Abstract
CD4+ T cells play a central role in orchestrating host immune responses against cancer as well as autoimmune and infectious diseases. Identification of major histocompatibility complex (MHC) class II-restricted helper T peptides is important for development of effective vaccines. The lack of effective methods to identify such T-cell peptides is a major hurdle in the use of antigen-specific CD4+ T cells in cancer vaccines. Here we describe a genetic targeting expression system for cloning genes encoding for MHC class II-restricted tumor antigens recognized by tumor-reactive CD4+ T cells. Helper T peptides are subsequently identified by using synthetic peptides to test their ability to stimulate CD4+ T cells.
| Original language | English (US) |
|---|---|
| Pages (from-to) | 227-235 |
| Number of pages | 9 |
| Journal | Methods |
| Volume | 29 |
| Issue number | 3 |
| DOIs | |
| State | Published - Mar 1 2003 |
Keywords
- Cancer vaccines
- CD4+ T cells
- cDNA library
- Helper T peptides
- Immunotherapy
- Major histocompatibility complex class II
- Targeting expression
- Tumor antigens
ASJC Scopus subject areas
- Molecular Biology
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