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1 ns of cytotoxic and decreased proportions of helper T lymphocytes.
2 often depends on proper cell fate choice by helper T lymphocytes.
3 ls or whether they are mediated by the aging helper T lymphocytes.
4 ion manifested by increased proliferation of helper T lymphocytes.
6 main target of HIV-1 infection is the CD4(+) helper T lymphocyte, a cell type that is responsible for
8 infection and tumors, is produced by CD4(+) helper T lymphocytes after stimulation by cultured dendr
9 e recognition, facilitating contacts between helper T lymphocytes and antigen-presenting cells as wel
10 its ability to induce CMV pp65-specific CTL, helper T lymphocytes, and antibodies in a phase I clinic
11 ic CD8(+) cytotoxic T lymphocytes and CD4(+) helper T lymphocytes can inhibit HBV replication in the
12 Most interestingly, the newly identified helper T lymphocyte epitopes encompass or lie proximal t
13 phocyte), CD8 (cytotoxic T lymphocyte), CD4 (helper T lymphocyte), HAM56 (macrophage), and CD20 (B ly
14 ntigens that specifically activate such CD4+ helper T lymphocytes have now been identified, including
15 tis B core Ag 18-27, linked to the universal helper T lymphocyte (HTL) epitope tetanus toxoid (TT) 83
16 rugs can be ascribed to a few immunodominant helper T lymphocyte (HTL) epitopes, and that reducing th
20 the localization of interleukin-2-producing helper T lymphocytes (HTL) following implantation of spo
21 Human immunodeficiency virus (HIV)-specific helper T lymphocytes (HTL) play a key role in the immune
24 ver, the exact role and specificity of these helper T lymphocytes in mediating allograft damage is pr
25 , graft-reactive cytolytic T lymphocytes and helper T lymphocytes in their spleens and grafts, and al
26 Immune recognition of pMHCII ligands by a helper T lymphocyte involves its antigen-specific T cell
27 T cell receptor-stimulated calcium influx in helper T lymphocytes occurs via channels activated as a
29 mphocyte precursor (CTLp) and IL-2-secreting helper T lymphocyte precursor (HTLp) frequency within gr
34 ons, and that the frequency and magnitude of helper T lymphocyte responses to each peptide is influen
35 ic parasite antigens inducing bovine CTL and helper T-lymphocyte responses for vaccine development ag
37 tigen-presenting cells (APC) with sensitized helper T lymphocytes (TC) producing Th2 cytokines may de
38 atment in patient 2, and numerous follicular helper T lymphocytes (TFH) within the follicular germina
40 In several diseases, an imbalance between helper T lymphocytes Th1 and Th2 and their cytokines has
42 the functions of immune cells, particularly helper T lymphocytes (Ths) and dendritic cells (DCs).
43 Most significantly, the peptide-reactive helper T lymphocytes were capable of recognizing various
44 ing their lytic activity on the tumor cells, helper T lymphocytes will be critical for the induction
45 nation induced virus-specific CTL and CD4(+) helper T lymphocytes with CTL frequencies as high as 20,
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