John M. Dye

ORCID: 0000-0002-0883-5016
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About
Contact & Profiles
Research Areas
  • Viral Infections and Outbreaks Research
  • Viral Infections and Vectors
  • SARS-CoV-2 and COVID-19 Research
  • Viral gastroenteritis research and epidemiology
  • Hepatitis B Virus Studies
  • Mosquito-borne diseases and control
  • COVID-19 epidemiological studies
  • Disaster Response and Management
  • COVID-19 Clinical Research Studies
  • Animal Virus Infections Studies
  • Virus-based gene therapy research
  • SARS-CoV-2 detection and testing
  • Respiratory viral infections research
  • vaccines and immunoinformatics approaches
  • Virology and Viral Diseases
  • Monoclonal and Polyclonal Antibodies Research
  • Fixed Point Theorems Analysis
  • Plant Virus Research Studies
  • Vector-Borne Animal Diseases
  • Optimization and Variational Analysis
  • Computational Drug Discovery Methods
  • Vaccine Coverage and Hesitancy
  • Influenza Virus Research Studies
  • Bacteriophages and microbial interactions
  • interferon and immune responses

United States Army Medical Research Institute of Infectious Diseases
2016-2025

United States Army
2022

The Geneva Foundation
2021

Uganda Virus Research Institute
2018

United States Department of the Army
2011-2015

Harvard University
2014

The Netherlands Cancer Institute
2014

Frederick Community College
2011

United States Army Medical Research and Development Command
2011

Medical University of South Carolina
2010

Seeking broad protection As scientists develop therapeutic antibodies and vaccines against severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2), the risk of emergent coronaviruses makes it important to also identify broadly protective antibodies. Wec et al. isolated characterized hundreds viral spike protein SARS-CoV-2 from memory B cells a survivor 2003 outbreak caused by related coronavirus, SARS-CoV. In both these viruses, facilitated entry binding angiotensin-converting enzyme...

10.1126/science.abc7424 article EN cc-by Science 2020-06-15

A decoy receptor for SARS-CoV-2 For severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) to enter human cells, the spike protein on surface of virus must bind host protein, angiotensin-converting enzyme (ACE2). soluble version is being explored as a therapeutic. Chan et al. used deep mutagenesis identify ACE2 mutants that more tightly and combined mutations further increase binding affinity (see Perspective by DeKosky). promising variant was engineered be stable dimer has protein; it...

10.1126/science.abc0870 article EN cc-by Science 2020-08-04

Severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2)-neutralizing monoclonal antibodies (mAbs) can reduce the risk of hospitalization from disease 2019 (COVID-19) when administered early. However, SARS-CoV-2 variants concern (VOCs) have negatively affected therapeutic use some authorized mAbs. Using a high-throughput B cell screening pipeline, we isolated LY-CoV1404 (bebtelovimab), highly potent spike glycoprotein receptor binding domain (RBD)-specific antibody. potently neutralizes...

10.1016/j.celrep.2022.110812 article EN cc-by-nc-nd Cell Reports 2022-04-25

Targeting sarbecoviruses As we continue to battle the COVID-19 pandemic, must confront possibility of new pathogenic coronaviruses emerging in humans future. With this mind, Rappazzo et al. isolated antibodies from a survivor 2003 severe acute respiratory syndrome coronavirus (SARS-CoV), used yeast display libraries introduce diversity into these antibodies, and then screened for binding SARS-CoV-2. One affinity-matured progeny strongly neutralized SARS-CoV-2, SARS-CoV, two SARS-related...

10.1126/science.abf4830 article EN cc-by Science 2021-01-25

10.1007/s00705-019-04247-4 article EN Archives of Virology 2019-05-14

How Lassa virus breaks and enters virus, which spreads from rodents to humans, infecting about half a million people every year, can lead deadly hemorrhagic fever. Like many viruses, binds cell surface receptors. Jae et al. now show that enter cell, the requires second receptor, this one inside infected cell. This requirement sheds light on “enigmatic resistance” of bird cells observed three decades ago. Although have intracellular receptor cannot bind stopping it in its tracks. Science ,...

10.1126/science.1252480 article EN Science 2014-06-26

The molecular composition and binding epitopes of the immunoglobulin G (IgG) antibodies that circulate in blood plasma after severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) infection are unknown. Proteomic deconvolution IgG repertoire to spike glycoprotein convalescent subjects revealed response is directed predominantly (>80%) against residing outside receptor domain (RBD). In one subject, just four lineages accounted for 93.5% response, including an amino (N)-terminal...

10.1126/science.abg5268 article EN cc-by Science 2021-05-04

Antibody therapies to prevent or limit filovirus infections have received modest interest in recent years, part because of early negative experimental evidence. We overcome the limitations this approach, leveraging use antibody from nonhuman primates (NHPs) that survived challenge filoviruses under controlled conditions. By using concentrated, polyclonal IgG these survivors, we treated filovirus-infected NHPs with multiple doses administered over clinical phase disease. In first study,...

