In vivo expansion of regulatory T cells with IL-2/IL-2 mAb complexes prevents anti-factor VIII immune responses in hemophilia A mice treated with factor VIII plasmid-mediated gene therapy.
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Animal models of hemophiliaLong-term tolerance to factor VIII is achieved by administration of interleukin-2/interleukin-2 monoclonal antibody complexes and low dosages of factor VIII.Treating human autoimmunity: current practice and future prospectsInhibitors - cellular aspects and novel approaches for tolerance.Development of Gene Transfer for Induction of Antigen-specific Tolerance.Fine epitope specificity of antibodies against interleukin-2 explains their paradoxical immunomodulatory effectspiggyBac-mediated phenotypic correction of factor VIII deficiencyGene therapy for haemophilia: prospects and challenges to prevent or reverse inhibitor formation.IL-2/α-IL-2 Complex Treatment Cannot Be Substituted for the Adoptive Transfer of Regulatory T cells to Promote Bone Marrow Engraftment.The immune system in Duchenne muscular dystrophy: Friend or foe.Strategies to target long-lived plasma cells for treating hemophilia A inhibitors.Anti-CD20 as the B-Cell Targeting Agent in a Combined Therapy to Modulate Anti-Factor VIII Immune Responses in Hemophilia a Inhibitor MiceProgress toward inducing immunologic tolerance to factor VIII.Inhibitors - genetic and environmental factors.Strategies for reducing inhibitor formation in severe haemophilia.In vivo induction of regulatory T cells for immune tolerance in hemophilia.Advances in Overcoming Immune Responses following Hemophilia Gene Therapy.Tilt balance towards regulation: evolving new strategy for treatment of hemophilia inhibitors.Increased CD8+ T-cell function following castration and immunization is countered by parallel expansion of regulatory T cells.Immune tolerance induced by platelet-targeted factor VIII gene therapy in hemophilia A mice is CD4 T cell mediated.Innovative Approaches for Immune Tolerance to Factor VIII in the Treatment of Hemophilia A.Platelet Gene Therapy Promotes Targeted Peripheral Tolerance by Clonal Deletion and Induction of Antigen-Specific Regulatory T Cells
P2860
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P2860
In vivo expansion of regulatory T cells with IL-2/IL-2 mAb complexes prevents anti-factor VIII immune responses in hemophilia A mice treated with factor VIII plasmid-mediated gene therapy.
description
2011 nî lūn-bûn
@nan
2011 թուականի Ապրիլին հրատարակուած գիտական յօդուած
@hyw
2011 թվականի ապրիլին հրատարակված գիտական հոդված
@hy
2011年の論文
@ja
2011年論文
@yue
2011年論文
@zh-hant
2011年論文
@zh-hk
2011年論文
@zh-mo
2011年論文
@zh-tw
2011年论文
@wuu
name
In vivo expansion of regulator ...... plasmid-mediated gene therapy.
@ast
In vivo expansion of regulator ...... plasmid-mediated gene therapy.
@en
type
label
In vivo expansion of regulator ...... plasmid-mediated gene therapy.
@ast
In vivo expansion of regulator ...... plasmid-mediated gene therapy.
@en
prefLabel
In vivo expansion of regulator ...... plasmid-mediated gene therapy.
@ast
In vivo expansion of regulator ...... plasmid-mediated gene therapy.
@en
P2093
P2860
P921
P356
P1433
P1476
In vivo expansion of regulator ...... plasmid-mediated gene therapy.
@en
P2093
Benjamin C Yen
Carol H Miao
Chao-Lien Liu
Peiqing Ye
P2860
P304
P356
10.1038/MT.2011.61
P577
2011-04-05T00:00:00Z