- Austin TX, US Erin WILLERT - Round Rock TX, US Sangeetha RAJAGOPALAN - Round Rock TX, US Garrett Lee ROBINSON - Austin TX, US Brigitte BRIESCHKE - Austin TX, US Jason KIM - Austin TX, US
International Classification:
A61K 39/00 A61K 47/68 C07K 14/25
Abstract:
The present invention provides cell-targeting molecules which can deliver a CD8+ T-cell epitope cargo to the MHC class I presentation pathway of a target cell. The cell-targeting molecules of the invention can be used to deliver virtually any CD8+ T-cell epitope from an extracellular space to the MHC class I pathway of a target cell, which may be a malignant cell and/or non-immune cell. The target cell can then display on a cell-surface the delivered CD8+ T-cell epitope complexed with MHC I molecule. The cell-targeting molecules of the invention have uses which include the targeted labeling and/or killing of specific cell-types within a mixture of cell-types, including within a chordate, as well as the stimulation of beneficial immune responses. The cell-targeting molecules of the invention have uses, e.g., in the treatment of a variety of diseases, disorders, and conditions, including cancers, tumors, growth abnormalities, immune disorders, and microbial infections.
De-Immunized, Shiga Toxin A Subunit Scaffolds And Cell-Targeting Molecules Comprising The Same
- Austin TX, US Erin WILLERT - Round Rock TX, US Garrett Lee ROBINSON - Austin TX, US Sangeetha RAJAGOPALAN - Round Rock TX, US Brigitte BRIESCHKE - Austin TX, US
International Classification:
C07K 14/25 C07K 19/00
Abstract:
The present invention relates to Shiga toxin A Subunit derived polypeptides and cell-targeting molecules comprising amino acid substitutions which equip the polypeptides with 1) de-immunization; 2) reduced, protease-cleavage sensitivity; and/or 3) a heterologous epitope cargo(s) while retaining Shiga toxin function(s), such as, e.g., potent cytotoxicity. Certain polypeptides of the invention exhibit reduced immunogenic potential in mammals and/or are capable of delivering an epitope to an MHC class molecule of a cell in which the polypeptide is present. Certain molecules comprising a polypeptide of the invention are well-tolerated by mammals while retaining one or more of the features mentioned above. The Shiga toxin polypeptides of the invention have uses as components of cell-targeting molecules for selectively killing specific cells; for selectively delivering cargos to specific cells, and as therapeutic and/or diagnostic molecules for treating and diagnosing a variety of conditions, including cancers, immune disorders, and microbial infections.
De-Immunized Shiga Toxin A Subunit Effector Polypeptides For Applications In Mammals
- Austin TX, US Erin Willert - Round Rock TX, US Garrett Lee Robinson - Austin TX, US Sangeetha Rajagopalan - Round Rock TX, US Brigitte Brieschke - Austin TX, US
The present invention relates to Shiga toxin effector polypeptides with reduced antigenic and/or immunogenic potential. Immunogenicity can be a limitation for the repeated administration to mammals of proteins and polypeptides derived from Shiga toxins. The Shiga toxin effector polypeptides of the present invention have uses as components of therapeutics, diagnostics, and immunization materials. The cytotoxic proteins of the present invention have uses for selective killing of specific cell types and as therapeutics for the treatment of a variety of diseases, including cancers, immune disorders, and microbial infections. The proteins of the present invention also have uses for detecting specific cell types, collecting diagnostic information, and monitoring the treatment of a variety of diseases, such as, e.g., cancers, immune disorders, and microbial infections.
Cell-Targeting Molecules Comprising De-Immunized, Shiga Toxin A Subunit Effectors And Cd8+ T-Cell Epitopes
- Austin TX, US Erin WILLERT - Round Rock TX, US Sangeetha RAJAGOPALAN - Round Rock TX, US Garrett Lee ROBINSON - Austin TX, US Brigitte BRIESCHKE - Austin TX, US Jason KIM - Austin TX, US
Assignee:
Molecular Templates, Inc. - Austin TX
International Classification:
A61K 39/00 A61K 47/68 C07K 14/25
Abstract:
The present invention provides cell-targeting molecules which can deliver a CD8+ T-cell epitope cargo to the MHC class I presentation pathway of a target cell. The cell-targeting molecules of the invention can be used to deliver virtually any CD8+ T-cell epitope from an extracellular space to the MHC class I pathway of a target cell, which may be a malignant cell and/or non-immune cell. The target cell can then display on a cell-surface the delivered CD8+ T-cell epitope complexed with MHC I molecule. The cell-targeting molecules of the invention have uses which include the targeted labeling and/or killing of specific cell-types within a mixture of cell-types, including within a chordate, as well as the stimulation of beneficial immune responses. The cell-targeting molecules of the invention have uses, e.g., in the treatment of a variety of diseases, disorders, and conditions, including cancers, tumors, growth abnormalities, immune disorders, and microbial infections.
