| Literature DB >> 12598896 |
Ulrike Seifert1, Concepción Marañón, Ayelet Shmueli, Jean-François Desoutter, Lisa Wesoloski, Katharina Janek, Peter Henklein, Susanne Diescher, Muriel Andrieu, Henri de la Salle, Toni Weinschenk, Hansjörg Schild, Diego Laderach, Anne Galy, Gaby Haas, Peter-M Kloetzel, Yuval Reiss, Anne Hosmalin.
Abstract
Most of the peptides presented by major histocompatibility complex (MHC) class I molecules require processing by proteasomes. Tripeptidyl peptidase II (TPPII), an aminopeptidase with endoproteolytic activity, may also have a role in antigen processing. Here, we analyzed the processing and presentation of the immunodominant human immunodeficiency virus epitope HIV-Nef(73-82) in human dendritic cells. We found that inhibition of proteasome activity did not impair Nef(73-82) epitope presentation. In contrast, specific inhibition of TPPII led to a reduction of Nef(73-82) epitope presentation. We propose that TPPII can act in combination with or independent of the proteasome system and can generate epitopes that evade generation by the proteasome-system.Entities:
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Year: 2003 PMID: 12598896 DOI: 10.1038/ni905
Source DB: PubMed Journal: Nat Immunol ISSN: 1529-2908 Impact factor: 25.606