Amnion epithelial cells - a novel therapy for ischemic stroke?

被引:25
作者
Evans, Megan A. [1 ]
Broughton, Brad R. S. [2 ]
Drummond, Grant R. [1 ]
Ma, Henry [3 ]
Phan, Thanh G. [3 ]
Wallace, Euan M. [4 ,5 ]
Lim, Rebecca [4 ,5 ]
Sobey, Christopher G. [1 ]
机构
[1] La Trobe Univ, Dept Physiol Anat & Microbiol, Melbourne, Vic, Australia
[2] Monash Univ, Dept Pharmacol, Biomed Discovery Inst, Cardiovasc Dis Program, Melbourne, Vic, Australia
[3] Monash Univ, Dept Med, Melbourne, Vic, Australia
[4] Hudson Inst Med Res, Ritchie Ctr, Melbourne, Vic, Australia
[5] Monash Univ, Dept Obstet & Gynaecol, Melbourne, Vic, Australia
关键词
ischemic stroke; cerebral infarction; stem cells; human amnion epithelial cells; inflammation; immunosuppression; brain repair; mouse; non-human primate;
D O I
10.4103/1673-5374.235223
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Stroke is a leading cause of death and disability and new therapies are desperately needed. Given the complex nature of ischemic brain injury, it has been postulated that cell-based therapies may be useful. However, cell resources, invasive extraction procedures, immunological rejection, tumorigenesis and ethical challenges make it unlikely that many stem cell types could serve as a practical source for therapy. By contrast, these issues do not pertain to human amnion epithelial cells (hAECs), which are placenta-derived stem cells. We recently assessed the effects of systemically delivered hAECs on stroke outcome using four animal models of stroke. We demonstrated that when injected intravenously after ischemia onset, hAECs migrate preferentially to the spleen and injured brain to limit apoptosis and inflammation, and attenuate early brain infiltration of immune cells, progression of infarction and systemic immunosuppression and to ultimately ameliorate functional deficits. When administration of hAECs is delayed by 1-3 days post-stroke, long-term functional recovery can still be enhanced in young and aged mice of either sex. Moreover, our proof-of-principle findings suggest that hAECs are effective at limiting post-stroke infarct development in non-human primates. Overall, the results suggest that hAECs could be a viable clinical stroke therapy.
引用
收藏
页码:1346 / 1349
页数:4
相关论文
共 12 条
[1]   Inflammation and Stroke: An Overview [J].
Anrather, Josef ;
Iadecola, Costantino .
NEUROTHERAPEUTICS, 2016, 13 (04) :661-670
[2]   Post-stroke inflammation and the potential efficacy of novel stem cell therapies: focus on amnion epithelial cells [J].
Broughton, Brad R. S. ;
Lim, Rebecca ;
Arumugam, Thiruma V. ;
Drummond, Grant R. ;
Wallace, Euan M. ;
Sobey, Christopher G. .
FRONTIERS IN CELLULAR NEUROSCIENCE, 2013, 6
[3]   Acute or Delayed Systemic Administration of Human Amnion Epithelial Cells Improves Outcomes in Experimental Stroke [J].
Evans, Megan A. ;
Lim, Rebecca ;
Kim, Hyun Ah ;
Chu, Hannah X. ;
Gardiner-Mann, Chantelle V. ;
Taylor, Kimberly W. E. ;
Chan, Christopher T. ;
Brait, Vanessa H. ;
Lee, Seyoung ;
Quynh Nhu Dinh ;
Vinh, Antony ;
Phan, Thanh G. ;
Srikanth, Velandai K. ;
Ma, Henry ;
Arumugam, Thiruma V. ;
Fann, David Y. ;
Poh, Luting ;
Hunt, Cameron P. J. ;
Pouton, Colin W. ;
Haynes, John M. ;
Selemidis, Stavros ;
Kwan, William ;
Teo, Leon ;
Bourne, James A. ;
Neumann, Silke ;
Young, Sarah ;
Gowing, Emma K. ;
Drummond, Grant R. ;
Clarkson, Andrew N. ;
Wallace, Euan M. ;
Sobey, Christopher G. ;
Broughton, Brad R. S. .
STROKE, 2018, 49 (03) :700-709
[4]   Recommendations for standards regarding preclinical neuroprotective and restorative drug development [J].
