Projects Offered

1 PhD project offered in the IPP winter call Molecular Biomedicine & Ageing

Scientific Background

Trained immunity has recently been discovered as a novel mechanism of immune cell memory in innate immune cells. Different to the adaptive immune system, innate cells do not develop into antigen-specific long lived memory cells that can be reactivated. Instead, it was found that epigenetic and metabolic changes in stem cells and progenitors are transmitting previous information (e.g. from prior infections) and change the general activation status of future generations of innate immune cells. Especially monocytes have been studied in the context of trained immunity, but other cell types like neutrophils and even epithelial cells contribute to trained immunity. 

These changes provide a more effective response to similar threats in the future, linked to pattern recognition pathways and cytokine production. As this re-activation is not antigen specific, it can also be triggered in response to other stimuli, potentially leading to broader beneficial but also detrimental effects. While trained immunity is not as specific or long-lasting as adaptive immune memory it still provides a faster, more robust reaction upon re-exposure in a non-antigen specific context.

PhD Project: Defining trained immunity in dendritic cells and their progenitors

In this PhD project we aim to study if dendritic cells also contribute to trained immunity. Dendritic cells play a fundamental role in antigen presentation and the priming of naive T cells. They are short lived and constantly replenished by stem cells within the bone marrow from where they are dispersed into tissues to sample and recognize pathogens. Several lineages of dendritic cells have been described, which originate from distinct progenitors. 

In this project you will establish protocols on how to isolate and differentiate different DC progenitors in vitro and in vivo, using both human and murine samples. Furthermore, you will investigate principles of central and peripheral trained immunity and perform molecular single-cell and omics approaches and define the cellular, molecular and functional changes of dendritic cells. These changes will be carefully compared to monocytes, which have been well studied in trained immunity and assess differences between different dendritic cell lineages. 

This PhD requires a strong background in immunology, previous experience with complex phenotyping of immune cells on a single-cell level and previous experience with either primary human or murine samples and cell isolation/characterization. 

If you are interested in this project, please select Mayer (DC Training) as your group preference in the IPP application platform.

Publications relevant to this project

Mayer JU, Hilligan KL, Chandler JS, Eccles DA, Old SI, Domingues RG, Yang J, Webb GR, Munoz-Erazo L, Hyde EJ, Wakelin KA, Tang SC, Chappell SC, von Daake S, Brombacher F, Mackay CR, Sher A, Tussiwand R, Connor LM, Ortega DG, Jankovic D, Gros GL, Hepworth MR, Lamiable O, Ronchese F. (2021) Homeostatic IL-13 in healthy skin directs dendritic cell differentiation to promote TH2 and inhibit TH17 cell polarization. Nat. Immunol.,1 (13). Link

Bosteels C, Neyt K, Vanheerswynghels M, van Helden MJ, Sichien D, Debeuf N, De Prijck S, Bosteels V, Vandamme N, Martens L, Saeys Y, Louagie E, Lesage M, Williams DL, Tang SC, Mayer JU, Ronchese F, Scott CL, Hammad H, Guilliams M, Lambrecht BN. (2020) Inflammatory Type 2 CDCs Acquire Features of CDC1s and Macrophages to Orchestrate Immunity to Respiratory Virus Infection. Immunity, 52 (6), 1039-1056 e9. Link

Netea MG, Domínguez-Andrés J, Barreiro LB, Chavakis T, Divangahi M, Fuchs E, Joosten LAB, van der Meer JWM, Mhlanga MM, Mulder WJM, Riksen NP, Schlitzer A, Schultze JL, Stabell Benn C, Sun JC, Xavier RJ, Latz E. (2020) Defining trained immunity and its role in health and disease. Nat Rev Immunol. (6):375-388 Link