摘要:
The present invention is directed to novel targeted heterodimeric fusion proteins comprising an IL-15/IL-15Rα Fc-fusion protein and a LAG-3 antibody fragment-Fc fusion protein.
摘要:
The present invention relates to methods and compositions for modulating T cells. The modulation includes suppressing or inducing regulatory T cells or cytotoxic T cells.
摘要:
The present disclosure relates to antibodies and polynucleotides encoding the same, that may be used to prevent, control, or reduce the activity of the complement pathway. In addition, the disclosure is directed to compositions and methods for diagnosing and treating diseases mediated by or involving complement C5. Specifically, the disclosure is related to C5 antibodies.
摘要:
Novel Heterodimeric IgG-Like Bispecific Antibodies (HILBAs) are provided herein. Such bispecific antibodies are similar to IgG in structure and, thus, do not exhibit a limited half-life like previous antibody fragment-based bispecifics. Moreover, such heterodimeric IgG-like bispecific antibodies advantageously do not entail complicated generation methods such as Fab arm exchange and common light chain methods. Unlike canonical IgG antibodies, the HILBAs described herein include at least one monomer that is from N- to C-terminus: a VH-scFv linker- VL-CL-domain linker-CH 1 -hinge - CH2-CH3.
摘要:
The present invention is directed to novel targeted heterodimeric fusion proteins comprising an IL-15/IL-15Rα Fc-fusion protein and a TIM-3 antibody fragment-Fc fusion protein.
摘要:
The present invention relates to rapid clearance molecules that bind target antigens and FcyRIIb with increased affinity as compared to parent molecules, said compositions being capable of causing accelerated clearance of such antigens. Such compositions are useful for treating a variety of disorders, including allergic diseases, atherosclerosis, and a variety of other conditions.
摘要:
The invention relates generally to compositions and methods for altering the isoelectric point of an antibody, and in some cases, resulting in improved plasma pharmacokinetics, e.g. increased serum half-life in vivo.