Hong Zhan

UCL Great Ormond Street Institute Of Child Health
London, ENG WC1N1EH, United Kingdom

Last Updated: 09/26/2026

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Found 13 publications

A phase 1 feasibility trial of BE-CAR33, an "off-the-shelf" base-edited CAR33 T cell therapy for acute myeloid leukemia.

A phase 1 feasibility trial of BE-CAR33, an "off-the-shelf" base-edited CAR33 T cell therapy for acute myeloid leukemia.

Journal: Science translational medicine

Published: August 19, 2026

Umbilical cord blood T cells can be isolated and enriched by CD62L selection for use in 'off the shelf' chimeric antigen receptor T-cell therapies to widen transplant options.

Umbilical cord blood T cells can be isolated and enriched by CD62L selection for use in 'off the shelf' chimeric antigen receptor T-cell therapies to widen transplant options.

Journal: Haematologica

Published: January 20, 2024

Base-Edited CAR7 T Cells for Relapsed T-Cell Acute Lymphoblastic Leukemia.

Base-Edited CAR7 T Cells for Relapsed T-Cell Acute Lymphoblastic Leukemia.

Journal: The New England journal of medicine

Published: June 14, 2023

Phase 1 clinical trial of CRISPR-engineered CAR19 universal T cells for treatment of children with refractory B cell leukemia.

Phase 1 clinical trial of CRISPR-engineered CAR19 universal T cells for treatment of children with refractory B cell leukemia.

Journal: Science translational medicine

Published: October 26, 2022

Deep sequencing reveals persistence of cell-associated mumps vaccine virus in chronic encephalitis.

Deep sequencing reveals persistence of cell-associated mumps vaccine virus in chronic encephalitis.

Journal: Acta neuropathologica

Published: August 11, 2016

Molecular remission of infant B-ALL after infusion of universal TALEN gene-edited CAR T cells.

Molecular remission of infant B-ALL after infusion of universal TALEN gene-edited CAR T cells.

Journal: Science translational medicine

Published: July 08, 2016

Automated manufacturing of chimeric antigen receptor T cells for adoptive immunotherapy using CliniMACS prodigy.

Automated manufacturing of chimeric antigen receptor T cells for adoptive immunotherapy using CliniMACS prodigy.

Journal: Cytotherapy

Published: March 16, 2016

Immunotherapy of HCC metastases with autologous T cell receptor redirected T cells, targeting HBsAg in a liver transplant patient.

Immunotherapy of HCC metastases with autologous T cell receptor redirected T cells, targeting HBsAg in a liver transplant patient.

Journal: Journal of hepatology

Published: June 04, 2014

Production and first-in-man use of T cells engineered to express a HSVTK-CD34 sort-suicide gene.

Production and first-in-man use of T cells engineered to express a HSVTK-CD34 sort-suicide gene.

Journal: PloS one

Published: May 13, 2013

Interferon-γ capture T cell therapy for persistent Adenoviraemia following allogeneic haematopoietic stem cell transplantation.

Interferon-γ capture T cell therapy for persistent Adenoviraemia following allogeneic haematopoietic stem cell transplantation.

Journal: British journal of haematology

Published: February 26, 2013

22q11.2 deletion syndrome with life-threatening adenovirus infection.

22q11.2 deletion syndrome with life-threatening adenovirus infection.

Journal: The Journal of pediatrics

Published: January 06, 2013

Lentiviral gene therapy against human immunodeficiency virus type 1, using a novel human TRIM21-cyclophilin A restriction factor.

Lentiviral gene therapy against human immunodeficiency virus type 1, using a novel human TRIM21-cyclophilin A restriction factor.

Journal: Human gene therapy

Published: August 23, 2012

Showing 1-12 of 13

Last Updated: 09/26/2026