3 results match your criteria: "VA Medical Centre Sacramento[Affiliation]"

Remission of psoriasis and psoriatic arthritis during bevacizumab therapy for renal cell cancer.

Indian J Dermatol

November 2014

Department of Internal Medicine, Division of Rheumatology, Allergy and Clinical Immunology, University of California Davis, School of Medicine, Davis, CA 95616, USA ; Department of Internal Medicine, Division of Rheumatology, Allergy and Clinical Immunology, University of California Davis, VA Medical Centre Sacramento, Mather, CA 95655, USA.

Bevacizumab, a monoclonal antibody against vascular endothelial growth factor (VEGF), is employed for treatment of several cancers and retinopathies. Although previous reports of remission of psoriasis with bevacizumab do exist, but its current experience for psoriatic arthritis (PsA) is still limited. In this report, we describe a patient with metastatic renal cell cancer, psoriasis and PsA, who experienced a complete remission of psoriasis and PsA during bevacizumab therapy without any other management for psoriasis and PsA.

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Severe combined immunodeficiency mouse-psoriatic human skin xenograft model: a modern tool connecting bench to bedside.

Indian J Dermatol Venereol Leprol

December 2014

Research, VA Medical Centre Sacramento; Department of Internal Medicine, Division of Rheumatology, Allergy and Clinical Immunology, University of California, Davis School of Medicine, Davis, CA 95616, USA.

Psoriasis is a multifactorial chronic inflammatory disease. Research into the pathogenesis of this disease is hindered by the lack of a proper animal model. Over the past two decades, many scientists were involved in the development of animal models that nearly mirror the immunopathogenesis of psoriasis.

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1,25-Dihydroxyvitamin D3-3-bromoacetate, a novel vitamin D analog induces immunosuppression through PI3K/Akt/mTOR signaling cascade.

Int Immunopharmacol

November 2013

Department of Internal Medicine/Rheumatology, Allergy and Clinical Immunology, School of Medicine, University of California Davis, Davis, CA 95616, USA; VA Medical Centre Sacramento, Mather, CA 95655, USA.

Purpose: The molecular mechanism responsible for the immunomodulatory effect of 1,25-dihydroxyvitamin D3 (Vit-D) is still not well elucidated. Unavoidable systemic toxicity of Vit-D has encouraged to develop more potent and less toxic Vit-D analogs, such as 1,25-dihydroxyvitamin D3-3-bromoacetate (BE). Our aim was to explore the immunosuppressive effect of BE and its molecular mechanism in autoimmune diseases.

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