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PMID: 7814868 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't Research Support, U.S. Gov't, P.H.S.

Variations in the number of peptide-MHC class I complexes required to activate cytotoxic T cell responses.

Journal of immunology (Baltimore, Md. : 1950) ·Vol. 154 ·No. 2 ·1995-01-15 ·Pages 567-76

Kageyama S, Tsomides TJ, Sykulev Y, Eisen HN

Abstract

We determined equilibrium constants for the binding of 16 peptides (based on four T cell epitopes) to three MHC class I proteins (A2, Kb, and Ld) on intact cells and estimated the number of accessible peptide-binding sites on these cells. From these results, and the concentrations of peptides required to sensitize target cells for lysis by CD8+ CTL, we conclude that the critical number of peptide-MHC complexes required per target cell for the activation of CTL responses varies with different combinations of peptide-MHC complexes and CTL clones from several thousand complexes to fewer than ten per target cell.

MeSH Terms
Amino Acid Sequence Animals Cell Line Cytotoxicity Tests, Immunologic H-2 Antigens/immunology HLA Antigens/immunology Histocompatibility Antigens Class I/immunology Humans Kinetics Lymphocyte Activation/immunology Mice Molecular Sequence Data Peptides/immunology Protein Binding/immunology T-Lymphocytes, Cytotoxic/immunology
Chemicals
H-2 Antigens HLA Antigens Histocompatibility Antigens Class I Peptides
Authors & Affiliations
4 authors, click to expand affiliations / ORCID
Kageyama S
Center for Cancer Research, Massachusetts Institute of Technology, Cambridge, MA 02139.
Tsomides T J
Sykulev Y
Eisen H N
Article Info
Journal
Journal of immunology (Baltimore, Md. : 1950)
Abbr.
J Immunol
ISSN
0022-1767
Published
1995-01-15
Pages
567-76
Language
English
Region
United States
NLM ID
2985117R
Subset
IM
Grants
NIAID NIH HHS · AI34247 · United States
NCI NIH HHS · CA60686 · United States
NCI NIH HHS · R35-CA42504 · United States
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