Cutting edge: Efficient MHC class I cross-presentation during early vaccinia infection requires the transfer of proteasomal intermediates between antigen donor and presenting cells
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作者:
Serna, A
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Fox Chase Canc Ctr, Div Basic Sci, Virol Working Grp, Philadelphia, PA 19111 USAFox Chase Canc Ctr, Div Basic Sci, Virol Working Grp, Philadelphia, PA 19111 USA
Serna, A
[1
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Ramirez, MC
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Fox Chase Canc Ctr, Div Basic Sci, Virol Working Grp, Philadelphia, PA 19111 USAFox Chase Canc Ctr, Div Basic Sci, Virol Working Grp, Philadelphia, PA 19111 USA
Ramirez, MC
[1
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Soukhanova, A
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Fox Chase Canc Ctr, Div Basic Sci, Virol Working Grp, Philadelphia, PA 19111 USAFox Chase Canc Ctr, Div Basic Sci, Virol Working Grp, Philadelphia, PA 19111 USA
Soukhanova, A
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Sigal, LJ
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Fox Chase Canc Ctr, Div Basic Sci, Virol Working Grp, Philadelphia, PA 19111 USAFox Chase Canc Ctr, Div Basic Sci, Virol Working Grp, Philadelphia, PA 19111 USA
Sigal, LJ
[1
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[1] Fox Chase Canc Ctr, Div Basic Sci, Virol Working Grp, Philadelphia, PA 19111 USA
Priming of CD8(+) T cells requires presentation of short peptides bound to MHC class I molecules of professional AM. Cross-presentation is a mechanism where by professional APC present on their own MHC class I molecules peptides derived from degradation of Ags synthesized by other Ag "donor cells." The mechanism of cross-presentation is poorly understood, and the nature of the transferred Ag is unknown. In this report, we demonstrate that the bulk of a cross-presented Ag transferred from donor cells recently infected with vaccinia virus are proteasomal products that are susceptible to peptidases within the donor cell cytosol and not full-length proteins or mature epitopes either free or bound to chaperones.