• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

超越自我保护:眼睛在生命早期指导系统性免疫耐受

Looking beyond Self-Protection: The Eyes Instruct Systemic Immune Tolerance Early in Life.

作者信息

Villafán Horacio, Gutiérrez-Ospina Gabriel

机构信息

Programa de Doctorado en Ciencias Biológicas, Unidad de Posgrado, Circuito de Posgrados, Ciudad Universitaria, Edificio D, 1erpiso, Coyoacán, Ciudad de México 04510, Mexico.

Departamento de Biología Celular y Fisiología, Instituto de Investigaciones Biomédicas, Universidad Nacional Autónoma de México, Ciudad de México 04510, Mexico.

出版信息

Brain Sci. 2023 Aug 30;13(9):1261. doi: 10.3390/brainsci13091261.

DOI:10.3390/brainsci13091261
PMID:37759864
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC10526493/
Abstract

The eyes provide themselves with immune tolerance. Frequent skin inflammatory diseases in young blind people suggest, nonetheless, that the eyes instruct a systemic immune tolerance that benefits the whole body. We tested this premise by using delayed skin contact hypersensitivity (DSCH) as a tool to compare the inflammatory response developed by sighted (S) and birth-enucleated (BE) mice against oxazolone or dinitrofluorobenzene at the ages of 10, 30 and 60 days of life. Adult mice enucleated (AE) at 60 days of age were also assessed when they reached 120 days of life. BE mice displayed exacerbated DSCH at 60 but not at 10 or 30 days of age. AE mice, in contrast, show no exacerbated DSCH. Skin inflammation in 60-day-old BE mice was hapten exclusive and supported by distinct CD8 lymphocytes. The number of intraepidermal T lymphocytes and migrating Langerhans cells was, however, similar between S and BE mice by the age of 60 days. Our observations support the idea that the eyes instruct systemic immune tolerance that benefits organs outside the eyes from an early age. The higher prevalence of inflammatory skin disorders reported in young people might then reflect reduced immune tolerance associated with the impaired functional morphology of the eyes.

摘要

眼睛自身具备免疫耐受性。然而,年轻盲人中频繁出现的皮肤炎症性疾病表明,眼睛会引导一种有益于全身的系统性免疫耐受。我们通过使用迟发性皮肤接触超敏反应(DSCH)作为工具,来比较有视力的(S)和出生时即摘除眼球的(BE)小鼠在10、30和60日龄时对恶唑酮或二硝基氟苯产生的炎症反应,以此来验证这一前提。60日龄时摘除眼球的成年小鼠(AE)在120日龄时也进行了评估。BE小鼠在60日龄时表现出加剧的DSCH,但在10日龄或30日龄时未出现。相比之下,AE小鼠未表现出加剧的DSCH。60日龄BE小鼠的皮肤炎症具有抗原特异性,并由不同的CD8淋巴细胞支持。然而,到60日龄时,S小鼠和BE小鼠的表皮内T淋巴细胞数量和迁移的朗格汉斯细胞数量相似。我们的观察结果支持这样一种观点,即眼睛从早期就引导系统性免疫耐受,使眼外器官受益。那么,年轻人中报告的炎症性皮肤病较高的患病率可能反映了与眼睛功能形态受损相关的免疫耐受性降低。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f39e/10526493/617d298863d2/brainsci-13-01261-g008.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f39e/10526493/6cdfb101f923/brainsci-13-01261-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f39e/10526493/5f797b30da83/brainsci-13-01261-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f39e/10526493/3ca8d605a35b/brainsci-13-01261-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f39e/10526493/cc5ffb6f30d0/brainsci-13-01261-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f39e/10526493/a0ceb4a314b5/brainsci-13-01261-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f39e/10526493/062974080f99/brainsci-13-01261-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f39e/10526493/64c857fc09f1/brainsci-13-01261-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f39e/10526493/617d298863d2/brainsci-13-01261-g008.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f39e/10526493/6cdfb101f923/brainsci-13-01261-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f39e/10526493/5f797b30da83/brainsci-13-01261-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f39e/10526493/3ca8d605a35b/brainsci-13-01261-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f39e/10526493/cc5ffb6f30d0/brainsci-13-01261-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f39e/10526493/a0ceb4a314b5/brainsci-13-01261-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f39e/10526493/062974080f99/brainsci-13-01261-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f39e/10526493/64c857fc09f1/brainsci-13-01261-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f39e/10526493/617d298863d2/brainsci-13-01261-g008.jpg