De-Immunized, Shiga Toxin A Subunit Scaffolds And Cell-Targeting Molecules Comprising The Same
- Austin TX, US Erin Willert - Round Rock TX, US Garrett Lee Robinson - Austin TX, US Sangeetha Rajagopalan - Round Rock TX, US Brigitte Brieschke - Austin TX, US
International Classification:
C07K 14/25 C07K 19/00
Abstract:
The present invention relates to Shiga toxin A Subunit derived polypeptides and cell-targeting molecules comprising amino acid substitutions which equip the polypeptides with 1) de-immunization; 2) reduced, protease-cleavage sensitivity; and/or 3) a heterologous epitope cargo(s) while retaining Shiga toxin function(s), such as, e.g., potent cytotoxicity. Certain polypeptides of the invention exhibit reduced immunogenic potential in mammals and/or are capable of delivering an epitope to an MHC class molecule of a cell in which the polypeptide is present. Certain molecules comprising a polypeptide of the invention are well-tolerated by mammals while retaining one or more of the features mentioned above. The Shiga toxin polypeptides of the invention have uses as components of cell-targeting molecules for selectively killing specific cells; for selectively delivering cargos to specific cells, and as therapeutic and/or diagnostic molecules for treating and diagnosing a variety of conditions, including cancers, immune disorders, and microbial infections.
Cell-Targeting Molecules Comprising De-Immunized, Shiga Toxin A Subunit Effectors And Cd8+ T-Cell Epitopes
- Austin TX, US Erin WILLERT - Round Rock TX, US Garrett Lee ROBINSON - Austin TX, US Brigitte BRIESCHKE - Austin TX, US Jason KIM - Austin TX, US
Assignee:
MOLECULAR TEMPLATES, INC. - Austin TX
International Classification:
C07K 14/25 A61K 47/68
Abstract:
The present invention provides cell-targeting molecules which can deliver a CD8+ T-cell epitope cargo to the MHC class I presentation pathway of a target cell. The cell-targeting molecules of the invention can be used to deliver virtually any CD8+ T-cell epitope from an extracellular space to the MHC class I pathway of a target cell, which may be a malignant cell and/or non-immune cell. The target cell can then display on a cell-surface the delivered CD8+ T-cell epitope complexed with MHC I molecule. The cell-targeting molecules of the invention have uses which include the targeted labeling and/or killing of specific cell-types within a mixture of cell-types, including within a chordate, as well as the stimulation of beneficial immune responses. The cell-targeting molecules of the invention have uses, e.g., in the treatment of a variety of diseases, disorders, and conditions, including cancers, tumors, growth abnormalities, immune disorders, and microbial infections.
De-Immunized, Shiga Toxin A Subunit Scaffolds And Cell-Targeting Molecules Comprising The Same
- Austin TX, US Erin WILLERT - Round Rock TX, US Garrett Lee ROBINSON - Austin TX, US Sangeetha RAJAGOPALAN - Round Rock TX, US Brigitte BRIESCHKE - Austin TX, US
Assignee:
Molecular Templates, Inc. - Austin TX
International Classification:
C07K 14/25 C07K 19/00
Abstract:
The present invention relates to Shiga toxin A Subunit derived polypeptides and cell-targeting molecules comprising amino acid substitutions which equip the polypeptides with 1) de-immunization; 2) reduced, protease-cleavage sensitivity; and/or 3) a heterologous epitope cargo(s) while retaining Shiga toxin function(s), such as, e.g., potent cytotoxicity. Certain polypeptides of the invention exhibit reduced immunogenic potential in mammals and/or are capable of delivering an epitope to an MHC class molecule of a cell in which the polypeptide is present. Certain molecules comprising a polypeptide of the invention are well-tolerated by mammals while retaining one or more of the features mentioned above. The Shiga toxin polypeptides of the invention have uses as components of cell-targeting molecules for selectively killing specific cells; for selectively delivering cargos to specific cells, and as therapeutic and/or diagnostic molecules for treating and diagnosing a variety of conditions, including cancers, immune disorders, and microbial infections.
De-Immunized Shiga Toxin A Subunit Effector Polypeptides For Applications In Mammals
- Georgetown TX, US Erin Willert - Round Rock TX, US Garrett Lee Robinson - Austin TX, US Sangeetha Rajagopalan - Round Rock TX, US Brigitte Brieschke - Austin TX, US
The present invention relates to Shiga toxin effector polypeptides with reduced antigenic and/or immunogenic potential. Immunogenicity can be a limitation for the repeated administration to mammals of proteins and polypeptides derived from Shiga toxins. The Shiga toxin effector polypeptides of the present invention have uses as components of therapeutics, diagnostics, and immunization materials. The cytotoxic proteins of the present invention have uses for selective killing of specific cell types and as therapeutics for the treatment of a variety of diseases, including cancers, immune disorders, and microbial infections. The proteins of the present invention also have uses for detecting specific cell types, collecting diagnostic information, and monitoring the treatment of a variety of diseases, such as, e.g., cancers, immune disorders, and microbial infections.
The worst mistake you can make is being too afraid to make one. Look for a limit, and you will find one. Creating a life worth living.
Bragging Rights:
Be humble.
Garrett Robinson
Education:
Hillsdale College - History
Tagline:
Interests include wine, ties, and books.
Garrett Robinson
Education:
State University of New York at Fredonia
Garrett Robinson
Education:
Midland
Garrett Robinson
Work:
J.O.B=Just Over Broke
Garrett Robinson
Tagline:
I'm all of my MCs. I'm also the Doctor. And Peter Pan. And Bert. And if you catch me on a weekend night, I'm a ninja.
Bragging Rights:
I've been to Gallifrey, Neverland, outside Time, survived several apocalypses, as well as saved the world from Frigids, Aeolus, Dissonant, Van Dal, and a future version of myself.
Garrett Robinson
Garrett Robinson
About:
I work on computers, hike, take photos, mountain bike, and stuff.