Vaccinology and Immunology Research Trials Unit, Women's and Children's Hospital, Adelaide, South Australia, Australia
Adelaide Medical School, The University of Adelaide, Adelaide, South Australia, Australia.
BMJ Open. 2024 May 8;14(5):e079144. doi: 10.1136/bmjopen-2023-079144.
The effectiveness of antibiotics for treating gonococcal infections is compromised due to escalating antibiotic resistance; and the development of an effective gonococcal vaccine has been challenging. Emerging evidence suggests that the licensed meningococcal B (MenB) vaccine, 4CMenB is effective against gonococcal infections due to cross-reacting antibodies and 95% genetic homology between the two bacteria, and that cause the diseases. This project aims to undertake epidemiological and genomic surveillance to evaluate the long-term protection of the 4CMenB vaccine against gonococcal infections in the Northern Territory (NT) and South Australia (SA), and to determine the potential benefit of a booster vaccine doses to provide longer-term protection against gonococcal infections.
This observational study will provide long-term evaluation results of the effectiveness of the 4CMenB vaccine against gonococcal infections at 4-7 years post 4CMenB programme implementation. Routine notifiable disease notifications will be the basis for assessing the impact of the vaccine on gonococcal infections. Pathology laboratories will provide data on the number and percentage of positive tests relative to all tests administered and will coordinate molecular sequencing for isolates. Genome sequencing results will be provided by SA Pathology and Territory Pathology/New South Wales Health Pathology, and linked with notification data by SA Health and NT Health. There are limitations in observational studies including the potential for confounding. Confounders will be analysed separately for each outcome/comparison.
The protocol and all study documents have been reviewed and approved by the SA Department for Health and Well-being Human Research Ethics Committee (HREC/2022/HRE00308), and the evaluation will commence in the NT on receipt of approval from the NT Health and Menzies School of Health Research Human Research Ethics Committee. Results will be published in peer-reviewed journals and presented at scientific meetings and public forums.
由于抗生素耐药性不断上升,抗生素治疗淋病感染的效果受到影响;而且,开发有效的淋病疫苗一直具有挑战性。新出现的证据表明,已获许可的脑膜炎 B 型(MenB)疫苗 4CMenB 由于交叉反应性抗体和两种细菌之间 95%的基因同源性,对淋病感染有效,这两种细菌可导致这两种疾病。本项目旨在开展流行病学和基因组监测,以评估 4CMenB 疫苗在北领地(NT)和南澳大利亚(SA)对淋病感染的长期保护作用,并确定加强疫苗剂量以提供更长时间的淋病感染保护的潜在益处。
本观察性研究将提供 4CMenB 疫苗接种方案实施后 4-7 年对淋病感染的有效性的长期评估结果。常规报告的传染病将作为评估疫苗对淋病感染影响的基础。病理学实验室将提供有关阳性测试数量和百分比的数据,相对于所有进行的测试,并将协调对分离株的分子测序。基因组测序结果将由南澳大利亚病理学和领地病理学/新南威尔士州卫生病理学提供,并由南澳大利亚卫生和北领地卫生通过 SA 健康和 NT 健康进行链接。观察性研究存在局限性,包括存在混杂因素的可能性。将分别分析每个结局/比较的混杂因素。
该方案和所有研究文件均已由南澳大利亚卫生部和福利部人类研究伦理委员会(HREC/2022/HRE00308)审查和批准,并且一旦收到北领地卫生和 Menzies 健康研究人类研究伦理委员会的批准,将在 NT 开始评估。结果将发表在同行评议的期刊上,并在科学会议和公共论坛上展示。