期刊
NEUROBIOLOGY OF DISEASE
卷 101, 期 -, 页码 27-39出版社
ACADEMIC PRESS INC ELSEVIER SCIENCE
DOI: 10.1016/j.nbd.2017.02.001
关键词
BCG; Vaccination; AD; Monocytes; IFN-gamma; Anti-inflammation
资金
- National Natural Science Foundation of China [31371130]
- Special Foundation of Education Department of Guangdong Province, China [2013-159]
- Medical Scientific Research Foundation of Guangdong Province, China [2013-159]
- Foundation of Medical Science and Technology Research of Guangdong Province [A2016273]
The immune system plays a crucial role in the progression of Alzheimer's disease (AD). Recently, immune-dependent cascade induced by systemic immune activation has been verified to play a beneficial role in AD mouse models. Here, we tested whether Bacillus Calmette-Guerin (BCG) immunization alters AD pathology and cognitive dysfunction in APP/PS1 AD mouse model, and with 4A beta 1-15 vaccination as positive control. It was found that BCG treatment reversed the cognitive decline to the extent observed in 4A beta 1-15group, but did not reduce the pamyloid (A beta) burden in the brain. Then, we demonstrated the enhanced recruitment of inflammation-resolving monocytes across the choroid plexus and perivascular spaces to cerebral sites of plaque pathology in APP/PS1 mice immunized with BCG. Furthermore, elevated splenocyte Foxp3+ regulatory T cell levels in the control APP/PS1 mice were down-regulated back to the wild-type (WT) levels by BCG treatment but not 4A beta 1-15 vaccination. In addition, BCG treatment induced the production of more circulating interferon (IFN)-gamma than the controls and 4A beta 1-15 vaccination. Though the similar reductions in brain levels of pro-inflammatory cytokines were observed in the BCG and 4A beta 1-15groups compared to the controls, only BCG had the great effect in upregulating cerebral anti-inflammatory cytokine levels as well as elevating the expression of neurotrophic factors in the brain of APP/PSI mice. Thus, it is suggested that BCG exerts a beneficial immunomodulatory effect in APP/PS1 mice through mitigation of systemic immune suppression, induction of IFN-'y response and alleviation of the neuroinflammatory response. (C) 2017 Elsevier Inc. All rights reserved.
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