Reprogrammed CD4+ T Cells That Express FoxP3+ Control Inhibitory Antibody Formation in Hemophilia A Mice
Author:
Publisher
Frontiers Media SA
Subject
Immunology,Immunology and Allergy
Reference88 articles.
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2. Gene therapy comes of age;Dunbar;Science,2018
3. Hemophilia B gene therapy with a high-specific-activity factor IX variant;George;N Engl J Med.,2017
4. AAV5-factor VIII gene transfer in severe hemophilia A;Rangarajan;N Engl J Med,2017
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2. Altered frequency of FOXP3+ regulatory T cells is associated with development of inhibitors in patients with severe hemophilia A;International Journal of Laboratory Hematology;2023-07-24
3. Immunogenicity of Recombinant Adeno-Associated Virus (AAV) Vectors for Gene Transfer;BioDrugs;2023-03-02
4. Suppression of anti-drug antibody formation against coagulation factor VIII by oral delivery of anti-CD3 monoclonal antibody in hemophilia A mice;Cellular Immunology;2023-03
5. Immune tolerance against infused FVIII in hemophilia A is mediated by PD-L1+ Tregs;Journal of Clinical Investigation;2022-11-15
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