459 related articles for article (PubMed ID: 16818784)
21. T cells from Leishmania major-susceptible BALB/c mice have a defect in efficiently up-regulating CXCR3 upon activation.
Barbi J; Brombacher F; Satoskar AR
J Immunol; 2008 Oct; 181(7):4613-20. PubMed ID: 18802063
[TBL] [Abstract][Full Text] [Related]
22. In situ analysis reveals physical interactions between CD11b+ dendritic cells and antigen-specific CD4 T cells after subcutaneous injection of antigen.
Ingulli E; Ulman DR; Lucido MM; Jenkins MK
J Immunol; 2002 Sep; 169(5):2247-52. PubMed ID: 12193689
[TBL] [Abstract][Full Text] [Related]
23. Clearance of influenza virus from the lung depends on migratory langerin+CD11b- but not plasmacytoid dendritic cells.
GeurtsvanKessel CH; Willart MA; van Rijt LS; Muskens F; Kool M; Baas C; Thielemans K; Bennett C; Clausen BE; Hoogsteden HC; Osterhaus AD; Rimmelzwaan GF; Lambrecht BN
J Exp Med; 2008 Jul; 205(7):1621-34. PubMed ID: 18591406
[TBL] [Abstract][Full Text] [Related]
24. Dendritic cell (DC)-based protection against an intracellular pathogen is dependent upon DC-derived IL-12 and can be induced by molecularly defined antigens.
Berberich C; Ramírez-Pineda JR; Hambrecht C; Alber G; Skeiky YA; Moll H
J Immunol; 2003 Mar; 170(6):3171-9. PubMed ID: 12626575
[TBL] [Abstract][Full Text] [Related]
25. Interleukin-4 Responsive Dendritic Cells Are Dispensable to Host Resistance Against
Osero BO; Cele Z; Aruleba RT; Maine RA; Ozturk M; Lutz MB; Brombacher F; Hurdayal R
Front Immunol; 2021; 12():759021. PubMed ID: 35154068
[TBL] [Abstract][Full Text] [Related]
26. Early production of IL-4 and induction of Th2 responses in the lymph node originate from an MHC class I-independent CD4+NK1.1- T cell population.
von der Weid T; Beebe AM; Roopenian DC; Coffman RL
J Immunol; 1996 Nov; 157(10):4421-7. PubMed ID: 8906817
[TBL] [Abstract][Full Text] [Related]
27. Directly transfected langerin+ dermal dendritic cells potentiate CD8+ T cell responses following intradermal plasmid DNA immunization.
Elnekave M; Furmanov K; Nudel I; Arizon M; Clausen BE; Hovav AH
J Immunol; 2010 Sep; 185(6):3463-71. PubMed ID: 20713888
[TBL] [Abstract][Full Text] [Related]
28. Inflammatory Dendritic Cells, Regulated by IL-4 Receptor Alpha Signaling, Control Replication, and Dissemination of
Hurdayal R; Nieuwenhuizen NE; Khutlang R; Brombacher F
Front Cell Infect Microbiol; 2019; 9():479. PubMed ID: 32039054
[TBL] [Abstract][Full Text] [Related]
29. MGL2 Dermal dendritic cells are sufficient to initiate contact hypersensitivity in vivo.
Kumamoto Y; Denda-Nagai K; Aida S; Higashi N; Irimura T
PLoS One; 2009; 4(5):e5619. PubMed ID: 19440334
[TBL] [Abstract][Full Text] [Related]
30. Langerhans cells promote early germinal center formation in response to Leishmania-derived cutaneous antigens.
Zimara N; Florian C; Schmid M; Malissen B; Kissenpfennig A; Männel DN; Edinger M; Hutchinson JA; Hoffmann P; Ritter U
Eur J Immunol; 2014 Oct; 44(10):2955-67. PubMed ID: 25070244
[TBL] [Abstract][Full Text] [Related]
31. Dendritic cells from malaria-infected mice are fully functional APC.
Perry JA; Rush A; Wilson RJ; Olver CS; Avery AC
J Immunol; 2004 Jan; 172(1):475-82. PubMed ID: 14688357
[TBL] [Abstract][Full Text] [Related]
32. Leishmania major: recruitment of Gr-1+ cells into draining lymph nodes during infection is important for early IL-12 and IFN gamma production.
dos Santos MS; Vaz Cardoso LP; Nascimento GR; Lino Rde S; Dorta ML; de Oliveira MA; Ribeiro-Dias F
Exp Parasitol; 2008 Jul; 119(3):403-10. PubMed ID: 18501355
[TBL] [Abstract][Full Text] [Related]
33. Imaging of the cross-presenting dendritic cell subsets in the skin-draining lymph node.
Kitano M; Yamazaki C; Takumi A; Ikeno T; Hemmi H; Takahashi N; Shimizu K; Fraser SE; Hoshino K; Kaisho T; Okada T
Proc Natl Acad Sci U S A; 2016 Jan; 113(4):1044-9. PubMed ID: 26755602
[TBL] [Abstract][Full Text] [Related]
34. Primary defect in UVB-induced systemic immunomodulation does not relate to immature or functionally impaired APCs in regional lymph nodes.
Gorman S; Tan JW; Thomas JA; Townley SL; Stumbles PA; Finlay-Jones JJ; Hart PH
J Immunol; 2005 Jun; 174(11):6677-85. PubMed ID: 15905507
[TBL] [Abstract][Full Text] [Related]
35. Epidermal and dermal dendritic cells display differential activation and migratory behavior while sharing the ability to stimulate CD4+ T cell proliferation in vivo.
Shklovskaya E; Roediger B; Fazekas de St Groth B
J Immunol; 2008 Jul; 181(1):418-30. PubMed ID: 18566408
[TBL] [Abstract][Full Text] [Related]
36. Activation of dendritic cells that cross-present tumor-derived antigen licenses CD8+ CTL to cause tumor eradication.
van Mierlo GJ; Boonman ZF; Dumortier HM; den Boer AT; Fransen MF; Nouta J; van der Voort EI; Offringa R; Toes RE; Melief CJ
J Immunol; 2004 Dec; 173(11):6753-9. PubMed ID: 15557168
[TBL] [Abstract][Full Text] [Related]
37. Antigen-presenting cells in human cutaneous leishmaniasis due to Leishmania major.
ElHassan AM; Gaafar A; Theander TG
Clin Exp Immunol; 1995 Mar; 99(3):445-53. PubMed ID: 7882568
[TBL] [Abstract][Full Text] [Related]
38. The early IL-4 response to Leishmania major and the resulting Th2 cell maturation steering progressive disease in BALB/c mice are subject to the control of regulatory CD4+CD25+ T cells.
Aseffa A; Gumy A; Launois P; MacDonald HR; Louis JA; Tacchini-Cottier F
J Immunol; 2002 Sep; 169(6):3232-41. PubMed ID: 12218142
[TBL] [Abstract][Full Text] [Related]
39. The immune response modifier and Toll-like receptor 7 agonist S-27609 selectively induces IL-12 and TNF-alpha production in CD11c+CD11b+CD8- dendritic cells.
Doxsee CL; Riter TR; Reiter MJ; Gibson SJ; Vasilakos JP; Kedl RM
J Immunol; 2003 Aug; 171(3):1156-63. PubMed ID: 12874201
[TBL] [Abstract][Full Text] [Related]
40. TNF controls the infiltration of dendritic cells into the site of Leishmania major infection.
Ritter U; Lechner A; Scharl K; Kiafard Z; Zwirner J; Körner H
Med Microbiol Immunol; 2008 Mar; 197(1):29-37. PubMed ID: 17661079
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]