相似文献

1
Looking beyond Self-Protection: The Eyes Instruct Systemic Immune Tolerance Early in Life.超越自我保护:眼睛在生命早期指导系统性免疫耐受
Brain Sci. 2023 Aug 30;13(9):1261. doi: 10.3390/brainsci13091261.
2
Oral administration of hapten inhibits in vivo induction of specific cytotoxic CD8+ T cells mediating tissue inflammation: a role for regulatory CD4+ T cells.口服半抗原可抑制体内介导组织炎症的特异性细胞毒性CD8 + T细胞的诱导:调节性CD4 + T细胞的作用。
J Immunol. 2000 Mar 1;164(5):2515-22. doi: 10.4049/jimmunol.164.5.2515.
3
Contact hypersensitivity is suppressed after sensitisation by dinitrofluorobenzene of early stage iso-skin grafts.在早期同种皮肤移植用二硝基氟苯致敏后,接触性超敏反应受到抑制。
Scand J Plast Reconstr Surg Hand Surg. 1996 Sep;30(3):169-75. doi: 10.3109/02844319609062810.
4
Local and systemic consequences of acute, low-dose ultraviolet B radiation are mediated by different immune regulatory mechanisms.急性低剂量紫外线B辐射的局部和全身影响是由不同的免疫调节机制介导的。
Eur J Immunol. 1994 Aug;24(8):1765-70. doi: 10.1002/eji.1830240807.
5
Inhibition of functional T cell priming and contact hypersensitivity responses by treatment with anti-secondary lymphoid chemokine antibody during hapten sensitization.在半抗原致敏期间用抗二级淋巴组织趋化因子抗体治疗可抑制功能性T细胞启动和接触性超敏反应。
J Immunol. 2000 May 15;164(10):5207-14. doi: 10.4049/jimmunol.164.10.5207.
6
Sensitizing capacity of Langerhans' cells obtained from ultraviolet-B-exposed murine skin.从紫外线B照射的小鼠皮肤中获取的朗格汉斯细胞的致敏能力。
Immunology. 1995 Dec;86(4):661-7.
7
Innate CD4+CD25+ regulatory T cells are required for oral tolerance and inhibition of CD8+ T cells mediating skin inflammation.先天性CD4+CD25+调节性T细胞是口腔耐受和抑制介导皮肤炎症的CD8+T细胞所必需的。
Blood. 2003 Nov 1;102(9):3295-301. doi: 10.1182/blood-2003-03-0727. Epub 2003 Jul 10.
8
Intravenously administered contact allergens coupled to syngeneic erythrocytes induce in mice tolerance rather than effector immune response.静脉注射与同基因红细胞偶联的接触性变应原可诱导小鼠产生耐受性而非效应性免疫反应。
Folia Med Cracov. 2019;59(1):61-73.
9
Galectin-1 Expression in CD8 T Lymphocytes Controls Inflammation in Contact Hypersensitivity.半乳糖凝集素-1 在 CD8+T 淋巴细胞中的表达控制接触性超敏反应中的炎症。
J Invest Dermatol. 2021 Jun;141(6):1522-1532.e3. doi: 10.1016/j.jid.2020.10.020. Epub 2020 Nov 9.
10
Sequential role of plasmacytoid dendritic cells and regulatory T cells in oral tolerance.浆细胞样树突状细胞和调节性T细胞在口服耐受中的顺序作用。
Gastroenterology. 2009 Sep;137(3):1019-28. doi: 10.1053/j.gastro.2009.03.055. Epub 2009 Apr 1.

本文引用的文献

1
Mast Cells Initiate Type 2 Inflammation through Tryptase Released by MRGPRX2/MRGPRB2 Activation in Atopic Dermatitis.肥大细胞通过 MRGPRX2/MRGPRB2 激活释放的类胰蛋白酶引发特应性皮炎的 2 型炎症。
J Invest Dermatol. 2024 Jan;144(1):53-62.e2. doi: 10.1016/j.jid.2023.06.201. Epub 2023 Jul 22.
2
Difelikefalin suppresses itch and reduces scratching independent of inflammation in a murine model of atopic dermatitis.在特应性皮炎小鼠模型中,地肤利法林可抑制瘙痒并减少搔抓,且与炎症无关。
J Allergy Clin Immunol. 2023 Oct;152(4):927-932. doi: 10.1016/j.jaci.2023.06.022. Epub 2023 Jul 13.
3
Circadian Regulation of the Neuroimmune Environment Across the Lifespan: From Brain Development to Aging.
生物钟对神经免疫环境的调控:从大脑发育到衰老。
J Biol Rhythms. 2023 Oct;38(5):419-446. doi: 10.1177/07487304231178950. Epub 2023 Jun 26.
4
Keratinocytes use FPR2 to detect and initiate antimicrobial skin defense.角质形成细胞利用 FPR2 来检测和启动抗菌皮肤防御。
Front Immunol. 2023 May 31;14:1188555. doi: 10.3389/fimmu.2023.1188555. eCollection 2023.
5
Advancing the understanding of allergic contact dermatitis: from pathophysiology to novel therapeutic approaches.增进对过敏性接触性皮炎的理解:从病理生理学到新型治疗方法。
Front Med (Lausanne). 2023 May 22;10:1184289. doi: 10.3389/fmed.2023.1184289. eCollection 2023.
6
Neuroimmune interactions in atopic and allergic contact dermatitis.特应性皮炎和过敏性接触性皮炎中的神经免疫相互作用。
J Allergy Clin Immunol. 2023 May;151(5):1169-1177. doi: 10.1016/j.jaci.2023.03.013.
7
Molecular Mechanisms of Neurogenic Inflammation of the Skin.皮肤神经源性炎症的分子机制。
Int J Mol Sci. 2023 Mar 5;24(5):5001. doi: 10.3390/ijms24055001.
8
Langerhans cells in the skin and oral mucosa: Brothers in arms?皮肤和口腔黏膜中的朗格汉斯细胞:同仇敌忾?
Eur J Immunol. 2023 Jul;53(7):e2149499. doi: 10.1002/eji.202149499. Epub 2023 May 31.
9
Anatomical contacts between sensory neurons and epidermal cells: an unrecognized anatomical network for neuro-immuno-cutaneous crosstalk.感觉神经元和表皮细胞之间的解剖接触:神经免疫皮肤串扰的未被识别的解剖网络。
Br J Dermatol. 2023 Feb 10;188(2):176-185. doi: 10.1093/bjd/ljac066.
10
Circadian Disruption and Consequences on Innate Immunity and Inflammatory Response.昼夜节律紊乱及其对先天免疫和炎症反应的影响。
Int J Mol Sci. 2022 Nov 8;23(22):13722. doi: 10.3390/ijms232213722.