Professor Dr Chiara Romagnani
- Section Microbiology and Immunology
- Location Berlin, Germany
- Election year 2024
Research
Research Priorities: innate immunity, chronic inflammation, chronic infection, innate lymphoid cells, natural killer cells
Chiara Romagnani is an Italian immunologist specialising in innate immunity. Her particular interest is in innate lymphoid cells (ILCs) and their dual role in wound healing and inflammation processes. Her working group succeeded in identifying signals that control the pro- and anti-inflammatory functions in ILCs. Another focus of her research is on natural killer cells (NK cells), lymphocytes, that contribute to the innate immune response.
The immune system consists of two closely intertwined components: innate (unspecific) and acquired (specific) defence. While the innate immune system reacts quickly and non-specifically, acquired defence works more slowly but in a targeted manner. Innate lymphoid cells, abbreviated as ILCs, are one of the cellular elements of the innate immune system. These cells undergo a multi-stage development process which begins in the blood-forming stem cells of the bone marrow. Under the influence of neighbouring cells the ILCs acquire specific effector functions – a process known as imprinting. These functions can be activated later and play a crucial role when it comes to infections or tissue damage.
The immune response of the ILCs can be influenced in at least three phases: during the differentiation, in the imprinting phase, and in the activation of the effector function in the tissue. For a long time, targeted intervention in these processes was impossible as the appropriate starting points were not known.
Chiara Romagnani and her team were able to identify signals that influence both the differentiation of the ILCs as well as the imprinting and activation of the effector functions. These investigations were carried out on the ILCs of healthy people as well as patients with chronic inflammatory diseases. In this way, Romagnani’s research was able to differentiate between signal pathways that initiate either the production of pro-inflammatory messenger substances, such as the tumour necrosis factor, or anti-inflammatory messenger substances, such as interleukin-22. By selectively blocking or activating the relevant receptors it could become possible to reduce the harmful effects of these cells. Chiara Romagnani and her team now plan to test whether chronic inflammation can be alleviated or even cured by targeted influencing of the identified receptors.
With her research on natural killer cells, the immunologist was able to prove that these cells have similar characteristics to classic memory cells, the B and T lymphocytes. Once activated they multiply into clones and survive for years. This knowledge could open up new possibilities of using these cells to fight specific viruses or tumour cells.
Chiara Romagnani’s research is a significant contribution to the improved understanding and treatment of infectious diseases, tumours, and inflammatory illnesses. At the same time she bridges the gap between basic and clinical research. She is particularly focused on implementing the obtained insights in a way that benefits patients.
Chiara Romagnani is an Italian immunologist specialising in innate immunity. Her particular interest is in innate lymphoid cells (ILCs) and their dual role in wound healing and inflammation processes. Her working group succeeded in identifying signals that control the pro- and anti-inflammatory functions in ILCs. Another focus of her research is on natural killer cells (NK cells), lymphocytes, that contribute to the innate immune response.
The immune system consists of two closely intertwined components: innate (unspecific) and acquired (specific) defence. While the innate immune system reacts quickly and non-specifically, acquired defence works more slowly but in a targeted manner. Innate lymphoid cells, abbreviated as ILCs, are one of the cellular elements of the innate immune system. These cells undergo a multi-stage development process which begins in the blood-forming stem cells of the bone marrow. Under the influence of neighbouring cells the ILCs acquire specific effector functions – a process known as imprinting. These functions can be activated later and play a crucial role when it comes to infections or tissue damage.
The immune response of the ILCs can be influenced in at least three phases: during the differentiation, in the imprinting phase, and in the activation of the effector function in the tissue. For a long time, targeted intervention in these processes was impossible as the appropriate starting points were not known.
Chiara Romagnani and her team were able to identify signals that influence both the differentiation of the ILCs as well as the imprinting and activation of the effector functions. These investigations were carried out on the ILCs of healthy people as well as patients with chronic inflammatory diseases. In this way, Romagnani’s research was able to differentiate between signal pathways that initiate either the production of pro-inflammatory messenger substances, such as the tumour necrosis factor, or anti-inflammatory messenger substances, such as interleukin-22. By selectively blocking or activating the relevant receptors it could become possible to reduce the harmful effects of these cells. Chiara Romagnani and her team now plan to test whether chronic inflammation can be alleviated or even cured by targeted influencing of the identified receptors.
