Department of Pathology, Otago Medical School, University of Otago, Dunedin, New Zealand.
Department of Pharmacology and Toxicology, School of Biomedical Sciences, University of Otago, Dunedin, New Zealand.
Immunology. 2021 May;163(1):98-104. doi: 10.1111/imm.13311. Epub 2021 Mar 1.
The role of antigen-presenting cells in the skin immune system, in particular Langerhans cells and dendritic cells, has not been well defined. We recently published a study in 'Immunology' where we reported that the loss of langerin-positive cells in the skin accelerated wound repair in the Lang-DTR mouse. The study published here by Li, et al. reports delayed wound closure following depletion of CD11c-positive cells in the CD11c-DTR mouse. In this commentary, we attribute the differences between these results to several factors that differ between the studies including the depletion of different cell populations; differences in the age and the sex of mice; differences in antibiotic use between the studies; and differences in the location of the biopsies that were taken. Here, we describe the impact of these differences on wound healing and conclude that further standardization of the wound model, and further characterization of the specific cells that are depleted in these mice, is necessary to better understand how antigen-presenting cells contribute to wound healing.
抗原呈递细胞在皮肤免疫系统中的作用,特别是朗格汉斯细胞和树突状细胞,尚未得到很好的定义。我们最近在《免疫学》上发表了一项研究,报告称皮肤中 langerin 阳性细胞的缺失加速了 Lang-DTR 小鼠的伤口修复。李等人在这里发表的研究报告称,在 CD11c-DTR 小鼠中耗尽 CD11c 阳性细胞后,伤口愈合延迟。在这篇评论中,我们将这些结果之间的差异归因于几个因素,包括研究之间不同的细胞群耗竭;不同年龄和性别的小鼠;研究之间抗生素使用的差异;以及进行活检的位置的差异。在这里,我们描述了这些差异对伤口愈合的影响,并得出结论,需要进一步规范伤口模型,并进一步表征这些小鼠中耗尽的特定细胞,以更好地了解抗原呈递细胞如何促进伤口愈合。