rdf:type |
|
lifeskim:mentions |
|
pubmed:issue |
6249
|
pubmed:dateCreated |
1990-1-4
|
pubmed:abstractText |
Cytotoxic T lymphocytes (CTL) constitute an essential part of the immune response against viral infections. Such CTL recognize peptides derived from viral proteins together with major histocompatibility complex (MHC) class I molecules on the surface of infected cells, and usually require in vivo priming with infectious virus. Here we report that synthetic viral peptides covalently linked to tripalmitoyl-S-glycerylcysteinyl-seryl-serine (P3CSS) can efficiently prime influenza-virus-specific CTL in vivo. These lipopeptides are able to induce the same high-affinity CTL as does the infectious virus. Our data are not only relevant to vaccine development, but also have a bearing on basic immune processes leading to the transition of virgin T cells to activated effector cells in vivo, and to antigen presentation by MHC class I molecules.
|
pubmed:commentsCorrections |
|
pubmed:language |
eng
|
pubmed:journal |
|
pubmed:citationSubset |
IM
|
pubmed:chemical |
|
pubmed:status |
MEDLINE
|
pubmed:month |
Nov
|
pubmed:issn |
0028-0836
|
pubmed:author |
|
pubmed:issnType |
Print
|
pubmed:day |
30
|
pubmed:volume |
342
|
pubmed:owner |
NLM
|
pubmed:authorsComplete |
Y
|
pubmed:pagination |
561-4
|
pubmed:dateRevised |
2006-11-15
|
pubmed:meshHeading |
pubmed-meshheading:2586628-Amino Acid Sequence,
pubmed-meshheading:2586628-Animals,
pubmed-meshheading:2586628-Antigen-Presenting Cells,
pubmed-meshheading:2586628-Cytotoxicity, Immunologic,
pubmed-meshheading:2586628-H-2 Antigens,
pubmed-meshheading:2586628-Lipoproteins,
pubmed-meshheading:2586628-Mice,
pubmed-meshheading:2586628-Molecular Sequence Data,
pubmed-meshheading:2586628-Peptide Fragments,
pubmed-meshheading:2586628-T-Lymphocytes, Cytotoxic,
pubmed-meshheading:2586628-Vaccines,
pubmed-meshheading:2586628-Vaccines, Synthetic,
pubmed-meshheading:2586628-Viral Proteins,
pubmed-meshheading:2586628-Viral Vaccines
|
pubmed:year |
1989
|
pubmed:articleTitle |
In vivo priming of virus-specific cytotoxic T lymphocytes with synthetic lipopeptide vaccine.
|
pubmed:affiliation |
Institut für Organische Chemie, Universität Tübingen.
|
pubmed:publicationType |
Journal Article,
Research Support, Non-U.S. Gov't
|