Humoral autoimmunity as a mediator of CNS repair

2001 ◽  
Vol 24 (11) ◽  
pp. S39-S44 ◽  
Author(s):  
Allan J Bieber ◽  
Arthur Warrington ◽  
Larry R Pease ◽  
Moses Rodriguez
2001 ◽  
Vol 24 ◽  
pp. 39-44 ◽  
Author(s):  
Allan J Bieber ◽  
Arthur Warrington ◽  
Larry R Pease ◽  
Moses Rodriguez

Cells ◽  
2021 ◽  
Vol 10 (5) ◽  
pp. 1078
Author(s):  
Debasish Roy ◽  
Andrea Tedeschi

Axons in the adult mammalian nervous system can extend over formidable distances, up to one meter or more in humans. During development, axonal and dendritic growth requires continuous addition of new membrane. Of the three major kinds of membrane lipids, phospholipids are the most abundant in all cell membranes, including neurons. Not only immature axons, but also severed axons in the adult require large amounts of lipids for axon regeneration to occur. Lipids also serve as energy storage, signaling molecules and they contribute to tissue physiology, as demonstrated by a variety of metabolic disorders in which harmful amounts of lipids accumulate in various tissues through the body. Detrimental changes in lipid metabolism and excess accumulation of lipids contribute to a lack of axon regeneration, poor neurological outcome and complications after a variety of central nervous system (CNS) trauma including brain and spinal cord injury. Recent evidence indicates that rewiring lipid metabolism can be manipulated for therapeutic gain, as it favors conditions for axon regeneration and CNS repair. Here, we review the role of lipids, lipid metabolism and ectopic lipid accumulation in axon growth, regeneration and CNS repair. In addition, we outline molecular and pharmacological strategies to fine-tune lipid composition and energy metabolism in neurons and non-neuronal cells that can be exploited to improve neurological recovery after CNS trauma and disease.


2000 ◽  
Vol 21 (6) ◽  
pp. 306-307 ◽  
Author(s):  
Abdelhadi Saoudi ◽  
Jean-Charles Guery ◽  
Mark De Baets

Neuron ◽  
2016 ◽  
Vol 91 (4) ◽  
pp. 728-738 ◽  
Author(s):  
Hedong Li ◽  
Gong Chen
Keyword(s):  

2021 ◽  
pp. ASN.2020060834
Author(s):  
Poh-Yi Gan ◽  
Jonathan Dick ◽  
Kim M. O’Sullivan ◽  
Virginie Oudin ◽  
Anne Cao Le ◽  
...  

BackgroundMyeloperoxidase ANCA-associated vasculitis is a major cause of ESKD. Efficacy of anti-CD20 mAb treatment was tested in a mouse model of the disease.MethodsMPO immunization induced anti-MPO autoimmunity, and a subnephritogenic dose of sheep anti-mouse GBM globulin triggered GN.ResultsAnti-CD20 mAb treatment increased the numbers and immunomodulatory capacity of MPO-specific T regulatory cells (Tregs) and attenuated T cell–mediated and humoral anti-MPO autoimmunity and GN. Disabling of Tregs negated the therapeutic benefit of anti-CD20 treatment. The mechanism of enhancement of Treg activity could be attributed to anti-CD20 mAb effects on inducing B cell apoptosis. Administering anti-CD20 mAb-induced apoptotic splenocytes to mice developing anti-MPO GN was as effective as anti-CD20 mAb treatment in inducing Tregs and attenuating both anti-MPO autoimmunity and GN. A nonredundant role for splenic macrophages in mediating the anti-CD20 mAb-induced immunomodulation was demonstrated by showing that administration of anti-CD20 mAb ex vivo–induced apoptotic splenocytes to unmanipulated mice attenuated autoimmunity and GN, whereas deletion of splenic marginal zone macrophages prevented anti-CD20 mAb-induced immunomodulation and treatment efficacy. Six days after administering anti-CD20 mAb to mice with murine anti-MPO GN, cell-mediated anti-MPO responses and GN were attenuated, and Tregs were enhanced, but ANCA levels were unchanged, suggesting humoral autoimmunity was redundant at this time point.ConclusionsCollectively, these data suggest that, as well as reducing humoral autoimmunity, anti-CD20 mAb more rapidly induces protective anti-MPO Treg-mediated immunomodulation by splenic processing of anti-CD20–induced apoptotic B cells.


2018 ◽  
Vol 72 (8) ◽  
pp. 955-956
Author(s):  
Panagiotis Antiochos ◽  
Peter Vollenweider ◽  
Sabrina Pagano ◽  
Nathalie Satta ◽  
Nicolas Vuilleumier
Keyword(s):  

2011 ◽  
pp. 367-382
Author(s):  
Willi Roman ◽  
Schwab Martin E.
Keyword(s):  

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