10.1073/pnas.1200409109 article EN Proceedings of the National Academy of Sciences 2012-03-12
Jens H. Kuhn Scott Adkins D. Alioto Sergey V. Alkhovsky Gaya K. Amarasinghe and 95 more Simon J. Anthony Tatjana Avšič‐Županc Marı́a A. Ayllón Justin Bahl Anne Balkema‐Buschmann Matthew J. Ballinger Tomáš Bartonička Christopher F. Basler Sina Bavari Martin Beer Dennis A. Bente Éric Bergeron Brian H. Bird Carol D. Blair Kim R. Blasdell Steven B. Bradfute Rachel Breyta Thomas Briese Paul A. Brown Ursula J. Buchholz Michael J. Buchmeier Alexander Bukreyev Felicity J. Burt Nıhal Buzkan Charles H. Calisher Mengji Cao Inmaculada Casas John Chamberlain Kartik Chandran Rémi N. Charrel Biao Chen Michela Chiumenti Il-Ryong Choi J. C. S. Clegg Ian Crozier John da Graça Elena Dal Bó Alberto M. R. Dávila Juan Carlos de la Torre Xavier de Lamballerie Rik L. de Swart Patrick L. Di Bello Nicholas Di Paola Francesco Di Serio Ralf G. Dietzgen M. Digiaro Valerian V. Dolja Olga Dolnik Michael Drebot Jan Felix Drexler Ralf Dürrwald Lucie Dufková William G. Dundon W. Paul Duprex John M. Dye Andrew J. Easton Hideki Ebihara Toufic Elbeaino Koray Ergünay Jorlan Fernandes Anthony R. Fooks Pierre Formenty Leonie F. Forth Ron A. M. Fouchier Juliana Freitas‐Astúa Selma Gago‐Zachert George F. Gao María Laura García Adolfo García-Sastre Aura R. Garrison Aiah A Gbakima Tracey Goldstein Jean‐Paul Gonzalez Anthony Griffiths Martin H. Groschup Stephan Günther Alexandro Guterres Roy A. Hall John Hammond M. Hassan Jussi Hepojoki Satu Hepojoki Udo Hetzel Roger Hewson Donata Hoffmann Seiji Hongo Dirk W. Höper Masayuki Horie Holly R. Hughes Timothy H. Hyndman Amara Jambai Rodrigo Jardim Dàohóng Jiāng Qi Jin Gilda B. Jonson

10.1007/s00705-020-04731-2 article EN Archives of Virology 2020-09-04

Global health is threatened by emerging viral infections, which largely lack effective vaccines or therapies. Targeting host pathways that are exploited multiple viruses could offer broad-spectrum solutions. We previously reported AAK1 and GAK, kinase regulators of the adaptor proteins AP1 AP2, essential for hepatitis C virus (HCV) infection, but underlying mechanism relevance to other in vivo infections remained unknown. Here, we have discovered AP2 cotraffic with HCV particles live cells....

10.1172/jci89857 article EN Journal of Clinical Investigation 2017-02-26

The newly emerged severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) highlights the urgent need for assays that detect protective levels of neutralizing antibodies. We studied relationship among anti-spike ectodomain (anti-ECD), anti–receptor-binding domain (anti-RBD) IgG titers, and SARS-CoV-2 virus neutralization (VN) titers generated by in vitro using convalescent plasma samples from 68 patients with COVID-19. report a strong positive correlation between both anti-RBD anti-ECD...

10.1172/jci141206 article EN Journal of Clinical Investigation 2020-09-10

Despite the success of severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) vaccines, there remains a need for more prevention and treatment options individuals remaining at risk disease 2019 (COVID-19). Monoclonal antibodies (mAbs) against viral spike protein have potential to both prevent treat COVID-19 reduce death. Here, we describe AZD7442, combination two mAbs, AZD8895 (tixagevimab) AZD1061 (cilgavimab), that simultaneously bind distinct, nonoverlapping epitopes on receptor...

10.1126/scitranslmed.abl8124 article EN Science Translational Medicine 2022-01-25

10.1007/s00705-018-3814-x article EN Archives of Virology 2018-04-11

Ebola virus disease causes widespread and highly fatal epidemics in human populations. Today, there is still great need for point-of-care tests diagnosis, patient management surveillance, both during post outbreaks. We present a test comprising an immunochromatographic strip smartphone reader, which detects semiquantifies Ebola-specific antibodies survivors. developed Sudan glycoprotein monoplex platform validated it using sera from 90 survivors 31 local noninfected controls. The performance...

10.1021/acsnano.7b07021 article EN cc-by ACS Nano 2018-01-05

Biological factors that influence the host range and spillover of Ebola virus (EBOV) other filoviruses remain enigmatic. While infect diverse mammalian cell lines, we report cells from African straw-colored fruit bats (Eidolon helvum) are refractory to EBOV infection. This could be explained by a single amino acid change in filovirus receptor, NPC1, which greatly reduces affinity EBOV-NPC1 interaction. We found signatures positive selection bat NPC1 concentrated at virus-receptor interface,...

10.7554/elife.11785 article EN public-domain eLife 2015-12-22
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