Project Details
SFB 650: Cellular Approaches for the Suppression of Unwanted Immune Reactions - From Bench to Bedside
Subject Area
Medicine
Term
from 2005 to 2016
Project identifier
Deutsche Forschungsgemeinschaft (DFG) - Project number 5486264
Diseases caused by the immune system such as autoimmunity, allergy and transplant rejection have major medical and economic implications. Presently available treatments are restricted to unspecific immuno-suppressants, i.e. drugs, which down-regulate the activities of the immune system. However, these drugs are limited in their effectiveness und are associated with significant side effects, long-term application cycles and - last but not least - very high costs.
This Collaborative Research Centre aims at developing new approaches to suppressing unwanted immune reactions selectively and to further develop concepts into medical treatments. In particular, it will be examined whether future therapies can utilise the cellular control mechanisms of the immune systems itself.
Several project groups investigate how regulatory lymphocytes suppress inflammatory immune reactions, and whether there are ways to use them for treating patients affected by autoimmune diseases or transplantation surgery. Other project groups are seeking to clarify under which conditions such regulatory cells are generated, which factors - substances synthesised or isolated from other organisms - support their development, which features are required to make them highly effective in vivo, and which molecular pathways are involved in the suppression of the immune reactions. The objective is to find ways either to increase the formation of those protective cells in vivo, or to use them for therapeutic treatments after isolation from patients and expansion in vitro. In addition, new ways to control the success or failure of treatment of patients by such novel therapies will be evaluated.
Project groups of this Collaborative Research Centre search for new treatments to be applied to rheumatic diseases, multiple sclerosis, transplantation medicine and allergies. Their common vision is the idea to use natural tolerance mechanisms - the ability of the immune system to regulate itself - for therapeutic purposes, i.e. to switch off unwanted immune reactions selectively and to return to a lasting immunological balance.
This Collaborative Research Centre aims at developing new approaches to suppressing unwanted immune reactions selectively and to further develop concepts into medical treatments. In particular, it will be examined whether future therapies can utilise the cellular control mechanisms of the immune systems itself.
Several project groups investigate how regulatory lymphocytes suppress inflammatory immune reactions, and whether there are ways to use them for treating patients affected by autoimmune diseases or transplantation surgery. Other project groups are seeking to clarify under which conditions such regulatory cells are generated, which factors - substances synthesised or isolated from other organisms - support their development, which features are required to make them highly effective in vivo, and which molecular pathways are involved in the suppression of the immune reactions. The objective is to find ways either to increase the formation of those protective cells in vivo, or to use them for therapeutic treatments after isolation from patients and expansion in vitro. In addition, new ways to control the success or failure of treatment of patients by such novel therapies will be evaluated.
Project groups of this Collaborative Research Centre search for new treatments to be applied to rheumatic diseases, multiple sclerosis, transplantation medicine and allergies. Their common vision is the idea to use natural tolerance mechanisms - the ability of the immune system to regulate itself - for therapeutic purposes, i.e. to switch off unwanted immune reactions selectively and to return to a lasting immunological balance.
DFG Programme
Collaborative Research Centres
Completed projects
- 01 - Induction of stable FOXP3+ regulatory T-cells (Project Head Hamann, Alf )
- 02 - Engineering resting B cells for the suppression of unwanted immunity (Project Head Fillatreau, Simon )
- 03 - Antigenspezifische Aktivierung von Suppressorzellen durch repetitive Epitopoligomere (Project Heads Falk, Kirsten ; Rötzschke, Olaf )
- 04 - Regulatory T cell induction by manipulation of transcription factors (Project Head Baumgraß, Ria )