Feinklestein, SP ;
Fisher, M ;
Furland, AJ ;
Goldstein, LB ;
Gorelick, PB ;
Kaste, M ;
Lees, KR ;
Traystman, RJ ;
Albers, GW ;
Anwer, UE ;
Ashwood, T ;
Barone, FC ;
Basta, SL ;
Bogousslavsky, J ;
Buchan, AM ;
Cady, WJ ;
Chan, PH ;
Clemens, JA ;
Cox, BF ;
Craddock, RE ;
Cramer, SC ;
del Zoppo, GJ ;
Dielrich, WD ;
Elliott, P ;
Faden, AI ;
Feuerstein, GZ ;
Ginsberg, MD ;
Gold, M ;
Greene, WL ;
Hall, ED ;
Hsu, CY ;
Hunter, AJ ;
Lai, M ;
Lesko, LM ;
Levy, DE ;
Li, FH ;
Locke, KW ;
Lodge, D ;
Lowe, D ;
Marcoux, FW ;
McCulloch, J ;
McDermott, J ;
Meibach, R ;
Messersmith, EK ;
Moseley, M ;
Moskowitz, MA ;
Mueller, AL ;
Munro, F ;
Nudo, RJ ;
Oeda, J .
STROKE, 1999, 30 (12) :2752-2758
[5]   Human amniotic epithelial cells ameliorate behavioral dysfunction and reduce infarct size in the rat middle cerebral artery occlusion model [J].
Liu, Tianjin ;
Wu, Jiacai ;
Huang, Qin ;
Hou, Yanan ;
Jiang, Zhihua ;
Zang, Shaoyun ;
Guo, Lihe .
SHOCK, 2008, 29 (05) :603-611
[6]   Heart Disease and Stroke Statistics-2016 Update A Report From the American Heart Association [J].
Mozaffarian, Dariush ;
Benjamin, Emelia J. ;
Go, Alan S. ;
Arnett, Donna K. ;
Blaha, Michael J. ;
Cushman, Mary ;
Das, Sandeep R. ;
de Ferranti, Sarah ;
Despres, Jean-Pierre ;
Fullerton, Heather J. ;
Howard, Virginia J. ;
Huffman, Mark D. ;
Isasi, Carmen R. ;
Jimenez, Monik C. ;
Judd, Suzanne E. ;
Kissela, Brett M. ;
Lichtman, Judith H. ;
Lisabeth, Lynda D. ;
Liu, Simin ;
Mackey, Rachel H. ;
Magid, David J. ;
McGuire, Darren K. ;
Mohler, Emile R., III ;
Moy, Claudia S. ;
Muntner, Paul ;
Mussolino, Michael E. ;
Nasir, Khurram ;
Neumar, Robert W. ;
Nichol, Graham ;
Palaniappan, Latha ;
Pandey, Dilip K. ;
Reeves, Mathew J. ;
Rodriguez, Carlos J. ;
Rosamond, Wayne ;
Sorlie, Paul D. ;
Stein, Joel ;
Towfighi, Amytis ;
Turan, Tanya N. ;
Virani, Salim S. ;
Woo, Daniel ;
Yeh, Robert W. ;
Turner, Melanie B. .
CIRCULATION, 2016, 133 (04) :E38-E360
[7]   Safety and effectiveness of stem cell therapies in early-phase clinical trials in stroke: a systematic review and meta-analysis [J].
Nagpal, Anjali ;
Choy, Fong Chan ;
Howell, Stuart ;
Hillier, Susan ;
Chan, Fiona ;
Hamilton-Bruce, Monica A. ;
Koblar, Simon A. .
STEM CELL RESEARCH & THERAPY, 2017, 8
[8]  
Phan TG, 2018, FRONT NEUROL
[9]   Translocation and dissemination of commensal bacteria in post-stroke infection [J].
Stanley, Dragana ;
Mason, Linda J. ;
Mackin, Kate E. ;
Srilchanta, Yogitha N. ;
Lyras, Dena ;
Prakash, Monica D. ;
Nurgali, Kulmira ;
Venegas, Andres ;
Hill, Michael D. ;
Moore, Robert J. ;
Wong, Connie H. Y. .
NATURE MEDICINE, 2016, 22 (11) :1277-1284
[10]   Amnion cell-mediated immune modulation following bleomycin challenge: controlling the regulatory T cell response [J].
Tan, Jean L. ;
Chan, Siow T. ;
Lo, Camden Y. ;
Deane, James A. ;
McDonald, Courtney A. ;
Bernard, Claude C. A. ;
Wallace, Euan M. ;
Lim, Rebecca .
STEM CELL RESEARCH & THERAPY, 2015, 6