Deep phenotyping of Tregs identifies an immune signature for idiopathic aplastic anemia and predicts response to treatment

Author:

Kordasti Shahram12ORCID,Costantini Benedetta12,Seidl Thomas1,Perez Abellan Pilar2,Martinez Llordella Marc3,McLornan Donal2,Diggins Kirsten E.4,Kulasekararaj Austin2,Benfatto Cinzia1,Feng Xingmin5,Smith Alexander12,Mian Syed A.1,Melchiotti Rossella6,de Rinaldis Emanuele6,Ellis Richard6,Petrov Nedyalko6,Povoleri Giovanni A. M.3,Chung Sun Sook1,Thomas N. Shaun B.1,Farzaneh Farzin1,Irish Jonathan M.4,Heck Susanne6,Young Neal S.5,Marsh Judith C. W.12,Mufti Ghulam J.12

Affiliation:

1. Department of Haematological Medicine, King's College London, London, United Kingdom;

2. Haematological Medicine, King's College Hospital, London, United Kingdom;

3. Division of Transplantation Immunology & Mucosal Biology, King's College London, London, United Kingdom;

4. Department of Cancer Biology, Vanderbilt University, Nashville, TN;

5. Hematology Branch, National Heart, Lung, and Blood Institute, National Institutes of Health, Bethesda, MD; and

6. National Institute for Health Research Biomedical Research Centre, King's College London, London, United Kingdom

Abstract

Key Points Mass cytometry reveals a Treg immune signature for AA and for response to antithymocyte globulin. AA Tregs in vitro are expandable, stable, and functional, with potential for future therapeutic options.

Publisher

American Society of Hematology

Subject

Cell Biology,Hematology,Immunology,Biochemistry

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