Overview
I am a dedicated investigator motivated by disease-focused immunology research that addresses clinically meaningful problems and improves patient health. My training includes biotechnology and pharmaceutical science (BS), microbiology and molecular biology (MS), T-cell biology (PhD), and postdoctoral training in B-cell immunology. This interdisciplinary path has provided a strong foundation in molecular immunology and diverse experimental approaches. I have specialized expertise in molecular biology and bioinformatics, which I leverage to tackle complex immunological problems in innovative ways. My five-year postdoctoral fellowship with Dr. Garnett Kelsoe in the Department of Integrative Immunobiology at Duke University was particularly formative, instilling a lasting commitment to scientific rigor and critical thinking.
My current work at the Duke Transplant Center focuses on understanding humoral allorecognition by profiling allogeneic HLA-specific B-cell responses in sensitized transplant candidates. We are working to define the phenotype, specificity, function, and B-cell receptor genetics of rare HLA-specific B cells, with the goal of clarifying the molecular basis of HLA immunogenicity and immunodominance. To enable this research, I have developed innovative platforms for efficient discovery and characterization of rare antigen-specific B cells—tools intended to be broadly applicable across immunology. I hope this work will inform improved strategies for immunological risk assessment and support better graft outcomes in transplant patients.
Current Duke Appointments & Affiliations
Recent Scholarly Works
Functional Convergence of Genetically Diverse B-Cell Receptors in Simian-HIV Infected Rhesus Macaques
Preprint · August 10, 2026 Germline-targeting or lineage-design vaccine strategies are being used to induce HIV broadly neutralizing antibody (bnAb) responses. These strategies assume that genetically diverse individuals respond similarly to the same immunogen by mobilizing ... Full text CiteFunctional Convergence of Genetically Diverse B-Cell Receptors in Simian-HIV Infected Rhesus Macaques
Preprint · August 10, 2026 Germline-targeting or lineage-design vaccine strategies are being used to induce HIV broadly neutralizing antibody (bnAb) responses. These strategies assume that genetically diverse individuals respond similarly to the same immunogen by mobilizing ... Full text CiteA novel immunoglobulin G- and immunoglobulin cleaving enzyme MG (IceMG), for antibody-mediated rejection.
Journal article Am J Transplant · June 2026 Antibody-mediated rejection remains a significant barrier to successful outcomes in both allotransplantation and xenotransplantation. In this study, we investigate the efficacy of a novel recombinant endopeptidase, IceMG, which simultaneously cleaves immun ... Full text Link to item CiteRecent Grants
Targeting the B Cell Response to Treat Antibody-Mediated Rejection
ResearchResearch Associate · Awarded by National Institute of Allergy and Infectious Diseases · 2021 - 2028Overcoming humoral rejection after xenotransplantation in sensitized nonhuman primate recipients
ResearchCo Investigator · Awarded by National Institute of Allergy and Infectious Diseases · 2023 - 2028ITN Adapt- HLA Specific Memory B Cell Assays
ResearchPrincipal Investigator · Awarded by Benaroya Research Institute at Virginia Mason · 2026 - 2027View All Grants