You are here: Department of Dermatology, Venerology and Allergology

​Research at the Department of Dermatology, Venereology, and Allergology

​​​Dermatological research at Leipzig University Hospital combines clinical questions with basic scientific approaches to better understand the pathophysiology, diagnostics, and treatment of skin diseases. Our research groups address a broad spectrum of topics—from inflammatory dermatoses to wound healing and tumor biology to immunological and allergological aspects. 

The focus is always on a translational medical approach: findings from basic research should contribute to long-term improvements in patient care.

Prof. Dr. med. Manfred Kunz

The research focus of the Kunz working group is on the molecular biological basis of malignant melanoma and the immunology of psoriasis and lupus erythematosus. In addition to genetic studies on human samples and corresponding mouse models, this also includes functional cell biological analyses of melanoma cells, keratinocytes, fibroblasts and T cells. In particular, we have recently been using single-cell sequencing technology (single-cell RNA-seq and single-cell ATAC-seq) and spatial sequencing. The results are being incorporated into a CAR T cell project on melanoma.
 

Group leader

Prof. Dr. med. Manfred Kunz
 

PhD and MD students

  • A.Stubenvoll (PhD)
  • C. Schultz (PhD)
  • M. Lingner Chango (PhD)
  • T. Reidenbach (MD)
  • A. Schönberg (MD)
 

Topics

  • Intracellular signal transduction
  • RNA interference
  • Cellular heterogeneity in melanoma, psoriasis and lupus erythematosus
  • Receptor-ligand interactions in immune processes
  • Chromatin structures in immune cells
  • CAR T cells​

Selected Publications​​

  • Stubenvoll A, Schmidt M, Moeller J, Chango MAL, Schultz C, Antoniadou O, Loeffler-Wirth H, Bernhart S, Große F, Thier B, Paschen A, Anderegg U, Simon JC, Ziemer M, Schoeder CT, Binder H, Kunz M. Single-cell transcriptomics and epigenomics point to CD58-CD2 interaction in controlling primary melanoma growth and immunity. Cancer Commun (Lond). 2025 Jan 15. doi: 10.1002/cac2.12651.
  • Karras F, Kunz M. Patient-derived melanoma models. Pathol Res Pract. 2024 Jul; 259:155231. doi: 10.1016/j.prp.2024.155231.
  • Frost B, Schmidt M, Klein B, Loeffler-Wirth H, Krohn K, Reidenbach T, Binder H, Stubenvoll A, Simon JC, Saalbach A, Kunz M. Single-cell transcriptomics reveals prominent expression of IL-14, IL-18, and IL-32 in psoriasis. Eur J Immunol. 2023 Nov;53(11):e2250354. doi: 10.1002/eji.202250354.
  • Klein B, Kunz M. Current concepts of photosensitivity in cutaneous lupus erythematosus. Front Med (Lausanne). 2022 Aug 25;9:939594. doi: 10.3389/fmed.2022.939594.
  • Saalbach A, Kunz M. Impact of Chronic Inflammation in Psoriasis on Bone Metabolism. Front Immunol. 2022 Jun 23;13:925503. doi: 10.3389/fimmu.2022.925503.
  • Klein B, Treudler R, Dumann K, Boldt A, Schumann I, Simon JC, Kunz M. Clinical response of CARD14-associated papulosquamous eruption to an anti-interleukin-17A antibody. Br J Dermatol. 2022 Sep;187(3):419-422. doi: 10.1111/bjd.21229.
  • Kunz M. Melanoma development: stage-dependent cancer competence of the melanocytic lineage. Signal Transduct Target Ther. 2021 Dec 20;6(1):433. doi: 10.1038/s41392-021-00854-3.
  • Reschke R, Gussek P, Boldt A, Sack U, Köhl U, Lordick F, Gora T, Kreuz M, Reiche K, Simon JC, Ziemer M, Kunz M. Distinct Immune Signatures Indicative of Treatment Response and Immune-Related Adverse Events in Melanoma Patients under Immune Checkpoint Inhibitor Therapy. Int J Mol Sci. 2021 Jul 27;22(15):8017. doi: 10.3390/ijms22158017
  • Kunz M, Brandl M, Bhattacharya A, Nobereit-Siegel L, Ewe A, Weirauch U, Hering D, Reinert A, Kalwa H, Guzman J, Weigelt K, Wach S, Taubert H, Aigner A. Nanoparticle-complexed antimiRs for inhibiting tumor growth and metastasis in prostate carcinoma and melanoma. J Nanobiotechnology. 2020 Nov 23;18(1):173. doi: 10.1186/s12951-020-00728-w.
  • Kunz M, Löffler-Wirth H, Dannemann M, Willscher E, Doose G, Kelso J, Kottek T, Nickel B, Hopp L, Landsberg J, Hoffmann S, Tüting T, Zigrino P, Mauch C, Utikal J, Ziemer M, Schulze HJ, Hölzel M, Roesch A, Kneitz S, Meierjohann S, Bosserhoff A, Binder H, Schartl M. RNA-seq analysis identifies different transcriptomic types and developmental trajectories of primary melanomas. Oncogene. 2018 Nov;37(47):6136-6151. doi: 10.1038/s41388-018-0385-y.​


