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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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Journal ArticleDOI

Sex differences in the therapeutic effects of anti-PDL2 neutralizing antibody on stroke

TL;DR: It is found that anti-PDL2 neutralizing antibody treatment of MCAO significantly reduced infarct volumes in male mice but had no protective effects in female mice even at a 5-fold increased dose of anti- PDL2 mAb.
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Episodic changes in T‐cell frequencies to myelin basic protein in patients with multiple sclerosis

TL;DR: With late-emerging CN previously probably had small-amplitude CN that was not clinically apparent, but would have been detectable with ophthalmoscopic examination, and the term “congenital” refers to a congenital predisposition for ocular motor instability rather than the exact time of its manifestation.
Patent

Partial mhc constructs and methods of use

TL;DR: In this article, isolated major histocompatibility complex (MHC) class II α 1 domain polypeptides and methods of use are discussed. And methods of evaluating efficacy of treatment or optimizing treatment of a subject with a poly-peptide including an MHC class IIα 1 domain or poly-protein, such as a β1α1 RTL.
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Prevention and treatment of experimental autoimmune encephalomyelitis with clonotypic CDR3 peptides: CD4(+) Foxp3(+) T-regulatory cells suppress interleukin-2-dependent expansion of myelin basic protein-specific T cells.

TL;DR: It is demonstrated that TCR CDR3 peptides from the transgenic TCR can provide a protective effect when therapy is initiated before the induction of experimental autoimmune encephalomyelitis (EAE) and can ameliorate the disease when administered after EAE onset.
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Multiple class I motifs revealed by sequencing naturally processed peptides eluted from rat T cell MHC molecules

TL;DR: In this paper, the authors characterized the Lewis rat Vbeta8.2+ T cell hybridoma C14/BW12-12A1 by FACS analysis and have used immunoaffinity chromatography to purify class I molecules from these cells.