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Innate Immunity
Prof. Dr. Chiara Romagnani
 

Innate Immunity

Prof. Dr. Chiara Romagnani

Charité - Universitätsmedizin Berlin (CBF)
Med. Klinik m.S. Gastroenterologie, Infektiologie und Rheumatologie
and
Deutsches Rheuma-Forschungszentrum Berlin
Work Group: Innate Immunity
Charitéplatz 1
10117 Berlin

romagnani@drfz.de
chiara.romagnani@charite.de
Phone: +49 (0)30 28460-681 Fax: +49 (0)30 28460-603 romagnani@drfz.de

CV and Key Publications

Scientific Career
  • 2020 W3 Professor „Immunology of Inflammation” at Charité Medical University and Chair of the Leibniz “Chronic Inflammation” Campus, Berlin
  • 2018 Primo Loco W3 in Immunology at the Medical Faculty of the Eberhard Karls Universität Tübingen
  • 2017-2020 W2-Heisenberg Professorship at the Charité Medical University, Berlin
  • 2009-2017 Group Leader at the Deutsche Rheumaforschungszentrum (DRFZ), Berlin
  • 2006 – 2009 PostDoc Charité and DRFZ, Berlin
Education
  • 2003 – 2006 PhD at the University of Genova, Italy
  • 1998 – 2003 Specialty in Oncology at the National Cancer Institute, Genoa, Italy
  • 1991 – 1998 Study of medicine at the University of Florence, Italy
Boards
  • Board of the German Society of Immunology (DGfI)
  • Executive Committee of the European Journal of Immunology (EJI)
  • Faculty Member Faculty of 1000 Research
  • Committee for the DGFI-Robert Koch Postdoc Prize
  • Chief Editor of Frontiers in Immunology – Specialty NK and ILCs (2017-2020)
Awards
  • 2017 DFG-Heisenberg Professorship
  • 2016 DFG-nominated member of AcademiaNet – “Expert Database for Outstanding Female Academics
    http://www.academia-net.de/
  • 2006 EMBO fellowship
Third Party Funding

Selection from 2016 ongoing

  • 2020-2023 Leibniz-Kooperative Exzellenz „Identification and modulation of new immune targets in juvenile idiopathic arthritis (JIA)“
  • 2016 – 2022 DFG SSP 1937/1 (RO3565/4-1; 4-2): Innate Lymphoid Cells: “Role of Innate lymphoid cells (ILC) and aryl hydrocarbon receptor (AhR) during pulmonary bacterial infections”
  • 2017-2020 DFG-Heisenberg Professorship at the Charité Medical University
  • 2018 – 2022 DFG-TRR 241 TP B02: “Signals mediating crosstalk of intestinal epithelial cells with innate lymphoid cells in inflammatory bowel diseases”
  • 2018 – 2022 DFG-TRR 241 Research Graduate Training (RTG)-Z01
  • 2019 Berlin Health Innovations (BHI) Validation Fund 2018 “Peptide-based vaccination targeting innate responses against viral infection and cancer”
Top Publications
  1. Hammer Q, Rückert T, Borst EM, Dunst J, Haubner A, Durek P, Heinrich F, Gasparoni G, Babic M, Tomic A, Pietra G, Nienen M, Blau IW, Hofmann J, Na IK, Prinz I, Koenecke C, Hemmati P, Babel N, Arnold R, Walter J, Thurley K, Mashreghi MF, Messerle M, Romagnani C. Peptide-specific recognition of human cytomegalovirus strains controls adaptive natural killer cells. Nat Immunol. 2018 May;19(5):453-463. doi: 10.1038/s41590-018-0082-6. Epub 2018 Apr 9. (I.F. 21)
  2. Diefenbach A, Colonna M, Romagnani C. The ILC World Revisited. Immunity. 2017 Mar 21;46(3):327-332. (I.F. 21)
  3. Montaldo E, Teixeira-Alves LG, Glatzer T, Hamann W, Babic M, Paclik D, Stölzel K, Gröne J, Lozza L, Juelke K, Matzmohr N, Loiacono F, Petronelli P, Huntington ND, Moretta L, Mingari MC and Romagnani C. Human RORgt+ CD34+ cells are lineage-specified progenitors of group 3 RORgt+ innate lymphoid cells. Immunity. 2014 Dec 18;41(6):988-1000. (I.F. 21)
  4. Luetke-Eversloh M, Hammer Q, Durek P, Nordström K, Gasparoni G, Pink M, Hamann A, Walter J, Chang HD, Dong J and Romagnani C. Human Cytomegalovirus Drives Epigenetic Imprinting of the IFNG Locus in NKG2Chi Natural Killer Cells. PLoS Pathog. 2014 Oct 16;10(10):e1004441. (I.F. 8.057)
  5. Glatzer T, Killig M, Meisig J, Ommert I, Luetke-Eversloh M, Babic M, Paclik D, Blüthgen N, Seidl R, Seifarth C, Gröne J, Lenarz M, Stölzel K, Fugmann D, Porgador A, Hauser A, Karlas A, Romagnani C. RORγt⁺ innate lymphoid cells acquire a proinflammatory program upon engagement of the activating receptor NKp44. Immunity. 2013 Jun 27;38(6):1223-35. (I.F. 21)
Romagnani lab
Identifying innate signals initiating and perpetuating chronic inflammation
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