Prof. Dr. rer. nat. Sandra Franz

​​Professor for Skin Regeneration

The research team at AG Franz is interested on the complexity of inflammatory and wound healing processes in the skin. We investigate the coordinated interaction of immune cells and skin cells during tissue repair and how changes in this cell-cell communication contribute to wound healing disorders in chronic wounds and skin fibrosis. In addition, we explore the influence of metabolic factors on skin tissue function and investigate how local changes in iron and metabolites influence cell growth and communication in skin homeostasis and tissue repair. Another research focus are biomaterial-based therapy strategies to support wound healing processes and skin regeneration. In interdisciplinary collaborations with materials scientists, we develop various biomaterials that can induce effective skin wound healing by modulating local immune responses and triggering repair programs in tissue cells.

Research focus Overview​


​Group leader

Prof. Dr. rer. nat. Sandra Franz
 

Scientists

Dr. Marta Torregrossa (Post-Doc)  
Dr. Ravinder Kandi (Post-Doc)
Jonathan Kessler (cand Dr. med)​​
 

Technicans

Elena Elter
Inka Forstreuter

Press release​

Relevant publications​​

  • Ertel A, Anderegg U, Franz S, Saalbach A. Dermal white adipose tissue derived IL-33 regulates interleukin 4/13 expression in myeloid cells during inflammation. J Invest Dermatol. 2023, doi: 10.1016/j.jid.2024.05.026​
  • ​​Ferrer RA, Torregrossa M, Franz S. Germ-free, carefree: injured skin uses IL-24 to kick-start repair independent of pathogen-recognition. Signal Transduct Target Ther. 2023, doi: 10.1038/s41392-023-01609-y.
  • Franz S, Ertel A, Engel KM, Simon JC, Saalbach A. Overexpression of S100A9 in obesity impairs macrophage differentiation via TLR4-NFkB-signaling worsening inflammation and wound healing. Theranostics. 2022, doi: 10.7150/thno.67174
  • Schmaus A, Rothley M, Schreiber C, Möller S, Roßwag S, Franz S, Garvalov BK, Thiele W, Spataro S, Herskind C, Prunotto M, Anderegg U, Schnabelrauch M, Sleeman J. Sulfated hyaluronic acid inhibits the hyaluronidase CEMIP and regulates the HA metabolism, proliferation and differentiation of fibroblasts. Matrix Biol. 2022, doi: 10.1016/j.matbio.2022.04.001
  • Hauck S, Zager P, Halfter N, Wandel E, Torregrossa M, Kakpenova A, Rother S, Ordieres M, Räthel S, Berg A, Möller S, Schnabelrauch M, Simon JC , Hintze V, Franz S. Collagen/hyaluronan based hydrogels releasing sulfated hyaluronan improve dermal wound healing in diabetic mice via reducing inflammatory macrophage activity. Bioact Mat. 2021, doi: 10.1016/j.bioactmat.2021.04.026
  • Torregrossa M, Kakpenova A, Simon JC, Franz S. Modulation of macrophage functions by ECM-inspired wound dressings – a promising therapeutic approach for chronic wounds. Biol Chem. 2021, aop, doi: 10.1515/hsz-2021-0145
  • Spiller S, Wippold T, Bellmann-Sickert K, Franz S, Saalbach A, Anderegg U,  Beck-Sickinger AG. Protease-Triggered Release of Stabilized CXCL12 from Coated Scaffolds in an Ex Vivo Wound Model. Pharmaceutics. 2021, doi: 10.3390/pharmaceutics13101597