- 05 - Immune modulation of allergic diseases by nuclear hormone receptor ligands (Project Heads Heine, Guido ; Radbruch, Andreas ; Worm, Margitta )
- 06 - Application of helminth-derived concepts to treat inflammatory diseases (Project Head Hartmann, Susanne )
- 08 - Modulation von chronischen Immunreaktionen über CD152 (CTLA-4) (Project Heads Brunner-Weinzierl, Monika Christine ; Burmester, Gerd-Rüdiger )
- 09 - Modulation der Funktion von CD4+ Effektor/Memory T-Zellen bei chronischen Autoimmunerkrankungen (Project Heads Lipp, Martin ; Müller, Gerd )
- 10 - Evaluation of the therapeutic potential of regulatory T cells in human and murine lupus (Project Heads Babel, Nina ; Riemekasten, Gabriela )
- 11 - Induktion und Stabilisierung des IL-10 Gedächtnisses von Tr1-Zellen für zelluläre immunregulatorische Therapien (Project Heads Radbruch, Andreas ; Sieper, Joachim ; Thiel, Andreas )
- 12 - Development of tailored protocols for tolerance induction by immunoablation and hematopoietic stem cell transplantation in autoimmune diseases (Project Heads Alexander, Tobias ; Arnold, Renate ; Hiepe, Falk )
- 13 - Induction of regulatory T-cell-responses by therapeutic modulation of antigen-presenting cells in multiple sclerosis (Project Heads Infante Duarte, Carmen ; Zipp, Frauke )
- 14 - Influence of the early immune monitoring profile on outcome (rejection / induction of tolerance) after liver transplantation (Project Heads Pascher, Andreas ; Sawitzki, Birgit )
- 16 - New generation anti-B cell therapy (Project Heads Dörner, Thomas ; Salama, Abdulgabar )
- 17 - Targeting of memory plasma cells in autoimmune diseases (Project Heads Burmester, Gerd-Rüdiger ; Hiepe, Falk ; Radbruch, Andreas )
- 18 - Treatment of immune disorders by a natural proteasome inhibitor (I-VSL#3) (Project Head Steinhoff, Ulrich )
- 20 - Exploiting NK cells for suppression of unwanted immune responses in transplantation (Project Heads Romagnani, Ph.D., Chiara ; Uharek, Lutz )
- 21 - Mast cell-driven down regulation of chronic inflammation (Project Heads Maurer, Marcus ; Metz, Martin )
- 22 - Antigen-specific regulatory T-cells for cellular therapies (Project Heads Sieper, Joachim ; Thiel, Andreas )
- 23 - Targeting of pathogenic T helper cells in chronic rheumatic inflammation (Project Heads Chang, Hyun-Dong ; Mashreghi, Mir-Farzin ; Radbruch, Andreas )
- 25 - Pro- and anti-inflammatory human Th17 cell functions - molecular targets and therapeutic intervention (Project Head Zielinski, Christina )
- 26 - Redirecting the antigen-specificity of polyclonal regulatory T cells to optimize their therapeutic efficacy and safety (Project Heads Fillatreau, Simon ; Scheffold, Alexander ; Uckert, Wolfgang )
- 28 - Suppression of autoreactive T cell responses by Th2 cells (Project Head Löhning, Max )
- MGK02 - Suppression of unwanted immune reactions (Project Heads Babel, Nina ; Löhning, Max ; Riemekasten, Gabriela )
- N01 - N01: Understanding and exploiting mechanisms controlling T cell tolerance, protective immune responses and autoimmunity (Project Head Geginat, Ph.D., Jens )
- V01 - Central tasks of the Collaborative Research Centre (Project Head Volk, Hans-Dieter )
- Z1 - Präparative Zellsortierung und Modifikation von regulatorischen Zellpopulationen (Project Heads Radbruch, Andreas ; Radtke, Hartmut ; Scheffold, Alexander )
- Z02 - Coordination of Clinical Trials and Development of GMP procedures for cell-based therapeutic approaches (Project Heads Reinke, Petra ; Volk, Hans-Dieter )
- Z03 - Histomorphological evaluation and in-situ analysis of regulatory and effector cells (Project Heads Heppner, Frank ; Kühl, Anja A. ; Loddenkemper, Christoph )
- Z04 - Set-up and evaluation of am human adaptive immune system in cord blood stem cell-transplanted mice - a model for translational projects (Project Heads Sawitzki, Birgit ; Volk, Hans-Dieter )
- Z06 - An integrated high-resolution immunophenotyping and computational biomarker discovery approach for monitoring clinical trials (Project Heads Grützkau, Ph.D., Andreas ; Häupl, Thomas ; Sawitzki, Birgit )
Applicant Institution
shared FU Berlin and HU Berlin through:
Charité - Universitätsmedizin Berlin
Charité - Universitätsmedizin Berlin
Co-Applicant Institution
Freie Universität Berlin; Humboldt-Universität zu Berlin
Participating Institution
Deutsches Rheuma-Forschungszentrum Berlin (DRFZ); Max-Delbrück-Centrum für Molekulare Medizin (MDC)
Spokesperson
Professor Dr. Hans-Dieter Volk