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Alan D. Salama

Researcher at University College London

Publications -  250
Citations -  10729

Alan D. Salama is an academic researcher from University College London. The author has contributed to research in topics: Vasculitis & Transplantation. The author has an hindex of 51, co-authored 236 publications receiving 9272 citations. Previous affiliations of Alan D. Salama include Royal Free Hospital & European Space Agency.

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Genetically Distinct Subsets within ANCA-Associated Vasculitis

TL;DR: This study confirms that the pathogenesis of ANCA-associated vasculitis has a genetic component, shows genetic distinctions between granulomatosis with polyang iitis and microscopic polyangiitis that are associated with ANCA specificity, and suggests that the response against the autoantigen proteinase 3 is a central pathogenic feature ofproteinase 3 ANCA -associated vasulitis.
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The programmed death-1 (PD-1) pathway regulates autoimmune diabetes in nonobese diabetic (NOD) mice.

TL;DR: A central role for PD-1–PD-L1 interaction in the regulation of induction and progression of autoimmune diabetes in the NOD mouse is demonstrated and the rationale to develop new therapies to target this costimulatory pathway in this disease is provided.
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Critical role of the programmed death-1 (PD-1) pathway in regulation of experimental autoimmune encephalomyelitis

TL;DR: The programmed death-1 (PD-1) costimulatory pathway plays a critical role in regulating peripheral tolerance in murine EAE and appears to be a major contributor to the resistance of disease induction in CD28-deficient mice.
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A multicenter survey of rituximab therapy for refractory antineutrophil cytoplasmic antibody-associated vasculitis

TL;DR: Rituximab was effective remission induction therapy for refractory ANCA-associated vasculitis in this study and there was no difference in efficacy between the 2 main treatment regimens.
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Regulatory functions of CD8+CD28– T cells in an autoimmune disease model

TL;DR: These are the first data establishing that regulatory CD8+CD28- T cells occur in normal mice and play a critical role in disease resistance in CD28-/- animals.