Liposome-mediated peptide loading of MHC-DR molecules in vivo.

Abstract:

:Amino acid residues 3-15 of mycobacterial HSP60 define a dominant T-cell epitope for HLA-DR3+ve humans and Mamu-DR3+ve rhesus monkeys. Our results show that Mamu-DR3 molecules on PBMC can be efficiently loaded in vivo with the above-mentioned peptides when they are intravenously injected encapsulated in liposomes, but not in the free form. Mamu-DR3 loading is abolished by encapsulation of a nonstimulatory peptide. These results have implications for the delivery of therapeutic peptides in vivo.

journal_name

FEBS Lett

journal_title

FEBS letters

authors

t Hart BA,Elferink DG,Drijfhout JW,Storm G,van Blooijs L,Bontrop RE,de Vries RR

doi

10.1016/s0014-5793(97)00493-6

subject

Has Abstract

pub_date

1997-06-02 00:00:00

pages

91-5

issue

1

eissn

0014-5793

issn

1873-3468

pii

S0014579397004936

journal_volume

409

pub_type

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