Project Details
TRR 359: Perinatal Development of Immune Cell Topology
Subject Area
Medicine
Biology
Biology
Term
since 2023
Project identifier
Deutsche Forschungsgemeinschaft (DFG) - Project number 491676693
Prenatal development of the immune system is orchestrated by cell-intrinsic programs that guide immune cell differentiation and instruct complex immunological solutions during organ development. At birth, separation from the mother triggers sudden, drastic challenges for the infant’s immune system, such as acquisition of microbiota, changes in oxygen tension and metabolism, and enteral nutrient exposure. The external stimuli and resultant alterations in tissue microenvironment are distinct for each organ and subanatomical site. Simultaneously, there is an influx of immune cells originating from definitive hematopoiesis. Aberrant perinatal immune development thus has severe consequences for tissue integrity and protection, microbiota composition and immune homeostasis. Yet the parameters regulating immune cell adaption during normal or aberrant perinatal development remain poorly defined. Tissue-specific information is limited and neonatal human samples are scarce. The proposed CRC TRR “Perinatal development of immune cell topology (PILOT)” aims to explore mechanisms that direct perinatal differentiation of immune cells and their cellular environment. PILOT will dissect how preprogrammed developmental traits and perinatal exogenous cues integrate to steer immune cell differentiation, establish immune homeostasis and provide immunity to infections. We will study subanatomical niches where structures with discrete functions meet, such as barrier tissues of intestine, lung and skin, and protected sites including the placenta. PILOT interlinks temporal and spatial aspects in two research areas. In Area A, “Response to exogenous cues”, the focus is on external factors that modulate immune cell repertoire development and drive diversification and adaptation of tissue-resident and circulating immune cells. Area B, “Preprogrammed development”, addresses cell-intrinsic programs that steer topology and function during perinatal immune cell development. Pioneering analytical tools, such as high-resolution imaging, single-cell transcriptome, epigenome and proteome analysis and in vivo fate mapping, will enable unique investigations of diverse and even small fetal and neonatal tissue niches. Using automated image analysis, unbiased data clustering and machine learning, PILOT will develop novel algorithms to elucidate how complex signals are integrated and translated to establish and maintain cellular immunity. These tools will be used not only in perinatal mouse and heterocellular in vitro models, but also in human neonatal biomaterial, thereby integrating translational perspectives into the consortium. Identification and modification of key parameters determining immunity around birth promises unique insights into how cellular immunity emerges through adaptation between host and environment on the global level, and microanatomically in the tissue. This will lay the foundation for PILOT’s ultimate goal: steering immunity for a better start and long-term health.
DFG Programme
CRC/Transregios
Current projects
- A01 - Nutrition, host metabolism and the antimicrobial response to enteric infection in the neonatal host (Project Head Hornef, Mathias Walter )
- A02 - Impact of neonatal CMV infection on lung macrophage development (Project Heads Henneke, Philipp ; Ruzsics, Zsolt )
- A03 - The role of S100-alarmins in the perinatal development of respiratory immunity (Project Heads Stark, Konstantin ; Viemann, Dorothee )
- A04 - Role of crosstalk between γδ T cells and Langerhans cells in driving their mutual differentiation in the postnatal niche (Project Heads Kierdorf, Katrin ; Sagar, Sagar )
- A05 - Long-lasting consequences of early-life influenza A virus infection for the tissue-resident memory T cell niche and susceptibility to secondary infections (Project Heads Bruder, Dunja ; Hühn, Jochen )
- A06 - Perinatal crosstalk of microbiota and intestinal macrophages in the control of mucosal pathogens (Project Heads Clavel, Thomas ; Erny, Daniel ; Henneke, Philipp )
- A07 - Effects of neonatal wildling microbiota on the immune response to vaccination (Project Heads Proietti, Ph.D., Michele ; Rosshart, Stephan Patrick )
- A08 - Immune trajectories defining early lung development in newborn infants (Project Heads Hilgendorff, Anne ; Schiller, Herbert )
- B01 - Perinatal fate decisions of macrophages in protected tissues (Project Head Prinz, Marco )
- B02 - Role of placenta-derived peptide PIF in perinatal immune cell regulation (Project Heads Immler, Roland ; Sperandio, Markus )
- B03 - Perinatal development of dermal macrophage diversity (Project Heads Kolter, Julia ; Preißl, Sebastian )
- B04 - Identification of fibroblast-immune interactions and skin topologies that shape scarless wound repair (Project Head Rinkevich, Ph.D., Yuval )
- B05 - Impact of intrauterine inflammation on neonatal dendritic cell development and function (Project Head Schraml-Schotta, Ph.D., Barbara )
- B06 - Genetic regulation of protein expression during immune cell development in human neonates (Project Heads Kim-Hellmuth, Sarah ; Nußbaum, Claudia Franziska )
- B07 - Development and functional implications of circadian leukocyte dynamics in early life (Project Heads Scheiermann, Christoph ; Sperandio, Markus )
- B09 - Effects of maternal hyperlipidemia on embryo-derived macrophages and perinatal immune development (Project Head Schulz, Christian )
- INF - Information infrastructure for research data management (Project Head Binder, Harald )
- MGK - CoPILOT, PILOT’s Integrated Research Training Group (Project Heads Kierdorf, Katrin ; Sperandio, Markus )
- Z01 - High-dimensional data analysis and data integration for quantitatively profiling perinatal immune cells (Project Heads Börries, Melanie ; Marr, Carsten )
- Z02 - Central administration and coordination (Project Head Henneke, Philipp )
Applicant Institution
Albert-Ludwigs-Universität Freiburg
Co-Applicant Institution
Ludwig-Maximilians-Universität München
Participating University
Julius-Maximilians-Universität Würzburg; Otto-von-Guericke-Universität Magdeburg; Rheinisch-Westfälische Technische Hochschule Aachen
Participating Institution
Helmholtz Zentrum München
Deutsches Forschungszentrum für Gesundheit und Umwelt; Helmholtz-Zentrum für Infektionsforschung (HZI); Helmholtz-Zentrum für Umweltforschung (UFZ)
Deutsches Forschungszentrum für Gesundheit und Umwelt; Helmholtz-Zentrum für Infektionsforschung (HZI); Helmholtz-Zentrum für Umweltforschung (UFZ)
Spokesperson
Professor Dr. Philipp Henneke