Use of Triplex CMV Vaccine in CAR T Cell Therapy
A method for treating a patient comprising: (a) providing a composition comprising a population of T cells expressing both a chimeric antigen receptor (CAR) and a T cell receptor specific for a cytomegalovirus (CMV) antigen; (b) administering the composition to the patient; and (c) administering to the patient a viral vector encoding: (i) CMV pp65 and (ii) a fusion protein comprising exon 4 of CMV protein IE I (e4) and exon 5 of CMV protein IE2 (e5) either prior to or subsequent to administering the composition comprising a population of T cells to the patient is described.
1 - 50 . (canceled)
51 . A method for treating a patient comprising:
(a) providing a composition comprising a population of T cells expressing both a chimeric antigen receptor (CAR) and a T cell receptor specific for a cytomegalovirus (CMV) antigen;
(b) administering the composition of part (a) to the patient; and
(c) administering to the patient a viral vector encoding:
(i) CMV pp65 and
(ii) a fusion protein comprising exon 4 of CMV protein IE1 (e4) and exon 5 of CMV protein IE2 (e5).
52 . The method of claim 51 , wherein the viral vector of part (a) is a MVA virus.
53 . The method of claim 52 , wherein expression of (i) CMV pp65 and (ii) the fusion protein comprising exon 4 of CMV protein IE1 (e4) and exon 5 of CMV protein IE2 (e5) is under the control of mH5 promoter.
54 . The method of claim 51 , wherein the patient is CMV-seronegative prior to treatment.
55 . The method of claim 51 , wherein the patient is CMV-seropositive prior to treatment.
56 . The method of claim 51 , wherein the CAR is targeted to CD19.
57 . The method of claim 51 , wherein the viral vector is administered to the patient both prior to and subsequent to the administration of the composition comprising a population of T cells.
58 . The method of claim 51 , wherein the step of providing a population of T cells expressing a CAR and a T cell receptor specific for a CMV antigen comprises:
(a1) providing PBMC or a T cell subpopulation from a CMV-seropositive human donor;
(a2) exposing the PBMC or the T cell subpopulation of part (a1) to at least one CMV antigen;
(a3) treating the exposed cells of part (a2) to produce a population of cells enriched for cells specific for CMV; and
(a4) transducing at least a portion of the enriched population of cells of part (a3) with a vector expressing a CAR.
59 . The method of claim 58 , wherein the step of treating the exposed cells to produce a population of cells enriched for cells specific for CMV comprises treating the cells to produce a population of cells enriched for cells expressing an activation marker.
60 . The method of claim 51 , wherein the step of providing a population of T cell expressing a CAR and a T cell receptor specific for a CMV antigen further comprises:
(a1) administering a viral vector encoding: (i) CMV pp65 and (ii) a fusion protein comprising exon 4 of CMV protein IE1 (e4) and exon 5 of CMV protein IE2 (e5) to a human donor to convert a CMV-seronegative human donor to one containing T cells responsive to CMV antigens pp65, IE1 and IE2;
(a2) obtaining PBMC from the CMV-seropositive human donor of (a1);
(a3) exposing the PBMC of (a2) to at least one CMV antigen;
(a4) treating the exposed cells of (a3) to produce a population of cells enriched for stimulated cells specific for CMV; and
(a5) transducing at least a portion of the enriched population of cells of (a4) with a vector expressing a CAR, thereby providing a population of T cell expressing a CAR and a T cell receptor specific for a CMV antigen.
61 . The method of claim 51 , wherein the step of providing a population of T cell expressing a CAR and a T cell receptor specific for a CMV antigen comprises:
(a1) administering a viral vector encoding: (i) CMV pp65 and (ii) a fusion protein comprising exon 4 of CMV protein IE1 (e4) and exon 5 of CMV protein IE2 (e5) to a CMV-positive human donor;
(a2) obtaining PBMC from the CMV-seropositive human donor of (a1);
(a3) exposing the PBMC of (a2) to at least one CMV antigen;
(a4) treating the exposed cells of (a3) to produce a population of cells enriched for stimulated cells specific for CMV;
(a5) transducing at least a portion of the enriched population of cells of (a4) with a vector expressing a CAR, thereby providing a population of T cell expressing a CAR and a T cell receptor specific for a CMV antigen.
62 . A method for preparing T cells expressing a CAR and a T cell receptor specific for a CMV antigen, the method comprising:
(a) administering a viral vector encoding: (i) CMV pp65 and (ii) a fusion protein comprising exon 4 of CMV protein IE1 (e4) and exon 5 of CMV protein IE2 (e5) to a CMV-positive human donor;
(b) obtaining PBMC from the CMV-seropositive human donor;
(c) exposing the PBMC to at least one CMV antigen;
(d) treating the exposed cells to produce a population of cells enriched for stimulated cells specific for CMV; and
(e) transducing at least a portion of the enriched population of cells with a vector expressing a CAR, thereby providing a population of T cell expressing a CAR and a T cell receptor specific for a CMV antigen.
63 . A method for preparing T cells expressing a CAR and a T cell receptor specific for a CMV antigen, the method comprising:
(a) administering a viral vector encoding: (i) CMV pp65 and (ii) a fusion protein comprising exon 4 of CMV protein IE1 (e4) and exon 5 of CMV protein IE2 (e5) to a CMV-positive human donor;
(b) obtaining PBMC from the CMV-seropositive human donor;
(c) (b) exposing the PBMC to at least one CMV antigen;
(d) treating the exposed cells to produce a population of cells enriched for stimulated cells specific for CMV; and
(e) transducing at least a portion of the enriched population of cells with a vector expressing a CAR, thereby providing a population of T cell expressing a CAR and a T cell receptor specific for a CMV antigen.
64 . The method of claim 51 , wherein the CAR is selective for an antigen selected from: CD19, CD123, CS1, BCMA, CD44v6, CD33, CD22, IL-13α2, PSA, HER-2, EGFRv3, CEA, and C7R.
65 . The method of claim 51 , wherein the CAR comprises: a scFv selective for a non-CMV antigen; a hinge/linker region; a transmembrane domain; a co-signaling domain; and CD3 ξ signaling domain.
66 . The method of claim 65 , wherein the co-signaling domain is selected from a CD28 co-signaling domain and a 4-IBB co-signaling domain.
67 . The method of claim 65 , wherein the transmembrane domain is selected from a CD28 transmembrane domain and a CD4 transmembrane