Patent number: 5019387
Filing date: Sep 8, 1987
Issue date: May 28, 1991
Inventors: Barton F. Haynes, Thomas J. Palker
Assignee: Duke University
Primary Examiner: Abdel A. Mohamed
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What is claimed is:
1. An essentially pure form of a hydrophilic peptide consisting essentially of an amino acid sequence of about 9 to 35 units in length and corresponding to at least one antigenic determinant of the envelope glycoprotein of human immunodeficiency virus (HIV) recognized by B lymphocytes, said peptide, when covalently linked to a carrier molecule, induces in a primate the production of high titers of antibodies that neutralize HIV.
2. The peptide according to claim 1, wherein said amino acid sequence corresponds to the SP-10 region of the envelope glycoprotein of HIV, or an antigenic portion thereof.
3. The peptide according to claim 2, wherein said amino acid sequence consists essentially of CTRPNNNTRKSIRIQRGpg, or an antigenic portion thereof.
4. An immunogenic conjugate that induces in a primate the production of high titers of antibodies that neutralize human immunodeficiency virus (HIV), said conjugate comprising a carrier molecule covalently attached to a hydrophilic peptide consisting essentially of an amino acid sequence of about 9 to 35 units in length and corresponding to at least the antigenic determinate of the envelope glycoprotein of HIV recognized by B lymphocytes.
5. The conjugate according to claim 4, wherein said carrier molecule comprises an amino acid sequence corresponding to a region of the envelope glycoprotein of HIV which region is distinct from said hydrophilic peptide and is recognized by T cells.
6. The conjugate according to claim 5, wherein said region is distinct from said hydrophilic peptic is T cell epitope T1 or T cell epitope T2, or an antigenic portion thereof.
7. The conjugate according to claim 4, wherein said carrier molecule is tetanus toxoid.
8. The conjugate according to claim 4, wherein said carrier molecule is covalently attached to said peptide through at least one spacer molecule.
9. The conjugate according to claim 8, wherein said spacer molecule consists of the dipeptide glycine-glycine.
10. The conjugate according to claim 4 wherein said peptide has an amino acid sequence corresponding to the SP-10 region of the envelope glycoprotein of HIV, or an antigenic portion thereof.
11. The conjugate according to claim 10 wherein said amino acid sequence consists essentially of CTRPNNNTRKSIRIQRGpg, or an antigenic portion thereof.
12. The conjugate according to claim 4, further comprising to the amino acid sequence FLGFLG which is covalently linked the C terminal of said peptide.
13. The conjugate according to claim 4 further comprising an amino acid sequence corresponding to a hypervariable region of the envelope protein of HIV isolates located C terminal to the SP-10 region of the envelope glycoprotein of HIV.
14. The conjugate according to claim 13 wherein said sequence corresponding to said hypervariable region is RAFVTIGKIGN and is directly linked to the C terminus of SP-10.
15. A method of producing immunity to HIV in a primate comprising administering to said primate at least one conjugate according to claim 4.