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Mitigating Coronavirus-Induced Acute Respiratory Distress Syndrome by Radiotherapy
被引:10
|作者:
Li, Jian Jian
[1
]
机构:
[1] Univ Calif Davis, Dept Radiat Oncol, NCI Designated Comprehens Canc Ctr, Sch Med, 4501 X St,Suite G0140, Sacramento, CA 95817 USA
来源:
关键词:
INDUCED ADAPTIVE RESPONSE;
CONVALESCENT PLASMA;
IONIZING-RADIATION;
HUMAN-LYMPHOCYTES;
T-CELLS;
CYTOKINE STORM;
NEOPLASTIC TRANSFORMATION;
RADIOADAPTIVE RESPONSE;
IN-VITRO;
X-RAYS;
D O I:
10.1016/j.isci.2020.101215
中图分类号:
O [数理科学和化学];
P [天文学、地球科学];
Q [生物科学];
N [自然科学总论];
学科分类号:
07 ;
0710 ;
09 ;
摘要:
The acute respiratory distress syndrome (ARDS) induced by SARS-CoV-2-mediated cytokine storm (CS) in lungs leads to the high mortality in COVID-19 patients. To reduce ARDS, an ideal approach is to diminish virus loading by activating immune cells for CS prevention or to suppress the overactive cytokine-releasing immune cells for CS inhibition. Here, a potential radiation-mediated CS regulation is raised by reevaluating the radiation-mediated pneumonia control in the 1920s, with the following latent advantages of lung radiotherapy (LR) in treatment of COVID-19: (1) radiation accesses poorly circulated tissue more efficiently than blood-delivered medications; (2) low-dose radiation (LDR)-mediated metabolic rewiring and immune cell activation inhibit virus loading; (3) pre-consumption of immune reserves by LDR decreases CS severity; (4) high-erdose radiation (HDR) within lung-tolerable doses relieves CS by eliminating in situ overactive cytokine-releasing cells. Thus, LDR and HDR or combined with antiviral and life-supporting modalities may mitigate SARS-CoV-2 and other virus-mediated ARDS.
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页数:11
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