Ibrahim Serag, Mohamed Abouzid, Mostafa Hossam El Din Moawad, Jaber H Jaradat, Mohamed Hendawy, Nada Ibrahim Hendi, Ibraheem M Alkhawaldeh, Judy Ahmed Abdullah, Mona Mahmoud Elsakka, Muneeb Ahmad Muneer, Marwa Aboelhassan Elnagar, Mohamed Adel Fakher, Aya J Elkenani, Abdallah Abbas
{"title":"Vaccines for Alzheimer's disease: a brief scoping review.","authors":"Ibrahim Serag, Mohamed Abouzid, Mostafa Hossam El Din Moawad, Jaber H Jaradat, Mohamed Hendawy, Nada Ibrahim Hendi, Ibraheem M Alkhawaldeh, Judy Ahmed Abdullah, Mona Mahmoud Elsakka, Muneeb Ahmad Muneer, Marwa Aboelhassan Elnagar, Mohamed Adel Fakher, Aya J Elkenani, Abdallah Abbas","doi":"10.1007/s10072-025-08073-2","DOIUrl":null,"url":null,"abstract":"<p><strong>Background: </strong>Alzheimer's disease (AD) is a neurodegenerative disorder and the most common cause of dementia among older adults. Existing treatments-such as cholinesterase inhibitors, N-methyl-D-aspartate receptor antagonists, and monoclonal antibodies targeting amyloid beta-can improve functional and neuropsychiatric outcomes but fail to prevent disease onset, halt progression, or adequately reduce amyloid-beta burden. Consequently, research efforts have shifted to primary prevention through immunization, although the efficacy of these strategies remains uncertain. This review explores the efficacy, safety, and adverse events of current immunotherapies for AD and discusses future research and clinical implications.</p><p><strong>Methods: </strong>A scoping review was conducted following the Preferred Reporting Items for Systematic Reviews and Meta-Analyses for Scoping Reviews (PRISMA-SR) checklist. A systematic search was carried out using PubMed, Scopus, and Web of Science.</p><p><strong>Results: </strong>A total of 145 studies were included. Preclinical research often employed transgenic mouse models to investigate AD pathology and vaccine benefits, while Phase I and II clinical trials centered on safety and preliminary efficacy in humans. Most studies were conducted in the USA, China, and Japan, highlighting these countries' strong clinical trial infrastructure. Vaccination frequently reduced amyloid-beta or tau pathology in preclinical settings, although cognitive outcomes were inconsistent. Clinical trials primarily focused on safety and immune response, with newer vaccines such as ABvac40 demonstrating encouraging results and minimal adverse events.</p><p><strong>Conclusion: </strong>Although AD vaccines show promise in preclinical settings, longer and more comprehensive clinical trials are necessary to determine their long-term efficacy and safety. Standardized protocols and efforts to reduce regional disparities in research would facilitate better comparability and generalizability of findings, thereby guiding the future development of effective immunotherapies for Alzheimer's disease.</p>","PeriodicalId":19191,"journal":{"name":"Neurological Sciences","volume":" ","pages":"2925-2950"},"PeriodicalIF":2.7000,"publicationDate":"2025-07-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Neurological Sciences","FirstCategoryId":"3","ListUrlMain":"https://doi.org/10.1007/s10072-025-08073-2","RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2025/3/20 0:00:00","PubModel":"Epub","JCR":"Q2","JCRName":"CLINICAL NEUROLOGY","Score":null,"Total":0}
引用次数: 0
Abstract
Background: Alzheimer's disease (AD) is a neurodegenerative disorder and the most common cause of dementia among older adults. Existing treatments-such as cholinesterase inhibitors, N-methyl-D-aspartate receptor antagonists, and monoclonal antibodies targeting amyloid beta-can improve functional and neuropsychiatric outcomes but fail to prevent disease onset, halt progression, or adequately reduce amyloid-beta burden. Consequently, research efforts have shifted to primary prevention through immunization, although the efficacy of these strategies remains uncertain. This review explores the efficacy, safety, and adverse events of current immunotherapies for AD and discusses future research and clinical implications.
Methods: A scoping review was conducted following the Preferred Reporting Items for Systematic Reviews and Meta-Analyses for Scoping Reviews (PRISMA-SR) checklist. A systematic search was carried out using PubMed, Scopus, and Web of Science.
Results: A total of 145 studies were included. Preclinical research often employed transgenic mouse models to investigate AD pathology and vaccine benefits, while Phase I and II clinical trials centered on safety and preliminary efficacy in humans. Most studies were conducted in the USA, China, and Japan, highlighting these countries' strong clinical trial infrastructure. Vaccination frequently reduced amyloid-beta or tau pathology in preclinical settings, although cognitive outcomes were inconsistent. Clinical trials primarily focused on safety and immune response, with newer vaccines such as ABvac40 demonstrating encouraging results and minimal adverse events.
Conclusion: Although AD vaccines show promise in preclinical settings, longer and more comprehensive clinical trials are necessary to determine their long-term efficacy and safety. Standardized protocols and efforts to reduce regional disparities in research would facilitate better comparability and generalizability of findings, thereby guiding the future development of effective immunotherapies for Alzheimer's disease.
背景:阿尔茨海默病(AD)是一种神经退行性疾病,是老年人痴呆症的最常见原因。现有的治疗方法,如胆碱酯酶抑制剂、n -甲基- d-天冬氨酸受体拮抗剂和靶向淀粉样蛋白-的单克隆抗体,可以改善功能和神经精神预后,但不能预防疾病的发生、停止进展或充分减少淀粉样蛋白-负担。因此,研究工作已转向通过免疫进行初级预防,尽管这些策略的效力仍不确定。这篇综述探讨了目前免疫疗法治疗AD的有效性、安全性和不良事件,并讨论了未来的研究和临床意义。方法:根据系统评价和范围评价荟萃分析首选报告项目(PRISMA-SR)清单进行范围评价。使用PubMed、Scopus和Web of Science进行系统检索。结果:共纳入145项研究。临床前研究通常采用转基因小鼠模型来研究阿尔茨海默病的病理和疫苗的益处,而I期和II期临床试验主要集中在人体的安全性和初步疗效上。大多数研究在美国、中国和日本进行,突出了这些国家强大的临床试验基础设施。尽管认知结果不一致,但在临床前接种疫苗通常会降低β淀粉样蛋白或tau蛋白病理。临床试验主要侧重于安全性和免疫反应,ABvac40等较新的疫苗显示出令人鼓舞的结果和最小的不良事件。结论:尽管阿尔茨海默病疫苗在临床前显示出希望,但需要更长时间和更全面的临床试验来确定其长期疗效和安全性。标准化的方案和减少研究区域差异的努力将促进更好的可比性和研究结果的普遍性,从而指导阿尔茨海默病有效免疫疗法的未来发展。
期刊介绍:
Neurological Sciences is intended to provide a medium for the communication of results and ideas in the field of neuroscience. The journal welcomes contributions in both the basic and clinical aspects of the neurosciences. The official language of the journal is English. Reports are published in the form of original articles, short communications, editorials, reviews and letters to the editor. Original articles present the results of experimental or clinical studies in the neurosciences, while short communications are succinct reports permitting the rapid publication of novel results. Original contributions may be submitted for the special sections History of Neurology, Health Care and Neurological Digressions - a forum for cultural topics related to the neurosciences. The journal also publishes correspondence book reviews, meeting reports and announcements.