  • Li H, Masieri FF, Schneider M, Kottek T, Hahnel S, Yamauchi K, Obradovic D, Seon J-K, Yun SJ, Ferrer RA, Franz S, Simon JC, Lethaus B, Savkovic V. Autologous, Non-Invasively Available Mesenchymal Stem Cells from the Outer Root Sheath of Hair Follicle Are Obtainable by Migration from Plucked Hair Follicles and Expandable in Scalable Amounts. Cells. 2020, doi: 10.3390/cells9092069
  • Gay D, Ghinatti G, Guerrero-Juarez CF, Ferrer RA, Ferri F, Murakami S, Gault N, Barroca V, Rombeau I, Mauffrey P, Irbah L, Treffeisen E, Franz S, Boissonnas A, Combadiere C, Plikus MV, Romeo P. Phagocytosis of Wnt inhibitor SFRP4 by late wound macrophages drives chronic Wnt activity for fibrotic skin healing. Sci Adv. 2019, doi: 10.1126/sciadv.aay3704
  • Herbert D, Franz S, Popkova Y, Anderegg U, Schiller J, Schwede K, Lorz A, Simon JC, Saalbach A. High-Fat Diet Exacerbates Early Psoriatic Skin Inflammation Independent of Obesity: Saturated Fatty Acids as Key Players. J Invest Dermatol. 2018, doi: 10.1016/j.jid.2018.03.1522
  • Lohmann N, Schirmer L, Atallah P, Wandel E, Ferrer RA, Werner C, Simon JC, Franz S*, Freudenberg U*,. Glycosaminoglycan-based hydrogels capture chemokines and rescue defective wound healing in mice. Sci Transl Med. 2017, doi: 10.1126/scitranslmed.aai9044 (*equal contribution)
  • Ferrer RA, Saalbach A, Grünwedel M, Lohmann N, Forstreuter I, Saupe S, Wandel E, Simon JC, Franz S. Dermal fibroblasts promote alternative macrophage activation improving impaired wound healing. J Invest Dermatol. 2017, doi: 10.1016/j.jid.2016.11.035
  • Jouy F, Lohmann N, Wandel E, Ruiz-Gómez G, Pisabarro MT, Beck-Sickinger AG, Schnabelrauch M, Moeller S, Simon JC, Kalkhof S, von Bergen M, Franz S. Sulfated hyaluronan attenuates inflammatory signaling pathways in macrophages involving induction of antioxidants. Proteomics. 2017, doi: 10.1002/pmic.201700082
  • Friedemann M, Kalbitzer L, Franz S, Moeller S, Schnabelrauch S, Simon JC, Pompe T,  Franke K. Instructing Human Macrophage Polarization by Stiffness and Glycosaminoglycan Functionalization in 3D Collagen Networks. Adv Healthc Mater. 2017, doi: 10.1002/adhm.201600967
  • Franz S, Allenstein F, Kajahn J, Forstreuter I, Hintze V,  Möller S, Simon JC. Artificial extracellular matrices composed of collagen I and high-sulfated hyaluronan promote phenotypic and functional modulation of human pro-inflammatory M1 macrophages. Acta Biomater 2013, doi: 10.1016/j.actbio.2012.11.016
  • Franz S, Rammelt S, Scharnweber D, Simon JC. Immune responses to implants – a review of the implications for the design of immunomodulatory biomaterials. Biomaterials. 2011, doi: 10.1016/j.biomaterials.2011.05.078​


AG Andrologie Prof. Paasch / Prof. Grunewald

The Paasch/Grunewald research group conducts research into the causes, treatment, and prevention of male infertility.

SCIENTIFIC DIRECTORS

Prof. Dr. Uwe Paasch and Prof. Dr. Sonja Grunewald

PhD Students

Janet Blaurock
Bo Henning Jedamski

Technical Staff

Nicole Schenk
Cornelia Schneider


Joint Projects:

BMBF Funding (LE-REP, CERES Network)
Fertitox Register​
Philipp-Rosenthal-Str., Haus 10
04103 Leipzig
Phone:
0341 - 97 18666
Fax:
0341 - 97 18609
Map