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.
209 related articles for article (PubMed ID: 11777943)
21. Tolerization of mice to Schistosoma mansoni egg antigens causes elevated type 1 and diminished type 2 cytokine responses and increased mortality in acute infection. Fallon PG; Dunne DW J Immunol; 1999 Apr; 162(7):4122-32. PubMed ID: 10201937 [TBL] [Abstract][Full Text] [Related]
22. Full development of Th2 immunity requires both innate and adaptive sources of CD154. Jenkins SJ; Perona-Wright G; MacDonald AS J Immunol; 2008 Jun; 180(12):8083-92. PubMed ID: 18523272 [TBL] [Abstract][Full Text] [Related]
23. Induction of cytotoxic effector cells towards cholangiocellular, pancreatic, and colorectal tumor cells by activation of the immune checkpoint CD40/CD40L on dendritic cells. Sadeghlar F; Vogt A; Mohr RU; Mahn R; van Beekum K; Kornek M; Weismüller TJ; Branchi V; Matthaei H; Toma M; Schmidt-Wolf IGH; Kalff JC; Strassburg CP; González-Carmona MA Cancer Immunol Immunother; 2021 May; 70(5):1451-1464. PubMed ID: 33180184 [TBL] [Abstract][Full Text] [Related]
24. Dendritic cell differentiation state and their interaction with NKT cells determine Th1/Th2 differentiation in the murine model of Leishmania major infection. Wiethe C; Debus A; Mohrs M; Steinkasserer A; Lutz M; Gessner A J Immunol; 2008 Apr; 180(7):4371-81. PubMed ID: 18354157 [TBL] [Abstract][Full Text] [Related]
25. In infection with Schistosoma mansoni, B cells are required for T helper type 2 cell responses but not for granuloma formation. Hernandez HJ; Wang Y; Stadecker MJ J Immunol; 1997 May; 158(10):4832-7. PubMed ID: 9144498 [TBL] [Abstract][Full Text] [Related]
26. CD40 ligand and CTLA-4 are reciprocally regulated in the Th1 cell proliferative response sustained by CD8(+) dendritic cells. Fallarino F; Grohmann U; Vacca C; Bianchi R; Fioretti MC; Puccetti P J Immunol; 2002 Aug; 169(3):1182-8. PubMed ID: 12133938 [TBL] [Abstract][Full Text] [Related]
27. Dendritic cell longevity and T cell persistence is controlled by CD154-CD40 interactions. Miga AJ; Masters SR; Durell BG; Gonzalez M; Jenkins MK; Maliszewski C; Kikutani H; Wade WF; Noelle RJ Eur J Immunol; 2001 Mar; 31(3):959-65. PubMed ID: 11241301 [TBL] [Abstract][Full Text] [Related]
28. Lipopolysaccharide modulation of dendritic cells is insufficient to mature dendritic cells to generate CTLs from naive polyclonal CD8+ T cells in vitro, whereas CD40 ligation is essential. Kelleher M; Beverley PC J Immunol; 2001 Dec; 167(11):6247-55. PubMed ID: 11714787 [TBL] [Abstract][Full Text] [Related]
29. Selective requirement for CD40-CD154 in drug-induced type 1 versus type 2 responses to trinitrophenyl-ovalbumin. Nierkens S; van Helden P; Bol M; Bleumink R; van Kooten P; Ramdien-Murli S; Boon L; Pieters R J Immunol; 2002 Apr; 168(8):3747-54. PubMed ID: 11937525 [TBL] [Abstract][Full Text] [Related]
30. CD40/CD154 interactions are required for the optimal maturation of skin-derived APCs and the induction of helminth-specific IFN-gamma but not IL-4. Hewitson JP; Jenkins GR; Hamblin PA; Mountford AP J Immunol; 2006 Sep; 177(5):3209-17. PubMed ID: 16920960 [TBL] [Abstract][Full Text] [Related]
31. Requirement for donor and recipient CD40 expression in cardiac allograft rejection: induction of Th1 responses and influence of donor-derived dendritic cells. Nathan MJ; Mold JE; Wood SC; Csencsits K; Lu G; Eichwald EJ; Bishop DK J Immunol; 2004 Jun; 172(11):6626-33. PubMed ID: 15153477 [TBL] [Abstract][Full Text] [Related]
32. Modulation of Th1/Th2 immune responses by killed Propionibacterium acnes and its soluble polysaccharide fraction in a type I hypersensitivity murine model: induction of different activation status of antigen-presenting cells. Squaiella-Baptistão CC; Teixeira D; Mussalem JS; Ishimura ME; Longo-Maugéri IM J Immunol Res; 2015; 2015():132083. PubMed ID: 25973430 [TBL] [Abstract][Full Text] [Related]
34. Th1 and Th2 CD4+ T cells provide help for B cell clonal expansion and antibody synthesis in a similar manner in vivo. Smith KM; Pottage L; Thomas ER; Leishman AJ; Doig TN; Xu D; Liew FY; Garside P J Immunol; 2000 Sep; 165(6):3136-44. PubMed ID: 10975827 [TBL] [Abstract][Full Text] [Related]
35. Dendritic cell expression of the Notch ligand jagged2 is not essential for Th2 response induction in vivo. Worsley AG; LeibundGut-Landmann S; Slack E; Phng LK; Gerhardt H; Reis e Sousa C; MacDonald AS Eur J Immunol; 2008 Apr; 38(4):1043-9. PubMed ID: 18350543 [TBL] [Abstract][Full Text] [Related]
36. A pivotal role for CD40-mediated IL-6 production by dendritic cells during IL-17 induction in vivo. Perona-Wright G; Jenkins SJ; O'Connor RA; Zienkiewicz D; McSorley HJ; Maizels RM; Anderton SM; MacDonald AS J Immunol; 2009 Mar; 182(5):2808-15. PubMed ID: 19234175 [TBL] [Abstract][Full Text] [Related]
37. The biological outcome of CD40 signaling is dependent on the duration of CD40 ligand expression: reciprocal regulation by interleukin (IL)-4 and IL-12. Lee BO; Haynes L; Eaton SM; Swain SL; Randall TD J Exp Med; 2002 Sep; 196(5):693-704. PubMed ID: 12208883 [TBL] [Abstract][Full Text] [Related]
38. Ox40 costimulation enhances the development of T cell responses induced by dendritic cells in vivo. De Smedt T; Smith J; Baum P; Fanslow W; Butz E; Maliszewski C J Immunol; 2002 Jan; 168(2):661-70. PubMed ID: 11777959 [TBL] [Abstract][Full Text] [Related]
39. Induction of Th2 responses and IgE is largely due to carbohydrates functioning as adjuvants on Schistosoma mansoni egg antigens. Okano M; Satoskar AR; Nishizaki K; Abe M; Harn DA J Immunol; 1999 Dec; 163(12):6712-7. PubMed ID: 10586068 [TBL] [Abstract][Full Text] [Related]
40. Commensal oral bacteria antigens prime human dendritic cells to induce Th1, Th2 or Treg differentiation. Kopitar AN; Ihan Hren N; Ihan A Oral Microbiol Immunol; 2006 Feb; 21(1):1-5. PubMed ID: 16390334 [TBL] [Abstract][Full Text] [Related] [Previous] [Next] [New Search]