Insoluble Aβ40 and Aβ42 levels were also elevated but did not reach statistical significance ( P > 0.21; Figure 2 C and D).
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Effects of human intravenous immunoglobulin on amyloid pathology and neuroinflammation in a mouse model of Alzheimer's disease.
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Mean GFAP immunopositive area for astrocyte reactivity was lower in hIVIG treated mice than in the saline group, but failed to reach statistical significance.
Nevertheless, even the longer hIVIG treatment did not reduce amyloid deposition but induced selective immunomodulation and enhanced neurogenesis, which both may be significant for the beneficial clinical effects of hIVIG in AD patients.