TY - JOUR
T1 - Exploring immunological specificity using synthetic peptide combinatorial libraries
AU - Pinilla, Clemencia
AU - Martin, Roland
AU - Gran, Bruno
AU - Appel, Jon R.
AU - Boggiano, Cesar
AU - Wilson, Darcy B.
AU - Houghten, Richard A.
PY - 1999/4
Y1 - 1999/4
N2 - The definition of epitopes for human B and T cells is fundamental for the understanding of the immune response mechanism and its role in the prevention and cause of human disease. This understanding can be applied to the design of diagnostics and synthetic vaccines. In recent years, the understanding of the specificity of B and T cells has been advanced significantly by the development and use of combinatorial libraries made up of thousands to millions of synthetic peptides. The use of this approach has had four major effects: first, the definition of high affinity ligands both for T cells and antibodies; second, the application of alternative means for identifying immunologically relevant peptides for use as potential preventive and therapeutic vaccines; third, a new appreciation of the requirements for TCR interactions with peptide-MHC complexes in immunogenicity; fourth, the establishment of new principles regarding the level of cross-reactivity in immunological recognition.
AB - The definition of epitopes for human B and T cells is fundamental for the understanding of the immune response mechanism and its role in the prevention and cause of human disease. This understanding can be applied to the design of diagnostics and synthetic vaccines. In recent years, the understanding of the specificity of B and T cells has been advanced significantly by the development and use of combinatorial libraries made up of thousands to millions of synthetic peptides. The use of this approach has had four major effects: first, the definition of high affinity ligands both for T cells and antibodies; second, the application of alternative means for identifying immunologically relevant peptides for use as potential preventive and therapeutic vaccines; third, a new appreciation of the requirements for TCR interactions with peptide-MHC complexes in immunogenicity; fourth, the establishment of new principles regarding the level of cross-reactivity in immunological recognition.
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U2 - 10.1016/S0952-7915(99)80033-8
DO - 10.1016/S0952-7915(99)80033-8
M3 - Article
C2 - 10322159
AN - SCOPUS:0032891125
SN - 0952-7915
VL - 11
SP - 193
EP - 202
JO - Current Opinion in Immunology
JF - Current Opinion in Immunology
IS - 2
ER -