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PMID: 9462514 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't

The duration of antigenic stimulation determines the fate of naive and effector T cells.

Immunity ·Vol. 8 ·No. 1 ·1998-01-00 ·Pages 89-95

Iezzi G, Karjalainen K, Lanzavecchia A

Abstract

It is known that T cells engage antigen-presenting cells (APCs) in a stable interaction that results in sustained TCR signaling. We show here that the duration of this process is critical in determining whether T cells will be activated or deleted. Whereas naive T cells require approximately 20 hr of sustained signaling to be committed to proliferation, effector T cells become committed after only 1 hr but die following activation if antigenic stimulation is prolonged. Costimulation by anti-CD28 facilitates T cell activation by decreasing the time of commitment and by protecting T cells from death. These findings explain in quantitative terms the essential requirement for professional APCs in T cell priming and show that the duration of antigenic stimulation is the major factor determining the fate of naive and effector T cells.

MeSH Terms
Animals Antigen-Presenting Cells/immunology,ultrastructure CD28 Antigens/immunology,pharmacology Cell Death/physiology Lymphocyte Activation/immunology Mice Mice, Inbred BALB C Receptors, Antigen, T-Cell/immunology,metabolism Receptors, Interleukin-2/biosynthesis Signal Transduction/physiology T-Lymphocytes, Regulatory/immunology,ultrastructure
Chemicals
CD28 Antigens Receptors, Antigen, T-Cell Receptors, Interleukin-2
Authors & Affiliations
3 authors, click to expand affiliations / ORCID
Iezzi G
Basel Institute for Immunology, Switzerland.
Karjalainen K
Lanzavecchia A
Article Info
Journal
Immunity
Abbr.
Immunity
ISSN
1074-7613
Published
1998-01-00
Pages
89-95
Language
English
Region
United States
NLM ID
9432918
Subset
IM
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