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Recent ancestry of Kyasanur Forest disease virus

Emerging infectious diseases, 2009-09, Vol.15 (9), p.1431-1437

2009

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Diagnosis of Kyasanur forest disease by nested RT-PCR, real-time RT-PCR and IgM capture ELISA

Journal of virological methods, 2012-12, Vol.186 (1-2), p.49-54

2012

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B cell focused transient immune suppression protocol for efficient AAV readministration to the liver

Molecular therapy. Methods & clinical development, 2024-03, Vol.32 (1), p.101216-101216, Article 101216

2024

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Engineering and In Vitro Selection of a Novel AAV3B Variant with High Hepatocyte Tropism and Reduced Seroreactivity

Molecular therapy. Methods & clinical development, 2020-12, Vol.19, p.347-361

2020

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Coagulation factor IX gene transfer to non-human primates using engineered AAV3 capsid and hepatic optimized expression cassette

Molecular therapy. Methods & clinical development, 2021-12, Vol.23, p.98-107

2021

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Immune Modulatory Cell Therapy for Hemophilia B Based on CD20-Targeted Lentiviral Gene Transfer to Primary B Cells

Molecular therapy. Methods & clinical development, 2017-06, Vol.5 (C), p.76-82

2017

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Immune Responses to Muscle-Directed Adeno-Associated Viral Gene Transfer in Clinical Studies

Human gene therapy, 2023-05, Vol.34 (9-10), p.365-371

2023

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Cas9-specific immune responses compromise local and systemic AAV CRISPR therapy in multiple dystrophic canine models

Nature communications, 2021-11, Vol.12 (1), p.6769-12, Article 6769

2021

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CAR- and TRuC-redirected regulatory T cells differ in capacity to control adaptive immunity to FVIII

Molecular therapy, 2021-09, Vol.29 (9), p.2660-2676

2021

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Key Role of Kupffer Cells in IL-1 Dependent Activation of CD8+ T Cell Responses to AAV Transgene Product in Liver

Blood, 2022-11, Vol.140 (Supplement 1), p.4928-4929

2022

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Effect of CpG Depletion of Vector Genome on CD8 + T Cell Responses in AAV Gene Therapy

Frontiers in immunology, 2021-05, Vol.12, p.672449-672449

2021

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Innate Immune Sensing of Adeno-Associated Virus Vectors

Human gene therapy, 2024-07, Vol.35 (13-14), p.451-463

2024

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IL-15 blockade and rapamycin rescue multifactorial loss of factor VIII from AAV-transduced hepatocytes in hemophilia A mice

Molecular therapy, 2022-12, Vol.30 (12), p.3552-3569

2022

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The Balance between CD8+ T Cell-Mediated Clearance of AAV-Encoded Antigen in the Liver and Tolerance Is Dependent on the Vector Dose

Molecular therapy, 2017-04, Vol.25 (4), p.880-891

2017

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TLR9-independent CD8+ T cell responses in hepatic AAV gene transfer through IL-1R1-MyD88 signaling

Molecular therapy, 2024-02, Vol.32 (2), p.325-339

2024

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Synergy between rapamycin and FLT3 ligand enhances plasmacytoid dendritic cell–dependent induction of CD4+CD25+FoxP3+ Treg

Blood, 2015-05, Vol.125 (19), p.2937-2947

2015

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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, Vol.385, p.104675-104675, Article 104675

2023

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Oral Anti-CD3 and Bioencapsulated FVIII Therapy Exhibit Distinct Mechanisms That Suppress Inhibitor Formation in Hemophilia a

Blood, 2022-11, Vol.140 (Supplement 1), p.11273-11274

2022

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B Cell Depletion Eliminates FVIII Memory B Cells and Enhances AAV8-coF8 Immune Tolerance Induction When Combined With Rapamycin

Frontiers in immunology, 2020-06, Vol.11, p.1293-1293

2020

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Gene Therapy With Regulatory T Cells: A Beneficial Alliance

