摘要:
The disclosure provides methods for immunizing a subject in need thereof with a prophylactic vaccine against an infectious disease, the method comprising enhancing the subject's immune responsiveness to the vaccine by administering to the subject an agent that transiently inhibits IL-10 production by follicular helper T ("Tfh") cells.
摘要:
Provided are methods of treatment, such as methods involving administering and/or determining dosing of, cell therapy, such as of cells engineered with a recombinant receptor, such as a T cell receptor (TCR) or chimeric antigen receptor (CAR). In some embodiments, the methods include determining a therapeutic range and/or window for dosing, for example, based on the estimated probabilities of risk of developing a toxicity and estimated probabilities of a treatment outcome or response, such as treatment, reduction nor amelioration of a sign or symptom thereof, or degree or durability thereof, following administration of the cell therapy or engineered cells. In some aspects, the methods involve administering an agent capable of modulating the engineered cells. Also provided are methods of ameliorating and/or treating a toxicity.
摘要:
Disclosed is a molecule comprising: (a) a first domain, which comprises a targeting moiety; (b) a second domain, which comprises an albumin binding domain (ABD), (c) a third domain, which comprises a furin cleavage sequence ("FCS"), which FCS is cleavable by furin; and (d) a fourth domain, which comprises an optionally substituted Domain III from Pseudomonas exotoxin A ("PE"). Related nucleic acids, recombinant expression vectors, host cells, populations of cells, pharmaceutical compositions, methods of producing the molecule, methods of treating or preventing cancer in a mammal, and methods of inhibiting the growth of a target cell are also disclosed.
摘要:
The invention relates to methods of using inhibitors of CSF-1 R for reducing microglial activation in the eye as well as treating an inflammation associated with an eye disease, such as age-related macular degeneration (AMD), retinitis pigmentosa and diabetic retinopathy. The methods can further comprise the administration of anti-VEGF antibody. In preferred embodiments, the CSF-1 R inhibitor is Pexidartinib (PLX3397).
摘要:
Provided herein are methods and compositions related to the treatment or prevention of cancer (e.g., by targeting a tumor in a subject with cancer) by administering to a subject an agent disclosed herein. In certain aspects, the disclosure relates to targeting tumors in a subject, and/or decreasing the number of tumor infiltrating T regulatory cells (TITRs) (e.g., TITRs present within a tumor) in a subject by administering to the subject an agent disclosed herein. Further provided herein are methods of identifying anti-cancer agents that decrease the number or activity of TITRs in a subject or in a tumor present in a subject. In some aspects, provided herein are methods for identifying TITRs in a subject (e.g., identifying TITRs in a tumor present in a subject).
摘要:
Methods are provided for the treatment of IL-6R related diseases involving a combination therapy. More specifically, specific dose regimens and pre-filled syringes are provided for subcutaneous administration, to subjects suffering an IL-6R related disease, of immunoglobulin single variable domains that bind IL-6R, in combination with at least one additional therapeutic agent, such as methotrexate.
摘要:
There is provided inter alia a polypeptide comprising an immunoglobulin chain variable domain which binds to IL-6R, wherein the immunoglobulin chain variable domain comprises three complementarity determining regions (CDR1-CDR3) and four framework regions (FR1-FR4), wherein CDR1-CDR3 and FR1-FR4 are as defined in the specification.
摘要:
Disclosed in this invention are human IgG Fc variants sequences that demonstrate low and no binding activities to Fc gamma receptor. The disclosed Fc variants are useful for making Fc fusion proteins and/or IgGs where low or no Fc effector function of the mentioned molecules are desirable.