With her research on natural killer cells, the immunologist was able to prove that these cells have similar characteristics to classic memory cells, the B and T lymphocytes. Once activated they multiply into clones and survive for years. This knowledge could open up new possibilities of using these cells to fight specific viruses or tumour cells.
Chiara Romagnani’s research is a significant contribution to the improved understanding and treatment of infectious diseases, tumours, and inflammatory illnesses. At the same time she bridges the gap between basic and clinical research. She is particularly focused on implementing the obtained insights in a way that benefits patients.
Career
- since 2023 Director, Institute of Medical Immunology, Charité – Universitätsmedizin Berlin as well as Professor, Berlin University Alliance (BUA), Charité – Universitätsmedizin Berlin and Freie Universität (FU) Berlin, Germany
- 2020-2023 Professor, Charité – Universitätsmedizin Berlin, Berlin, Germany
- 2017-2020 Heisenberg Professor “Innate Mechanism of Chronic Inflammation”, Department of Gastroenterology, Infectious Diseases and Rheumatology, Charité – Universitätsmedizin Berlin, Berlin, Germany
- since 2010 Group Leader, Deutsches Rheuma-Forschungszentrum (DRFZ)
- 2006-2009 Postdoctoral Fellow, Institute of Immunology, Charité – Universitätsmedizin Berlin, Berlin, Germany
- and DRFZ
- 2003-2006 PhD in Immunology, University of Genoa, Genoa, Italy
- 1999-2002 Medical Specialist in Oncology, National Cancer Institute, University of Genoa, Genoa, Italy
- 1991-1998 Degree in Human Medicine and Doctorate (MD), Università degli Studi di Firenze, Florence, Italy
Functions
- since 2024 Member, Review Board “Microbiology, Virology, Immunology”, German Research Foundation (DFG), Germany
- since 2022 Member, Review Panel “Life Sciences”, European Research Council (ERC)
- since 2022 Editor in Chief, European Journal of Immunology
- since 2020 Spokesperson, PhD Programme, Center of Infection Biology and Immunity (ZIBI), Berlin, Germany
- since 2020 Member, Advisory Board, Immunity
- since 2019 Member, Committee, Robert Koch Postdoctoral Award, Robert Koch Foundation, Berlin, Germany
- since 2018 Member, Executive Board, German Society for Immunology(DGfI), Germany
Projects
- since 2022 Principal Investigator, Advanced Research Grant “MEM-CLONK – Imprinting and clonality of human NK cell memory”, ERC
- since 2021 Co-Speaker, Else Kröner-Promotionskolleg “Rethinking Health”, Else Kröner-Fresenius Foundation, Homborg vor der Höhe, Germany
- 2020-2024 Speaker, Leibniz ScienceCampus “Chronic Inflammation”, Leibniz Association, Berlin
- since 2018 Member, Steering Committee, Transregio (TRR) 241 “Immune-Epithelial Communication in Inflammatory Bowel Diseases”, DFG, Germany
- since 2018 Speaker, Integrated Research Training Group (iRTG) “Intestinal Inflammation – From Bench to Bedside”, TRR 241, DFG, Germany
- since 2018 Project Head, Subproject “Signals mediating crosstalk of intestinal epithelial cells with innate lymphoid cells in inflammatory bowel diseases”, TRR 241, DFG, Germany
- 2016-2023 Project Head, Subproject “Role of innate lymphoid cells (ILC) and the aryl hydrocarbon receptor in pulmonary bacterial infections”, Priority Programme (PP) 1937, DFG, Germany
- 2016-2022 Member, Steering Committee, PP 1937 “Innate Lymphoid Cells”, DFG, Germany
Honours and Memberships
- since 2024 Member, German National Academy of Sciences Leopoldina, Germany
- 2017-2020 Heisenberg Professorship “Innate Mechanism of Chronic Inflammation”, DFG, Germany
- 2016 Member, AcademiaNet. The Portal to Excellent Women Academics, Swiss National Science Foundation (SNSF), Switzerland
- 2006 Fellowship, European Molecular Biology Organization (EMBO)