ライフサイエンスコーパス: T-lymphocyte subset

1 continuous activation/proliferation of this T-lymphocyte subset.

2 on robust generation of functionally diverse T lymphocyte subsets.

3 nd vitamin A on birth outcomes and counts of T lymphocyte subsets.

4 eptors expressed on natural killer cells and T lymphocyte subsets.

5 killer lymphocytes and dysfunction of other T lymphocyte subsets.

6 iltrating CD4 and CD8 lymphocytes and CXCR3+ T-lymphocyte subsets.

7 of pro- and anti-inflammatory cytokines and T-lymphocyte subsets.

8 ansferred IL-9-secreting CD8+ Tc9 (cytotoxic T lymphocyte subset 9) cells exert greater persistence a

9 We compared T lymphocyte subsets among HIV-HHV-8+ and HIV-HHV-8- inf

10 cluster of differentiation (CD)8alpha/beta+ T lymphocyte subset and the percentage of CD8alpha/beta+

11 sion allows the detection of discrete CD8(+) T lymphocyte subsets and may be useful for assessing the

12 ted numbers of human CD4(+) naive and memory T lymphocyte subsets and skin- and gut-homing memory T c

13 a before and after ART initiation, examining T-lymphocyte subsets and inflammatory biomarkers in peri

14 g to the spleen index, thymus index, splenic T-lymphocyte subsets, and other immune-related cytokines

15 procedures in which absolute cell counts of T lymphocyte subsets are calculated from observed percen

16 In parallel, T lymphocyte subsets, as key constituents of the adaptiv

17 D8(+), central memory CD4(+), and regulatory T-lymphocyte subsets at enrollment was not associated wi

18 The evolutionary conservation of T lymphocyte subsets bearing alphabeta TCRs using invari

19 cells affecting both memory and naive CD4(+) T lymphocyte subsets following administration by either

20 kout mice revealed a requirement for the CD4 T lymphocyte subset for the complete rejection of tumors

21 ue characteristics of B, CD4(+) T and CD8(+) T-lymphocyte subsets from monozygotic twins, we quantify

22 represent the first analysis of the role of T lymphocyte subsets in immunity to spotted fever group

23 We decided to evaluate the role of T lymphocyte subsets in tumor immunity induced by recomb

24 However, they are the most abundant T-lymphocyte subset in some epithelial barriers such as

25 used to characterize functional activity of T-lymphocyte subsets in humans infected with T. gondii.

26 The role of T-lymphocyte subsets in recovery from foot-and-mouth dis

27 The importance of T-lymphocyte subsets in the control of poxvirus infectio

28 We examined the dynamics of specific B- and T-lymphocyte subsets induced by primary series vaccinati

29 e because of (a) reduction in CCR5 and CXCR3 T-lymphocyte subset infiltration into the graft, (b) att

30 define this population as a distinct memory T-lymphocyte subset, intermediate between naive and cent

31 arthritis is the segregation of CD4 and CD8 T lymphocyte subsets into distinct microdomains within t

32 However, the T-lymphocyte subsets involved in the pathophysiology of

33 Determination of T-lymphocyte subsets is a simple and effective parameter

34 Transfer of specific T lymphocyte subsets isolated from the spleens of health

35 from B6.C-H2bm12 mice were transplanted into T lymphocyte subset knockout recipients and T lymphocyte

36 T lymphocyte subsets, monocytes and neutrophils from org

37 ntrols the differentiation and function of a T lymphocyte subset, NK1+ natural T cells, proposed to r

38 naive, unactivated CD26(low) CD45RA+ CD45R0- T lymphocyte subset of peripheral blood lymphocytes.

39 No modification of memory T lymphocytes subsets or numbers was observed in the per

40 Adoptive transfer of T lymphocyte subset populations into nude recipients con

41 We further identified a CD4(+) T lymphocyte subset producing IFN-gamma together with a

42 Circulating T-lymphocyte subset profiles in conventional HIV- BDD we

43 iously shown that gammadeltaT cells, a small T lymphocyte subset, reduce acute inflammatory lung dama

44 PG27 largely normalized splenic T lymphocyte subsets, reduced allospecific cytotoxic T l

45 Flow cytometric analyses of T lymphocyte subsets revealed that the proportions of Fc

46 ly, in vivo depletion of either CD4+ or CD8+ T lymphocyte subsets significantly prolonged survival in

47 Recently, the T lymphocyte subset T(H)17 was shown to play a role in r

48 nt increases in the frequency of CD4 and CD8 T lymphocyte subsets, T cell activation markers CXCR3, C

49 We show that NFATx mRNA was expressed in all T lymphocyte subsets tested and was highest in CD4+CD8+

50 advances in the understanding of the diverse T lymphocyte subsets that provide acute and long-term pr

51 the differentiation and function of several T lymphocyte subsets that provide immunity to infection,

52 staining was significantly reduced on CD8(+) T lymphocyte subsets that showed immunophenotypic eviden

53 infectivity assays, using live sorted CD4(+) T lymphocyte subsets, that 30-90% of circulating naive c

54 The precise role and contributions of T lymphocyte subsets to CAV development remains unknown.

55 o investigate the ability of distinct CD4(+) T lymphocyte subsets to enter and persist in non-lymphoi

56 The relative contributions of T-lymphocyte subsets to host defense in cattle infected

57 We evaluated mucosal T lymphocyte subsets, virus-specific cellular responses,

58 termine if distinct alphabeta and gammadelta T-lymphocyte subsets were involved in the response of th

59 The three T-lymphocyte subsets were positively correlated with CD4

60 Here we identified colonic CD4(+) and CD8(+) T lymphocyte subsets with gene expression profiles resem

61 reconstituted different quantities of CD4(+) T lymphocyte subsets with preferential expansion of CXCR

62 We analyzed the kinetics of T-lymphocyte subsets within the first 8 months posttrans