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05129nam a2201237Ia 4500 |
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10.1111-odi.12813 |
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220706s2018 CNT 000 0 und d |
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|a 1354523X (ISSN)
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|a Immunohistopathological characterization and the impact of topical immunomodulatory therapy in oral chronic graft-versus-host disease: A pilot study
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|b Blackwell Publishing Ltd
|c 2018
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|z View Fulltext in Publisher
|u https://doi.org/10.1111/odi.12813
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|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.
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|a Administration, Topical
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|a adult
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|a Adult
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|a aged
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|a Aged
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|a Antigens, CD
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|a apoptosis
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|a Article
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|a biomarkers
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|a CD103 antigen
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|a CD163 antigen
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|a CD20 antigen
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|a CD3 antigen
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|a CD4 antigen
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|a CD8 antigen
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|a cell infiltration
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|a chronic graft versus host disease
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|a chronic graft-versus-host disease
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|a chronic lymphatic leukemia
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|a chronic myeloid leukemia
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|a clinical article
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|a controlled study
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|a dexamethasone
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|a Dexamethasone
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|a exocytosis
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|a female
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|a Female
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|a forkhead transcription factor
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|a Forkhead Transcription Factors
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|a FOXP3 protein, human
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|a glucocorticoid
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|a Glucocorticoids
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|a graft versus host reaction
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|a Graft vs Host Disease
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|a histopathology
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|a human
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|a human tissue
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|a Humans
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|a immunohistochemistry
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|a Immunohistochemistry
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|a immunology
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|a immunomodulation
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|a Immunomodulation
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|a immunopathology
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|a immunosuppressive agent
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|a Immunosuppressive Agents
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|a immunosuppressive treatment
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|a leukocyte antigen
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|a lichenoid
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|a macrophage
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|a Macrophages
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|a male
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|a Male
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|a mast cell
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|a metabolism
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|a middle aged
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|a Middle Aged
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|a mouth disease
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|a Mouth Diseases
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|a myelodysplastic syndrome
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|a myeloproliferative disorder
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|a neutrophil
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|a nonhodgkin lymphoma
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|a oral biopsy
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|a oral mucosa
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|a PADGEM protein
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|a pathology
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|a peripheral blood stem cell transplantation
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|a pilot study
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|a platelet endothelial cell adhesion molecule 1
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|a prednisone
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|a priority journal
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|a rapamycin
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|a sclerosis
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|a stem cell factor receptor
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|a T lymphocyte
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|a t6 antigen
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|a tacrolimus
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|a Tacrolimus
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|a T-Lymphocytes
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|a topical drug administration
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|a topical therapy
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|a transcription factor FOXP3
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|a young adult
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|a Young Adult
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|a Larson, A.
|e author
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|a Lerman, M.
|e author
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|a Motta, A.C.F.
|e author
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|a Murphy, G.F.
|e author
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|a Soiffer, R.J.
|e author
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|a Treister, N.S.
|e author
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|a Woo, S.-B.
|e author
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|a Zhan, Q.
|e author
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|t Oral Diseases
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