The use of carboxyfluorescein diacetate succinimidyl ester to determine the site, duration and cell type responsible for antigen presentation in vivo
Open Access
- 1 December 1999
- journal article
- review article
- Published by Wiley in Immunology & Cell Biology
- Vol. 77 (6), 539-543
- https://doi.org/10.1046/j.1440-1711.1999.00868.x
Abstract
This report examines the use of 5-(and-6)-carboxyfluorescein diacetate succinimidyl ester (CFSE) to determine the site, duration and cell type responsible for antigen presentation in vivo. Evidence that CFSE-labelled T cells can be used to determine where various types of antigens are presented, including auto-antigens, oral antigens and cell-associated foreign antigens, is provided. Using this technique, the length of time antigen is presented after acquisition by APC was measured. Finally, CFSE labelling was used to identify the origin of the APC responsible for different forms of antigen presentation.Keywords
This publication has 19 references indexed in Scilit:
- Signalling through CD30 protects against autoimmune diabetes mediated by CD8 T cellsNature, 1999
- Defective TCR expression in transgenic mice constructed using cDNA‐based α‐ and β‐chain genes under the control of heterologous regulatory elementsImmunology & Cell Biology, 1998
- Induction of Autoimmune Diabetes by Oral Administration of AutoantigenScience, 1996
- Determination of lymphocyte division by flow cytometryJournal of Immunological Methods, 1994
- T cell receptor antagonist peptides induce positive selectionCell, 1994
- Virus infection triggers insulin-dependent diabetes mellitus in a transgenic model: Role of anti-self (virus) immune responseCell, 1991
- Ablation of “tolerance” and induction of diabetes by virus infection in viral antigen transgenic miceCell, 1991
- New fluorescent dyes for lymphocyte migration studiesJournal of Immunological Methods, 1990
- Class I-restricted processing and presentation of exogenous cell-associated antigen in vivo.The Journal of Experimental Medicine, 1990
- Introduction of soluble protein into the class I pathway of antigen processing and presentationCell, 1988