Neurodegenerative disease treatments by direct TNF reduction, SB623 cells, maraviroc and irisin and MCC950, from an inflammatory perspective - a Commentary

被引:11
作者
Clark, I. A. [1 ]
Vissel, B. [2 ,3 ]
机构
[1] Australian Natl Univ, Res Sch Biol, Canberra, ACT, Australia
[2] Univ Technol, Fac Sci, Ctr Neurosci & Regenerat Med, Sydney, NSW, Australia
[3] St Vincents Ctr Appl Med Res, Sydney, NSW, Australia
关键词
Neurodegenerative disease; TNF; SB623; cells; maraviroc; irisin; MCC950; TUMOR-NECROSIS-FACTOR; TRAUMATIC BRAIN-INJURY; MESENCHYMAL STEM-CELLS; ALPHA SYNTHESIS INHIBITOR; LONG-TERM POTENTIATION; ALZHEIMERS-DISEASE; SYNAPTIC PLASTICITY; CLINICAL-OUTCOMES; CEREBROSPINAL-FLUID; NLRP3; INFLAMMASOME;
D O I
10.1080/14737175.2019.1618710
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Introduction: The importance of excessive cerebral tumor necrosis factor (TNF) concentrations as one of the central tenets of the pathogenesis of the neurodegenerative diseases is now widely known, but variably accepted. Areas covered: Here we update the field by including material that is freely available on the large databases, particularly PubMed. We include the therapeutic outcomes with etanercept (a widely used specific anti-TNF biological), XPro1595 (a new double negative TNF inhibitor), 3,6(1)-dithiothalidomide, implanted SB623 stem cells, maraviroc (a CCR5 inhibitor used to treat AIDS), MCC950 (an NLRP3 inhibitor), and changes in the hormone irisin. Expert opinion: Remarkably, considering the ample literature that links SB623 cells, maraviroc, MCC950 and irisin to TNF, these publications do not mention this cytokine, and therefore not their implicit involvement with controlling its cerebral levels. With regard to developments demonstrated by MCC950, we note that DAMPs and PAMPs recognize and activate both TLRs and inflammasomes in these disease states. Here, as in other illnesses, data suggests that preventing a pathogenic interaction could be achieved through shutting down either of these arms of innate immunity.
引用
收藏
页码:535 / 543
页数:9
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