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Editorial introductions. 编辑介绍。
IF 2.8 3区 医学 Q2 RESPIRATORY SYSTEM Pub Date : 2025-05-01 Epub Date: 2025-03-27 DOI: 10.1097/MCP.0000000000001164
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引用次数: 0
Pleural infection: controversies on the therapeutic strategies. 胸膜感染:治疗策略之争。
IF 2.8 3区 医学 Q2 RESPIRATORY SYSTEM Pub Date : 2025-05-01 Epub Date: 2025-02-17 DOI: 10.1097/MCP.0000000000001157
Ken K P Chan, Estee P M Lau, Y C Gary Lee

Purpose of review: Management of pleural infection remains heterogeneous worldwide. This review highlights current controversies in therapeutic strategies for pleural infection, focusing particularly on recent studies and their implications.

Recent findings: The introduction of intrapleural therapy combining alteplase [a tissue plasminogen activator (tPA)] and deoxyribonuclease (DNase) has revolutionized treatment practices, though the optimal delivery and dosing regimen is an area of active investigation. Variations to simplify administration protocols and/or to lower the required drug doses have been published. Most were exploratory studies, but the variations showed maintained therapeutic efficacy.Whether intrapleural alteplase/DNase or video-assisted thoracoscopic surgery (VATS) is superior is a topic of debate. Retrospective comparative analyses between the two revealed no clear benefits on all-cause mortality from either approach. Pilot randomized trials have been published and further full-scale, head-to-head trials are underway.

Summary: Effective management of pleural infection involves adequate pleural drainage and appropriate antibiotic use. This review outlines the current evidence (and its limitations) and highlights knowledge gaps in optimizing the therapeutic strategies.

回顾的目的:胸膜感染的管理在世界范围内仍然存在差异。这篇综述强调了目前胸膜感染治疗策略的争议,特别关注最近的研究及其意义。近期发现:胸腔内联合阿替普酶[一种组织型纤溶酶原激活剂(tPA)]和脱氧核糖核酸酶(DNase)治疗的引入已经彻底改变了治疗实践,尽管最佳的递送和给药方案是一个积极研究的领域。简化给药方案和/或降低所需药物剂量的变化已经公布。大多数是探索性研究,但变异显示维持治疗效果。胸膜内注射阿替普酶/ dna酶或视频辅助胸腔镜手术(VATS)孰优孰优是一个有争议的话题。两种方法之间的回顾性比较分析显示,两种方法对全因死亡率都没有明显的好处。试点随机试验已经公布,进一步的全面面对面试验正在进行中。总结:胸腔感染的有效管理包括充分的胸腔引流和适当的抗生素使用。本综述概述了目前的证据(及其局限性),并强调了优化治疗策略的知识差距。
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引用次数: 0
Community acquired pneumonia due to antibiotic resistant- Streptococcus pneumoniae : diagnosis, management and prevention. 耐药肺炎链球菌引起的社区获得性肺炎:诊断、管理和预防。
IF 2.8 3区 医学 Q2 RESPIRATORY SYSTEM Pub Date : 2025-05-01 Epub Date: 2025-02-07 DOI: 10.1097/MCP.0000000000001153
Grace C Y Lui, Christopher K C Lai

Purpose of review: A resurgence of pneumococcal pneumonia has been observed after a marked reduction in the early COVID-19 pandemic. Penicillin-nonsusceptible Streptococcus pneumoniae is regarded as a WHO priority pathogen.

Recent findings: Overall antibiotic resistance rates in S. pneumoniae have increased due to increase in antibiotic consumption and changes in serotype distribution, partly driven by the rollout of pneumococcal vaccination. Isolates from pneumococcal pneumonia have higher resistance rates than those from invasive pneumococcal disease. New antibiotics have been approved for treatment of community-acquired pneumonia, and are active against multidrug-resistant S. pneumoniae . Pneumococcal vaccines in both children and adults are effective in reducing the burden of pneumococcal pneumonia in adults, though some circulating vaccine and nonvaccine serotypes are driving antibiotic resistance.

