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17β-雌二醇可减轻流感嗜血杆菌引起的中耳炎症反应。

17β-estradiol Attenuates the Middle Ear Inflammatory Response to Nontypeable Haemophilus influenzae.

机构信息

Department of Otolaryngology and Communication Sciences, Medical College of Wisconsin, Milwaukee, Wisconsin, U.S.A.

Department of Pediatrics Quantitative Health Sciences, Medical College of Wisconsin, Milwaukee, Wisconsin, U.S.A.

出版信息

Laryngoscope. 2024 Aug;134(8):3815-3819. doi: 10.1002/lary.31343. Epub 2024 Feb 24.

Abstract

OBJECTIVES

17β-estradiol (E2) is a steroidal hormone with immunomodulatory functions that play a role in infectious and inflammatory diseases. E2 was recently identified as the leading upstream regulator of differentially expressed genes in a comparative RNA sequencing study of pediatric patients with otitis media (OM) versus OM-free counterparts and may therefore play a role in the inflammatory response to bacterial otopathogens during pediatric OM. This study examined the effect of E2 on bacterial-induced inflammatory cytokine expression in an in vitro pediatric OM model.

METHODS

An immortalized middle ear (ME) epithelial cell line, ROM-SV40, was developed from a pediatric recurrent OM patient. The culture was exposed to E2 at physiological levels for 1-48 h prior to 6 h-stimulation with nontypeable Haemophilus influenzae (NTHi) whole cell lysate. TNFA, IL1B, IL6, and IL8 were assayed by qPCR and ELISA.

RESULTS

E2 pretreatment (24 h) abrogated NTHi induction of IL6; a longer pretreatment (1-10 nM, 48 h) abrogated IL1B induction (p < 0.05). E2 pretreatment (5 nM, 48 h) abrogated NTHi-induced IL8 secretion (p = 0.017).

CONCLUSION

E2 pretreatment partially rescued NTHi-induced cytokine production by ME epithelia. These data support a role for E2 in moderating the excessive inflammatory response to middle ear infection that contributes to OM pathophysiology.

LEVELS OF EVIDENCE

NA Laryngoscope, 134:3815-3819, 2024.

摘要

目的

17β-雌二醇(E2)是一种具有免疫调节功能的甾体激素,在感染和炎症性疾病中发挥作用。E2 最近在一项小儿中耳炎(OM)患者与无 OM 对照组的比较 RNA 测序研究中被确定为差异表达基因的主要上游调节剂,因此可能在小儿 OM 期间对细菌耳病原体的炎症反应中发挥作用。本研究通过体外小儿 OM 模型研究了 E2 对细菌诱导的炎症细胞因子表达的影响。

方法

从一名小儿复发性 OM 患者中建立了永生化中耳(ME)上皮细胞系 ROM-SV40。在 6 小时非定型流感嗜血杆菌(NTHi)全细胞裂解物刺激前,将培养物用生理水平的 E2 预处理 1-48 小时。通过 qPCR 和 ELISA 测定 TNFA、IL1B、IL6 和 IL8。

结果

E2 预处理(24 小时)阻断了 NTHi 诱导的 IL6;更长的预处理(1-10 nM,48 小时)阻断了 IL1B 的诱导(p<0.05)。E2 预处理(5 nM,48 小时)阻断了 NTHi 诱导的 IL8 分泌(p=0.017)。

结论

E2 预处理部分挽救了 ME 上皮细胞中 NTHi 诱导的细胞因子产生。这些数据支持 E2 在调节中耳感染引起的过度炎症反应中的作用,该反应有助于 OM 病理生理学。

证据水平

无。喉科学,134:3815-3819,2024。

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