{"id":19799,"date":"2025-10-02T06:13:50","date_gmt":"2025-10-02T06:13:50","guid":{"rendered":"https:\/\/www.drfz.de\/?p=19799"},"modified":"2025-10-02T06:13:51","modified_gmt":"2025-10-02T06:13:51","slug":"epigenetic-imprints-of-immune-memory-across-the-human-body","status":"publish","type":"post","link":"https:\/\/www.drfz.de\/en\/neuigkeiten\/epigenetic-imprints-of-immune-memory-across-the-human-body\/","title":{"rendered":"Epigenetic Imprints of Immune Memory across the Human Body"},"content":{"rendered":"\n

Epigenetic programming of immune cells: permanent tissue residence and protection against infections<\/strong><\/strong><\/h2>\n\n\n\n

A remarkable collaborative study by the research teams of Andreas Radbruch at the German Rheumatology Research Centre Berlin, an institute of the Leibniz Association, and J\u00f6rn Walter at the University of the Saarland, together with scientists from the Charit\u00e9 University Medicine and Berlin Institute of Health, has discovered how immune cells are epigenetically imprinted to provide protection against repeated infections by pathogens and to persist in tissues. The findings are published in the journal Immunity & Inflammation recently<\/em>.<\/p>\n\n\n\n

T lymphocytes are an essential component of this \u201cImmunological Memory\u201d.  This study shows that \u201cmemory T lymphocytes\u201d modify the genes they need to survive and persist in specific tissues, as well as the genes required to mount protective responses. The mechanism involves epigenetic imprinting through demethylation of particular cytosine bases, which flags these genes for transcription factors. While this process optimizes immunity against pathogens, it can also become misdirected, contributing to diseases, such as allergies and chronic inflammation.<\/p>\n\n\n\n

The authors present the first comprehensive atlas of genome-wide demethylation patterns in memory T lymphocytes across human bone marrow, intestine, spleen, lung, skin, and blood. The findings show that memory T lymphocytes are differentially imprinted for residency and survival in each individual tissue. This atlas provides a valuable resource to identify molecular pathways critical for long-term immune maintenance and to explore novel options for treatment of chronic immune-mediated diseases.<\/p>\n\n\n\n

According to Dr. Jun Dong from the German Rheumatology Research Centre Berlin, corresponding author of the study: \u201cOur results reveal that T lymphocytes are not only imprinted for recall responses but also for residency in particular tissues. Their epigenetic imprint offers a unique opportunity to track them during secondary and chronic immune responses. We are gaining new insights into the division of labor in immunological memory\u2014both in protective immunity and in immune-mediated diseases such as rheumatic disorders<\/em>.\u201d<\/p>\n\n\n\n

The study was supported by the German Research Foundation (DFG), the Leibniz Collaborative Excellence Programme, the China Scholarship Council (CSC), the Chinesisch-Deutsches Zentrum f\u00fcr Wissenschaftsf\u00f6rderung (CDZ, DFG), the European Research Council (ERC), and the German Epigenome Programme \u2018DEEP\u2019.<\/p>\n\n\n\n

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Original publication<\/h2>\n \n \n
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\n \n Original publication<\/a>\n\n Deng, X., Du, W., Gasparoni, G. et al. Methylomes of human CD4 and CD8 memory T lymphocytes reveal tissue-specific epigenetic signatures for maintenance and recall function. Immun. Inflamm. 1, 13 (2025). https:\/\/doi.org\/10.1007\/s44466-025-00009-x<\/span>\n \n \n <\/span>\n <\/a>\n <\/div>\n <\/div>\n <\/div>\n <\/div>\n <\/section>\n\n\n\n\n
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Cell Biology<\/h2>\n \n
Radbruch lab<\/div>\n \n \n
\n learn more<\/span><\/a> <\/div>\n <\/div>\n\n
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Prof. Dr. rer. nat. Andreas Radbruch<\/h2>\n
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\n Programme Area 1, PA 1 \u2013 Cell and Tissue Rheumatology <\/p>\n

\n Group leader: Cell Biology <\/p>\n <\/div>\n <\/div>\n\n

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radbruch@drfz.de<\/a><\/p>\n <\/div>\n Prof. Dr. rer. nat. Andreas Radbruch<\/span><\/a>\n<\/article> <\/div>\n <\/div>\n <\/section>\n\n\n\n

Acknowlegements<\/h3>\n\n\n\n

The study was supported by the German Research Foundation (DFG), the Leibniz Collaborative Excellence Programme, the China Scholarship Council (CSC), the Chinesisch-Deutsches Zentrum f\u00fcr Wissenschaftsf\u00f6rderung (CDZ, DFG), the European Research Council (ERC), and the German Epigenome Programme \u2018DEEP\u2019.<\/p>\n\n\n\n

Tissue illustrations was generated using BioRender.<\/p>\n\n\n\n

<\/p>\n","protected":false},"excerpt":{"rendered":"

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