Abstract:
:Several studies have proposed cerebral malaria (CM) as a CD4+ and CD8+ T lymphocyte-mediated disease. However, there are no data regarding the recruitment and/or persistence of these cells in the CNS following the phase of infection resolution. Glutamate-mediate excitotoxicity has also been implicated in CM. Blockade of glutamate NMDA receptors by its noncompetitive antagonist MK801 modulates cytokine and neurotrophic factors expression preventing cognitive and depressive-like behavior in experimental CM. Herein, we aim to investigate the role of T lymphocytes in later outcomes in CM, and whether the protective role of MK801 is associated with T lymphocytes response.
journal_name
J Neuroimmunoljournal_title
Journal of neuroimmunologyauthors
de Miranda AS,Ferreira RN,Vieira ÉLM,Abreu LKS,Brant F,Vieira LB,Ribeiro FM,Machado FS,Rachid MA,Teixeira ALdoi
10.1016/j.jneuroim.2019.02.002subject
Has Abstractpub_date
2019-05-15 00:00:00pages
5-11eissn
0165-5728issn
1872-8421pii
S0165-5728(19)30016-5journal_volume
330pub_type
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