Abstract
We have found that a small number of purified Th2-biased Abeta-specific T cells are sufficient to provide profound cognitive and pathological benefits in an APP+PS1 mouse model for Alzheimer's disease. Six weeks after receiving T cell infusions, cognitively-impaired mice performed significantly better in working memory tasks, which correlated with higher plasma levels of soluble Abeta. Pathological analysis of the hippocampus revealed a 30% decrease of plaque-associated microglia and less vascular amyloidosis in T cell treated mice. The infusion of Abeta-specific Th2 cells also reduced plasma levels of IFN-gamma, TNF-alpha, GM-CSF, IL-2 and IL-4, which are elevated in untreated APP+PS1 mice. No significant immune cell infiltration and no anti-Abeta antibody titers occurred in the T cell treated mice. These results demonstrate that Abeta-specific Th2 cells are sufficient to reverse cognitive impairment and provide multiple pathological benefits in an Alzheimer's mouse model.
MeSH Terms
Adoptive Transfer
Alzheimer Disease/physiopathology,therapy
Amyloid beta-Peptides/blood,immunology
Amyloidosis/therapy
Animals
Cognition Disorders/physiopathology,therapy
Disease Models, Animal
Granulocyte-Macrophage Colony-Stimulating Factor/blood
Hippocampus/physiopathology
Interferon-gamma/blood
Interleukin-2/blood
Interleukin-4/blood
Maze Learning/physiology
Memory Disorders/physiopathology,therapy
Mice
Mice, Transgenic
Microglia/physiology
Th2 Cells/immunology,transplantation
Tumor Necrosis Factor-alpha/blood
Chemicals
Amyloid beta-Peptides
Interleukin-2
Tumor Necrosis Factor-alpha
Interleukin-4
Interferon-gamma
Granulocyte-Macrophage Colony-Stimulating Factor
Authors & Affiliations
6 authors, click to expand affiliations / ORCID
Cao Chuanhai
The Johnnie B. Byrd Sr. Alzheimer's Center and Research Institute, Tampa, FL 33613, USA.
Arendash Gary W
Dickson Alexander
Mamcarz Malgorzata B
Lin Xiaoyang
Ethell Douglas W
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