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本文引用的文献

1
Damage-associated molecular patterns (DAMPs) released after burn are associated with inflammation and monocyte activation.烧伤后释放的损伤相关分子模式(DAMPs)与炎症和单核细胞激活有关。
Burns. 2017 Mar;43(2):297-303. doi: 10.1016/j.burns.2016.10.001. Epub 2016 Oct 27.
2
Silver Sulfadiazine Retards Wound Healing and Increases Hypertrophic Scarring in a Rabbit Ear Excisional Wound Model.在兔耳切除伤口模型中,磺胺嘧啶银会延缓伤口愈合并增加肥厚性瘢痕形成。
J Burn Care Res. 2017 Jan/Feb;38(1):e418-e422. doi: 10.1097/BCR.0000000000000406.
3
S100A12 Induced in the Epidermis by Reduced Hydration Activates Dermal Fibroblasts and Causes Dermal Fibrosis.水合作用降低诱导表皮产生的S100A12激活真皮成纤维细胞并导致真皮纤维化。
J Invest Dermatol. 2017 Mar;137(3):650-659. doi: 10.1016/j.jid.2016.10.040. Epub 2016 Nov 10.
4
Serum Decorin, Interleukin-1β, and Transforming Growth Factor-β Predict Hypertrophic Scarring Postburn.血清核心蛋白聚糖、白细胞介素-1β和转化生长因子-β可预测烧伤后增生性瘢痕形成。
J Burn Care Res. 2016 Nov/Dec;37(6):356-366. doi: 10.1097/BCR.0000000000000271.
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Hypertrophic scarring: the greatest unmet challenge after burn injury.肥厚性瘢痕形成:烧伤后最大的未解决挑战。
Lancet. 2016 Oct 1;388(10052):1427-1436. doi: 10.1016/S0140-6736(16)31406-4.
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The metabolic stress response to burn trauma: current understanding and therapies.烧伤创伤的代谢应激反应:当前的认识与治疗方法
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7
Scavenging nucleic acid debris to combat autoimmunity and infectious disease.清除核酸碎片以对抗自身免疫和传染病。
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Microbial Ecology of the Human Skin.人体皮肤微生物生态学。
Microb Ecol. 2018 Jul;76(1):113-120. doi: 10.1007/s00248-016-0789-6. Epub 2016 May 31.
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Early versus Delayed Excision and Grafting of Full-Thickness Burns in a Porcine Model: A Randomized Study.猪模型中全层烧伤早期与延迟切除及植皮的随机研究
Plast Reconstr Surg. 2016 Jun;137(6):972e-979e. doi: 10.1097/PRS.0000000000002161.
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The role of neutrophils in immune dysfunction during severe inflammation.中性粒细胞在严重炎症期间免疫功能障碍中的作用。
Crit Care. 2016 Mar 23;20:73. doi: 10.1186/s13054-016-1250-4.

Toll样受体信号通路在烧伤创面愈合与瘢痕形成中的作用

Toll-Like Receptor Signaling in Burn Wound Healing and Scarring.

作者信息

D'Arpa Peter, Leung Kai P

机构信息

The Geneva Foundation, Tacoma, Washington.

Dental and Craniofacial Trauma Research and Tissue Regeneration Directorate, US Army Institute of Surgical Research, JBSA Fort Sam Houston, Texas.

出版信息

Adv Wound Care (New Rochelle). 2017 Oct 1;6(10):330-343. doi: 10.1089/wound.2017.0733.

DOI:10.1089/wound.2017.0733
PMID:29062590
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5649422/
Abstract

Damage-associated molecular patterns (DAMPs) and pathogen-associated molecular patterns (PAMPs) emanate from burn-injured tissue and enter systemic circulation. Locally and systemically, they activate pattern-recognition receptors, including toll-like receptors (TLRs), to stimulate cytokine secretion, which in the severest burns typically results in extreme systemic cytokine levels, a dysfunctioning immune system, infection, impaired healing, and excessive scarring. This system-wide disruption of homeostasis can advance to life-threatening, multiorgan dysfunction syndrome. Knowledge of DAMP- and PAMP-TLR signaling may lead to treatments that ameliorate local and systemic inflammation and reduce scarring and other burn injury sequela. Many PAMPs and DAMPs, the TLRs they activate, and their downstream signaling molecules have been shown to contribute to local and systemic inflammation and tissue damage following burn injury. Whether TLR-pathway-targeting treatments applied at different times postburn injury might improve scarring remains an open question. The evaluation of this question requires the use of appropriate preclinical and clinical burn models carried out until after mature scar has formed. After TLR-pathway-targeting treatments are evaluated in porcine burn wound models and their safety is demonstrated, they can be tested in proof-of-concept clinical burn wound models.

摘要

损伤相关分子模式(DAMPs)和病原体相关分子模式(PAMPs)源自烧伤组织并进入体循环。在局部和全身,它们激活模式识别受体,包括Toll样受体(TLRs),以刺激细胞因子分泌,在最严重的烧伤中,这通常会导致全身细胞因子水平极高、免疫系统功能失调、感染、愈合受损和过度瘢痕形成。这种全系统的内稳态破坏可发展为危及生命的多器官功能障碍综合征。对DAMP和PAMP-TLR信号传导的了解可能会带来改善局部和全身炎症、减少瘢痕形成和其他烧伤后遗症的治疗方法。许多PAMPs和DAMPs、它们激活的TLRs及其下游信号分子已被证明在烧伤后导致局部和全身炎症以及组织损伤。烧伤后不同时间应用靶向TLR途径的治疗是否能改善瘢痕形成仍是一个悬而未决的问题。对这个问题的评估需要使用合适的临床前和临床烧伤模型,并持续到成熟瘢痕形成之后。在猪烧伤创面模型中评估靶向TLR途径的治疗并证明其安全性后,可在概念验证临床烧伤创面模型中进行测试。