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



Aiming for Cure and Preventive Initiatives in Psoriatic Disease: Building Synergy at NPF, GRAPPA, and PPACMAN.

Current rheumatology reports

Bell S, Merola JF, Webster DE, Pennington SR, Liao W, Ogdie A, FitzGerald O, Ritchlin C, Scher JU

Immunopathogenesis of hidradenitis suppurativa and response to anti-TNFa therapy.

JCI insight

Lowe MM, Naik HB, Clancy S, Pauli M, Smith KM, Bi Y, Dunstan R, Gudjonsson J, Paul M, Harris HW, Kim EA, Shin US, Ahn R, Liao W, Hansen SL, Rosenblum M

A review of current phase III clinical trials of plaque psoriasis: Underrepresentation of non-white subjects and need for reform.

The British journal of dermatology

Reddy VD, Myers BA, Chan SY, Thibodeaux QG, Brownstone ND, Bhutani T, Liao W, Lester JC, Koo JY

Safety and Effectiveness of Anti-Tumor Necrosis Factor-Alpha Biosimilar Agents in the Treatment of Psoriasis.

American journal of clinical dermatology

Reynolds KA, Pithadia DJ, Lee EB, Liao W, Wu JJ