Frontiers in immunology, 2018-03, Vol.9, p.554-554

2018

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PB1-F2 Protein Does Not Impact the Virulence of Triple-Reassortant H3N2 Swine Influenza Virus in Pigs but Alters Pathogenicity and Transmission in Turkeys

Journal of virology, 2016-01, Vol.90 (1), p.222-231

2016

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Role of Small Intestine and Gut Microbiome in Plant-Based Oral Tolerance for Hemophilia

Frontiers in immunology, 2020-05, Vol.11, p.844

2020

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Distinct functions and transcriptional signatures in orally induced regulatory T cell populations

Frontiers in immunology, 2023-10, Vol.14, p.1278184-1278184

2023

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Incorporation of Host Complement Regulatory Proteins into Newcastle Disease Virus Enhances Complement Evasion

Journal of Virology, 2012-12, Vol.86 (23), p.12708-12716

2012

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TLR9-Activating CpG-B ODN but Not TLR7 Agonists Triggers Antibody Formation to Factor IX in Muscle Gene Transfer

Human gene therapy. Part B. Methods, 2019-06, Vol.30 (3), p.81-92

2019

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Recent ancestry of Kyasanur Forest disease virus

Diagnosis of Kyasanur forest disease by nested RT-PCR, real-time RT-PCR and IgM capture ELISA

B cell focused transient immune suppression protocol for efficient AAV readministration to the liver

Engineering and In Vitro Selection of a Novel AAV3B Variant with High Hepatocyte Tropism and Reduced Seroreactivity

Coagulation factor IX gene transfer to non-human primates using engineered AAV3 capsid and hepatic optimized expression cassette

Immune Modulatory Cell Therapy for Hemophilia B Based on CD20-Targeted Lentiviral Gene Transfer to Primary B Cells

Immune Responses to Muscle-Directed Adeno-Associated Viral Gene Transfer in Clinical Studies

Cas9-specific immune responses compromise local and systemic AAV CRISPR therapy in multiple dystrophic canine models

CAR- and TRuC-redirected regulatory T cells differ in capacity to control adaptive immunity to FVIII

Key Role of Kupffer Cells in IL-1 Dependent Activation of CD8+ T Cell Responses to AAV Transgene Product in Liver

Effect of CpG Depletion of Vector Genome on CD8 + T Cell Responses in AAV Gene Therapy

Innate Immune Sensing of Adeno-Associated Virus Vectors

IL-15 blockade and rapamycin rescue multifactorial loss of factor VIII from AAV-transduced hepatocytes in hemophilia A mice

The Balance between CD8+ T Cell-Mediated Clearance of AAV-Encoded Antigen in the Liver and Tolerance Is Dependent on the Vector Dose

TLR9-independent CD8+ T cell responses in hepatic AAV gene transfer through IL-1R1-MyD88 signaling

Synergy between rapamycin and FLT3 ligand enhances plasmacytoid dendritic cell–dependent induction of CD4+CD25+FoxP3+ Treg

Suppression of anti-drug antibody formation against coagulation factor VIII by oral delivery of anti-CD3 monoclonal antibody in hemophilia A mice

Oral Anti-CD3 and Bioencapsulated FVIII Therapy Exhibit Distinct Mechanisms That Suppress Inhibitor Formation in Hemophilia a

B Cell Depletion Eliminates FVIII Memory B Cells and Enhances AAV8-coF8 Immune Tolerance Induction When Combined With Rapamycin

Gene Therapy With Regulatory T Cells: A Beneficial Alliance

PB1-F2 Protein Does Not Impact the Virulence of Triple-Reassortant H3N2 Swine Influenza Virus in Pigs but Alters Pathogenicity and Transmission in Turkeys

Role of Small Intestine and Gut Microbiome in Plant-Based Oral Tolerance for Hemophilia

Distinct functions and transcriptional signatures in orally induced regulatory T cell populations

Incorporation of Host Complement Regulatory Proteins into Newcastle Disease Virus Enhances Complement Evasion

TLR9-Activating CpG-B ODN but Not TLR7 Agonists Triggers Antibody Formation to Factor IX in Muscle Gene Transfer

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