140 related articles for article (PubMed ID: 11813165)
1. Specific role for cathepsin S in the generation of antigenic peptides in vivo.
Plüger EB; Boes M; Alfonso C; Schröter CJ; Kalbacher H; Ploegh HL; Driessen C
Eur J Immunol; 2002 Feb; 32(2):467-76. PubMed ID: 11813165
[TBL] [Abstract][Full Text] [Related]
2. Cathepsin D, but not cathepsin B, releases T cell stimulatory fragments from lysozyme that are functional in the context of multiple murine class II MHC molecules.
van Noort JM; Jacobs MJ
Eur J Immunol; 1994 Sep; 24(9):2175-80. PubMed ID: 8088334
[TBL] [Abstract][Full Text] [Related]
3. Asparagine endopeptidase is not essential for class II MHC antigen presentation but is required for processing of cathepsin L in mice.
Maehr R; Hang HC; Mintern JD; Kim YM; Cuvillier A; Nishimura M; Yamada K; Shirahama-Noda K; Hara-Nishimura I; Ploegh HL
J Immunol; 2005 Jun; 174(11):7066-74. PubMed ID: 15905550
[TBL] [Abstract][Full Text] [Related]
4. Individual cathepsins degrade immune complexes internalized by antigen-presenting cells via Fcgamma receptors.
Driessen C; Lennon-Duménil AM; Ploegh HL
Eur J Immunol; 2001 May; 31(5):1592-601. PubMed ID: 11465117
[TBL] [Abstract][Full Text] [Related]
5. Cathepsin B-Deficient Mice Resolve Leishmania major Inflammation Faster in a T Cell-Dependent Manner.
Rasid O; Mériaux V; Khan EM; Borde C; Ciulean IS; Fitting C; Manoury B; Cavaillon JM; Doyen N
PLoS Negl Trop Dis; 2016 May; 10(5):e0004716. PubMed ID: 27182703
[TBL] [Abstract][Full Text] [Related]
6. Differential regulation of cathepsin S and cathepsin L in interferon gamma-treated macrophages.
Beers C; Honey K; Fink S; Forbush K; Rudensky A
J Exp Med; 2003 Jan; 197(2):169-79. PubMed ID: 12538657
[TBL] [Abstract][Full Text] [Related]
7. Threshold detection of self-antigen/MHC class II complexes formed in vivo: constitutive presentation of an immunodominant epitope of hen egg lysozyme (HEL) in HEL-transgenic mice.
Kanost D; Basten A; McCluskey J
Int Immunol; 1993 Aug; 5(8):893-902. PubMed ID: 8398984
[TBL] [Abstract][Full Text] [Related]
8. Antigen presentation by dendritic cells focuses T cell responses against immunodominant peptides: studies in the hen egg-white lysozyme (HEL) model.
Gapin L; Bravo de Alba Y; Casrouge A; Cabaniols JP; Kourilsky P; Kanellopoulos J
J Immunol; 1998 Feb; 160(4):1555-64. PubMed ID: 9469410
[TBL] [Abstract][Full Text] [Related]
9. A role for cathepsin L and cathepsin S in peptide generation for MHC class II presentation.
Hsieh CS; deRoos P; Honey K; Beers C; Rudensky AY
J Immunol; 2002 Mar; 168(6):2618-25. PubMed ID: 11884425
[TBL] [Abstract][Full Text] [Related]
10. Cytosolic targeting of hen egg lysozyme gives rise to a short-lived protein presented by class I but not class II major histocompatibility complex molecules.
Calin-Laurens V; Forquet F; Mottez E; Kanellopoulos J; Godeau F; Kourilsky P; Gerlier D; Rabourdin-Combe C
Eur J Immunol; 1991 Mar; 21(3):761-9. PubMed ID: 2009914
[TBL] [Abstract][Full Text] [Related]
11. Presentation on class II MHC molecules of endogenous lysozyme targeted to the endocytic pathway.
Parra-López CA; Lindner R; Vidavsky I; Gross M; Unanue ER
J Immunol; 1997 Mar; 158(6):2670-9. PubMed ID: 9058800
[TBL] [Abstract][Full Text] [Related]
12. Destructive proteolysis by cysteine proteases in antigen presentation of ovalbumin.
Rodriguez GM; Diment S
Eur J Immunol; 1995 Jul; 25(7):1823-7. PubMed ID: 7621859
[TBL] [Abstract][Full Text] [Related]
13. Processing of endogenously synthesized hen egg-white lysozyme retained in the endoplasmic reticulum or in secretory form gives rise to a similar but not identical set of epitopes recognized by class II-restricted T cells.
Adorini L; Guéry JC; Fuchs S; Ortiz-Navarrete V; Hämmerling GJ; Momburg F
J Immunol; 1993 Oct; 151(7):3576-86. PubMed ID: 7690807
[TBL] [Abstract][Full Text] [Related]
14. Simultaneous presentation and cross-presentation of immune-stimulating complex-associated cognate antigen by antigen-specific B cells.
Robson NC; Donachie AM; Mowat AM
Eur J Immunol; 2008 May; 38(5):1238-46. PubMed ID: 18398931
[TBL] [Abstract][Full Text] [Related]
15. mAb against hen egg-white lysozyme regulate its presentation to CD4(+) T cells.
Guermonprez P; Lo-Man R; Sedlik C; Rojas MJ; Poljak RJ; Leclerc C
Int Immunol; 1999 Nov; 11(11):1863-72. PubMed ID: 10545490
[TBL] [Abstract][Full Text] [Related]
16. Novel physiological functions of cathepsins B and L on antigen processing and osteoclastic bone resorption.
Katunuma N; Matsunaga Y; Matsui A; Kakegawa H; Endo K; Inubushi T; Saibara T; Ohba Y; Kakiuchi T
Adv Enzyme Regul; 1998; 38():235-51. PubMed ID: 9762356
[TBL] [Abstract][Full Text] [Related]
17. Cathepsin L maturation and activity is impaired in macrophages harboring M. avium and M. tuberculosis.
Nepal RM; Mampe S; Shaffer B; Erickson AH; Bryant P
Int Immunol; 2006 Jun; 18(6):931-9. PubMed ID: 16636015
[TBL] [Abstract][Full Text] [Related]
18. Constraints in antigen processing result in unresponsiveness to a T cell epitope of hen egg lysozyme in C57BL/6 mice.
Kim BS; Jang YS
Eur J Immunol; 1992 Mar; 22(3):775-82. PubMed ID: 1372259
[TBL] [Abstract][Full Text] [Related]
19. Endogenous and exogenous forms of the same antigen are processed from different pools to bind MHC class II molecules in endocytic compartments.
Bonifaz LC; Arzate S; Moreno J
Eur J Immunol; 1999 Jan; 29(1):119-31. PubMed ID: 9933093
[TBL] [Abstract][Full Text] [Related]
20. Monovalent ligation of the B cell receptor induces receptor activation but fails to promote antigen presentation.
Kim YM; Pan JY; Korbel GA; Peperzak V; Boes M; Ploegh HL
Proc Natl Acad Sci U S A; 2006 Feb; 103(9):3327-32. PubMed ID: 16492756
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