Summary: Continual surveillance of serotype and resistance patterns of S. pneumoniae causing pneumonia in adult populations is important after the introduction of new pneumococcal vaccines. Novel pneumococcal vaccine platforms are needed to overcome the threats of serotype replacement and antibiotic resistance.

回顾目的:在COVID-19早期大流行显著减少后,观察到肺炎球菌肺炎再次出现。青霉素不敏感肺炎链球菌被视为世卫组织的重点病原体。最近的发现:肺炎链球菌的总体抗生素耐药率有所增加,这是由于抗生素用量的增加和血清型分布的变化,部分原因是肺炎球菌疫苗接种的推广。肺炎球菌肺炎分离株的耐药率高于侵袭性肺炎球菌疾病分离株。新的抗生素已被批准用于治疗社区获得性肺炎,并对耐多药肺炎链球菌具有活性。儿童和成人使用肺炎球菌疫苗可有效减轻成人肺炎球菌肺炎的负担,尽管一些循环疫苗和非疫苗血清型正在推动抗生素耐药性。摘要:在引入新的肺炎球菌疫苗后,对成人人群中引起肺炎的肺炎链球菌的血清型和耐药模式进行持续监测非常重要。需要新的肺炎球菌疫苗平台来克服血清型替代和抗生素耐药性的威胁。
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引用次数: 0
Comorbidities and multimorbidity in asthma. 哮喘的合并症和多病。
IF 2.8 3区 医学 Q2 RESPIRATORY SYSTEM Pub Date : 2025-05-01 Epub Date: 2025-03-06 DOI: 10.1097/MCP.0000000000001162
Diego J Maselli, Jesse Sherratt, Sandra G Adams

Purpose of review: To describe the associations between asthma and relevant comorbidities, and appraise the latest evidence on the management strategies of asthmatics with comorbid conditions.

Recent findings: Conditions such as allergic rhinitis, chronic rhinosinusitis with and without nasal polyps, gastroesophageal reflux disease, obesity, chronic obstructive pulmonary disease, bronchiectasis, anxiety and depression have been linked to worse outcomes in asthma. Recognition and treatment of these conditions is important in asthma, particularly in those with uncontrolled or severe asthma. Biologics for asthma have been effective in those with chronic rhinosinusitis with nasal polyps and chronic obstructive pulmonary disease (COPD), with emerging evidence in bronchiectasis. Weight loss programs with diet and exercise improve asthma control. Anxiety and depression are often unrecognized in patients with asthma.

Summary: Comorbid conditions have been recognized as important factors in the diagnosis and treatment of asthma, particularly in patients who have severe disease and remain uncontrolled. Comorbidities in asthma are correlated with poor quality of life and asthma control, increased healthcare utilization and their treatment is associated with improved outcomes.

综述的目的:描述哮喘与相关合并症之间的关系,并评价哮喘合并合并症的治疗策略的最新证据。最近的研究发现:过敏性鼻炎、伴有或不伴有鼻息肉的慢性鼻窦炎、胃食管反流疾病、肥胖、慢性阻塞性肺病、支气管扩张、焦虑和抑郁等疾病与哮喘的预后恶化有关。识别和治疗这些情况对哮喘很重要,特别是对那些不受控制或严重哮喘的人。治疗哮喘的生物制剂对慢性鼻窦炎合并鼻息肉和慢性阻塞性肺疾病(COPD)患者有效,支气管扩张也有新的证据。节食和运动相结合的减肥计划可以改善哮喘的控制。哮喘患者的焦虑和抑郁常被忽视。摘要:合并症已被认为是哮喘诊断和治疗的重要因素,特别是在病情严重且未得到控制的患者中。哮喘合并症与生活质量差和哮喘控制相关,增加医疗保健利用及其治疗与改善预后相关。
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引用次数: 0
Novel biomarkers in asthma. 哮喘的新生物标志物。
IF 2.8 3区 医学 Q2 RESPIRATORY SYSTEM Pub Date : 2025-05-01 Epub Date: 2025-02-14 DOI: 10.1097/MCP.0000000000001155
Nikita Agrawal, Monica Kraft

