Note to users. If you're seeing this message, it means that your browser cannot find this page's style/presentation instructions -- or possibly that you are using a browser that does not support current Web standards. Find out more about why this message is appearing, and what you can do to make your experience of our site the best it can be.
IMMUNOLOGY: Antigen Presentation--Losing Its Shine in the Absence of GILT
Colin Watts
T cell activation requires presentation of antigen by antigen-presenting cells (APCs). Before the antigen can be presented on the APC surface, it must be processed within the endosomes and lysosomes of APCs into short peptides, which are then assembled into complexes with MHC class II molecules. In a Perspective, Watts identifies the enzyme GILT as a necessary component for efficient processing of antigen containing disulfide bonds (Maric et al.).
The author is in the School of Life Sciences, University of Dundee, Dundee DD1 5EH, UK. E-mail: c.watts{at}dundee.ac.uk
The editors suggest the following Related Resources on Science sites:
In Science Magazine
REPORTS
Maja Maric, Balasubramanian Arunachalam, Uyen T. Phan, Chen Dong, Wendy S. Garrett, Kurt S. Cannon, Christopher Alfonso, Lars Karlsson, Richard A. Flavell, and Peter Cresswell (9 November 2001) Science294 (5545), 1361.
[DOI: 10.1126/science.1065500] |Abstract »|Full Text »|PDF »|Supplemental Data »
THIS ARTICLE HAS BEEN CITED BY OTHER ARTICLES:
Inhibitory Fragment from the p41 Form of Invariant Chain Can Regulate Activity of Cysteine Cathepsins in Antigen Presentation.
M. Mihelic, A. Dobersek, G. Guncar, and D. Turk (2008)
J. Biol. Chem.
283, 14453-14460
|Abstract »|Full Text »|PDF »
Molecular profiling of diffuse large B-cell lymphoma identifies robust subtypes including one characterized by host inflammatory response.
S. Monti, K. J. Savage, J. L. Kutok, F. Feuerhake, P. Kurtin, M. Mihm, B. Wu, L. Pasqualucci, D. Neuberg, R. C. T. Aguiar, et al. (2005)
Blood
105, 1851-1861
|Abstract »|Full Text »|PDF »
Genomic analysis of the host response to hepatitis B virus infection.
S. Wieland, R. Thimme, R. H. Purcell, and F. V. Chisari (2004)
PNAS
101, 6669-6674
|Abstract »|Full Text »|PDF »