ライフサイエンスコーパス: T-cell type

1 identifying LDN5-like T cells as a distinct T cell type.

2 All of the lymphoid tumors tested were of T cell type.

3 gain represented the predominant gamma delta T cell type.

4 and delta chains is critical for determining T cell type.

5 g diagnosed with lymphoma, especially of the T-cell type.

6 t stem, hematopoietic stem and primary human T cell types.

7 nt effects on TFH cells and, possibly, other T cell types.

8 e shown to activate TGF-beta1 in several non-T cell types.

9 r T cells depended on targeting a third (non-T) cell type.

10 R beta mRNA expression were observed in both T-cell types.

11 siveness in transient assays in monocyte and T-cell types.

12 cross all six primary sclerosing cholangitis T-cell types.

13 and increased T helper type 1 (Th1)/Th17 and T cell type 1 (Tc1)/Tc17 skin infiltration.

14 In multimarker analysis, the helper T cell type 1 (TH1)-related markers interferon-gamma, IL

15 ansion of antigen-specific regulatory CD4(+) T cell type 1 (TR1)-like cells in different mouse models

16 tion from a helper T cell Type 2 to a helper T cell Type 1 cytokine-biased profile in bronchoalveolar

17 IFN-gamma-dependent networks (perhaps helper T cell type 1 responses) while minimizing the effect of

18 ree groups of genes associated with a CD4(+) T-cell type-1 (Th1) immune response and three clusters l

19 in-10 (IL-10) is an anti-inflammatory helper T cell type 2 (Th2) cytokine that modulates Th1-type cyt

20 IL-13, a helper T cell type 2 (Th2) cytokine, transforms cultured airway

21 as immune deviation in childhood to a helper T cell type 2 (Th2) subtype of CD4(+) cells.

22 ading to the generation of Th2 and cytotoxic T cell type 2 cells but not for IL-4 expression in cells

23 f CD8+ T cells into IL-4-secreting cytotoxic T cell type 2 cells.

24 cumsporozoite protein (CSP) ratios, a helper T cell type 2 cytokine, correlated with higher odds of m

25 Helper T cell type 2 responses in IFN-gamma(-/-) mice correspon

26 s associated with a transition from a helper T cell Type 2 to a helper T cell Type 1 cytokine-biased

27 increased and sustained production of helper T cell Type 2-associated cytokines by splenocytes of HDM

28 In circulating T cells, type 2 cytokine production was elevated in MA,

29 Conversely, eosinophils, Th2 T cells, type 2 innate lymphoid cells, and possibly Foxp

30 eated DCs containing naive allogeneic CD4(+) T cells: type 2 cytokines (IL-6 and IL-13) increased whi

31 lighting the underappreciated role of helper T-cell type 2-related pathways.

32 that the role of each pathway depends on the T cell type and differentiation stage.

33 Other PB T cell types and plasma cytokines were determined by flo

34 DC) subsets in initial activation of the two T cell types and their co-operation.

35 ly increased risk for NHL, especially of the T-cell type and primarily localized in the gut (EATL); (

36 risk for non-Hodgkin lymphoma, especially of T-cell type and primarily localized in the gut.

37 w the antitumor functions of specific CD4(+) T cell types are induced while limiting their protumorig

38 renewing tissues, terminally differentiated (TD) cell types are typically specified through the actio

39 risk for B-cell tumors at all or even to all T-cell types but only to a particular type of T-cell tum

40 tor induction of nuclear factor of activated T cells type c-1 and cathepsin K expression is defective

41 tional activator nuclear factor of activated T cells type c-1, associated with increased gene promote

42 induced lung eosinophilia and type 2 helper T-cell-type cytokines in orally sensitized mice.

43 rstand why X4 HIV-1 strains infection affect T-cell types differently during AIDS development and ind

44 d week 5, the predominance of one particular T cell type emerged, supporting the conclusion that tran

45 ely to be critical in various differentiated T cell types, even when triggered by the same stimulus.

46 destabilizes TCRalpha proteins in all other T cell types examined.

47 reactive T cells, these apparently disparate T cell types generally show simplified patterns of T cel

48 roenvironment is characterized by regulatory T cells, type II macrophages, myeloid-derived suppressor

49 subset, which represents a major gammadelta T cell type in the lymphoid organs and blood of mice, to

50 ongoing cross-talk between distinct effector T cell types in the lungs may contribute to a protective

51 e larger in CD8 Memory T cells than in other T-cell types, indicating an association between T-cell c

52 level ratio, consistent with a type 2 helper T-cell-type inflammatory response, and subacute fibrosis

53 the induction of the IL-17-producing CD8(+) T cell type is largely epitope specific and that this sp

54 on with TGF-beta1, generating another CD8(+) T-cell type lacking both NKG2D and 4-1BB.

55 Brain biopsy confirmed active, T-cell type MS.

56 opathological analysis revealed lymphomas of T-cell type, often comprising a minor B-cell component.

57 Both T-cell types produced IL-17, IL-22, and IFN-gamma, but o

58 ) correlated with the disease resistance and T-cell-type response.

59 ther than the currently proposed specialized T-cell types that have a known lifespan of days.

60 gh there are differences between innate-like T cell types, they share metabolic and functional featur

61 to define unique biomarkers associated with T cell types throughout the progression of ID.

62 dy aims to clarify the contributions of each T cell type to the regulation of squamous cell carcinoma

63 the disease induced by each of the effector T cell types to suppression by polyclonal regulatory T c

64 robe the temporal secretion patterns of each T cell type using real-time binding analyses for direct

65 and the level determines the development of T cell types, which are either protective or pathogenic.

66 sion pattern of GRAIL in other murine CD4(+) T cell types with a described anergic phenotype.

67 ther, our analyses unveil a unique cutaneous T cell type within the native skin microenvironment and