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 Appointments & Affiliations
Recent Publications
Profiling Allogeneic HLA-specific B-cell Responses Utilizing a 64-plex Single-HLA Reporter Cell Panel.
Preprint · January 20, 2026 Full text Link to item CiteFunctional Convergence of Genetically Diverse B-Cell Receptors in Simian-HIV Infected Rhesus Macaques.
Preprint · January 12, 2026 Full text Link to item CiteA Novel IgG- and IgM-Cleaving Endopeptidase, IceMG, for Antibody-Mediated Rejection.
Journal Article Am J Transplant · October 22, 2025 Antibody-mediated rejection (AMR) remains a significant barrier to successful outcomes in both allo- and xenotransplantation. In this study, we investigate the efficacy of a novel recombinant endopeptidase, IceMG, which simultaneously cleaves IgG and IgM i ... 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 - 2028The impact of targeting CD40-CD154 pathway in nonhuman primate vascularized composite allograft model
ResearchCo Investigator · Awarded by National Institutes of Health · 2024 - 2025View All Grants