Sex
Defining female–male differences in immune states, responses and molecular phenotypes.
FEMMUNITYX · BONN
Across hormonal states, metabolism, environment and time.
We use human systems immunology to understand how sex and female physiology shape immune variation — from population-level differences to hormonal dynamics within individuals and tissue-resolved immunity.
Explore our research ↓OUR VISION
Female immunity emerges at the intersection of sex, hormones, metabolism, environment and time.
We use systems immunology to understand how these dimensions shape immune states across individuals and physiological contexts — connecting population-level sex differences with longitudinal variation within women and, ultimately, tissue-resolved immunity.
INTEGRATED RESEARCH PROGRAM
Immune sex differences are not fixed. We investigate how endocrine, metabolic and environmental contexts interact with sex to shape immune phenotypes — and how these relationships change across female physiology.
Defining female–male differences in immune states, responses and molecular phenotypes.
Understanding how changing endocrine environments intersect with immune-cell states and function.
Mapping interactions between metabolic state, nutrition and immune regulation.
Studying immune variation across nutritional, microbiome and population contexts.
Following immune variation across hormonal states, time and biological compartments.
RESEARCH PROGRAMS
Our projects approach immune variation at complementary scales — from population and metabolic diversity, through longitudinal female physiology, to controlled experimental systems and computational integration.
TransMic / TransInf
TransMic and TransInf investigate how nutrition, microbiome composition and metabolic state shape human immune function across populations and metabolic contexts.
Within FemmunityX, we extend these questions to immune sex differences — asking whether diet, obesity, insulin resistance, microbiome composition and food-derived metabolites influence immune function differently in females and males.
Partners: KCMC (Tanzania), Radboud UMC (The Netherlands), INSERM & Sorbonne Université (France), University of Florence & Meyer Children’s Hospital (Italy), RSS-URCN (Burkina Faso)
Funding: JPI-HDHL · BMFTR
Femmunity
Femmunity investigates how hormonal rhythms shape immune variation across female physiology. We use the natural menstrual cycle and hormonal contraceptive use as models of changing endocrine environments and follow immune variation longitudinally.
The program is expanding from peripheral immunity toward the reproductive tissue environment, allowing us to ask which immune features remain stable, which are hormonally dynamic, and how immune states differ across biological compartments.
Partner: Jr. Prof. Marie-Christine Simon, University of Bonn
Explore the Femmunity Study →HormoneX
We are developing experimental approaches to investigate how human immune cells respond directly to changing hormonal environments ex vivo.
This emerging work complements our human studies by moving toward controlled investigation of hormone–immune interactions.
InformatYX
InformatYX is our developing computational framework for analysing immune data through a sex-aware and physiology-aware lens.
We develop analytical workflows and resources that integrate sex, hormonal state, metabolism, population context and physiology into the interpretation of high-dimensional immune data.
FLAGSHIP STUDY
The Femmunity Study explores how the immune system is shaped by hormonal rhythms in female physiology. Using the menstrual cycle and hormonal contraceptive use as models of changing endocrine environments, we follow immune variation over time and across biological compartments.
Our goal is to move beyond the idea of a single female immune baseline and instead understand which immune features remain stable, which are hormonally dynamic, and how these dynamics extend from peripheral blood toward the reproductive tissue environment.
Partner: Jr. Prof. Marie-Christine Simon, University of Bonn
Join the Femmunity Study →Prefer to call? +49 228 4330 2707
01 · NATURAL CYCLE
Longitudinal immune profiling alongside natural hormonal and metabolic variation.
02 · HORMONAL MODULATION
Investigating how exogenous hormonal states intersect with immune and metabolic trajectories.
03 · TISSUE INTERFACE
Using menstrual fluid and single-cell omics to investigate immune biology at the reproductive tissue interface.
WHERE THIS LEADS
Connecting immune states across physiology, time and tissue creates a path toward identifying coordinated patterns — and ultimately the drivers — of female immune variation.
HOW WE WORK
SELECTED SCIENCE
Marcus Altfeld, Camila Consiglio, Darragh Duffy, Molly Ingersoll, Cliona O'Farrelly, Tal Pecht✉, Tal Shay & Helena Soares
Calling for sex and gender to become integral dimensions of immunological research — a central step toward understanding immune variation and developing more precise and equitable medicine.
Read paper ↗Godfrey S. Temba*, Tal Pecht*, Vesla I. Kullaya, Nadira Vadaq, Mary V. Mosha, Thomas Ulas, Sneha Kanungo, Liesbeth van Emst, Lorenzo Bonaguro, Jonas Schulte-Schrepping, Elias Mafuru, Paolo Lionetti, Musa M. Mhlanga, Andre J. van der Ven, Duccio Cavalieri, Leo A. B. Joosten, Reginald A. Kavishe, Blandina T. Mmbaga, Joachim L. Schultze, Mihai G. Netea & Quirijn de Mast
Revealing how profoundly diet can reshape human immune and metabolic states, and providing a foundation for asking how these responses intersect with sex and female physiology.
Read paper ↗Alina Schieren, Sandra Koch, Tal Pecht & Marie-Christine Simon
Exploring how physiological hormonal fluctuations across the menstrual cycle interact with glucose metabolism and the gut microbiome — key biological dimensions of dynamic female physiology.
Read paper ↗Godfrey S. Temba, Nadira Vadaq, Vesla Kullaya, Tal Pecht, Paolo Lionetti, Duccio Cavalieri, Joachim L. Schultze, Reginald Kavishe, Leo A. B. Joosten, Andre J. van der Ven, Blandina T. Mmbaga, Mihai G. Netea & Quirijn de Mast
Demonstrating how environment, diet and population context contribute to variation in the human inflammatory system — reinforcing the need to understand immunity as a dynamic, context-dependent phenotype.
Read paper ↗Godfrey S. Temba*, Vesla I. Kullaya*, Tal Pecht*, et al.
Showing how lifestyle, nutrition and metabolism shape systemic inflammation in healthy individuals — highlighting the remarkable plasticity of the human immune system across environments.
Read paper ↗Tal Pecht, Anna C. Aschenbrenner, Thomas Ulas & Antonella Succurro
Examining computational approaches for understanding biological heterogeneity across populations and individual cells — a conceptual foundation for studying complex and dynamic immune variation.
Read paper ↗PEOPLE
We are an interdisciplinary team within the Systems Medicine Department at DZNE, bringing together human immunology, female physiology, molecular biology and computational approaches. Together, we study immune variation across scales — from human cohorts and longitudinal physiology to molecular and systems-level analysis.
Sex differences · female immunity · systems immunology
Sex differences · immunometabolism · systems immunology
Estrogen signaling · immune regulation
Reproductive immunology · systems immunology
JOIN FEMMUNITYX
We welcome researchers and students interested in human immunology, female physiology, immunometabolism, single-cell biology and computational systems approaches.