Improving TCR Gene Therapy for Treatment of Haematological Malignancies

Adoptive immunotherapy using TCR gene modified T cells may allow separation of beneficial Graft versus tumour responses from harmful GvHD. Improvements to this include methods to generate high avidity or high affinity TCR, improvements in vector design and reduction in mispairing. Following adoptive...

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Main Authors: Emma Nicholson, Sara Ghorashian, Hans Stauss
Format: Article
Language:English
Published: Wiley 2012-01-01
Series:Advances in Hematology
Online Access:http://dx.doi.org/10.1155/2012/404081
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author Emma Nicholson
Sara Ghorashian
Hans Stauss
author_facet Emma Nicholson
Sara Ghorashian
Hans Stauss
author_sort Emma Nicholson
collection DOAJ
description Adoptive immunotherapy using TCR gene modified T cells may allow separation of beneficial Graft versus tumour responses from harmful GvHD. Improvements to this include methods to generate high avidity or high affinity TCR, improvements in vector design and reduction in mispairing. Following adoptive transfer, TCR transduced T cells must be able to survive and persist in vivo to give most effective antitumour responses. Central memory or naive T cells have both been shown to be more effective than effector cells at expanding and persisting in vivo. Lymphodepletion may enhance persistence of transferred T cell populations. TCR gene transfer can be used to redirect CD4 helper T cells, and these could be used in combination with CD8+ tumour specific T cells to provide help for the antitumour response. Antigen specific T regulatory T cells can also be generated by TCR gene transfer and could be used to suppress unwanted alloresponses.
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institution Kabale University
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series Advances in Hematology
spelling doaj-art-ea8270d6a2c8448eb1dbafdbbefc859e2025-02-03T01:04:26ZengWileyAdvances in Hematology1687-91041687-91122012-01-01201210.1155/2012/404081404081Improving TCR Gene Therapy for Treatment of Haematological MalignanciesEmma Nicholson0Sara Ghorashian1Hans Stauss2Department of Immunology, Royal Free Hospital, University College London, Hampstead Campus, Rowland Hill Street, London NW3 2QG3, UKDepartment of Immunology, Royal Free Hospital, University College London, Hampstead Campus, Rowland Hill Street, London NW3 2QG3, UKDepartment of Immunology, Royal Free Hospital, University College London, Hampstead Campus, Rowland Hill Street, London NW3 2QG3, UKAdoptive immunotherapy using TCR gene modified T cells may allow separation of beneficial Graft versus tumour responses from harmful GvHD. Improvements to this include methods to generate high avidity or high affinity TCR, improvements in vector design and reduction in mispairing. Following adoptive transfer, TCR transduced T cells must be able to survive and persist in vivo to give most effective antitumour responses. Central memory or naive T cells have both been shown to be more effective than effector cells at expanding and persisting in vivo. Lymphodepletion may enhance persistence of transferred T cell populations. TCR gene transfer can be used to redirect CD4 helper T cells, and these could be used in combination with CD8+ tumour specific T cells to provide help for the antitumour response. Antigen specific T regulatory T cells can also be generated by TCR gene transfer and could be used to suppress unwanted alloresponses.http://dx.doi.org/10.1155/2012/404081
spellingShingle Emma Nicholson
Sara Ghorashian
Hans Stauss
Improving TCR Gene Therapy for Treatment of Haematological Malignancies
Advances in Hematology
title Improving TCR Gene Therapy for Treatment of Haematological Malignancies
title_full Improving TCR Gene Therapy for Treatment of Haematological Malignancies
title_fullStr Improving TCR Gene Therapy for Treatment of Haematological Malignancies
title_full_unstemmed Improving TCR Gene Therapy for Treatment of Haematological Malignancies
title_short Improving TCR Gene Therapy for Treatment of Haematological Malignancies
title_sort improving tcr gene therapy for treatment of haematological malignancies
url http://dx.doi.org/10.1155/2012/404081
work_keys_str_mv AT emmanicholson improvingtcrgenetherapyfortreatmentofhaematologicalmalignancies
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AT hansstauss improvingtcrgenetherapyfortreatmentofhaematologicalmalignancies