Immunogenic peptides
The invention provides relatively short immunogenic peptides derived from CD19 and CD20 antigens, and biologically active variants thereof, which elicit an immune response. Nucleic acids encoding the immunogenic peptides and antibodies specific for the peptides are also provided. The immunogenic peptides can be included in pharmaceutical compositions, such as cancer vaccines, and used for the treatment of cancer.
1. An isolated leukemic antigen consisting of a fragment of CD19 (SEQ ID NO:13) or a variant thereof having one, two, or three conservative or nonconservative amino acid substitutions that is capable of stimulating a cytotoxic T-lymphocyte reaction against a cell expressing CD19, wherein the fragment is
(a) 11 to 80 amino acids in length or
(b) 9 to 80 amino acids in length and comprises the amino acid sequence RLLFFLLFL (SEQ ID NO: 1), TLAYLIFCL (SEQ ID NO: 2), LLFLTPMEV (SEQ ID NO: 3), KLMSPKLYV (SEQ ID NO: 4), or LLFFLLFLV (SEQ ID NO: 5).
2. The isolated leukemic antigen of claim 1 wherein the fragment of CD19 antigen is immunologically recognized by MHC restricted T-lymphocytes that are HLA-A2.1 restricted.
3. The isolated leukemic antigen of claim 2 wherein the fragment of CD19 antigen or variant thereof is 9 to 80 amino acids in length and comprises the amino acid sequence RLLFFLLFL (SEQ ID NO: 1), TLAYLIFCL (SEQ ID NO: 2), LLFLTPMEV (SEQ ID NO: 3), KLMSPKLYV (SEQ ID NO: 4), or LLFFLLFLV (SEQ ID NO: 5).
4. The isolated leukemic antigen of claim 3 wherein the fragment of the CD19 antigen is 9 to 30 amino acids in length.
5. A pharmaceutical composition comprising the isolated leukemic antigen of claim 1 and one or more co-immunostimulatory molecules.
6. A pharmaceutical composition comprising the isolated leukemic antigen of claim 1 and a pharmaceutically acceptable carrier thereby forming the pharmaceutical composition.
7. An isolated leukemic antigen consisting of a fragment of CD19 (SEQ ID NO:13) or a variant thereof, wherein the variant has one or two conservative or nonconservative amino acid substitutions, wherein the fragment or variant is immunologically recognized by MHC restricted T-lymphocytes that are HLA-A2.1 restricted and is capable of stimulating a cytotoxic T-lymphocyte reaction against cells expressing CD19, and wherein the fragment or variant thereof is
(a) 11 to 40 amino acids in length and comprises two anchor amino acids, wherein the anchor amino acids comprise a leucine or isoleucine residue separated from a valine residue by six amino acids; or
(b) 9 to 40 amino acids in length and comprises the amino acid sequence RLLFFLLFL (SEQ ID NO: 1), TLAYLIFCL (SEQ ID NO: 2), LLFLTPMEV (SEQ ID NO: 3), KLMSPKLYV (SEQ ID NO: 4), or LLFFLLFLV (SEQ ID NO: 5).
8. The isolated leukemic antigen of claim 7 wherein the fragment of the CD19 or CD20 antigen is 9 to 15 amino acids in length and comprises the amino acid sequence RLLFFLLFL (SEQ ID NO: 1), TLAYLIFCL (SEQ ID NO: 2), LLFLTPMEV (SEQ ID NO: 3), KLMSPKLYV (SEQ ID NO: 4), or LLFFLLFLV (SEQ ID NO: 5.
9. A pharmaceutical composition comprising the isolated leukemic antigen of claim 7 in combination with one or more co-immunostimulatory molecules.