Immunohistopathological characterization and the impact of topical immunomodulatory therapy in oral chronic graft-versus-host disease: A pilot study

Objective: To characterize the immunohistopathological features of oral chronic graft-versus-host disease (cGVHD), and the impact of topical immunomodulatory therapy on the infiltrating cells. Material and Methods: Paired oral cGVHD biopsies obtained before (n = 12) and 1 month after treatment (n = ...

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Main Authors: Larson, A. (Author), Lerman, M. (Author), Motta, A.C.F (Author), Murphy, G.F (Author), Soiffer, R.J (Author), Treister, N.S (Author), Woo, S.-B (Author), Zhan, Q. (Author)
Format: Article
Language:English
Published: Blackwell Publishing Ltd 2018
Subjects:
Online Access:View Fulltext in Publisher
LEADER 05129nam a2201237Ia 4500
001 10.1111-odi.12813
008 220706s2018 CNT 000 0 und d
020 |a 1354523X (ISSN) 
245 1 0 |a Immunohistopathological characterization and the impact of topical immunomodulatory therapy in oral chronic graft-versus-host disease: A pilot study 
260 0 |b Blackwell Publishing Ltd  |c 2018 
856 |z View Fulltext in Publisher  |u https://doi.org/10.1111/odi.12813 
520 3 |a Objective: To characterize the immunohistopathological features of oral chronic graft-versus-host disease (cGVHD), and the impact of topical immunomodulatory therapy on the infiltrating cells. Material and Methods: Paired oral cGVHD biopsies obtained before (n = 12) and 1 month after treatment (n = 12) with topical dexamethasone (n = 8) or tacrolimus (n = 4) were characterized by immunohistochemistry using a panel of CD1a, CD3, CD4, CD8, CD20, CD31, CD62E, CD103, CD163, c-kit, and FoxP3. Controls included acute GVHD (aGVHD; n = 3), oral lichen planus (OLP; n = 5), and normal tissues (n = 5). Results: Oral cGVHD specimens prior to treatment were mainly characterized by basal cell squamatization, lichenoid inflammation, sclerosis, apoptosis, and lymphocytic exocytosis. The infiltrating cells in oral cGVHD primarily consisted of CD3+, CD4+, CD8+, CD103+, CD163+, and FoxP3+ cells, which were higher than in normal tissues. Topical dexamethasone or tacrolimus reduced neutrophilic exocytosis, basal cell squamatization, and lichenoid inflammation in oral cGVHD, and dexamethasone reduced the number of CD4+ and CD103+ cells. Conclusion: The high expression of CD3, CD4, CD8, CD103, CD163, and FoxP3 confirms that oral cGVHD is largely T-cell-driven with macrophage participation. The impact of topical immunomodulatory therapy was variable, reducing histological inflammatory features, but with a weak clinicopathological correlation. Topical dexamethasone reduced the expression of CD4 and CD103, which may offer novel therapeutic targets. © 2017 John Wiley & Sons A/S. Published by John Wiley & Sons Ltd. 
650 0 4 |a Administration, Topical 
650 0 4 |a adult 
650 0 4 |a Adult 
650 0 4 |a aged 
650 0 4 |a Aged 
650 0 4 |a Antigens, CD 
650 0 4 |a apoptosis 
650 0 4 |a Article 
650 0 4 |a biomarkers 
650 0 4 |a CD103 antigen 
650 0 4 |a CD163 antigen 
650 0 4 |a CD20 antigen 
650 0 4 |a CD3 antigen 
650 0 4 |a CD4 antigen 
650 0 4 |a CD8 antigen 
650 0 4 |a cell infiltration 
650 0 4 |a chronic graft versus host disease 
650 0 4 |a chronic graft-versus-host disease 
650 0 4 |a chronic lymphatic leukemia 
650 0 4 |a chronic myeloid leukemia 
650 0 4 |a clinical article 
650 0 4 |a controlled study 
650 0 4 |a dexamethasone 
650 0 4 |a Dexamethasone 
650 0 4 |a exocytosis 
650 0 4 |a female 
650 0 4 |a Female 
650 0 4 |a forkhead transcription factor 
650 0 4 |a Forkhead Transcription Factors 
650 0 4 |a FOXP3 protein, human 
650 0 4 |a glucocorticoid 
650 0 4 |a Glucocorticoids 
650 0 4 |a graft versus host reaction 
650 0 4 |a Graft vs Host Disease 
650 0 4 |a histopathology 
650 0 4 |a human 
650 0 4 |a human tissue 
650 0 4 |a Humans 
650 0 4 |a immunohistochemistry 
650 0 4 |a Immunohistochemistry 
650 0 4 |a immunology 
650 0 4 |a immunomodulation 
650 0 4 |a Immunomodulation 
650 0 4 |a immunopathology 
650 0 4 |a immunosuppressive agent 
650 0 4 |a Immunosuppressive Agents 
650 0 4 |a immunosuppressive treatment 
650 0 4 |a leukocyte antigen 
650 0 4 |a lichenoid 
650 0 4 |a macrophage 
650 0 4 |a Macrophages 
650 0 4 |a male 
650 0 4 |a Male 
650 0 4 |a mast cell 
650 0 4 |a metabolism 
650 0 4 |a middle aged 
650 0 4 |a Middle Aged 
650 0 4 |a mouth disease 
650 0 4 |a Mouth Diseases 
650 0 4 |a myelodysplastic syndrome 
650 0 4 |a myeloproliferative disorder 
650 0 4 |a neutrophil 
650 0 4 |a nonhodgkin lymphoma 
650 0 4 |a oral biopsy 
650 0 4 |a oral mucosa 
650 0 4 |a PADGEM protein 
650 0 4 |a pathology 
650 0 4 |a peripheral blood stem cell transplantation 
650 0 4 |a pilot study 
650 0 4 |a platelet endothelial cell adhesion molecule 1 
650 0 4 |a prednisone 
650 0 4 |a priority journal 
650 0 4 |a rapamycin 
650 0 4 |a sclerosis 
650 0 4 |a stem cell factor receptor 
650 0 4 |a T lymphocyte 
650 0 4 |a t6 antigen 
650 0 4 |a tacrolimus 
650 0 4 |a Tacrolimus 
650 0 4 |a T-Lymphocytes 
650 0 4 |a topical drug administration 
650 0 4 |a topical therapy 
650 0 4 |a transcription factor FOXP3 
650 0 4 |a young adult 
650 0 4 |a Young Adult 
700 1 |a Larson, A.  |e author 
700 1 |a Lerman, M.  |e author 
700 1 |a Motta, A.C.F.  |e author 
700 1 |a Murphy, G.F.  |e author 
700 1 |a Soiffer, R.J.  |e author 
700 1 |a Treister, N.S.  |e author 
700 1 |a Woo, S.-B.  |e author 
700 1 |a Zhan, Q.  |e author 
773 |t Oral Diseases