{"id":8375,"date":"2024-08-29T12:40:00","date_gmt":"2024-08-29T12:40:00","guid":{"rendered":"https:\/\/www.drfz.de\/news\/neuer-ausloeser-fuer-nierenschaeden-bei-lupus-identifiziert\/"},"modified":"2025-02-14T14:29:31","modified_gmt":"2025-02-14T14:29:31","slug":"neuer-ausloeser-fuer-nierenschaeden-bei-lupus-identifiziert","status":"publish","type":"post","link":"https:\/\/www.drfz.de\/en\/neuigkeiten\/neuer-ausloeser-fuer-nierenschaeden-bei-lupus-identifiziert\/","title":{"rendered":"New cause of kidney damage in lupus identified"},"content":{"rendered":"\n

Researchers at Charit\u00e9 \u2013 Universit\u00e4tsmedizin Berlin, the German Rheumatology Research Center (DRFZ) and the Max Delbr\u00fcck Center (MDC) have discovered that specialised immune cells, known as innate lymphoid cells (ILC), play a key role in kidney damage (lupus nephritis) in lupus patients. These cells exacerbate the organ damage that was mainly associated to autoantibodies until now. The study, published in Nature<\/em>, challenges traditional views and could influence future antibody therapies for lupus. Lupus affects around five million people worldwide, mainly young women, and can lead to severe kidney damage.<\/p>\n\n\n\n

The research team led by Antigoni Triantafyllopoulou and Andreas Diefenbach, both Charit\u00e9-liaison group leaders at the DRFZ, and Masatoshi Kanda from the MDC, in cooperation with Mir-Farzin Mashreghi from the DRFZ, examined the entire kidney cell repertoire  using single-cell RNA sequencing. They analysed almost 100,000 kidney and immune cells to identify the circuits controlled by the ILCs in order to understand the mechanism of lupus nephritis.<\/p>\n\n\n\n

Until now, it was assumed that autoantibodies alone cause kidney inflammation. However, this study has shown that specialised ILC with the receptor NKp46, play a key role in triggering kidney damage. These cells produce the protein GM-CSF, which leads to the proliferation of macrophages that cause tissue damage. By blocking NKp46, the kidney damage was significantly reduced, even though the amount of autoantibodies did not change.<\/p>\n\n\n\n

These findings could lead to the development of new antibody therapies to prevent severe kidney damage in lupus patients.<\/p>\n\n\n\n

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Link to Charit\u00e9 press lelease<\/a><\/div>\n<\/div>\n\n\n\n
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Prof. Antigoni Triantafyllopoulou, MD<\/h2>\n
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\n Programme Area 1, PA 1 \u2013 Cell and Tissue Rheumatology <\/p>\n

\n Group leader: Macrophage biology and innate cellular networks in chronic inflammatory diseases <\/p>\n Liaison working group with Charit\u00e9 – Rheumatology and Clinical Immunology<\/p>\n <\/div>\n <\/div>\n\n

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triantafyllopoulou@drfz.de<\/a><\/p>\n <\/div>\n Prof. Antigoni Triantafyllopoulou, MD<\/span><\/a>\n<\/article>\n\n

\n \"\" <\/div>\n
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Prof. Dr. Andreas Diefenbach<\/h2>\n
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\n Programme Area 1, PA 1 \u2013 Cell and Tissue Rheumatology <\/p>\n

\n Group leader: Developmental and Mucosal Immunology <\/p>\n Liaison working group with Charit\u00e9 – Microbiology, Infectious Diseases and Immunology,<\/p>\n <\/div>\n <\/div>\n\n

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andreas.diefenbach@charite.de<\/a><\/p>\n <\/div>\n Prof. Dr. Andreas Diefenbach<\/span><\/a>\n<\/article> <\/div>\n <\/div>\n <\/section>\n\n\n\n

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\n \n original publication<\/a>\n\n Biniaris-Georgallis SI, Aschman T, Stergioula K, Schreiber F, Jafari V, Taranko A, Karmalkar T, Kasapi A, Lenac Rovis T, Jelencic V, Bejarano DA, Fabry L, Papacharalampous M, Mattiola I, Molgora M, Hou J, Hublitz KW, Heinrich F, Guerra GM, Durek P, Patone G, Lindberg EL, Maatz H, H\u00f6lsken O, Kr\u00f6nke G, Mortha A, Voll RE, Clarke AJ, Hauser AE, Colonna M, Thurley K, Schlitzer A, Schneider C, Stamatiades EG, Mashreghi MF, Jonjic S, H\u00fcbner N, Diefenbach A, Kanda M, Triantafyllopoulou A. Amplification of autoimmune organ damage by NKp46-activated ILC1. Nature. 2024 Aug 13. doi: 10.1038\/s41586-024-07907-x. Epub ahead of print. PMID: 39137897.<\/span>\n \n \n <\/span>\n <\/a>\n <\/div>\n <\/div>\n <\/div>\n <\/div>\n <\/section>\n\n","protected":false},"excerpt":{"rendered":"

Researchers at Charit\u00e9 \u2013 Universit\u00e4tsmedizin Berlin, the German Rheumatology Research Center (DRFZ) and the Max Delbr\u00fcck Center (MDC) have discovered that specialised immune cells, known\u2026<\/p>\n","protected":false},"author":9,"featured_media":4741,"comment_status":"closed","ping_status":"closed","sticky":false,"template":"","format":"standard","meta":{"_acf_changed":false,"footnotes":""},"categories":[291],"tags":[413,492,459],"programme-area-tax":[179],"working-group-tax":[245,254],"class_list":["post-8375","post","type-post","status-publish","format-standard","has-post-thumbnail","hentry","category-publications","tag-macrophages-in-chronic-inflammation","tag-program-area-1","tag-triantafyllopoulou-en","programme-area-tax-programme-area-1","working-group-tax-developmental-and-mucosal-immunology","working-group-tax-macrophage-biology-and-innate-cellular-networks-in-chronic-inflammatory-diseases"],"acf":[],"yoast_head":"\nNew cause of kidney damage in lupus identified - DRFZ<\/title>\n<meta name=\"robots\" content=\"index, follow, max-snippet:-1, max-image-preview:large, max-video-preview:-1\" \/>\n<link rel=\"canonical\" href=\"https:\/\/www.drfz.de\/en\/neuigkeiten\/neuer-ausloeser-fuer-nierenschaeden-bei-lupus-identifiziert\/\" \/>\n<meta property=\"og:locale\" content=\"en_US\" \/>\n<meta property=\"og:type\" content=\"article\" \/>\n<meta property=\"og:title\" content=\"New cause of kidney damage in lupus identified - DRFZ\" \/>\n<meta property=\"og:description\" content=\"Researchers at Charit\u00e9 \u2013 Universit\u00e4tsmedizin Berlin, the German Rheumatology Research Center (DRFZ) and the Max Delbr\u00fcck Center (MDC) have discovered that specialised immune cells, known\u2026\" \/>\n<meta property=\"og:url\" content=\"https:\/\/www.drfz.de\/en\/neuigkeiten\/neuer-ausloeser-fuer-nierenschaeden-bei-lupus-identifiziert\/\" \/>\n<meta property=\"og:site_name\" content=\"DRFZ\" \/>\n<meta property=\"article:publisher\" 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