Literature DB >> 18534912

Immunotherapy for neurological diseases.

Pablo Villoslada1, Beatriz Moreno, Ignacio Melero, Jose L Pablos, Gianvito Martino, Antonio Uccelli, Xavier Montalban, Jesus Avila, Serge Rivest, Laia Acarin, Stanley Appel, Samia J Khoury, Patrick McGeer, Isidro Ferrer, Mario Delgado, Jose Obeso, Michal Schwartz.   

Abstract

The burden of neurological diseases in western societies has accentuated the need to develop effective therapies to stop the progression of chronic neurological diseases. Recent discoveries regarding the role of the immune system in brain damage coupled with the development of new technologies to manipulate the immune response make immunotherapies an attractive possibility to treat neurological diseases. The wide repertoire of immune responses and the possibility to engineer such responses, as well as their capacity to promote tissue repair, indicates that immunotherapy might offer benefits in the treatment of neurological diseases, similar to the benefits that are being associated with the treatment of cancer and autoimmune diseases. However, before applying such strategies to patients it is necessary to better understand the pathologies to be targeted, as well as how individual subjects may respond to immunotherapies, either in isolation or in combination. Due to the powerful effects of the immune system, one priority is to avoid tissue damage due to the activity of the immune system, particularly considering that the nervous system does not tolerate even the smallest amount of tissue damage.

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Year:  2008        PMID: 18534912     DOI: 10.1016/j.clim.2008.04.003

Source DB:  PubMed          Journal:  Clin Immunol        ISSN: 1521-6616            Impact factor:   3.969


  20 in total

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Review 3.  A deadly spread: cellular mechanisms of α-synuclein transfer.

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5.  Viral-like brain inflammation during development causes increased seizure susceptibility in adult rats.

Authors:  M A Galic; K Riazi; A K Henderson; S Tsutsui; Q J Pittman
Journal:  Neurobiol Dis       Date:  2009-08-04       Impact factor: 5.996

6.  Selective MyD88-dependent pathway inhibition by the cyanobacterial natural product malyngamide F acetate.

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7.  Advances in imaging of new targets for pharmacological intervention in stroke: real-time tracking of T-cells in the ischaemic brain.

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Review 8.  New immunological approaches in treating and diagnosing CNS diseases.

Authors:  Kathy Guo; Damir Janigro
Journal:  Pharm Pat Anal       Date:  2013-05

9.  Expression of the protein chaperone, clusterin, in spinal cord cells constitutively and following cellular stress, and upregulation by treatment with Hsp90 inhibitor.

Authors:  Samantha Zinkie; Benoit J Gentil; Sandra Minotti; Heather D Durham
Journal:  Cell Stress Chaperones       Date:  2013-04-19       Impact factor: 3.667

Review 10.  Heterogeneity of microglial activation in the innate immune response in the brain.

Authors:  Carol A Colton
Journal:  J Neuroimmune Pharmacol       Date:  2009-08-05       Impact factor: 4.147

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