Purpose of review: Asthma is a common global respiratory disease characterized by airway inflammation. It is a heterogenous group of disorders with overlapping biological mechanisms. This review will discuss the current state of the use of biomarkers in asthma with an eye to the future. The identification of biomarkers has advanced our understanding of inflammatory pathways in asthma and aided in development of targeted therapies. However, even with similar inflammatory biomarkers, not all patients respond uniformly. Thus, further research into novel biomarkers in asthma is needed.

Recent findings: Recent literature highlights several key themes in biomarker research for asthma. Biomarkers can be derived from various sources, including sputum, blood, urine, and exhaled breath. Historically, studies have focused on eosinophilic inflammation, yet total blood eosinophil counts do not capture asthma pathology and treatment responses. Recent investigations explore eosinophil activity as well as eosinophil subpopulations based on surface protein expressions. Mast cell involvement, their mediators, and club cell secretory protein are further being examined across different asthma molecular phenotypes.

Summary: The complexity of inflammatory pathways in asthma, influenced by various factors, underscores the inadequacy of relying on a single biomarker at one time point. Continued research is essential to identify appropriate biomarkers.

综述目的:哮喘是一种以气道炎症为特征的全球常见呼吸系统疾病。它是一组具有重叠生物学机制的异质性疾病。这篇综述将讨论生物标志物在哮喘中的应用现状,并着眼于未来。生物标志物的鉴定提高了我们对哮喘炎症途径的理解,并有助于靶向治疗的发展。然而,即使具有相似的炎症生物标志物,也不是所有患者的反应都一致。因此,需要进一步研究哮喘的新型生物标志物。最近的发现:最近的文献强调了哮喘生物标志物研究的几个关键主题。生物标志物可以从各种来源获得,包括痰、血液、尿液和呼出的气体。历史上,研究主要集中在嗜酸性粒细胞炎症,但总血嗜酸性粒细胞计数不能捕获哮喘病理和治疗反应。最近的研究探讨了基于表面蛋白表达的嗜酸性粒细胞活性以及嗜酸性粒细胞亚群。肥大细胞的参与、它们的介质和俱乐部细胞分泌蛋白在不同的哮喘分子表型中被进一步研究。摘要:哮喘炎症通路的复杂性,受各种因素的影响,强调了在一个时间点依赖单一生物标志物的不足。持续的研究对于确定合适的生物标志物至关重要。
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引用次数: 0
Mucosal-associated invariant T-cells in pulmonary pathophysiology. 肺部病理生理学中的粘膜相关不变 T 细胞
IF 2.8 3区 医学 Q2 RESPIRATORY SYSTEM Pub Date : 2025-05-01 Epub Date: 2025-03-19 DOI: 10.1097/MCP.0000000000001163
Jéssica Kamiki, Carolina M Gorgulho, Joana R Lérias, Markus J Maeurer

Purpose of review: Mucosal-associated invariant T-cells (MAIT) have been associated with lung cancer and pulmonary infections. The treatment of patients with cancer or infections includes host-directed therapies (HDTs). MAIT play a role in shaping the 'milieu interne' in cancer and infections and this review addresses the biology of MAIT in pulmonary pathophysiology.

Recent findings: MAIT represent an attractive target for therapy in pulmonary malignancies and infections. T-cells are often difficult to exploit therapeutically due to the diversity of both T-cell receptor (TCR) repertoire and its ligandome. MAIT-cells are restricted by the major histocompatibility complex class I-related gene protein (MR1) that presents nondefined tumor-associated targets, bacterial products, vitamin and drug derivates. Due to their plasticity in gene expression, MAIT are able to conversely switch from IFN-γ to IL-17 production. Both cytokines play a key role in protective immune responses in infections and malignancies. MAIT-derived production of interleukin (IL)-17/TGF-β shapes the tumor micro-environment (TME), including tissue re-modelling leading to pulmonary fibrosis and recruitment of neutrophils. MAIT contribute to the gut-lung axis associated with clinical improved responses of patients with cancer to checkpoint inhibition therapy. MAIT are at the crossroad of HDTs targeting malignant and infected cells. Clinical presentations of overt inflammation, protective immune responses and tissue re-modeling are reviewed along the balance between Th1, Th2, Th9, and Th17 responses associated with immune-suppression or protective immune responses in infections.

