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Immunoelectron microscopy of acute graft versus host disease of the skin after allogeneic bone marrow transplantation.

机译:同种异体骨髓移植后皮肤的急性移植物抗宿主病的免疫电子显微镜检查。

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摘要

AIMS--To clarify the pathological mechanisms of acute cutaneous graft versus host disease (GvHD) following allogeneic bone marrow transplantation. METHODS--Skin biopsy specimens from five patients were examined by immunoelectron microscopy. A panel of monoclonal antibodies against T cell and natural killer cell subpopulations was used, including anti-CD4, -CD8, -CD16b, -CD56, -CD57, and -TCR delta 1 antibodies. RESULTS--All the specimens contained CD8+ cells, CD4+ cells, and CD56+ cells infiltrating the epidermis. Cells stained with anti-CD16b, -CD57, or -TCR delta 1 were very sparse or absent. Most of the CD8+ cells in the epidermis displayed morphological features of activated cytotoxic T lymphocytes and apposition of such cells to degenerating keratinocytes was shown. CD4+ cells outnumbered CD8+ cells in the epidermis in all five cases. Noticeable intercellular as well as intracellular oedema of keratinocytes was observed at the site of prominent CD4+ cell infiltration, suggesting that these also have a role as actual effector cells by secreting cytotoxic cytokines. CD56+ cells infiltrating the epidermis did not exhibit the characteristic ultrastructural morphology of the natural killer cells thus far examined, and their lineage remained uncertain. CONCLUSIONS--These data provide direct evidence that CD8+ cytotoxic T cells attack keratinocytes, and further suggest that CD4+ cells as well as CD56+ cells participate in the cellular pathogenesis of acute cutaneous GvHD.
机译:目的-为了阐明同种异体骨髓移植后急性皮肤移植物抗宿主疾病(GvHD)的病理机制。方法-通过免疫电子显微镜检查了五名患者的皮肤活检标本。使用了一组针对T细胞和天然杀伤细胞亚群的单克隆抗体,包括抗CD4,-CD8,-CD16b,-CD56,-CD57和-TCR delta 1抗体。结果-所有标本均包含浸润表皮的CD8 +细胞,CD4 +细胞和CD56 +细胞。用抗CD16b,-CD57或-TCR delta 1染色的细胞非常稀疏或缺失。表皮中的大多数CD8 +细胞均表现出活化的细胞毒性T淋巴细胞的形态特征,并显示了此类细胞与变性角质形成细胞的结合。在所有五种情况下,表皮中的CD4 +细胞均超过CD8 +细胞。在突出的CD4 +细胞浸润部位观察到了明显的角质形成细胞间和细胞内水肿,表明它们还通过分泌细胞毒性细胞因子而起着实际效应细胞的作用。到目前为止,渗透到表皮的CD56 +细胞并未表现出自然杀伤细胞的特征性超微结构形态,并且其谱系仍然不确定。结论-这些数据提供了CD8 +细胞毒性T细胞攻击角质形成细胞的直接证据,并进一步表明CD4 +细胞以及CD56 +细胞参与急性皮肤GvHD的细胞发病机制。

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