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US 6,632,435 B1Granted
CTL epitope analogs
AssigneeCity of Hope
InventorDon J. Diamond
Life of this patent
Estimating the term…
Abstract
We have screened the HCMV-specific T cell clone, 33F4, with a nonamer PS-SCL based on SEQ ID NO: 1, and described a series of analog peptides that are recognized with greater affinity than the native peptide sequence.
Claims5
A peptide selected from group consisting of SEQ ID NO:
- 38, 52 and 64′ produced according to the steps of:
- (a) providing a sequence of a human-cytomegalovirus-cytotoxic-T-lymphocyte epitope and a combinatorial peptide library which contains peptide analogs of said viral-cytotoxic-T-lymphocyte epitope;
- (b) screening said combinatorial peptide library for immunogenicity;
- (c) analyzing the results of said screening to select one or more peptide analogs which may have improved immunogenicity relative to the native human-cytomegalovirus-cytotoxic-T-lymphocyte epitope;
- (d) assaying said one or more peptide analogs for immunogenicity;
- (e) analyzing the results of the assay in step (d);
- (f) selecting one or more highly immunogenic peptide analogs based on the analysis of step (e);
- (g) assaying said highly immunogenic peptide analogs for broad recognition of MHC allele subtypes;
- (h) analyzing the results of the assay in step (g);
- (i) selecting one or more highly immunogenic peptide analogs with retained breadth of recognition of MHC allele subtypes relative to the native human-cytomegalovirus-cytotoxic-T-lymphocyte epitoPe based on the analysis of the earlier steps;
- and
- (j) synthesizing the peptide selected in step (i) wherein said peptide is selected from the group consisting of SEQ ID NOS:
- 38, 52 and 64′ wherein said peptide is selected from the group consistin of SEQ ID NOS:
- 38, 52 and 64.
11 more elements
A peptide which is selected from the group consisting of SEQ ID NOS:
- 38, 52 and 64.
A peptide of SEQ ID NO:
- 38.
A peptide of SEQ ID NO:
- 52.
A peptide of SEQ ID NO:
- 64.
Dependencies are inferred from the claim text.