Abstract
The critical role of costimulatory signals in T-cell activation and the complexity of T-cell costimulatory pathways involved make a detailed understanding of this system a challenging task. By taking advantage of the unique chemical properties of CFSE, we and others have developed an in vivo model that allows quantitative analysis of T-cell activation at a single-cell level. This model involves labeling of donor T-cells with the tracking dye CFSE and adoptively transferring into lethally irradiated allogeneic hosts. T-cells proliferating in the host mice can be explicitly analyzed upon recovery. By using mice deficient for certain costimulatory molecules as a source of donor cells or by treating the host mice with reagents that block certain costimulatory pathways, this CFSE model is extremely useful in studying the role of T-cell costimulatory signals in activation, survival, and effector differentiation of alloreactive T-cells in vivo.
| Original language | English (US) |
|---|---|
| Pages (from-to) | 409-420 |
| Number of pages | 12 |
| Journal | Methods in molecular medicine |
| Volume | 109 |
| State | Published - 2005 |
ASJC Scopus subject areas
- Molecular Medicine
Divisions
- Abdominal Transplant
Fingerprint
Dive into the research topics of 'Study of T-cell costimulatory blockade in vivo at a single-cell level.'. Together they form a unique fingerprint.Cite this
- APA
- Standard
- Harvard
- Vancouver
- Author
- BIBTEX
- RIS