Overview
Dr. Kevin Wiehe is the director of research, director of computational biology and co-director of the Quantitative Research Division at the Duke Human Vaccine Institute (DHVI). He has over 20 years of experience in the field of computational biology and has expertise in computational structural biology, computational genomics, and computational immunology.
For the past decade, he has applied his unique background to developing computational approaches for studying the B cell response in both the infection and vaccination settings. He has utilized his expertise in computational structural biology to structurally model and characterize HIV and influenza antibody recognition. Dr. Wiehe has utilized his expertise in computational genomics and computational immunology to develop software to analyze large scale next generation sequencing data of antibody repertoires as well as develop computational programs for estimating antibody mutation probabilities. Dr. Wiehe has shown that low probability antibody mutations can act as rate-limiting steps in the development of broadly neutralizing antibodies in HIV.
Through his PhD, postdoc work, and now his roles at DHVI, Dr. Wiehe always approaches the analysis and the scientific discovery process from a structural biology perspective. Supporting the Duke Center for HIV Structural Biology (DCHSB), Dr. Wiehe will conduct antibody sequence analysis for antibodies used in computational and molecular modeling analyses conducted.
Current Appointments & Affiliations
Recent Publications
Vaccine induction of heterologous HIV-1-neutralizing antibody B cell lineages in humans.
Journal Article Cell · November 13, 2025 Full text Link to item CiteWhole-Thorax Irradiation Induces Persistent T Cell Clonal Dysregulation in Pediatric Rhesus Macaques.
Journal Article Radiat Res · October 1, 2025 The thymus is critical for the development and selection of T cells with a diverse range of non-self-reactive antigen receptors. Both the thymus and circulating T cells can be damaged by acute exposure to ionizing radiation, leading to dose-dependent lymph ... Full text Link to item CiteAcquisition of quaternary trimer interaction as a key step in the lineage maturation of a broad and potent HIV-1 neutralizing antibody.
Journal Article Structure · August 7, 2025 Although most broadly neutralizing antibodies (bNAbs) specific for the CD4-binding site (CD4-BS) of HIV-1 interact with a single gp120 protomer, a few mimic the quaternary binding mode of CD4, making contact with a second protomer through elongated heavy c ... Full text Link to item CiteRecent Grants
Persistent Immunogenicity of IDLV delivering membrane tethered Native-Like HIV-1 Envelope Trimers
ResearchInvestigator · Awarded by National Institute of Allergy and Infectious Diseases · 2025 - 2030Translating germline-targeting HIV Env SOSIP immunization of infants: targeting bnAbs in early life
ResearchPrincipal Investigator · Awarded by Weill Cornell Medicine · 2025 - 2030Genetic and Structural Basis for Virus Neutralization
ResearchInvestigator · Awarded by National Institute of Allergy and Infectious Diseases · 2024 - 2029View All Grants