitted "natural" regulatory T cells and CD4(+)CD25(-)GITR(low) p

4 okines and decreased baseline frequencies of natural regulatory T cells but not interleukin 10 or tra

5 subset of human CD4(+)CD25(high)FoxP3(high) natural regulatory T cells (DR(+) Tregs) that induces mo

6 h elevated T helper 2 cytokines and aberrant natural regulatory T cell function and is unique in havi

7 Smad3 was found to be dispensable for natural regulatory T cell function.

8 ve thymic development and selection and lack natural regulatory T cells, implicating a breakdown of b

9 ncreased adaptive T regulatory cells but not natural regulatory T cells in LTB.

10 tive CD4(+) T cells into disease-suppressing natural regulatory T cells, in a beta56-67-regulated man

11 cells lacked many of the characteristics of natural regulatory T cells, including Foxp3.

12 significantly increased expression of Foxp3 (natural regulatory T cell marker) and regulatory effecto

13 ecifically activating CD4(+)CD25(Hi)FoxP3(+) natural regulatory T cells (nT(Regs)).

14 opment, including the generation of Foxp3(+) natural regulatory T cells (nTreg cells) and the continu

15 Natural regulatory T cells (nTreg) play a central role i

16 T-bet is essential for natural regulatory T cells (nTreg) to regulate Th1 infla

17 ith thymic-derived Foxp3 regulatory T cells (natural regulatory T cells (nTreg)).

18 th thymic-derived Foxp3+ regulatory T cells (natural regulatory T cells (nTreg)).

19 lls that arise from the thymus, analogous to natural regulatory T cells (nTreg).

20 es contain inherent pathways, in the form of natural regulatory T-cells (nTreg), that globally dampen

21 relationship between the TCR repertoires of natural regulatory T cells (nTregs) and conventional CD4

22 n a loss of peripheral tolerance mediated by natural regulatory T cells (nTregs) and development of a

23 a decline in both the functional capacity of natural regulatory T cells (nTregs) and in PLP(139-151)-

24 The low number of natural regulatory T cells (nTregs) in the circulation s

25 udies have failed to investigate the role of natural regulatory T cells (nTregs) on the mitigation of

26 Natural regulatory T cells (nTregs) play an important ro

27 Natural regulatory T cells (nTregs) that develop in the

28 can use TGF-beta produced by thymus-derived natural regulatory T cells (nTregs) to convert them to T

29 to augmented global reconstitution of CD4(+) natural regulatory T cells (nTregs), CD4(+) induced Treg

30 on of the cytokine IL-10 and the activity of natural regulatory T cells (nTregs).

31 elected, negatively selected, or selected as natural regulatory T cells (nTregs).

32 "Natural" regulatory T cells (nTregs) that express the tr

33 autoimmunity through negative regulation of natural regulatory T cell numbers by inhibiting the deve

34 h a significant increase in proliferation of natural regulatory T cells, resulting in an increase in

35 CD4(+)CD25(+)Foxp3(+) natural regulatory T cells (T reg cells) maintain self-t

36 The thymic natural regulatory T cell (Treg) compartment of NOD mice

37 TFR are natural regulatory T cells (TREG) that migrate into the

38 not observe human CD83 on unstimulated human natural regulatory T cells (Treg), in contrast to report

39 S2 as being preferentially expressed in both natural regulatory T cells (Tregs) and inducible Tregs (

40 stitutively expressed on dendritic cells and natural regulatory T cells (Tregs) but only detected on

41 Therapeutic CD4(+)Foxp3(+) natural regulatory T cells (Tregs) can control experimen

42 Natural regulatory T cells (Tregs) constitutively expres

43 This decrease was the result of increased natural regulatory T cells (Tregs) generated by high vir

44 Natural regulatory T cells (Tregs) participate in respon

45 cial role in the development and function of natural regulatory T cells (Tregs).

46 tion factor, Foxp3, is a master regulator of natural regulatory T cells (Tregs).

47 recipient mice was examined, a deficiency in natural regulatory T cells was noted.