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Theodore Tselios

Researcher at University of Patras

Publications -  85
Citations -  1790

Theodore Tselios is an academic researcher from University of Patras. The author has contributed to research in topics: Epitope & Peptide. The author has an hindex of 23, co-authored 76 publications receiving 1594 citations. Previous affiliations of Theodore Tselios include University of Ioannina & Burnet Institute.

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Multiple Sclerosis: Immunopathology and Treatment Update

TL;DR: Go back to the basics to understand the immunopathophysiology of MS to gain insights in the development of new improved drug treatments and present current disease-modifying therapies for the treatment of MS.
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Round and round we go : Cyclic peptides in disease

TL;DR: Important cyclic peptide compounds used as synthetic immunogens, transmembrane ion channels, antigens for Herpes Simplex Virus, and potential immunotherapeutic vaccines for diabetes are reviewed.
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Transmembrane tumour necrosis factor is neuroprotective and regulates experimental autoimmune encephalomyelitis via neuronal nuclear factor-κB

TL;DR: Evidence that the soluble and transmembrane forms of tumour necrosis factor exert opposing deleterious and beneficial effects, respectively, in a multiple sclerosis model is presented and it is suggested that selective inhibition of soluble tumour Necrosis factor may provide a new way forward for the treatment of multiple sclerosis and possibly other inflammatory central nervous system disorders.
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Review cyclic peptides on a merry‐go‐round; towards drug design

TL;DR: The rational design and synthesis of cyclic peptide analogues has turned into an alternative approach for improved biological activity in the case of metabolically unstable peptide ligands.
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Antagonistic Effects of Human Cyclic MBP87-99 Altered Peptide Ligands in Experimental Allergic Encephalomyelitis and Human T-Cell Proliferation

TL;DR: Two cyclic analogues of the immunodominant myelin basic protein peptide, designed by NMR and molecular modeling data on human MBP(87-99) and its linear antagonist peptide analogue, inhibited EAE in Lewis rats and decreased inflammation in the spinal cord.