Suppr超能文献

白细胞介素-1受体拮抗剂抑制早期肉芽组织形成。

IL-1 Receptor Antagonist Inhibits Early Granulation Formation.

作者信息

Nicolli Elizabeth A, Ghosh Ankona, Haft Sunny, Frank Renee, Saunders Cecil James, Cohen Noam, Mirza Natasha

机构信息

Department of Otorhinolaryngology-Head & Neck Surgery, University of Pennsylvania, Philadelphia, Pennsylvania, USA.

Department of Otorhinolaryngology-Head & Neck Surgery, University of California San Diego, San Diego, California, USA.

出版信息

Ann Otol Rhinol Laryngol. 2016 Apr;125(4):284-9. doi: 10.1177/0003489415610588. Epub 2015 Nov 1.

Abstract

PURPOSE

Using a functional model of airway granulation tissue in laryngotracheal stenosis, we investigated changes in histopathology and inflammatory markers within granulation tissue in response to an interleukin-1 receptor antagonist (IL-1Ra). This study allows us to further delineate the immune response to wound healing and potentially identify treatment markers.

METHODS

Laryngotracheal complexes (LTCs) of donor mice underwent direct airway injury. The LTCs were transplanted into subcutaneous tissue of recipient mice in 2 groups: IL-1Ra treated and untreated. The IL-1Ra-treated arm received daily intraperitoneal injections of IL-1Ra for 3 weeks. The LTCs were then harvested. Granulation formation was measured. The mRNA expression of transforming growth factor (TGF) beta and IL-1 was quantified using real-time reverse transcript polymerase chain reaction.

RESULTS

There were statistically significant differences in lamina propria thickness. There were no statistically significant changes in mRNA expression of TGF-β and IL-1β between the treated and untreated specimens.

CONCLUSIONS

Using a previously described murine model, we delineate inflammatory markers that can be targeted for potential therapy. While the levels of inflammatory markers do not change significantly, the lamina propria thickness shows that the effects of IL-1 have been inhibited. The early use of the IL-1Ra will inhibit the efficacy of IL-1 in the inflammatory cascade and can prevent early granulation formation.

摘要

目的

利用喉气管狭窄气道肉芽组织的功能模型,我们研究了肉芽组织中组织病理学和炎症标志物在白细胞介素-1受体拮抗剂(IL-1Ra)作用下的变化。本研究使我们能够进一步描绘对伤口愈合的免疫反应,并有可能识别治疗标志物。

方法

供体小鼠的喉气管复合体(LTCs)遭受直接气道损伤。将LTCs移植到受体小鼠的皮下组织中,分为两组:IL-1Ra治疗组和未治疗组。IL-1Ra治疗组每天腹腔注射IL-1Ra,持续3周。然后收获LTCs。测量肉芽形成情况。使用实时逆转录聚合酶链反应定量转化生长因子(TGF)β和IL-1的mRNA表达。

结果

固有层厚度存在统计学显著差异。治疗组和未治疗组标本中TGF-β和IL-1β的mRNA表达无统计学显著变化。

结论

使用先前描述的小鼠模型,我们描绘了可作为潜在治疗靶点的炎症标志物。虽然炎症标志物水平没有显著变化,但固有层厚度表明IL-1的作用已被抑制。早期使用IL-1Ra将抑制IL-1在炎症级联反应中的作用,并可防止早期肉芽形成。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验