These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
123 related articles for article (PubMed ID: 14510978)
21. Freshly isolated Langerhans cells negatively regulate naïve T cell activation in response to peptide antigen through cell-to-cell contact. Imai Y; Hayashi N; Yasuda K; Tsutsui H; Mizutani H; Nakanishi K J Dermatol Sci; 2008 Jul; 51(1):19-29. PubMed ID: 18367382 [TBL] [Abstract][Full Text] [Related]
22. The role of epidermal cells in the induction of delayed-type hypersensitivity to alloantigens. Tamaki K; Furue M J Invest Dermatol; 1985 Jul; 85(1):20-4. PubMed ID: 3891874 [TBL] [Abstract][Full Text] [Related]
23. Inhibition of functional T cell priming and contact hypersensitivity responses by treatment with anti-secondary lymphoid chemokine antibody during hapten sensitization. Engeman TM; Gorbachev AV; Gladue RP; Heeger PS; Fairchild RL J Immunol; 2000 May; 164(10):5207-14. PubMed ID: 10799880 [TBL] [Abstract][Full Text] [Related]
24. Cutaneous hypersensitivities to hapten are controlled by IFN-gamma-upregulated keratinocyte Th1 chemokines and IFN-gamma-downregulated langerhans cell Th2 chemokines. Mori T; Kabashima K; Yoshiki R; Sugita K; Shiraishi N; Onoue A; Kuroda E; Kobayashi M; Yamashita U; Tokura Y J Invest Dermatol; 2008 Jul; 128(7):1719-27. PubMed ID: 18239613 [TBL] [Abstract][Full Text] [Related]
25. The role of antigen-presenting cells in the regulation of delayed-type hypersensitivity. II. Epidermal Langerhans' cells and peritoneal exudate macrophages. Morikawa Y; Furotani M; Matsuura N; Kakudo K Cell Immunol; 1993 Nov; 152(1):200-10. PubMed ID: 8242760 [TBL] [Abstract][Full Text] [Related]
26. The differential role of CD86 and CD80 co-stimulatory molecules in the induction and the effector phases of contact hypersensitivity. Nuriya S; Yagita H; Okumura K; Azuma M Int Immunol; 1996 Jun; 8(6):917-26. PubMed ID: 8671681 [TBL] [Abstract][Full Text] [Related]
33. Skin application of the nonsteroidal anti-inflammatory drug ketoprofen downmodulates the antigen-presenting ability of Langerhans cells in mice. Atarashi K; Kabashima K; Akiyama K; Tokura Y Br J Dermatol; 2008 Aug; 159(2):306-13. PubMed ID: 18565185 [TBL] [Abstract][Full Text] [Related]
34. Modification of LC phenotype and suppression of contact hypersensitivity response by stress. Hosoi J; Tsuchiya T; Denda M; Ashida Y; Takashima A; Granstein RD; Koyama J J Cutan Med Surg; 1998 Oct; 3(2):79-84. PubMed ID: 9822780 [TBL] [Abstract][Full Text] [Related]
35. The glucocorticoid-induced TNF receptor-related protein (GITR)-GITR ligand pathway acts as a mediator of cutaneous dendritic cell migration and promotes T cell-mediated acquired immunity. Kamimura Y; Iwai H; Piao J; Hashiguchi M; Azuma M J Immunol; 2009 Mar; 182(5):2708-16. PubMed ID: 19234165 [TBL] [Abstract][Full Text] [Related]
36. Induction of sensitization and tolerance in contact sensitivity with haptenated epidermal cells in the guinea-pig. Baker D; Parker D; Healey DG; Turk JL Immunology; 1987 Dec; 62(4):659-64. PubMed ID: 2448230 [TBL] [Abstract][Full Text] [Related]
37. GammadeltaT cells regulate the development of hapten-specific CD8+ effector T cells in contact hypersensitivity responses. Guan H; Zu G; Slater M; Elmets C; Xu H J Invest Dermatol; 2002 Jul; 119(1):137-42. PubMed ID: 12164936 [TBL] [Abstract][Full Text] [Related]