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BCG 疫苗接种对巴西成年医护人员结核分枝杆菌感染的影响:一项嵌套临床试验。

Effect of BCG vaccination against Mycobacterium tuberculosis infection in adult Brazilian health-care workers: a nested clinical trial.

机构信息

Universidade Federal de Mato Grosso do Sul-UFMS, Campo Grande, Mato Grosso do Sul, Brazil.

Infectious Diseases Group, Murdoch Children's Research Institute, Parkville, VIC, Australia; Department of Paediatrics, The University of Melbourne, Parkville, VIC, Australia.

出版信息

Lancet Infect Dis. 2024 Jun;24(6):594-601. doi: 10.1016/S1473-3099(23)00818-6. Epub 2024 Feb 26.

Abstract

BACKGROUND

The effectiveness of BCG vaccine for adult pulmonary tuberculosis remains uncertain. In this study, we aimed to evaluate the effect of vaccination with BCG-Denmark to prevent initial and sustained interferon-γ release assay conversion in Brazilian health-care workers.

METHODS

This substudy is a nested randomised controlled trial embedded within the BRACE trial (NCT04327206). Specifically, this substudy enrolled Brazilian health-care workers (aged ≥18 years) from three sites in Brazil (Manaus, Campo Grande, and Rio de Janeiro) irrespective of previously receiving BCG vaccination. Participants were excluded if they had contraindications to BCG vaccination, more than 1 month of treatment with specific tuberculosis treatment drugs, previous adverse reactions to BCG, recent BCG vaccination, or non-compliance with assigned interventions. Those eligible were randomly assigned (1:1) to either the BCG group (0·1 mL intradermal injection of BCG-Denmark [Danish strain 1331; AJ Vaccines, Copenhagen]) or the placebo group (intradermal injection of 0·9% saline) using a web-based randomisation process in variable-length blocks (2, 4, or 6), and were stratified based on the study site, age (<40, ≥40 to <60, ≥60 years), and comorbidity presence (diabetes, chronic respiratory disease, cardiac condition, hypertension). Sealed syringes were used to prevent inadvertent disclosure of group assignments. The QuantiFERON-TB Gold (QFT) Plus test (Qiagen; Hilden, Germany) was used for baseline and 12-month tuberculosis infection assessments. The primary efficacy outcome was QFT Plus conversion (≥0·35 IU/mL) by 12 months following vaccination in participants who had a negative baseline result (<0·35 IU/mL).

FINDINGS

Between Oct 7, 2020, and April 12, 2021, 1985 (77·3%) of 2568 participants were eligible for QFT Plus assessment at 12 months and were included in this substudy; 996 (50·2%) of 1985 were in the BCG group and 989 (49·8%) were in the placebo group. Overall, 1475 (74·3%) of 1985 participants were women and 510 (25·7%) were men, and the median age was 39 years (IQR 32-47). During the first 12 months, QFT Plus conversion occurred in 66 (3·3%) of 1985 participants, with no significant differences by study site (p=0·897). Specifically, 34 (3·4%) of 996 participants had initial QFT conversion in the BCG group compared with 32 (3·2%) of 989 in the placebo group (risk ratio 1·09 [95% CI 0·67-1·77]; p=0·791).

INTERPRETATION

BCG-Denmark vaccination did not reduce initial QFT Plus conversion risk in Brazilian health-care workers. This finding underscores the need to better understand tuberculosis prevention in populations at high risk.

FUNDING

Bill & Melinda Gates Foundation, the Minderoo Foundation, Sarah and Lachlan Murdoch, the Royal Children's Hospital Foundation, Health Services Union NSW, the Peter Sowerby Foundation, SA Health, the Insurance Advisernet Foundation, the NAB Foundation, the Calvert-Jones Foundation, the Modara Pines Charitable Foundation, the United Health Group Foundation, Epworth Healthcare, and individual donors.

TRANSLATION

For the Portuguese translation of the abstract see Supplementary Materials section.

摘要

背景

卡介苗(BCG)疫苗对成人肺结核的有效性仍不确定。本研究旨在评估接种丹麦卡介苗(BCG-Denmark)预防巴西卫生保健工作者初始和持续干扰素-γ释放试验(IGRA)转化的效果。

方法

本亚研究是 BRACE 试验(NCT04327206)中的一项嵌套随机对照试验。具体来说,本亚研究纳入了来自巴西三个地点(马瑙斯、坎波格兰德和里约热内卢)的巴西卫生保健工作者(年龄≥18 岁),无论他们之前是否接种过 BCG 疫苗。如果参与者有 BCG 疫苗接种禁忌、正在接受特定的结核病治疗药物治疗 1 个月以上、之前对 BCG 有不良反应、最近接种过 BCG 疫苗或不遵守分配的干预措施,则将其排除在外。符合条件的参与者被随机分配(1:1)到 BCG 组(0.1mL 皮内注射丹麦株 1331 卡介苗[丹麦疫苗,哥本哈根])或安慰剂组(皮内注射 0.9%生理盐水),使用基于网络的随机化过程,以可变长度的块(2、4 或 6)进行分组,并根据研究地点、年龄(<40、≥40 至<60、≥60 岁)和合并症存在情况(糖尿病、慢性呼吸道疾病、心脏状况、高血压)进行分层。使用密封注射器防止意外披露分组情况。使用 QuantiFERON-TB Gold(QFT)Plus 试验(Qiagen;德国黑尔德)进行基线和 12 个月的结核病感染评估。主要疗效终点是接种后 12 个月时 QFT Plus 转换(≥0.35IU/mL),即在基线时结果为阴性(<0.35IU/mL)的参与者。

结果

2020 年 10 月 7 日至 2021 年 4 月 12 日,共有 2568 名参与者中有 1985 名(77.3%)有资格在 12 个月时进行 QFT Plus 评估,并纳入本亚研究;1985 名参与者中,996 名(50.2%)在 BCG 组,989 名(49.8%)在安慰剂组。总体而言,1985 名参与者中有 1475 名(74.3%)为女性,510 名(25.7%)为男性,中位年龄为 39 岁(IQR 32-47)。在最初的 12 个月中,1985 名参与者中有 66 名(3.3%)发生了 QFT Plus 转换,不同研究地点之间没有显著差异(p=0.897)。具体来说,BCG 组有 34 名(3.4%)参与者出现初始 QFT 转换,安慰剂组有 32 名(3.2%)参与者出现初始 QFT 转换(风险比 1.09[95%CI 0.67-1.77];p=0.791)。

解释

丹麦卡介苗(BCG-Denmark)疫苗接种并不能降低巴西卫生保健工作者初始 QFT Plus 转换风险。这一发现强调了需要更好地了解高危人群中的结核病预防。

资助

比尔及梅琳达·盖茨基金会、米尔杜拉基金会、萨拉和拉克兰·默多克、皇家儿童医院基金会、新南威尔士州卫生服务工会、彼得·索伯里基金会、南澳大利亚州卫生署、保险顾问网络基金会、澳大利亚国家银行基金会、卡尔弗特-琼斯基金会、莫达拉松树慈善基金会、联合健康集团基金会、伊普沃思医疗保健公司和个人捐赠者。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6186/11111441/3db9966f461b/gr1.jpg

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