Abstract
T-cell activation and response to antigen follows presentation by major histocompatibility complex (MHC)-compatible antigen-presenting cells (APC). Activation requires a number of separate but interrelated receptor-ligand interactions between the T cell and APC. Some of these interactions can be mimicked by other molecules, such as lectins, antibodies, or synthetic peptides. We discuss the potential use of conjugates to activate T cells, and describe a new class of heteroconjugates for stimulation or modulation of antigen-specific T-cell activity. These heteroconjugates contain an antigen-specific epitope coupled to a T-cell ligand, which replaces some functions of the APC. Such heteroconjugates would bind and supply two signals to T cells, one through the antigen-recognition site of the T-cell receptor and the other through receptors required for activation. Natural heteroconjugates of this type have been identified, for example in a small peptide derived from a Mycobacterium leprae protein.1 Coupling of these two signaling moieties into a single soluble molecule may allow antigen-specific T-cell activation without the need for processing and presentation by antigen-presenting cells and without MHC restriction. Conjugates of this type may be useful for the study of T-cell activation, the development of new antigen-specific diagnostic materials and immunomodulators, and possibly a new class of vaccines.
| Original language | English (US) |
|---|---|
| Pages (from-to) | 91-102 |
| Number of pages | 12 |
| Journal | Vaccine Research |
| Volume | 5 |
| Issue number | 2 |
| State | Published - Jan 1 1996 |
| Externally published | Yes |
UN SDGs
This output contributes to the following UN Sustainable Development Goals (SDGs)
-
SDG 3 Good Health and Well-being
ASJC Scopus subject areas
- Immunology
- Microbiology (medical)
Fingerprint
Dive into the research topics of 'A new approach to T-cell activation: Natural and synthetic conjugates capable of activating T cells'. Together they form a unique fingerprint.Cite this
- APA
- Standard
- Harvard
- Vancouver
- Author
- BIBTEX
- RIS