TCR affinity for p/MHC formed by tumor antigens that are self-proteins: impact on efficacy and toxicity.
TCR affinity for p/MHC formed by tumor antigens that are self-proteins: impact on efficacy and toxicity.
Curr Opin Immunol. 2015 Jan 22;33C:16-22
Authors: Stone JD, Harris DT, Kranz DM
Abstract
Recent studies have shown that the range of affinities of T cell receptors (TCRs) against non-mutated cancer peptide/class I complexes are lower than TCR affinities for foreign antigens. Raising the affinity of TCRs for optimal activity of CD8 T cells, and for recruitment of CD4 T cell activity against a class I antigen, provides opportunities for more robust adoptive T cell therapies. However, TCRs with enhanced affinities also risk increased reactivity with structurally related self-peptides, and off-target toxicities. Careful selection of tumor peptide antigens, in silico proteome screens, and in vitro peptide specificity assays will be important in the development of the most effective, safe TCR-based adoptive therapies.
PMID: 25618219 [PubMed - as supplied by publisher]
Source: Current Opinion in Immunology - Category: Allergy & Immunology Authors: Stone JD, Harris DT, Kranz DM Tags: Curr Opin Immunol Source Type: research