基本信息
views: 6
Career Trajectory
Bio
Research in the Stauss lab focusses on T cell immunology, with a particular focus on the role of the T cell receptor (TCR) in the recognition of cancer antigens.
Research summary
Cancer is a major health problem worldwide with WHO projections predicting an increase in incidence by 57% from 14 million cases in 2012 to 22 million cases by 2032. We are interested in exploring the role of the immune system in tumour development, and whether novel forms of immunotherapy can be used to treat cancer.
The research of our group is focussed on T cell immunology, with a particular focus the role of the T cell receptor (TCR) in the recognition of cancer antigens. We were amongst the first to show that cytotoxic T cells can selectively attack cancer cells by recognising point mutations in transforming proteins expressed in tumours (J Exp Med. 1993; 177:1493). We have since developed strategies to isolate monoclonal TCR that are specific for tumour antigens, and we use these TCR for gene therapy to redirected the specificity of patient T cells and equip them with the ability to selectively recognize and attack cancer cells.
The use of TCR gene therapy to produce antigen-specific cytotoxic and helper T cells is one area of active research in our group. We also use TCR and chimeric antigen receptor (CAR) gene transfer to produce antigen-specific regulatory T cells. This provides the opportunity to achieve highly selective immune suppression and treat autoimmune conditions without the need for systemic immune suppression.
We use gene transfer technologies to direct the functional profile of therapeutic T cells. We have developed genetic switches to enhance or suppress the metabolic activity of T cells, and this promote effector function or memory formation. Transfer of genes encoding transcription factors is used to drive Th1, Th2 or Th17 differentiation of adoptively transferred T cells. We perform studies with human T cells in vitro, and in immunodeficient mice in vivo. Murine models are used for mechanistic studies and to test therapeutic interventions in appropriate disease models.
Research summary
Cancer is a major health problem worldwide with WHO projections predicting an increase in incidence by 57% from 14 million cases in 2012 to 22 million cases by 2032. We are interested in exploring the role of the immune system in tumour development, and whether novel forms of immunotherapy can be used to treat cancer.
The research of our group is focussed on T cell immunology, with a particular focus the role of the T cell receptor (TCR) in the recognition of cancer antigens. We were amongst the first to show that cytotoxic T cells can selectively attack cancer cells by recognising point mutations in transforming proteins expressed in tumours (J Exp Med. 1993; 177:1493). We have since developed strategies to isolate monoclonal TCR that are specific for tumour antigens, and we use these TCR for gene therapy to redirected the specificity of patient T cells and equip them with the ability to selectively recognize and attack cancer cells.
The use of TCR gene therapy to produce antigen-specific cytotoxic and helper T cells is one area of active research in our group. We also use TCR and chimeric antigen receptor (CAR) gene transfer to produce antigen-specific regulatory T cells. This provides the opportunity to achieve highly selective immune suppression and treat autoimmune conditions without the need for systemic immune suppression.
We use gene transfer technologies to direct the functional profile of therapeutic T cells. We have developed genetic switches to enhance or suppress the metabolic activity of T cells, and this promote effector function or memory formation. Transfer of genes encoding transcription factors is used to drive Th1, Th2 or Th17 differentiation of adoptively transferred T cells. We perform studies with human T cells in vitro, and in immunodeficient mice in vivo. Murine models are used for mechanistic studies and to test therapeutic interventions in appropriate disease models.
