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全身性白癜风患者的 CD8+ 细胞毒性 T 淋巴细胞的整体激活与调节性 T 细胞的损伤有关。

Global activation of CD8+ cytotoxic T lymphocytes correlates with an impairment in regulatory T cells in patients with generalized vitiligo.

机构信息

Departments of dermatology, Zhongshan Hospital, Fudan University, Shanghai, China.

出版信息

PLoS One. 2012;7(5):e37513. doi: 10.1371/journal.pone.0037513. Epub 2012 May 23.

DOI:10.1371/journal.pone.0037513
PMID:22649532
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3359382/
Abstract

Melanocyte-specific CD8(+) cytotoxic T lymphocytes (CTLs) play a pivotal role in vitiligo-induced depigmentation. Yet, the mechanisms underlying the high frequency of generalized autoimmune disorders associated with generalized vitiligo (GV) are unknown. We hypothesized that an imbalance between activated CD8(+) CTLs and regulatory T cells (Tregs) exists in patients with GV . Assessment of the circulating CD8(+) CTLs and Tregs by flow cytometric analysis revealed an obvious expansion of CD8(+) CTLs and a concomitant decrease in Treg cells in GV patients. The percentages of skin infiltrating CD8(+) CTLs and Tregs were evaluated by immunohistochemistry and revealed dramatically increased numbers of both CD8(+) CTLs and Tregs in the perilesional skin of GV patients. However, peripheral Tregs were impaired in their ability to suppress the proliferation and cytolytic capacity of autologous CD8(+) T cells, suggesting that a functional failure of Tregs and the hyper-activation of CD8(+) CTLs may contribute to progressive GV. Our data indicate that reduced numbers and impaired function of natural Tregs fail to control the widespread activation of CD8(+) CTLs, which leads to the destruction of melanocytes and contributes to the elevated frequency of various associated autoimmune diseases. This knowledge furthers our understanding of the mechanisms of immune tolerance that are impaired in GV patients and may aid in the future development of effective immunotherapy for GV patients.

摘要

黑素细胞特异性 CD8(+)细胞毒性 T 淋巴细胞 (CTL) 在白癜风诱导的色素脱失中起关键作用。然而,与广泛白癜风 (GV) 相关的全身性自身免疫性疾病高发的机制尚不清楚。我们假设 GV 患者中存在激活的 CD8(+)CTLs 和调节性 T 细胞 (Tregs) 之间的失衡。通过流式细胞术分析评估循环中的 CD8(+)CTLs 和 Tregs,发现 GV 患者的 CD8(+)CTLs 明显扩增,同时 Treg 细胞减少。通过免疫组织化学评估皮肤浸润的 CD8(+)CTLs 和 Tregs,发现 GV 患者皮损周围皮肤中 CD8(+)CTLs 和 Tregs 的数量明显增加。然而,外周 Tregs 抑制自身 CD8(+)T 细胞增殖和细胞毒性的能力受损,这表明 Tregs 功能衰竭和 CD8(+)CTLs 的过度激活可能导致 GV 的进行性发展。我们的数据表明,天然 Tregs 的数量减少和功能受损不能控制 CD8(+)CTLs 的广泛激活,这导致黑色素细胞的破坏,并导致各种相关自身免疫性疾病的高发。这一知识增进了我们对 GV 患者免疫耐受机制受损的理解,并可能有助于未来为 GV 患者开发有效的免疫治疗方法。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b52c/3359382/98c296b9be5e/pone.0037513.g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b52c/3359382/76902cc99fa0/pone.0037513.g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b52c/3359382/e6fcc31ec34a/pone.0037513.g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b52c/3359382/ae83f1d58927/pone.0037513.g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b52c/3359382/98c296b9be5e/pone.0037513.g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b52c/3359382/76902cc99fa0/pone.0037513.g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b52c/3359382/e6fcc31ec34a/pone.0037513.g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b52c/3359382/ae83f1d58927/pone.0037513.g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b52c/3359382/98c296b9be5e/pone.0037513.g004.jpg

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