Highly networked immunogen composition
AssigneesThe General Hospital Corporation, Massachusetts Eye and Ear Infirmary
InventorsBruce D. Walker, Gaurav D. Gaiha, Elizabeth Rossin
Life of this patent
Estimating the term…
Loading patent…
AssigneesThe General Hospital Corporation, Massachusetts Eye and Ear Infirmary
InventorsBruce D. Walker, Gaurav D. Gaiha, Elizabeth Rossin
Estimating the term…
A method of preventing or treating HIV in a subject includes selecting two or more HIV CTL epitopes from an HIV proteome that have a network score that meets a threshold value. The network score for a given epitope can be determined by generating at least one network representing protein structure, calculating a set of network parameters, combining the network parameters to determine a network score for each amino acid residue in the protein structure, generating a network score for each of a plurality of epitopes as a weighted linear combination of the amino acid residues of the epitopes, and selecting two or more epitopes according to their network score. An effective amount of a T cell immunogen composition and a pharmaceutically acceptable carrier is administered to the subject. The T cell immunogen composition includes the two or more selected HIV CTL epitopes.
A multi-epitope T cell immunogen composition comprising two highly networked human immunodeficiency virus (HIV) cytotoxic T lymphocyte (CTL) epitopes, wherein the two highly networked HIV CTL epitopes are human leukocyte antigen (HLA)-B*57 KAFSPEVIPMF (KF11) (SEQ ID NO:201) and HLA-B*57 TSTLQEQIGW (TW10) (SEQ ID NO:202), or wherein the amino acid sequences of the highly networked HIV CTL epitopes have at least about 75% to about 99% homology to the amino acid sequences of HLA-B*57 KF11 and HLA-B*57 TW10.
A multi-epitope T cell immunogen composition comprising two or more highly networked HIV CTL epitopes, wherein the two highly networked HIV CTL epitopes are HLA-B*57 KAFSPEVIPMF (KF11) (SEQ ID NO:201) and HLA-B*57 TSTLQEQIGW (TW10) (SEQ ID NO:202), and further comprising at least ten HIV CTL epitopes, wherein the ten HIV CTL epitopes are HLA-A*11 AVDLSHFLK (AK9) (SEQ ID NO:
A multi-epitope T cell immunogen composition comprising two highly networked HIV CTL epitopes HLA-B*57 KAFSPEVIPMF (KF11) (SEQ ID NO:201) and HLA-B*57 TSTLQEQIGW (TW10) (SEQ ID NO:202), or amino acid sequences having at least about 75% to about 99% homology to the amino acid sequences of HLA-B*57 KF11 of and HLA-B*57 TW10 and further comprising two highly networked HIV CTL epitopes restricted by HLA-E*101 and HLA-E*103, wherein the two highly networked HIV CTL epitopes are selected from HLA-E*101/E*103 SALSEGATP (SEQ ID NO:
An RNA vector comprising a multi-epitope T cell immunogen, wherein the vector comprises a sequence comprising two or more highly networked HIV CTL epitopes, wherein the two or more highly networked HIV CTL epitopes each have a network score from 3.04 to 9.05.
A viral vector comprising a multi-epitope T cell immunogen, wherein the vector comprises a sequence comprising two or more highly networked HIV CTL epitopes, wherein the two or more highly networked HIV CTL epitopes each have a network score from 3.04 to 9.05, and wherein the viral vector is selected from the group consisting of a human adenovirus, a rhesus adenovirus, adeno-associated virus, Gorilla adenovirus, modified Ankara virus, herpesvirus, and a cytomegalovirus (CMV) viral vector.
Dependencies are inferred from the claim text.