Summary: MAIT shape the TME in pulmonary malignancies and infections. Drugs targeting the TME and HDTs affect MAIT that can be explored to achieve improved clinical results while curbing overt tissue-damaging immune responses.

综述目的:粘膜相关不变性t细胞(MAIT)与肺癌和肺部感染有关。癌症或感染患者的治疗包括宿主定向疗法(HDTs)。MAIT在形成癌症和感染的“环境间隙”中发挥作用,本文综述了MAIT在肺部病理生理学中的生物学作用。最新发现:MAIT是肺部恶性肿瘤和感染治疗的一个有吸引力的靶点。由于t细胞受体(TCR)库及其配体的多样性,t细胞通常难以用于治疗。mait细胞受到主要组织相容性复合体i类相关基因蛋白(MR1)的限制,MR1呈现不确定的肿瘤相关靶点、细菌产物、维生素和药物衍生物。由于它们在基因表达中的可塑性,MAIT能够反过来从IFN-γ切换到IL-17的产生。这两种细胞因子在感染和恶性肿瘤的保护性免疫反应中起关键作用。mait衍生的白介素(IL)-17/TGF-β的产生塑造了肿瘤微环境(TME),包括导致肺纤维化和中性粒细胞募集的组织重塑。MAIT有助于与癌症患者对检查点抑制治疗的临床改善反应相关的肠-肺轴。MAIT是靶向恶性和感染细胞的HDTs的十字路口。临床表现的明显炎症,保护性免疫反应和组织重建沿着Th1, Th2, Th9和Th17反应之间的平衡与免疫抑制或保护性免疫反应在感染中进行了回顾。总结:MAIT影响肺部恶性肿瘤和感染的TME。靶向TME和HDTs的药物可以影响MAIT,从而在抑制明显的组织损伤性免疫反应的同时获得更好的临床结果。
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引用次数: 0
Respiratory syncytial virus pulmonary infections in adults - disease burden and prevention. 成人呼吸道合胞病毒肺部感染——疾病负担和预防。
IF 2.8 3区 医学 Q2 RESPIRATORY SYSTEM Pub Date : 2025-05-01 Epub Date: 2024-12-23 DOI: 10.1097/MCP.0000000000001151
Grant W Waterer, Mark Metersky

Purpose of review: We highlight the evolving understanding of the burden of respiratory syncytial virus (RSV) in older adults and recent data on the three new vaccines.

Recent findings: As well as a greater recognition of the amount of RSV infection in adults, and especially over 60 years of age, there has been a significant amount of study detailing the postacute burden including excess cardiovascular disease and loss of physical and cognitive functioning. Three new RSV vaccines now have published data for two seasons, and while direct comparison is not possible due to differences in the timing, methodology and populations studies, all show good efficacy with no serious side effects of concern.

Summary: RSV causes a substantial amount of morbidity and mortality in older adults with both acute and longer term impacts. With effective vaccines now available clinicians should be advocating with their patients to prevent RSV infection.

