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不可分型流感嗜血杆菌和卡他莫拉菌疫苗在慢性阻塞性肺疾病中的安全性和有效性:一项随机对照试验的系统评价和荟萃分析

The safety and efficacy of non-typeable Haemophilus influenzae and Moraxella catarrhalis vaccine in chronic obstructive pulmonary disease: a systematic review and meta-analysis of randomized controlled trials.

作者信息

Shuai Tiankui, Liu Jing, Dong Meijun, Wu Peng, Zhang Lu, Feng Zhouzhou, Li Wenqiang, Liu Jian

机构信息

Department of Emergency Critical Care Medicine, The First Hospital of Lanzhou University, Lanzhou, Gansu, China.

The First Clinical Medical College, Lanzhou University, Lanzhou, Gansu, China.

出版信息

Front Med (Lausanne). 2025 Apr 4;12:1572726. doi: 10.3389/fmed.2025.1572726. eCollection 2025.

Abstract

BACKGROUND

Non-typeable Haemophilus influenzae (NTHi) and Moraxella catarrhalis (Mcat) are major pathogens implicated in bacterial exacerbations of chronic obstructive pulmonary disease (COPD). Their involvement contributes to antibiotic resistance and poses significant immune challenges, underscoring the need for targeted vaccine strategies. This systematic review and meta-analysis assessed the safety and efficacy of NTHi-Mcat/NTHi vaccines in COPD patients.

RESEARCH DESIGN AND METHODS

Randomized controlled trials (RCTs) assessing the safety and efficacy of NTHi-Mcat/NTHi vaccines for COPD were systematically searched across four databases (PubMed, CENTRAL, Embase, and Medline) from inception to October 2024. Meta-analyses were conducted using random-effects or fixed-effects models, with subgroup analyses to investigate possible sources of heterogeneity.

RESULTS

This analysis included eight RCTs involving 1,574 participants, primarily conducted in Europe ( = 3) and Australia ( = 2), with interventions administered orally or intramuscularly at varying frequencies (twice or three times). The Meta-analyses revealed that the NTHi-Mcat/NTHi vaccine did not affect the incidence of acute exacerbations of COPD (relative risk (RR): 1.02, 95% confidence interval (CI): 0.76 to 1.36), all-cause mortality (RR: 0.91, 95% CI: 0.38 to 2.21), and hospitalization rate (RR: 0.50, 95% CI: 0.09 to 2.77). Regarding safety, the NTHi-Mcat/NTHi vaccine did not significantly increase the risk of serious adverse events (RR: 1.00, 95% CI: 0.84 to 1.19) or grade 3 serious events (RR: 1.20, 95% CI: 0.93 to 1.53). However, it was associated with a higher risk of local and systemic reactions, including pain (RR: 5.33, 95% CI: 1.98 to 14.33), swelling (RR: 12.15, 95% CI: 4.67 to 31.67), redness (first dose: RR: 12.74, 95% CI: 3.48 to 46.59; second dose: RR: 11.55, 95% CI: 3.90 to 34.22), headaches (RR: 1.20, 95% CI: 1.00 to 1.43), erythema (RR: 15.38, 95% CI: 5.64 to 41.92), and fever (after the second dose: RR: 2.33, 95% CI: 1.24 to 4.38).

CONCLUSION

Although the NTHi-Mcat/NTHi vaccines were well-tolerated in COPD patients, they did not significantly reduce the risk of exacerbations or mortality. These findings suggest that further research is needed to validate these results and identify potential subgroups that may derive clinical benefit.

SYSTEMATIC REVIEW REGISTRATION

The study was registered in PROSPERO (ID: CRD42023381488).

摘要

背景

不可分型流感嗜血杆菌(NTHi)和卡他莫拉菌(Mcat)是慢性阻塞性肺疾病(COPD)细菌感染加重的主要病原体。它们的感染会导致抗生素耐药性,并带来重大的免疫挑战,这凸显了针对性疫苗策略的必要性。本系统评价和荟萃分析评估了NTHi-Mcat/NTHi疫苗在COPD患者中的安全性和有效性。

研究设计与方法

从数据库建立至2024年10月,在四个数据库(PubMed、CENTRAL、Embase和Medline)中系统检索评估NTHi-Mcat/NTHi疫苗对COPD安全性和有效性的随机对照试验(RCT)。采用随机效应或固定效应模型进行荟萃分析,并进行亚组分析以探究异质性的可能来源。

结果

该分析纳入了八项RCT,涉及1574名参与者,主要在欧洲(3项)和澳大利亚(2项)开展,干预措施通过口服或肌肉注射,频率各异(两次或三次)。荟萃分析显示,NTHi-Mcat/NTHi疫苗不影响COPD急性加重的发生率(相对风险(RR):1.02,95%置信区间(CI):0.76至1.36)、全因死亡率(RR:0.91,95%CI:0.38至2.21)和住院率(RR:0.50,95%CI:0.09至2.77)。在安全性方面,NTHi-Mcat/NTHi疫苗未显著增加严重不良事件风险(RR:1.00,95%CI:0.84至1.19)或3级严重事件风险(RR:1.20,95%CI:0.93至1.53)。然而,它与局部和全身反应的较高风险相关,包括疼痛(RR:5.33,95%CI:1.98至14.33)、肿胀(RR:12.15,95%CI:4.67至31.67)、发红(首剂:RR:12.74,95%CI:3.48至46.59;第二剂:RR:11.55,95%CI:3.90至34.22)、头痛(RR:1.20,95%CI:1.00至1.43)、红斑(RR:15.38,95%CI:5.64至41.92)和发热(第二剂后:RR:2.33,95%CI:1.24至4.

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/76dd/12006075/4a3f6c8f0a3d/fmed-12-1572726-g001.jpg

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