Enhanced immune response to an antigen by a composition of a recombinant virus expressing the antigen with a recombinant virus expressing an immunostimulatory molecule
AssigneeThe United States of America, as represented by the Secretary, Department of Health and Human Services
InventorsJeffrey Schlom, Judith Kantor, James W. Hodge
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Abstract
The present invention is a composition of recombinant virus which has incorporated into its genome or portion thereof a gene encoding an antigen to a disease causing agent and a recombinant virus which has incorporated into its genome or portion thereof a gene encoding an immunostimulatory molecule(s) for the purpose of stimulating an immune response against the disease causing agent. Methods of treatment of diseases such as cancer and diseases caused by pathogenic microorganisms is provide using the composition.
Claims24
A composition comprising a first recombinant virus which has incorporated into a viral genome or infectable portion thereof one or more genes encoding a tumor-associated antigen of a cancer and a second recombinant virus which has incorporated into a viral genome or infectable portion thereof one or more genes or DNA sequences encoding B7.1, B7.2, or B7.1 and B7.2, wherein the composition is able to coinfect a host cell resulting in coexpression of the antigen-encoding genes and the B7.1, B7.2, or B7.1 and B7.2encoding genes or DNA sequences.
A composition comprising (i) a first recombinant virus comprising a recombinant virus genome, or an infectable portion thereof, having incorporated therein exogenous DNA encoding a tumor-associated antigen, or an immunogenic segment thereof, selected from the group consisting of oncofetal antigens, MART-1, MAGE-1, MAGE-3, gp100, tyrosinase, CEA, PSA, CA-125, erb-2, Muc-1, Muc-2, point-mutated ras, point-mutated p53 and TAG-72, and (ii) a second recombinant virus comprising a recombinant virus genome, or an infectable portion thereof, having incorporated therein exogenous DNA encoding B7.1 B7.2, or B7.1 and B7.2;
- wherein the composition is able to co-infect a host cell resulting in co-expression of the antigen-encoding DNA and the B7.1, B7.2, or B7.1 and B7.2-encoding DNA and further wherein the co-expression causes an enhanced cellular immune response against cells expressing tumor-associated antigen.
A composition comprising (i) a first recombinant virus comprising a recombinant virus genome, or an injectable portion thereof, having incorporated therein exogenous DNA encoding carcinoembryonic antigen (CEA), prostate specific antigen (PSA), MUC-1 antigen or an immunogenic portion thereof, and (ii) a second recombinant virus comprising a recombinant virus genome, or an infectable portion thereof, having incorporated therein exogenous DNA encoding B7.1, B7.2, or B7.1 and B7.2;
- wherein the composition is able to co-infect a host cell resulting in co-expression of the antigen-encoding DNA and the B7.1, B7.2, or B7.1 and B7.2-encoding DNA and further wherein the co-expression causes an enhanced cellular immune response against cells expressing the CEA, PSA or MUC-1 antigens.
A composition comprising (i) a first recombinant virus comprising a recombinant virus genome, or an infectable portion thereof, having incorporated therein exogenous DNA encoding a tumor-associated antigen or an immunogenic portion thereof, selected from the group consisting of oncofetal antigens, MART-1, MAGE-1, MAGS3, gp100, tyrosinase, CEA, PSA, CA-125, erb-3, MUC-1, MUC-2, point-mutated ras, point mutated p53 and TAG-72, said tumor-associated antigen is expressed in cancer, said cancer selected from the group consisting of non-Hodgkin Lymphoma, leukemia, Hodgkins lymphoma, lung cancer, liver cancer, melanoma, adenocarcinoma, thymoma, and sarcoma, and (ii) a second recombinant virus comprising a recombinant virus genome, or an infectable portion thereof, having incorporated therein exogenous DNA encoding B7.1, B7.2, or B7.1 and B7.2, wherein tie composition is able to co-infect a host cell resulting in co-expression of the antigen-encoding DNA and the B7.1, B7.2, or B7.1 and B7.2-encoding DNA and further wherein the co-expression causes an enhanced cellular immune response against the cells expressing tumor-associated antigen.
A recombinant virus comprising a recombinant virus genome, or an infectable portion thereof, having incorporated therein one or more genes encoding a tumor-associated antigen of a cancer and one or more genes or DNA sequences encoding B7.1, B7.2, or B7.1 and B7.2.
The recombinant virus according to 15 wherein the antigen is carcinoembryonic antigen (CEA).
A recombinant virus comprising a recombinant virus genome, or an infectable portion thereof, having incorporated therein exogenous DNA encoding a tumor-associated antigen or immunogenic portion thereof, said antigen selected from the group consisting of oncofetal antigens, MART-1, MAGE-1, MAGE-3, gp100, tyrosinase, CEA, PSA, CA-125, erb-2, Muc-1, Muc-2, point-mutated ras, point-mutated p53 and TAG-72, and exogenous DNA encoding B7.1, B7.2, or B7.1 and B7.2, wherein the virus is able to infect a host cell resulting in co-expression of the antigen-encoding DNA and the B7.1, B7.2, or B7.1 and B7.2-encoding DNA and further wherein the co-expression causes an enhanced cellular immune response against the cells expressing tumor-associated antigen.
A recombinant virus comprising a recombinant virus genome, or an infectable portion thereof, having incorporated therein exogenous DNA encoding a tumor-associated antigen or immunogenic portion thereof, said antigen selected from the group consisting of carcinoembryonic antigen (CEA), prostate specific antigen (PSA) and MUC-1, and exogenous DNA encoding B7.1, B7.2, or B7.1 and B7.2, wherein the virus is able to infect a host cell resulting in co-expression of the antigen-encoding DNA and the B7.1, B7.2 or B7.1 and B7.2-encoding DNA and further wherein the co-expression causes an enhanced cellular immune response against cells expressing CEA, PSA, MUC-1 or immunogenic portion thereof.
Dependencies are inferred from the claim text.