综述的目的:我们强调对老年人呼吸道合胞病毒(RSV)负担的不断发展的认识以及三种新疫苗的最新数据。最近的发现:除了对成人,特别是60岁以上的成年人RSV感染数量的更多认识外,已经有大量的研究详细说明了急性后负担,包括过度心血管疾病和身体和认知功能的丧失。三种新的RSV疫苗现已公布了两个季节的数据,虽然由于时间、方法和人群研究的差异而无法进行直接比较,但所有疫苗都显示出良好的疗效,没有严重的副作用。总结:RSV在老年人中引起大量的急性和长期影响的发病率和死亡率。现在有了有效的疫苗,临床医生应该提倡患者预防呼吸道合胞病毒感染。
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引用次数: 0
An updated review of pulmonary radiological features of acute and chronic COVID-19. 急性和慢性肺部COVID-19肺部影像学特征的最新综述
IF 2.8 3区 医学 Q2 RESPIRATORY SYSTEM Pub Date : 2025-05-01 Epub Date: 2025-02-04 DOI: 10.1097/MCP.0000000000001152
Raya Tcheroyan, Peter Makhoul, Scott Simpson

Purpose of review: Significant progress has been made in our understanding of the acute and chronic clinical and radiological manifestations of coronavirus-19 (COVID-19). This article provides an updated review on pulmonary COVID-19, while highlighting the key imaging features that can identify and distinguish acute COVID-19 pneumonia and its chronic sequelae from other diseases.

Recent findings: Acute COVID-19 pneumonia typically presents with manifestations of organizing pneumonia on computed tomography (CT). In cases of severe disease, patients clinically progress to acute respiratory distress syndrome, which manifests as diffuse alveolar damage on CT. The most common chronic imaging finding is ground-glass opacities, which commonly resolves, as well as subpleural bands and reticulation. Pulmonary fibrosis is an overall rare complication of COVID-19, with characteristic features, including architectural distortion, and traction bronchiectasis.

Summary: Chest CT can be a helpful adjunct tool in both diagnosing and managing acute COVID-19 pneumonia and its chronic sequelae. It can identify high-risk cases and guide decision-making, particularly in cases of severe or complicated disease. Follow-up imaging can detect persistent lung abnormalities associated with long COVID and guide appropriate management.

综述目的:我们对冠状病毒-19 (COVID-19)的急慢性临床和放射学表现的认识取得了重大进展。本文综述了肺部COVID-19的最新进展,同时强调了能够识别和区分急性COVID-19肺炎及其慢性后遗症与其他疾病的关键影像学特征。近期发现:急性COVID-19肺炎在计算机断层扫描(CT)上典型表现为组织肺炎。病情严重时,临床进展为急性呼吸窘迫综合征,CT表现为弥漫性肺泡损伤。最常见的慢性影像表现为磨玻璃混浊,通常会消退,同时还有胸膜下带和网状影。肺纤维化是COVID-19的一种罕见并发症,其特征包括结构扭曲和牵引性支气管扩张。胸部CT可作为诊断和治疗急性COVID-19肺炎及其慢性后遗症的辅助工具。它可以识别高风险病例并指导决策,特别是在严重或复杂疾病的情况下。随访影像可以发现与长冠相关的持续性肺部异常,并指导适当的治疗。
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引用次数: 0
Recent evidence for stepping down severe asthma therapies. 减少严重哮喘治疗的最新证据。
IF 2.8 3区 医学 Q2 RESPIRATORY SYSTEM Pub Date : 2025-05-01 Epub Date: 2025-02-28 DOI: 10.1097/MCP.0000000000001156
Eric Merrell, Sandhya Khurana

Purpose of review: Biologics have proven safe and effective for severe asthma. Their introduction has offered hope for patients and prescribers with a growing list of novel medications and indications. While 'step-up' indications for biologic initiation are well described in guidelines, 'step-down' strategy remains poorly understood and thus guidance is limited. In this opinion article we aim to focus on recent practice changing evidence for stepping-down severe asthma management, tools for the assessment of biologic efficacy, propose a framework for the step-down of biologic and nonbiologic therapies and suggest topics of interest for future research.

Recent findings: Clinical tools have been developed to aid in assessing biologic response. Some patients experience marked improvement and may enter a period of clinical remission or even complete remission. Following positive response, add-on therapy may safely be approached for taper or withdrawal.

Summary: There is limited consensus but growing evidence for stepping-down therapies in patients who achieve clinical response and/or remission after biologic initiation. Further structured guidance would benefit clinicians who face clinical uncertainty when deciding to step-down therapy in patients with well controlled asthma.

