摘要:
Interleukin-10 muteins and other interleukin-10 - related molecules are described, as well as methods of identifying interleukin-10 muteins and other interleukin-10 - related molecules. Also described herein are modifications of the foregoing, which modifications may enhance a property (e.g., half-life) of the muteins or other molecules compared to human interleukin-10. Particular interleukin-10 muteins and related molecules have comparable immunogenicity to human interleukin-10 and/or bioactivity at least comparable to human interleukin-10. Pharmaceutical compositions and methods of use are also described herein.
摘要:
The present disclosure provides methods and compositions relating to isolated CD8+ T cells expressing a disease antigen-specific T cell receptor, as well as nucleic acids encoding the Vα and Vβ polypeptide pairs of T cell receptors (TCRs) of such disease antigen-specific T cells. Such disease antigen-specific CD8+ T cells are obtainable from the periphery (e.g., blood) of a subject having a disease amenable to treatment with an IL-10 agent. The present disclosure also contemplates therapeutic methods and compositions relating to administration of isolated disease antigen-specific CD8+ T cells to a subject, as well as therapeutic methods and compositions relating to CD8+ T cells genetically modified to express a disease antigen-specific TCR and/or chimeric antigen receptor.
摘要:
Interleukin-15 muteins and other interleukin-15 - related molecules are described, as well as methods of identifying interleukin-15 muteins and other interleukin-15 - related molecules. Also described herein are modifications of the foregoing, which modifications may enhance a property (e.g., half-life) of the muteins or other molecules compared to human interleukin-15. Pharmaceutical compositions and methods of use are also described herein.
摘要:
The present disclosure provides polypeptide binding molecules that bind to Programmed Cell Death-1 (PD-1) and inhibit PD-1 interaction with both Programmed Cell Death Ligand-1 (PD-L1) and/or Programmed Cell Death Ligand-2 (PD-L2). The present disclosure further provides pharmaceutical formulations comprising the molecules of the present invention. The present disclosure further provides methods of use of such polypeptide binding molecules in the treatment of various disorders and diseases. The present disclosure further provides recombinant nucleic acid sequences encoding such polypeptide binding molecules and cells transformed therewith. The present disclosure also provides methods of use of the molecules of the present invention in the diagnosis, prevention and treatment of various disorders or conditions in subjects including but not limited to the treatment of neoplastic disorders including but not limited to cancer.