Research Interests
Papers共 340 篇Author StatisticsCo-AuthorSimilar Experts
By YearBy Citation主题筛选期刊级别筛选合作者筛选合作机构筛选
时间
引用量
主题
期刊级别
合作者
合作机构
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
Yiya Zhong,Hans J. Stauss
Cellsno. 10 (2024): 797-797
FRONTIERS IN IMMUNOLOGY (2024)
HUMAN GENE THERAPYno. 21-22 (2023): A30-A30
Cited0Views0Bibtex
0
0
Neurology® neuroimmunology & neuroinflammationno. 5 (2023)
crossref(2023)
Adriana S. Albuquerque,Jesmeen Maimaris, Alexander J McKenna,Jonathan Lambourne,Fernando Moreira,Sarita Workman,Karyn Mégy,Ilenia Simeoni,Hana Lango Allen,Zoe Adhya,Hana Alachkar,Ariharan Anantharachagan,Richard Antrobus,Gururaj Arumugakani,Chiara Bacchelli,Helen Baxendale,Claire Bethune,Shahnaz Bibi, Barbara Boardman,Claire Booth, Michael Browning, Mary Brownlie,Siobhan O. Burns, Anita Chandra,Hayley Clifford,Nichola Cooper,Sophie Davies,John Dempster,Lisa Devlin, Rainer Döffinger,Elizabeth Drewe,David Edgar,William Egner,Tariq El‐Shanawany,Bobby Gaspar, Rohit Ghurye,Kimberly C. Gilmour,Sarah Goddard, Pavel Gordins,Sofia Grigoriadou,Scott Hackett,Rosie Hague,Lorraine Harper, G. Thomas Hayman,Archana Herwadkar,Stephen Hughes,Aarnoud Huissoon,Stephen Jolles, Julie R. Jones,Peter Kelleher,Nigel Klein, Taco W. Kuijpers,Dinakantha Kumararatne,James Laffan,Sara Lear,Hilary Longhurst,Lorena Lorenzo,Ania Manson,Elizabeth McDermott, Hazel Millar,Anoop Mistry, Valerie Morrisson,Sai Murng, Iman Nasir,Sergey Nejentsev,Sadia Noorani,Éric Oksenhendler,Mark Ponsford,Waseem Qasim, Ellie Quinn,Isabella Quinti,Alexander Richter,Crina Samarghitean,Ravishankar Sargur,Sinisa Savic, Suranjith L. Seneviratne, Carrock Sewall,Fiona Shackley, Kenneth Smith,Emily Staples,Hans J. Stauss,Cathal Steele,James Thaventhiran,Moira Thomas,Adrian J. Thrasher, Stephen R. Welch,Lisa Willcocks,Austen Worth, Nigel Yeatman,Patrick Yong,Sofie Ashford,John S. Bradley, Debra Fletcher, Tracey Hammerton, Roger James,Nathalie Kingston,Willem H. Ouwehand,Christopher Penkett,F. Lucy Raymond,Kathleen Stirrups, Marijke Veltman, Timothy M. Young,Matthew Brown, Naomi Clements-Brod, John M. Davis,Eleanor Dewhurst,Marie Erwood,Amy Frary,Rachel Linger,Jennifer Martin,Sofia Papadia,Karola Rehnström,William Astle,Antony Attwood,Marta Bleda,Keren Carss,Louise Daugherty,Sri V. V. Deevi,Stefan Gräf,Daniel Greene, Csaba Halmagyi,Matthias Haimel,Fengyuan Hu, Vera Matser,Stuart Meacham,Olga Shamardina, Catherine Titterton,Salih Tuna,Ernest Turro, Ping Yu, Julie von Ziegenweldt, Abigail Furnell,Rutendo Mapeta, Simon Staines, Jonathan Stephens,Deborah Whitehorn,Paula Rayner-Matthews, C. Ian F. Watt,Emma Morris
HUMAN GENE THERAPYno. 21-22 (2023): A13-A13
Cited0Views0Bibtex
0
0
HUMAN GENE THERAPYno. 21-22 (2023): A36-A36
Cited0Views0Bibtex
0
0
Load More
Author Statistics
#Papers: 343
#Citation: 11416
H-Index: 55
G-Index: 96
Sociability: 7
Diversity: 4
Activity: 105
Co-Author
Co-Institution
D-Core
- 合作者
- 学生
- 导师
Data Disclaimer
The page data are from open Internet sources, cooperative publishers and automatic analysis results through AI technology. We do not make any commitments and guarantees for the validity, accuracy, correctness, reliability, completeness and timeliness of the page data. If you have any questions, please contact us by email: report@aminer.cn