Methods and compositions useful in generating non canonical cd8+ t cell responses

Abstract

Methods of inducing a CD8+ T cell response to a heterologous antigen in which at least 10% of the CD8+ T cells are MHC-E restricted are disclosed. The method involves immunizing with a CMV vector that does not express UL128 and UL130 proteins. Also disclosed are recombinant CMV vectors comprising nucleic acids encoding a heterologous protein antigen, a UL40 protein, and a US28 protein but that do not express an active UL128 and UL130 protein. Also disclosed are recombinant CMV vectors comprising nucleic acids encoding a heterologous protein antigen, but that do not express an active UL40 protein, UL128 protein, UL130 protein, and optionally a US28 protein. Also disclosed are recombinant CMV vectors comprising nucleic acids encoding a heterologous protein antigen, but that do not express an active US28 protein, UL128 protein, UL130 protein, and optionally a UL40 protein.

1 . A recombinant cytomegalovirus (CMV) vector comprising:
 (1) a first nucleic acid sequence encoding at least one heterologous antigen;   (2) a second nucleic acid sequence encoding at least one active UL40 protein, or an ortholog or homolog thereof; and   (3) a third nucleic acid sequence encoding at least one active US28 protein, or an ortholog or homolog thereof;   wherein the CMV vector does not express an active UL128 protein, or an ortholog thereof, and does not express an active UL130 protein, or an ortholog thereof.   
     
     
         2 . The recombinant CMV vector of  claim 1 , wherein the at least one heterologous antigen comprises a pathogen-specific antigen, a tumor antigen, a tissue-specific antigen, or a host self-antigen. 
     
     
         3 . (canceled) 
     
     
         4 . The recombinant CMV vector of  claim 2 , wherein the pathogen-specific antigen is derived from a pathogen selected from the group consisting of: human immunodeficiency virus, simian immunodeficiency virus, herpes simplex virus, hepatitis B virus, hepatitis C virus, papillomavirus,  Plasmodium  parasites, and  Mycobacterium tuberculosis.    
     
     
         5 . (canceled) 
     
     
         6 . The recombinant CMV vector of  claim 1 , wherein the CMV vector does not express an active UL128 or UL130 protein, or orthologs thereof, due to the presence of one or more mutations in the nucleic acid sequence encoding UL128 or UL130, or orthologs thereof. 
     
     
         7 . The recombinant CMV vector of  claim 6 , wherein the one or more mutations in the nucleic acid sequence encoding UL128 or UL130, or orthologs thereof, are selected from the group consisting of: point mutations, frameshift mutations, truncation mutations, and deletion of all of the nucleic acid sequence encoding the protein. 
     
     
         8 . (canceled) 
     
     
         9 . The recombinant CMV vector of  claim 1 , wherein the CMV vector further comprises at least one inactivating mutation in one or more viral genes encoding viral proteins that are essential, non-essential, or augmenting for growth in vivo. 
     
     
         10 . The recombinant CMV vector of  claim 9 , wherein the at least one inactivating mutation is selected from the group consisting of: point mutation, frameshift mutation, truncation mutation, and deletion of all of the nucleic acid sequence encoding the viral protein. 
     
     
         11 . The recombinant CMV vector of  claim 9 , wherein the at least one inactivating mutation is in UL82 (pp71). 
     
     
         12 . The recombinant CMV vector of  claim 9 , wherein the at least one inactivating mutation is in US11. 
     
     
         13 . The recombinant CMV vector of  claim 1 , wherein the CMV vector is a human CMV (HCMV) or rhesus CMV (RhCMV) vector. 
     
     
         14 . A method of generating an MHC-E-restricted CD8 +  T cell response to at least one heterologous antigen in a subject, the method comprising administering to the subject the recombinant CMV vector of  claim 1  in an amount effective to elicit an MHC-E-restricted CD8 +  T cell response to the at least one heterologous antigen in the subject. 
     
     
         15 - 18 . (canceled) 
     
     
         19 . The method of  claim 14 , wherein the subject has been previously exposed to CMV. 
     
     
         20 . The method of  claim 14 , wherein the subject is a human or nonhuman primate. 
     
     
         21 - 62 . (canceled) 
     
     
         63 . A method of generating CD8 +  T cells that recognize MHC-E-peptide complexes, the method comprising:
 (1) administering to a subject the recombinant CMV vector of  claim 1  in an amount effective to generate a set of CD8 +  T cells that recognize MHC-E/peptide complexes; 
 (2) identifying a first CD8 +  TCR from the set of CD8 +  T cells, wherein the first CD8 +  TCR recognizes a MHC-E/heterologous antigen-derived peptide complex; 
 (3) isolating one or more CD8 +  T cells from the subject; and 
 (4) transfecting the one or more CD8 +  T cells with an expression vector, wherein the expression vector comprises a nucleic acid sequence encoding a second CD8 +  TCR and a promoter operably linked to the nucleic acid sequence encoding the second CD8 +  TCR, wherein the second CD8 +  TCR comprises CDR3α and CDR3β of the first CD8 +  TCR, thereby generating one or more transfected CD8 +  T cells that recognize a MHC-E/heterologous antigen-derived peptide complex. 
 
     
     
         64 - 101 . (canceled) 
     
     
         102 . A CD8 +  T cell generated by the method of  claim 63 . 
     
     
         103 - 104 . (canceled) 
     
     
         105 . The CD8 +  T cell of  claim 102 , wherein the at least one heterologous antigen of the recombinant CMV vector comprises a pathogen-specific antigen. 
     
     
         106 . The CD8 +  T cell of  claim 105 , wherein the pathogen-specific antigen is derived from a pathogen selected from the group consisting of: human immunodeficiency virus, simian immunodeficiency virus, herpes simplex virus, hepatitis B virus, hepatitis C virus, papillomavirus,  Plasmodium  parasites, and  Mycobacterium tuberculosis.    
     
     
         107 - 109 . (canceled) 
     
     
         110 . A method of treating a pathogenic infection, the method comprising administering the CD8 +  T cell of  claim 105  to a subject. 
     
     
         111 - 112 . (canceled) 
     
     
         113 . A method of treating a pathogenic infection, the method comprising administering the CD8 +  T cell of  claim 106  to a subject. 
     
     
         114 . The method of  claim 113 , wherein the pathogen-specific antigen is derived from a human immunodeficiency virus.