CD38-binding proteins comprising de-immunized Shiga toxin A subunit effectors
AssigneesMolecular Templates, Inc., Millennium Pharmaceuticals, Inc.
InventorsNibedita Chattopadhyay, Eric Poma, Erin Willert
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AssigneesMolecular Templates, Inc., Millennium Pharmaceuticals, Inc.
InventorsNibedita Chattopadhyay, Eric Poma, Erin Willert
Estimating the term…
The instant invention provides binding proteins (“CD38-binding proteins”) which each comprise (1) a CD38-binding region for cell-targeting and (2) a Shiga toxin A Subunit effector polypeptide (“Shiga toxin effector polypeptide”). The Shiga toxin effector polypeptide components of the CD38-binding proteins may comprise a combination of mutations relative to a wild-type Shiga toxin sequence providing (1) de-immunization and/or (2) a reduction in protease sensitivity; wherein each Shiga toxin effector polypeptide retains one or more Shiga toxin function, such as, e.g., stimulating cellular internalization, directing intracellular routing, catalytic activity, and/or potent cytotoxicity. The CD38-binding proteins may have one or multiple uses, e.g., the selective killing of a specific CD38-expressing cell-type; and more generally, for the diagnosis and treatment of cancers and disorders involving CD38-expressing cells, e.g., in CD38-positive hematopoietic cancers such as multiple myeloma.
A method of treating or slowing the progression of multiple myeloma in a subject in need thereof, the method comprising administering to the subject an effective amount of a pharmaceutical composition comprising a CD38-binding fusion protein, wherein the CD38-binding fusion protein comprises:
A method of treating or slowing the progression of multiple myeloma in a subject in need thereof, the method comprising administering to the subject an effective amount of a pharmaceutical composition comprising a CD38-binding fusion protein, wherein the CD38-binding fusion protein comprises a polypeptide having the sequence of SEQ ID NO:
Dependencies are inferred from the claim text.