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Arthur A. Vandenbark

Researcher at Oregon Health & Science University

Publications -  134
Citations -  7372

Arthur A. Vandenbark is an academic researcher from Oregon Health & Science University. The author has contributed to research in topics: Experimental autoimmune encephalomyelitis & T cell. The author has an hindex of 41, co-authored 134 publications receiving 6920 citations. Previous affiliations of Arthur A. Vandenbark include Veterans Health Administration & United States Department of Veterans Affairs.

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Regulatory CD8+CD122+ T-cells predominate in CNS after treatment of experimental stroke in male mice with IL-10-secreting B-cells

TL;DR: A major neuroprotective role for IL-10+ B-cells is demonstrated in treating MCAO in male WT mice at a time point well beyond the ~4 h tPA treatment window, leading to the generation of a dominant IL- 10+CD8+CD122+ Treg population associated with spleen preservation and reduced CNS inflammation.
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CCR6: a biomarker for Alzheimer's-like disease in a triple transgenic mouse model

TL;DR: The authors' data demonstrate increased expression of CCR6 in the brain and peripheral immune organs of both pre-symptomatic and symptomatic 3xTg-AD mice, strongly suggesting an ongoing inflammatory process that precedes onset of clinical AD-like disease.
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Treatment of passive experimental autoimmune encephalomyelitis in SJL mice with a recombinant TCR ligand induces IL-13 and prevents axonal injury.

TL;DR: Pronounced IL-13 levels coupled with marked reduction in IL-6 levels secreted by PLP-specific T cells from blood after treatment of mice with RTL401 indicate that IL- 13 and IL- 6 may be useful markers for following effects of RTL therapy in future clinical trials in multiple sclerosis.
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Regulation of Encephalitogenic T Cells with Recombinant TCR Ligands

TL;DR: Clinical effects of recombinant TCR ligands (RTLs) comprised of the rat RT1.B β1α1 domains covalently linked to the 72–89 peptide of guinea pig myelin basic protein (RTl-201), to the corresponding 72– 89 peptide from rat myelinbasic protein ( RTL-200), or to cardiac myosin peptide CM-2 (RT L-203).