Specific tolerization of active cytolytic T lymphocyte responses in vivo with soluble peptides
Details
Serval ID
serval:BIB_A7383A0BF272
Type
Article: article from journal or magazin.
Collection
Publications
Institution
Title
Specific tolerization of active cytolytic T lymphocyte responses in vivo with soluble peptides
Journal
Cellular Immunology
ISSN
0008-8749 (Print)
Publication state
Published
Issued date
04/1996
Volume
169
Number
1
Pages
16-23
Notes
Journal Article
Research Support, Non-U.S. Gov't --- Old month value: Apr 10
Research Support, Non-U.S. Gov't --- Old month value: Apr 10
Abstract
A promising approach toward preventing and treating autoimmune disease involves identifying the mediating antigen and then tolerizing the autoreactive T cells with the corresponding antigen. For success, this method will require the specific tolerization of active helper or CTL responses while maintaining the integrity of the immune system. In this report, we selectively eliminated an ongoing CTL response by administering soluble peptide. BALB/c mice were immunized with two H-2Kd-restricted immunodominant CTL epitopes derived from HIV and malaria together with a T helper epitope to elicit a strong CTL response. Beginning 3 days later, mice were injected 3 times at 3-day intervals with 500 micrograms of only one or both of these epitopes in PBS. Following these injections, only one of two active CTL responses was tolerized without affecting T helper cells. This tolerization state requires antigen for its maintenance, may be retolerized upon return, and is not due to active or antigen-driven bystander suppression. This study suggests that soluble peptides may be utilized to treat or prevent autoimmune diseases caused by autoreactive CTLs.
Keywords
Amino Acid Sequence
Animals
Female
HIV/immunology
Immunodominant Epitopes/immunology
Lymphocyte Activation/*drug effects
Mice
Mice, Inbred BALB C
Molecular Sequence Data
Peptides/*pharmacology
T-Lymphocytes, Cytotoxic/*immunology
Pubmed
Web of science
Create date
24/01/2008 14:55
Last modification date
20/08/2019 15:12