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2. Involvement of NO in contact hypersensitivity. Ross R; Gillitzer C; Kleinz R; Schwing J; Kleinert H; Förstermann U; Reske-Kunz AB Int Immunol; 1998 Jan; 10(1):61-9. PubMed ID: 9488156 [TBL] [Abstract][Full Text] [Related]
3. 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]
4. Osteopontin is involved in the initiation of cutaneous contact hypersensitivity by inducing Langerhans and dendritic cell migration to lymph nodes. Weiss JM; Renkl AC; Maier CS; Kimmig M; Liaw L; Ahrens T; Kon S; Maeda M; Hotta H; Uede T; Simon JC J Exp Med; 2001 Nov; 194(9):1219-29. PubMed ID: 11696588 [TBL] [Abstract][Full Text] [Related]
5. Langerhans cells are required for UVR-induced immunosuppression. Schwarz A; Noordegraaf M; Maeda A; Torii K; Clausen BE; Schwarz T J Invest Dermatol; 2010 May; 130(5):1419-27. PubMed ID: 20090769 [TBL] [Abstract][Full Text] [Related]
6. Dermal dendritic cells, and not Langerhans cells, play an essential role in inducing an immune response. Fukunaga A; Khaskhely NM; Sreevidya CS; Byrne SN; Ullrich SE J Immunol; 2008 Mar; 180(5):3057-64. PubMed ID: 18292528 [TBL] [Abstract][Full Text] [Related]
7. CCR8 regulates contact hypersensitivity by restricting cutaneous dendritic cell migration to the draining lymph nodes. Yabe R; Shimizu K; Shimizu S; Azechi S; Choi BI; Sudo K; Kubo S; Nakae S; Ishigame H; Kakuta S; Iwakura Y Int Immunol; 2015 Apr; 27(4):169-81. PubMed ID: 25344933 [TBL] [Abstract][Full Text] [Related]
8. Effect of topical application of lipopolysaccharide on contact hypersensitivity. Tanaka M; Kohchi C; Inagawa H; Ikemoto T; Hara-Chikuma M Biochem Biophys Res Commun; 2022 Jan; 586():100-106. PubMed ID: 34837833 [TBL] [Abstract][Full Text] [Related]
9. Dynamics and function of Langerhans cells in vivo: dermal dendritic cells colonize lymph node areas distinct from slower migrating Langerhans cells. Kissenpfennig A; Henri S; Dubois B; Laplace-Builhé C; Perrin P; Romani N; Tripp CH; Douillard P; Leserman L; Kaiserlian D; Saeland S; Davoust J; Malissen B Immunity; 2005 May; 22(5):643-54. PubMed ID: 15894281 [TBL] [Abstract][Full Text] [Related]
10. IL-36α is involved in hapten-specific T-cell induction, but not local inflammation, during contact hypersensitivity. Numata T; Yoshizaki T; Yamaguchi S; Shimura E; Iwakura Y; Harada K; Sudo K; Tsuboi R; Nakae S Biochem Biophys Res Commun; 2018 Nov; 506(3):429-436. PubMed ID: 30352688 [TBL] [Abstract][Full Text] [Related]
11. An inhibitory immunoreceptor, Allergin-1, suppresses FITC-induced type 2 contact hypersensitivity. Almeida MS; Shibagaki S; Tahara-Hanaoka S; Shibayama S; Shibuya A Biochem Biophys Res Commun; 2021 Nov; 579():146-152. PubMed ID: 34601199 [TBL] [Abstract][Full Text] [Related]
12. Selective 5-lipoxygenase expression in Langerhans cells and impaired dendritic cell migration in 5-LO-deficient mice reveal leukotriene action in skin. Doepping S; Funk CD; Habenicht AJ; Spanbroek R J Invest Dermatol; 2007 Jul; 127(7):1692-700. PubMed ID: 17392829 [TBL] [Abstract][Full Text] [Related]
13. Visualization and characterization of migratory Langerhans cells in murine skin and lymph nodes by antibodies against Langerin/CD207. Stoitzner P; Holzmann S; McLellan AD; Ivarsson L; Stössel H; Kapp M; Kämmerer U; Douillard P; Kämpgen E; Koch F; Saeland S; Romani N J Invest Dermatol; 2003 Feb; 120(2):266-74. PubMed ID: 12542532 [TBL] [Abstract][Full Text] [Related]
14. TGF-beta is required to maintain the pool of immature Langerhans cells in the epidermis. Kel JM; Girard-Madoux MJ; Reizis B; Clausen BE J Immunol; 2010 Sep; 185(6):3248-55. PubMed ID: 20713882 [TBL] [Abstract][Full Text] [Related]
16. Enhanced contact hypersensitivity in human monocyte chemoattractant protein-1 transgenic mouse. Mizumoto N; Iwabichi K; Nakamura H; Ato M; Shibaki A; Kawashima T; Kobayashi H; Iwabuchi C; Ohkawara A; Onoé K Immunobiology; 2001 Dec; 204(4):477-93. PubMed ID: 11776402 [TBL] [Abstract][Full Text] [Related]
17. IL-10-producing Langerhans cells and regulatory T cells are responsible for depressed contact hypersensitivity in grafted skin. Yoshiki R; Kabashima K; Sugita K; Atarashi K; Shimauchi T; Tokura Y J Invest Dermatol; 2009 Mar; 129(3):705-13. PubMed ID: 18843293 [TBL] [Abstract][Full Text] [Related]
18. Identification of a novel population of Langerin+ dendritic cells. Bursch LS; Wang L; Igyarto B; Kissenpfennig A; Malissen B; Kaplan DH; Hogquist KA J Exp Med; 2007 Dec; 204(13):3147-56. PubMed ID: 18086865 [TBL] [Abstract][Full Text] [Related]
19. Effect of skin sensitizers on inducible nitric oxide synthase expression and nitric oxide production in skin dendritic cells: role of different immunosuppressive drugs. Cruz MT; Neves BM; Gonçalo M; Figueiredo A; Duarte CB; Lopes MC Immunopharmacol Immunotoxicol; 2007; 29(2):225-41. PubMed ID: 17849269 [TBL] [Abstract][Full Text] [Related]
20. Dendritic cell-derived nitric oxide inhibits the differentiation of effector dendritic cells. Si C; Zhang R; Wu T; Lu G; Hu Y; Zhang H; Xu F; Wei P; Chen K; Tang H; Yeretssian G; Xiong H Oncotarget; 2016 Nov; 7(46):74834-74845. PubMed ID: 27556858 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]