David T. Evans



Pathology & Laboratory Medicine (School of Medicine and Public Health)
David Evans University of Wisconsin AIDS Vaccine Research Laboratory

Contact Information

  • (608) 265-1485

Other web pages

Pathology and Laboratory Medicine

Aligned research focus:

Virology and immunology, innate immunity, host-pathogen interactions

Organ system/disease focus:

Human and simian immunodeficiency viruses

Research description

My research program is directed towards understanding host-pathogen interactions for human and simian immunodeficiency viruses. Current areas of investigation include (1) mechanisms of lentiviral resistance to tetherin/BST-2, (2) the role of KIR and MHC class I polymorphisms in regulating NK cell responses, (3) ADCC as a mechanism of protection, and (4) single-cycle SIV as an experimental AIDS vaccine approach.

Tetherin (BST-2 or CD317) is an interferon-inducible transmembrane protein that interferes with the detachment of enveloped viruses from infected cells. We identified Nef as the viral gene product of SIV that counteracts restriction by tetherin in Old World monkeys, and found that this activity is dependent on a five amino acid sequence that is missing from the cytoplasmic domain of human tetherin (Jia & Serra-Moreno et al. 2009. PLoS Pathog.). The absence of sequences in human tetherin that confer susceptibility to Nef explains why this activity was ultimately acquired by the Vpu and Env proteins of HIV-1 and HIV-2 respectively. We also identified compensatory changes in the cytoplasmic tail of Env that restore resistance to tetherin in a nef-deleted strain of SIV that regained a pathogenic phenotype in rhesus macaques (Serra-Moreno et al. 2011. Cell Host Microbe). This finding is entirely consistent with the adaptation of HIV-2 Env for antagonism of human tetherin, and provides the most direct evidence to date that the ability to counteract restriction by tetherin is important for lentiviral pathogenesis. More recently, we investigated the mechanism of tetherin antagonism by Nef, and found that this activity is dependent on a physical interaction between Nef and tetherin and on clathrin-mediated endocytosis (Serra-Moreno et al. 2013. PLoS Pathog.).

Natural killer (NK) cells recognize and kill infected or malignant cells without prior antigenic stimulation and thus provide an important innate immune defense against infectious agents and tumors. NK cell responses are regulated in part through interactions between highly polymorphic killer cell immunoglobulin-like receptors (KIRs) expressed on NK cells and their MHC class I ligands on target cells. Genetic evidence indicates that KIR and MHC class I polymorphisms play an important role in determining the rate of disease progression in HIV-1 infected individuals. However, the immunological mechanisms underlying these observations are poorly understood. We recently identified an interaction between an inhibitory KIR and a common MHC class I molecule in the rhesus macaque that is modulated by SIV peptides (Colantonio et al. 2011. PLoS Pathog.). One implication of these observations is that viruses may acquire changes in epitopes that increase the binding of MHC class I ligands to inhibitory KIRs as a mechanism of innate immune evasion to prevent the activation of certain NK cell subsets

The role of ADCC in HIV-1 or SIV infection is poorly understood due in part to limitations of methods for measuring this immune response. We therefore developed a novel assay for measuring antibody titers capable of directing ADCC against virus-infected cells (Alpert et al. 2012. J. Virol.). Data obtained with this assay suggest that the time-dependent maturation of protection in macaques inoculated with nef-deleted, live-attenuated SIV is associated with an increase in ADCC titers to the challenge virus (Alpert et al. 2012. PLoS Pathog.). This assay was also selected by the US Military HIV Research Program as one of six primary assays for the immune correlates analysis of the phase III RV144 vaccine trial (or “Thai trial”) to determine if ADCC activity differed for HIV-infected versus uninfected vaccine recipients (Haynes et al. 2012. N. Engl. J. Med.). Current projects are now directed towards understanding the molecular mechanisms of HIV-1 and SIV resistance to ADCC.


magna cum laude
Cornell University
1997Ph.D.Cellular & Molecular BiologyUniversity of Wisconsin

Selected references:

Schafer JL, Colantonio AD, Neidermyer WJ, Dudley DM, Connole M, O’Connor DH, Evans DT. KIR3DL01 recognition of Bw4 ligands in the rhesus macaque: Maintenance of Bw4 specificity since the divergence of apes and old world monkeys. J. Immunol.. 2014. 192: 1907-1917.

Arias JF, Heyer LN, von Bredow B, Weisgrau KL, Moldt B, Burton DR, Rakasz EG, Evans DT. Tetherin antagonism by Vpu protects HIV-infected cells from antibody-dependent cell-mediated cytotoxicity. Proc. Natl. Acad. Sci. U.S.A.. 2014. 111: 6425-6430.

Serra-Moreno R, Zimmermann K, Stern LJ, Evans DT. Tetherin/BST-2 antagonism by Nef depends on a direct physical interaction between Nef and tetherin, and on clathrin-mediated endocytosis. PLoS Pathog. 2013. 9: e1003487.

Evans DT, Elder JH, Desrosiers RC. Nonhuman lentiviruses. In: Fields Virology, Sixth Edition. Knipe DM, Howley PM (eds). Lippincott Williams & Wilkins, Philadelphia, PA. 2013

Evans DT and Silvestri G. Non-human Primate Models in AIDS Research. Curr. Opin. HIV AIDS. 2013. 8: 255-261.