Journal of Clinical Immunology

, Volume 34, Supplement 1, pp 74–79 | Cite as

Clinical Trials of Intravenous Immunoglobulin for Alzheimer’s Disease

  • Norman RelkinEmail author


The human polyclonal IgG antibody preparation known as Intravenous Immunoglobulin (IVIG) has been under study as a potential treatment for Alzheimer’s disease (AD) since 2002. Preclinical and clinical studies have shown that IVIG has anti-amyloid and immune modulatory properties relevant to treating neurodegenerative disorders. In early stage AD clinical trials, IVIG was found to reduce cognitive decline and increase brain glucose metabolism. Unfortunately, IVIG failed to meet primary outcome objectives in the North American Phase 3 clinical trial in mild to moderate AD. However, positive cognitive signals were observed in pre-planned subgroup analyses among APOE-ε4 carriers and moderately impaired AD patients. Biomarker studies revealed dose dependent increases in plasma and CSF immunoglobulins and decreases in beta amyloid-42 levels. In addition, IVIG treatment was generally safe and well-tolerated. These findings suggest that naturally occurring human anti-amyloid antibodies may play a physiologic role in the clearance of aggregated amyloid proteins. While the results of clinical trials to date do not provide support for the use of IVIG to treat AD at the doses tested, additional studies of IVIG’s mechanisms are warranted and may guide the development of more effective therapies for AD in the future.


Human intravenous immunoglobulin polyclonal IgG alzheimer’s disease beta amyloid immunotherapy clinical trials 



The author acknowledges the support of the National Institute on Aging through a grant to the Alzheimer’s disease Cooperative Study Group and Baxter for its support of all phases of the US studies of IVIG for Alzheimer’s.


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Copyright information

© Springer Science+Business Media New York 2014

Authors and Affiliations

  1. 1.Department of Neurology and Brain Mind Research InstituteWeill Cornell Medical CollegeNew YorkUSA

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