Wilson Liao, MD

Associate Professor
Department of Dermatology
Research Overview: 

Background: Psoriasis is a common cutaneous and systemic inflammatory disease that represents a fascinating intersection between genetics, immunology, microbiology, and metabolism. Over forty genetic loci contributing to psoriasis susceptibility have been identified. The affected genes result in abnormal responses of both the innate and adaptive immune system, influencing diverse cell types such as keratinocytes, T cells, dendritic cells, NK cells, and macrophages. Psoriasis may be triggered by a number of bacterial and viral infections and it is likely that psoriasis is influenced by microbiota residing on the skin and in the gut. Patients with psoriasis have systemic inflammation leading to increased risk of heart attack, stroke, type 2 diabetes, metabolic syndrome, and other autoimmune diseases. Due to the accessibility of skin for sampling, psoriasis represents an attractive model system to study multiple facets of human biology.  The Liao laboratory utilizes a translational approach in which patient data and biosamples from the clinic are directly studied in the laboratory.

Major goals: (i) Understand the genetic and environmental determinants of psoriasis; (ii) Identify biomarkers to predict psoriasis prognosis and therapeutic response

Ongoing projects:

  1. Identification of novel psoriasis genes. We use genome-wide association data, exome and whole genome sequencing data, and functional mapping methods to identify both common and rare susceptibility variants in psoriasis.
  2. Analysis of whole transcriptome expression networks. Using RNA-seq data of both whole skin and skin cell subtypes, we construct gene expression modules to describe networks of coding genes, non-coding genes, and human genome repetitive elements.
  3. Role of diet and microbiome. We combine epidemiologic surveys of diet with microbial profiling of the skin and gut in psoriasis to explore the role of these factors in modulating psoriasis severity, systemic inflammation, and associated co-morbidities.
  4. Autoimmune disease and HIV-1 control. Our lab has identified a link between the genetic determinants of autoimmune disease (psoriasis, Crohn’s) and immunologic control of HIV-1 replication. Evolutionarily, beneficial adaptation leading to heightened immune responses against retroviruses may have detrimentally increased risk of autoimmune disease. We are exploring how the genetic and immunologic features of psoriasis relate to an antiviral state.
Primary Thematic Area: 
Human Genetics
Secondary Thematic Area: 
Virology & Microbial Pathogenesis
Research Summary: 
Integrated Genomic and Environmental Analysis of Inflammatory Skin Disease

Websites

Publications: 

Layilin Anchors Regulatory T Cells in Skin.

Journal of immunology (Baltimore, Md. : 1950)

Mehta P, Gouirand V, Boda DP, Zhang J, Gearty SV, Zirak B, Lowe MM, Clancy S, Boothby I, Mahuron KM, Fries A, Krummel MF, Mankoo P, Chang HW, Liu J, Moreau JM, Scharschmidt TC, Daud A, Kim E, Neuhaus IM, Harris HW, Liao W, Rosenblum MD

Review of Apremilast Combination Therapies in the Treatment of Moderate to Severe Psoriasis.

Journal of drugs in dermatology : JDD

Ivanic MG, Thatiparthi A, Walia S, Liao W, Wu JJ

New Frontiers in Psoriatic Disease Research, Part I: Genetics, Environmental Triggers, Immunology, Pathophysiology, and Precision Medicine.

The Journal of investigative dermatology

Yan D, Gudjonsson JE, Le S, Maverakis E, Plazyo O, Ritchlin C, Scher JU, Singh R, Ward NL, Bell S, Liao W

Large-Scale Imputation of KIR Copy Number and HLA Alleles in North American and European Psoriasis Case-Control Cohorts Reveals Association of Inhibitory KIR2DL2 With Psoriasis.

Frontiers in immunology

Ahn R, Vukcevic D, Motyer A, Nititham J, Squire DM, Hollenbach JA, Norman PJ, Ellinghaus E, Nair RP, Tsoi LC, Oksenberg J, Foerster J, Lieb W, Weidinger S, Franke A, Elder JT, Jorgenson E, Leslie S, Liao W

Nail Psoriasis: A Review of Effective Therapies and Recommendations for Management.

Dermatology and therapy

Hadeler E, Mosca M, Hong J, Brownstone N, Bhutani T, Liao W