综述目的:生物制剂已被证明对严重哮喘是安全有效的。它们的引入为患者和处方医生带来了希望,因为他们有越来越多的新药物和适应症。虽然指南中对生物起始的“逐步”适应症有很好的描述,但“逐步”策略仍然知之甚少,因此指南是有限的。在这篇观点文章中,我们的目标是关注最近的实践改变严重哮喘管理的证据,评估生物疗效的工具,提出生物和非生物治疗的框架,并提出未来研究的兴趣主题。最近的发现:临床工具已经开发出来,以帮助评估生物反应。有些患者症状明显改善,可能进入临床缓解期,甚至完全缓解期。积极反应后,附加治疗可以安全地逐渐减少或停药。总结:对于在生物起始治疗后达到临床反应和/或缓解的患者,目前的共识有限,但证据越来越多。进一步的结构化指导将使临床医生在决定对控制良好的哮喘患者减少治疗时面临临床不确定性。
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引用次数: 0
Non-T2 asthma. Non-T2哮喘。
IF 2.8 3区 医学 Q2 RESPIRATORY SYSTEM Pub Date : 2025-05-01 Epub Date: 2025-03-27 DOI: 10.1097/MCP.0000000000001154
Emily K Duffus, Fernando Holguin, Deepa Rastogi

Purpose of review: This review provides a comprehensive overview of the non-T asthma phenotypes. Asthma is an umbrella term that defines a complex group of heterogenous airway disorders, which are broadly categorized into predominantly T2 or non-T2 phenotypes depending on the presence and levels of airway and systemic biomarkers associated with a T2 inflammatory response. Individuals with predominant T2 asthma have greater numbers of peripheral blood eosinophils, exhaled nitric oxide and IgE. These patients have more atopy and earlier onset asthma. In contrast, the absence or low levels of these biomarkers define non-T2 asthma. This is a heterogenous group with a later onset of asthma that is also more commonly associated with obesity and with females.

Recent findings: This article summarizes new information regarding the plasticity that exists between T2 and non-T2 mechanisms, including their role in exacerbation-prone and nonexacerbating asthma, and many of the risk factors associated with the non-T2 phenotype, such as viral infections, ambient air pollution exposure, smoking, genetic and metabolic factors. It also provides new information on the immunological and metabolic mechanisms associated with non-T2 asthma. We also discuss how to manage this asthma phenotype and how treatment responses differ for these patients.

Summary: Non-T2 asthma defines a heterogenous group of asthma phenotypes. However, acknowledging that the absence of T2 biomarkers is influenced by several factors is important and can longitudinally change in relation to exacerbations, particularly in children.

综述目的:本综述提供了非t型哮喘表型的全面概述。哮喘是一个总称,定义了一组复杂的异质性气道疾病,根据与T2炎症反应相关的气道和全身生物标志物的存在和水平,其大致分为主要的T2或非T2表型。以T2哮喘为主的个体外周血嗜酸性粒细胞、呼出一氧化氮和IgE数量较多。这些患者有更多的特应性和早发性哮喘。相比之下,这些生物标志物的缺失或低水平定义了非t2哮喘。这是一个异质性的群体,哮喘发病较晚,而且与肥胖和女性更常见。最新发现:本文总结了T2和非T2机制之间存在的可塑性的新信息,包括它们在易加重和非加重哮喘中的作用,以及与非T2表型相关的许多危险因素,如病毒感染、环境空气污染暴露、吸烟、遗传和代谢因素。它还提供了与非t2哮喘相关的免疫和代谢机制的新信息。我们还讨论了如何管理这种哮喘表型以及这些患者的治疗反应如何不同。总结:非t2型哮喘定义了一组异质性哮喘表型。然而,认识到T2生物标志物的缺失受到几个因素的影响是很重要的,并且与恶化有关,特别是在儿童中,可以纵向改变。
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引用次数: 0
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Current Opinion in Pulmonary Medicine
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