Patent classifications
A61K40/17
ENGINEERED CHIMERIC FUSION PROTEIN COMPOSITIONS AND METHODS OF USE THEREOF
Compositions and methods for making and using engineered cells, such as, engineered myeloid cells that express a chimeric fusion protein that has a binding domain capable to binding surface molecules on target cells such as diseased cells.
METHODS FOR TREATING NEOPLASTIC DISEASES
A method of treating a cancer, the method comprising: providing a modified macrophage or monocyte that contains an exogenous nucleic acid sequence encoding a Hom- 1 polypeptide or a fragment thereof that contains the Hom-1 homeobox domain, wherein the modified macrophage or monocyte expresses the Hom-1 polypeptide or the fragment thereof; and administering the modified macrophage or monocyte to a subject with a cancer.
METHODS FOR TREATING NEOPLASTIC DISEASES
A method of treating a cancer, the method comprising: providing a modified macrophage or monocyte that contains an exogenous nucleic acid sequence encoding a Hom- 1 polypeptide or a fragment thereof that contains the Hom-1 homeobox domain, wherein the modified macrophage or monocyte expresses the Hom-1 polypeptide or the fragment thereof; and administering the modified macrophage or monocyte to a subject with a cancer.
EX-VIVO PROLIFERATION OF HUMAN PHAGOCYTIC CELLS
The invention provides human phagocytic cells which are not tumorigenic, yet still capable of cell division ex-vivo, such as in cell culture. A culture containing these cells can be expanded manyfold, that is the cell number in such a culture can be increased by a factor of 10 or more. The cells show characteristics of functional phagocytes in a differentiated state and are capable to alleviate pathological defects in in vivo models.
EX-VIVO PROLIFERATION OF HUMAN PHAGOCYTIC CELLS
The invention provides human phagocytic cells which are not tumorigenic, yet still capable of cell division ex-vivo, such as in cell culture. A culture containing these cells can be expanded manyfold, that is the cell number in such a culture can be increased by a factor of 10 or more. The cells show characteristics of functional phagocytes in a differentiated state and are capable to alleviate pathological defects in in vivo models.
Compositions and methods for selective phagocytosis of human cancer cells
The present invention relates to compositions and methods that provide novel therapies in cancer. The invention includes a phagocytic cell modified with a repressor of signal regulatory protein-alpha (SIRP) and bound to a targeting antibody to enhance phagocytic activity of the phagocytic cell toward tumor tissue. Methods of enhancing phagocytic activity and treating a tumor are also included.
Compositions and methods for selective phagocytosis of human cancer cells
The present invention relates to compositions and methods that provide novel therapies in cancer. The invention includes a phagocytic cell modified with a repressor of signal regulatory protein-alpha (SIRP) and bound to a targeting antibody to enhance phagocytic activity of the phagocytic cell toward tumor tissue. Methods of enhancing phagocytic activity and treating a tumor are also included.
Myeloid Cells Overexpressing BCL2
The present invention relates to isolated modified myeloid cell, a progenitor thereof, or a progeny thereof, encoding an antigen recognizing receptor, wherein said myeloid cell or progenitor thereof has been further modified to overexpress BCL2. The present invention further relates to therapeutic application in particular in the field of adoptive therapy of said modified myeloid cells.
Myeloid Cells Overexpressing BCL2
The present invention relates to isolated modified myeloid cell, a progenitor thereof, or a progeny thereof, encoding an antigen recognizing receptor, wherein said myeloid cell or progenitor thereof has been further modified to overexpress BCL2. The present invention further relates to therapeutic application in particular in the field of adoptive therapy of said modified myeloid cells.
UTILIZING THE INNATE IMMUNE SYSTEM TO DELIVER THERAPEUTIC AGENTS
In one aspect, the invention provides a composition comprising at least one monocyte comprising an agent that increases monocyte homing to a site of injury, and an effective amount of a drug. In another aspect, the invention provides a method of using the composition to deliver a drug to a site of injury.