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

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

4 on robust generation of functionally diverse T lymphocyte subsets.

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

29 T lymphocyte subsets, monocytes and neutrophils from org

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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