269 related articles for article (PubMed ID: 15030573)
21. Ethanol affects the generation, cosignaling molecule expression, and function of plasmacytoid and myeloid dendritic cell subsets in vitro and in vivo.
Lau AH; Abe M; Thomson AW
J Leukoc Biol; 2006 May; 79(5):941-53. PubMed ID: 16478920
[TBL] [Abstract][Full Text] [Related]
22. Limited costimulatory molecule expression on renal tubular epithelial cells impairs T cell activation.
Waeckerle-Men Y; Starke A; Wahl PR; Wüthrich RP
Kidney Blood Press Res; 2007; 30(6):421-9. PubMed ID: 17975322
[TBL] [Abstract][Full Text] [Related]
23. Semi-allogeneic dendritic cells can induce antigen-specific T-cell activation, which is not enhanced by concurrent alloreactivity.
Wells JW; Cowled CJ; Darling D; Guinn BA; Farzaneh F; Noble A; Galea-Lauri J
Cancer Immunol Immunother; 2007 Dec; 56(12):1861-73. PubMed ID: 17487489
[TBL] [Abstract][Full Text] [Related]
24. Glycogen synthase kinase 3 activity during development of bone marrow-derived dendritic cells (DCs) essential for the DC function to induce T helper 2 polarization.
Ono T; Yanagawa Y; Iwabuchi K; Nonomura K; Onoé K
Immunology; 2007 Oct; 122(2):189-98. PubMed ID: 17490435
[TBL] [Abstract][Full Text] [Related]
25. Role of dendritic cells in the priming of CD4+ T lymphocytes to peptide antigen in vivo.
Levin D; Constant S; Pasqualini T; Flavell R; Bottomly K
J Immunol; 1993 Dec; 151(12):6742-50. PubMed ID: 7903097
[TBL] [Abstract][Full Text] [Related]
26. Selective antigen presenting activity of cortical thymic epithelial cells against CD4+ T cells associated with both lack of costimulatory molecules and inefficient presentation of MHC-peptide ligands.
Kaneda R; Iwabuchi K; Kasai M; Murakami M; Uede T; Onoé K
Cell Immunol; 1997 Nov; 181(2):163-71. PubMed ID: 9398403
[TBL] [Abstract][Full Text] [Related]
27. B7/CD28-dependent and -independent induction of CD40 ligand expression.
Ding L; Green JM; Thompson CB; Shevach EM
J Immunol; 1995 Dec; 155(11):5124-32. PubMed ID: 7594521
[TBL] [Abstract][Full Text] [Related]
28. Preparation of fully activated dendritic cells capable of priming tumor-specific cytotoxic T lymphocytes in patients with metastatic cancer using penicillin-killed streptococcus pyogenes (OK432) and anti-CD40 antibody.
Kontani K; Teramoto K; Ozaki Y; Sawai S; Tezuka N; Ishida H; Kajino K; Fujino S; Yamauchi A; Taguchi O; Kannagi R; Yokomise H; Ogasawara K
Oncol Rep; 2007 Apr; 17(4):895-902. PubMed ID: 17342333
[TBL] [Abstract][Full Text] [Related]
29. Herpes simplex virus (HSV) amplicon-mediated codelivery of secondary lymphoid tissue chemokine and CD40L results in augmented antitumor activity.
Tolba KA; Bowers WJ; Muller J; Housekneckt V; Giuliano RE; Federoff HJ; Rosenblatt JD
Cancer Res; 2002 Nov; 62(22):6545-51. PubMed ID: 12438249
[TBL] [Abstract][Full Text] [Related]
30. CD40 activation boosts T cell immunity in vivo by enhancing T cell clonal expansion and delaying peripheral T cell deletion.
Maxwell JR; Campbell JD; Kim CH; Vella AT
J Immunol; 1999 Feb; 162(4):2024-34. PubMed ID: 9973474
[TBL] [Abstract][Full Text] [Related]
31. Concerted antigen presentation by dendritic cells and B cells is necessary for optimal CD4 T-cell immunity in vivo.
Kleindienst P; Brocker T
Immunology; 2005 Aug; 115(4):556-64. PubMed ID: 16011524
[TBL] [Abstract][Full Text] [Related]
32. Ketamine inhibits maturation of bone marrow-derived dendritic cells and priming of the Th1-type immune response.
Ohta N; Ohashi Y; Fujino Y
Anesth Analg; 2009 Sep; 109(3):793-800. PubMed ID: 19690248
[TBL] [Abstract][Full Text] [Related]
33. Split peripheral tolerance: CD40 ligation blocks tolerance induction for CD8 T cells but not for CD4 T cells in response to intestinal antigens.
Chung Y; Ko SY; Ko HJ; Kang CY
Eur J Immunol; 2005 May; 35(5):1381-90. PubMed ID: 15827964
[TBL] [Abstract][Full Text] [Related]
34. Dendritic cells genetically engineered to express IL-4 exhibit enhanced IL-12p70 production in response to CD40 ligation and accelerate organ allograft rejection.
Kaneko K; Wang Z; Kim SH; Morelli AE; Robbins PD; Thomson AW
Gene Ther; 2003 Jan; 10(2):143-52. PubMed ID: 12571643
[TBL] [Abstract][Full Text] [Related]
35. Interferon-beta enhances monocyte and dendritic cell expression of B7-H1 (PD-L1), a strong inhibitor of autologous T-cell activation: relevance for the immune modulatory effect in multiple sclerosis.
Schreiner B; Mitsdoerffer M; Kieseier BC; Chen L; Hartung HP; Weller M; Wiendl H
J Neuroimmunol; 2004 Oct; 155(1-2):172-82. PubMed ID: 15342209
[TBL] [Abstract][Full Text] [Related]
36. A role for CD40 expression on CD8+ T cells in the generation of CD8+ T cell memory.
Bourgeois C; Rocha B; Tanchot C
Science; 2002 Sep; 297(5589):2060-3. PubMed ID: 12242444
[TBL] [Abstract][Full Text] [Related]
37. Structure and duration of contact between dendritic cells and T cells are controlled by T cell activation state.
Rothoeft T; Balkow S; Krummen M; Beissert S; Varga G; Loser K; Oberbanscheidt P; van den Boom F; Grabbe S
Eur J Immunol; 2006 Dec; 36(12):3105-17. PubMed ID: 17111349
[TBL] [Abstract][Full Text] [Related]
38. B lymphocytes can be competent antigen-presenting cells for priming CD4+ T cells to protein antigens in vivo.
Constant S; Schweitzer N; West J; Ranney P; Bottomly K
J Immunol; 1995 Oct; 155(8):3734-41. PubMed ID: 7561077
[TBL] [Abstract][Full Text] [Related]
39. Polarization of naive T cells into Th1 or Th2 by distinct cytokine-driven murine dendritic cell populations: implications for immunotherapy.
Feili-Hariri M; Falkner DH; Morel PA
J Leukoc Biol; 2005 Sep; 78(3):656-64. PubMed ID: 15961574
[TBL] [Abstract][Full Text] [Related]
40. MHC class II-expressing hepatocytes function as antigen-presenting cells and activate specific CD4 T lymphocyutes.
Herkel J; Jagemann B; Wiegard C; Lazaro JF; Lueth S; Kanzler S; Blessing M; Schmitt E; Lohse AW
Hepatology; 2003 May; 37(5):1079-85. PubMed ID: 12717388
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]
