PMID- 31290564 OWN - NLM STAT- MEDLINE DCOM- 20191113 LR - 20200108 IS - 1346-8138 (Electronic) IS - 0385-2407 (Linking) VI - 46 IP - 9 DP - 2019 Sep TI - Infliximab reduces activated myeloid dendritic cells, different macrophage subsets and CXCR3-positive cells in granuloma annulare. PG - 808-811 LID - 10.1111/1346-8138.14981 [doi] AB - Disseminated granuloma annulare (GA) is a rare granulomatous dermatitis of unknown etiology. Treatment is often challenging and lack of a uniformly effective treatment, adds to the disease morbidity. Tumor necrosis factor (TNF)-alpha is an important cytokine in granuloma formation and previous reports have shown improvement of disseminated GA with anti-TNF-alpha therapy. Nevertheless, the underlying mechanism of actions of TNF-alpha inhibitors in GA remains unclear. Our aim was to evaluate alterations in the inflammatory infiltrate in a patient who experienced complete clearance of GA after treatment with infliximab. A skin biopsy was obtained before and 24 weeks after treatment with infliximab 5 mg/kg at weeks 0, 2, 6, 14 and 24. Immunohistochemical stains were performed in pre- and post-treatment biopsy specimens using CD1a, CD4, CD8, CD11c, CD32, CD68, CD69, CD163, CD183 and human leukocyte antigen (HLA)-DR to characterize alterations of the infiltrates. Parallel with clinical improvement, we observed a marked decrease in myeloid (CD11c) dendritic cells, different macrophage subsets (CD68, CD32, CD163) and T cells. In addition, a marked reduction of activation markers (HLA-DR, CD69) and CD183(+) (CXCR3) cells was observed in post-treatment biopsy specimens. In conclusion, the clinical improvement of disseminated GA by infliximab is paralleled by inhibition of activated myeloid dendritic cells, different macrophage subsets and type 1 T cells. CI - (c) 2019 Japanese Dermatological Association. FAU - Burgler, Christina AU - Burgler C AUID- ORCID: 0000-0003-1412-1869 AD - Department of Dermatology and Venereology, Inselspital, Bern University Hospital, University of Bern, Bern, Switzerland. FAU - Vinay, Keshavamurthy AU - Vinay K AD - Department of Dermatology, Venereology and Leprology, Postgraduate Institute of Medical Education and Research, Chandigarh, India. FAU - Hafliger, Stefanie AU - Hafliger S AD - Department of Dermatology and Venereology, Inselspital, Bern University Hospital, University of Bern, Bern, Switzerland. FAU - Klotgen, Hans-Wilhelm AU - Klotgen HW AD - Department of Dermatology and Venereology, Inselspital, Bern University Hospital, University of Bern, Bern, Switzerland. FAU - Yawalkar, Nikhil AU - Yawalkar N AD - Department of Dermatology and Venereology, Inselspital, Bern University Hospital, University of Bern, Bern, Switzerland. LA - eng PT - Case Reports PT - Journal Article DEP - 20190710 PL - England TA - J Dermatol JT - The Journal of dermatology JID - 7600545 RN - 0 (CXCR3 protein, human) RN - 0 (Dermatologic Agents) RN - 0 (Receptors, CXCR3) RN - 0 (TNF protein, human) RN - 0 (Tumor Necrosis Factor-alpha) RN - B72HH48FLU (Infliximab) SB - IM MH - Aged MH - Biopsy MH - Dendritic Cells/*drug effects/immunology/metabolism MH - Dermatologic Agents/*pharmacology/therapeutic use MH - Granuloma Annulare/*drug therapy/immunology/pathology MH - Humans MH - Infliximab/*pharmacology/therapeutic use MH - Macrophages/*drug effects/immunology/metabolism MH - Male MH - Receptors, CXCR3/immunology/metabolism MH - Skin/cytology/drug effects/pathology MH - Treatment Outcome MH - Tumor Necrosis Factor-alpha/antagonists & inhibitors/immunology OTO - NOTNLM OT - T cells OT - dendritic cells OT - granuloma annulare OT - infliximab OT - macrophages EDAT- 2019/07/11 06:00 MHDA- 2019/11/14 06:00 CRDT- 2019/07/11 06:00 PHST- 2018/12/21 00:00 [received] PHST- 2019/05/21 00:00 [accepted] PHST- 2019/07/11 06:00 [pubmed] PHST- 2019/11/14 06:00 [medline] PHST- 2019/07/11 06:00 [entrez] AID - 10.1111/1346-8138.14981 [doi] PST - ppublish SO - J Dermatol. 2019 Sep;46(9):808-811. doi: 10.1111/1346-8138.14981. Epub 2019 Jul 10.