Skip to main content

Research Repository

Advanced Search

Optimising Adoptive T Cell Therapy Following Allogeneic Hematopoietic Stem Cell Transplantation

Ghorashian, Sara; Wright, Graham; Thomas, Sharyn; Hart, Daniel P.; King, Judy; Voisine, Cecile; Pospori, Constandina; Perro, Mario; Cesco-Gaspere, Michela; Holler, Angelika; Gao, Liquan; Xue, Shao-An; Morris, Emma C.; Chakraverty, Ronjon; Stuass, Hans J.

Authors

Sara Ghorashian

Sharyn Thomas

Daniel P. Hart

Judy King

Cecile Voisine

Constandina Pospori

Mario Perro

Michela Cesco-Gaspere

Angelika Holler

Liquan Gao

Shao-An Xue

Emma C. Morris

Ronjon Chakraverty

Hans J. Stuass



Contributors

Yair Reisner
Editor

Massimo F. Martelli
Editor

Abstract

Allogeneic hematopoietic stem cell transplantation (HSCT) is carried out to correct genetic disorders of the hematopoietic system, as well as to treat hematopoietic malignancies. Adoptive Tcell therapy has great potential as an adjunct to this treatment modality, and clinical trials have already demonstrated the feasibility and efficacy of this approach. It offers two therapeutic effects in this setting:
(1) Augmentation of anti-tumor responses, such as in the setting of relapsed disease; (2) Prevention and treatment of transplant-related infections.
Underlying the therapeutic efficacy of adoptive T cell therapy is the demonstration of a graft-vs-leukemia/lymphoma (GvL) effect

Acceptance Date May 5, 2009
Online Publication Date May 1, 2015
Publication Date Jan 1, 2010
Deposit Date May 4, 2020
Pages 373-395
Book Title Bone Marrow Transplantation Across Major Genetic Barriers
DOI https://doi.org/10.1142/9789814271271_0016
Public URL http://researchrepository.napier.ac.uk/Output/2658343
Publisher URL https://www.worldscientific.com/doi/abs/10.1142/9789814271271_0016