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Amyloid-Β Peptide-Targeting Immunotherapy in Alzheimer Disease: A Systematic Review of Clinical Studies Publisher



Mosleh H1 ; Ghayyem H2 ; Sharifpour S3 ; Eyvani K4 ; Niknejad S5 ; Davoodi A5 ; Zarebidoki A6 ; Ahmadian S7 ; Kohandel K8 ; Eghbaldoost A9 ; Pour MJ10 ; Binaei S11 ; Abbasi AS4 ; Kosari M12
Authors
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Authors Affiliations
  1. 1. Hearing Disorder Research Center, Loghman Hakim Hospital, Shahid Beheshti University of Medical Sciences, Tehran, Iran
  2. 2. Student Research Committee, School of Medicine, Shahid Beheshti University of Medical Sciences, Tehran, Iran
  3. 3. Department of Internal Medicine, Faculty of Medicine, Tehran Medical Sciences Branch, Islamic Azad University, Tehran, Iran
  4. 4. Student Research Committee, School of Medicine, Guilan University of Medical Sciences, Rasht, Iran
  5. 5. Noncommunicable Diseases Research Center, Fasa University of Medical Sciences, Fasa, Iran
  6. 6. Student Research Committee, Shahid Sadoughi University of Medical Sciences, Yazd, Iran
  7. 7. Department of Internal Medicine, School of Medicine, Isfahan University of Medical Sciences, Isfahan, Iran
  8. 8. Multiple Sclerosis Researcher Center, Neuroscience Institute, Tehran University of Medical Sciences, Tehran, Iran
  9. 9. Student Research Committee, Golestan University of Medical Sciences, Gorgan, Iran
  10. 10. Institue of Biology and Medicine, Taras Shevchenko National University of Kyiv, Kyiv, Ukraine
  11. 11. Endocrinology and Metabolism Research Center, Hormozgan University of Medical Sciences, Bandar Abbas, Iran
  12. 12. Department of Neurology, Tongji Medical College, Tongji Hospital, Huazhong University of Science and Technology, Wuhan, China

Source: Caspian Journal of Neurological Sciences Published:2024


Abstract

Background: Amyloid-β (Aβ) peptide accumulation in the brain is a pathological hallmark of Alzheimer disease (AD). Because of the relationship between the Aβ plaque formation and AD progression, targeting Aβ has been advocated as a treatment strategy for this disease. Several studies have focused on immunotherapy methods, such as different vaccination approaches. Materials & Methods: In this systematic review, we explored the main features of the vaccines used to date, including their efficiency in inducing anti-Aβ antibodies and removing Aβ plaques. We also summarized the reported clinical outcomes and mortality rates. A total of 29 articles written in English that describe human clinical trials using three different vaccines (AN1792, CAD106 and AADVac) were reviewed. Results: Based on these studies, most of the patients who received one of these vaccines showed a significant anti-Aβ antibody response at some point during the trial. Several studies reported a decline in Aβ plaque load and an increase in Aβ phagocytosis in different brain regions. The time intervals between the initial vaccination and the booster doses vary among studies, but a 30-day interval has been suggested as the most appropriate by most studies. Meningoencephalitis, microhemorrhages, amyloid encephalopathy, allergic dermatitis and atrial fibrillation have been reported as the most common adverse effects in vaccinated patients. Conclusion: Clinical investigations have shown improved functional and cognitive outcomes, such as the mini-mental state examination score (MMSE), for vaccinated patients compared to the control groups. However, more human clinical studies are needed for a more conclusive evaluation of the properties of different vaccines. © 2024 The Author(s); This is an open access article distributed under the terms of the Creative Commons Attribution License (CC-By-NC: https://creativecommons.org/licenses/by-nc/4.0/ legalcode.en), which permits use, distribution, and reproduction in any medium, provided the original work is properly cited and is not used for commercial purposes.