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Bio
Group Leader: Dr Ronjon Chakraverty
Introduction
The Transplantation Immunology Group is based at the Hampstead Campus and forms part of a large Immunotherapy Programme at UCL. Our research involves both pre-clinical, translational and phase I/II projects that aim to develop innovative strategies to improve the anti-tumour effects of blood and bone marrow transplantation. We work closely with the groups of Professor Hans Stauss/Dr. Emma Morris (Tumour Immunology, Cellular and Gene Therapy), and Dr. Clare Bennett (Dendritic Cell Immunotherapy), with a number of fellows or PhD students working on joint projects.
Research
Following blood or bone marrow transplantation, donor T cells that have been infused as part of the graft or given at a later time point, become activated in response to antigenic differences between the donor and the recipient. This effect can be co-opted to generate anti-tumour activity, an effect termed the ‘graft-versus-tumour’ (GVT) response. Alternatively, donor T cells may react against normal tissues, leading to graft-versus-host disease (GVHD). See figure below:
Graft-versus-host-disease
These outcomes depend upon how donor T cells recognize antigen and this, in turn is influenced by nature of the cells presenting antigen. We are interested in how distinct non-haematopoietic and haematopoietic cell populations in the recipient influence the development of donor T cell immunity after transplantation. This research offers the opportunity to develop new approaches to manipulating antigen presentation for therapeutic benefit e.g. following vaccination.
Ultimately, durable anti-tumour immunity requires that T cells with anti-tumour reactivity engraft and then persist long-term in the recipient. By exploring clinically relevant models, we are examining the mechanisms that influence the long-term survival of anti-tumour T cells such that they can provide long-term immune surveillance. An improved understanding of the pathways that regulate this property of ‘memory’ is helping us to engineer T cells that can maintain their functions over long periods.
Introduction
The Transplantation Immunology Group is based at the Hampstead Campus and forms part of a large Immunotherapy Programme at UCL. Our research involves both pre-clinical, translational and phase I/II projects that aim to develop innovative strategies to improve the anti-tumour effects of blood and bone marrow transplantation. We work closely with the groups of Professor Hans Stauss/Dr. Emma Morris (Tumour Immunology, Cellular and Gene Therapy), and Dr. Clare Bennett (Dendritic Cell Immunotherapy), with a number of fellows or PhD students working on joint projects.
Research
Following blood or bone marrow transplantation, donor T cells that have been infused as part of the graft or given at a later time point, become activated in response to antigenic differences between the donor and the recipient. This effect can be co-opted to generate anti-tumour activity, an effect termed the ‘graft-versus-tumour’ (GVT) response. Alternatively, donor T cells may react against normal tissues, leading to graft-versus-host disease (GVHD). See figure below:
Graft-versus-host-disease
These outcomes depend upon how donor T cells recognize antigen and this, in turn is influenced by nature of the cells presenting antigen. We are interested in how distinct non-haematopoietic and haematopoietic cell populations in the recipient influence the development of donor T cell immunity after transplantation. This research offers the opportunity to develop new approaches to manipulating antigen presentation for therapeutic benefit e.g. following vaccination.
Ultimately, durable anti-tumour immunity requires that T cells with anti-tumour reactivity engraft and then persist long-term in the recipient. By exploring clinically relevant models, we are examining the mechanisms that influence the long-term survival of anti-tumour T cells such that they can provide long-term immune surveillance. An improved understanding of the pathways that regulate this property of ‘memory’ is helping us to engineer T cells that can maintain their functions over long periods.
Research Interests
Papers共 218 篇Author StatisticsCo-AuthorSimilar Experts
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Ronjon Chakraverty,Emma Kempshall,Fiona Dignan,Adrian Bloor,Matthew Collin,Kavita Raj, Jeff Davies,Victoria Potter,Ram Malladi, Siobhan Smith,Simon Gates,Charlotte Gaskell,Rebecca Bishop,Andrea Hodgkinson, Gabrielle Smith
BMJ OPENno. 1 (2025)
Francesca Emily Sillito,Angelika Holler, Aideen T O'Neill, Lauren A Callender, Sian M Henson,Hans Stauss,Ronjon Chakraverty
Bloodno. Supplement 1 (2024): 7196-7196
BONE MARROW TRANSPLANTATION (2024): 253-253
Cited0Views0Bibtex
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0
Hermione E. Allen, Andrew Mcintyre,Jesus Gutierrez-Abril,Amy A. Kirkwood,Daniel Leongamornlert,Rodothea Amerikanou,Emily A. Cutler,Aditi Dey,Richard Burt,Ronjon Chakraverty,Adele Kay Fielding
BLOOD (2024): 1454-1455
Daniel North,Ronjon Chakraverty
Foram Khatsuria,Christel McMullan,Olalekan Lee Aiyegbusi,Karen L Shaw, Roshina Iqbal,Francesca Kinsella,Keith Wilson, Lester Pyatt, Marlene Lewis, Sophie M R Wheldon,David Burns,Ronjon Chakraverty,Melanie Calvert,Sarah E Hughes
The Lancet Oncologyno. 10 (2024): e476-e488
Andrew McIntyre,Maria Cuadrado, Joshua Hughes, Aideen O'Neill, William Wilson,Darren Edwards, Ka Man Mak, Jessica Hunt,Laura Clifton-Hadley,Adrian Bloor,Andrew Clark,Anne Parker,Maria Gilleece,Richard Lovell,Alexander M. Martin,Ann Hunter,Deborah Richardson,John Snowden,Stephen Robinson,Ben Uttenthal,Charles Crawley,Mark Lowdell,Karl Peggs,Persephone Borrow,Ronjon Chakraverty
BONE MARROW TRANSPLANTATION (2024): 53-54
Cited0Views0Bibtex
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0
Foram Khatsuria,Melanie Calvert,Christel McMullan,Karen Shaw,Olalekan Lee Aiyegbusi, Roshina Iqbal,Francesca Kinsella,Keith Wilson,David Burns, Lester Pyatt, Marlene Lewis, Sophie Wheldon,Ronjon Chakraverty,Sarah Hughes
QUALITY OF LIFE RESEARCH (2024): S162-S163
Cited0Views0Bibtex
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0
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Author Statistics
#Papers: 218
#Citation: 8337
H-Index: 42
G-Index: 90
Sociability: 7
Diversity: 3
Activity: 47
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