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Monika C. Wolkers,Nathalie Brouwenstijn,*Arnold H. Bakker,*Mireille Toebes,Ton N. M. Schumacher
Activated CD8+ T cells detect virally infected cells and tumorcells by recognition of major histocompatibility complex classIbound peptides derived from degraded, endogenously producedproteins. In contrast, CD8+ T cell activation often occurs throughinteraction with specialized antigen-presenting cells displayingpeptides acquired from an exogenous cellular source, a processtermed cross-priming. Here, we observed a marked inefficiencyin exogenous presentation of epitopes derived from signal sequencesin mouse models. These data indicate that certain virus- andtumor-associated antigens may not be detected by CD8+ T cellsbecause of impaired cross-priming. Such differences in the abilityto cross-present antigens should form important considerationsin vaccine design.
Division of Immunology, Netherlands Cancer Institute, Plesmanlaan 121, 1066 CX Amsterdam, Netherlands.
* These authors contributed equally to this work.
To whom correspondence should be addressed. E-mail: t.schumacher{at}nki.nl
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