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Exp Dermatol ; 30(12): 1814-1819, 2021 12.
Article in English | MEDLINE | ID: mdl-34223669

ABSTRACT

Graft-versus-host disease (GvHD) is a major complication following stem-cell or solid-organ transplantation. Accurate diagnosis of cutaneous GvHD is challenging, given that drug eruptions and viral rashes may present with similar clinical/histological manifestations. Specific markers are not available. We performed the histological examination of biopsy samples from acute GvHD (aGvHD; n = 54), Stevens-Johnson syndrome/toxic epidermal necrolysis (SJS/TEN; n = 27), maculopapular drug eruption (MDE; n = 26) and healthy controls (n = 26). Samples of aGvHD showed a decrease in Langerhans cells (LC, p = 0.0001) and an increase in macrophages (MΦ, p = 0.0001) compared to healthy skin. Compared to SJS/TEN, MDE and healthy skin, aGvHD biopsies contained greater numbers of CD4+ and CD8+ T cells. The majority of CD4+ T-helper cells were localized in the upper dermis, whereas cytotoxic CD8+ T cells were found in the epidermis. Increased numbers of CD56+ natural killer (NK) cells in the upper dermis of aGvHD skin (p = 0.007) were not observed in controls or SJS/TEN and MDE. There were no differences in elafin staining between aGvHD and the latter two conditions. Acute GvHD appears to have a distinct inflammatory cell profile (T cells/NK cells) that may aid establishing in a more accurate diagnosis, especially when used to rule out differential diagnoses such as SJS/TEN or MDE.


Subject(s)
Graft vs Host Disease/diagnosis , Organ Transplantation , Skin/pathology , Biomarkers , CD8-Positive T-Lymphocytes/metabolism , Case-Control Studies , Diagnosis, Differential , Drug Eruptions/diagnosis , Drug Eruptions/immunology , Drug Eruptions/pathology , Graft vs Host Disease/immunology , Graft vs Host Disease/pathology , Humans , Killer Cells, Natural/metabolism , Stevens-Johnson Syndrome/diagnosis , Stevens-Johnson Syndrome/immunology
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