Human-monoclonal-antibody therapy protects nonhuman primates against advanced Lassa fever
Thomas Geisbert and colleagues show that a cocktail of monoclonal antibodies protects cynomolgus monkeys from lethal Lassa fever virus infection, including when administration is delayed by more than a week after viral challenge. There are no approved treatments for Lassa fever, which is endemic to...
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Published in | Nature medicine Vol. 23; no. 10; pp. 1146 - 1149 |
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Main Authors | , , , , , , , , , , , , , , , , , , |
Format | Journal Article |
Language | English |
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01.10.2017
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Abstract | Thomas Geisbert and colleagues show that a cocktail of monoclonal antibodies protects cynomolgus monkeys from lethal Lassa fever virus infection, including when administration is delayed by more than a week after viral challenge.
There are no approved treatments for Lassa fever, which is endemic to the same regions of West Africa that were recently devastated by Ebola. Here we show that a combination of human monoclonal antibodies that cross-react with the glycoproteins of all four clades of Lassa virus is able to rescue 100% of cynomolgus macaques when treatment is initiated at advanced stages of disease, including up to 8 d after challenge. |
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AbstractList | Thomas Geisbert and colleagues show that a cocktail of monoclonal antibodies protects cynomolgus monkeys from lethal Lassa fever virus infection, including when administration is delayed by more than a week after viral challenge.There are no approved treatments for Lassa fever, which is endemic to the same regions of West Africa that were recently devastated by Ebola. Here we show that a combination of human monoclonal antibodies that cross-react with the glycoproteins of all four clades of Lassa virus is able to rescue 100% of cynomolgus macaques when treatment is initiated at advanced stages of disease, including up to 8 d after challenge. Thomas Geisbert and colleagues show that a cocktail of monoclonal antibodies protects cynomolgus monkeys from lethal Lassa fever virus infection, including when administration is delayed by more than a week after viral challenge. There are no approved treatments for Lassa fever, which is endemic to the same regions of West Africa that were recently devastated by Ebola. Here we show that a combination of human monoclonal antibodies that cross-react with the glycoproteins of all four clades of Lassa virus is able to rescue 100% of cynomolgus macaques when treatment is initiated at advanced stages of disease, including up to 8 d after challenge. There are no approved treatments for Lassa fever, which is endemic to the same regions of West Africa that were recently devastated by Ebola. Here we show that a combination of human monoclonal antibodies that cross-react with the glycoproteins of all four clades of Lassa virus is able to rescue 100% of cynomolgus macaques when treatment is initiated at advanced stages of disease, including up to 8 d after challenge. There are no approved treatments for Lassa fever, which is endemic to the same regions of West Africa that were recently devastated by Ebola. Here we show that a combination of human monoclonal antibodies that cross-react with the glycoproteins of all four clades of Lassa virus is able to rescue 100% of cynomolgus macaques when treatment is initiated at advanced stages of disease, including up to 8 d after challenge.There are no approved treatments for Lassa fever, which is endemic to the same regions of West Africa that were recently devastated by Ebola. Here we show that a combination of human monoclonal antibodies that cross-react with the glycoproteins of all four clades of Lassa virus is able to rescue 100% of cynomolgus macaques when treatment is initiated at advanced stages of disease, including up to 8 d after challenge. |
Audience | Academic |
Author | Heinrich, Megan L Borisevich, Viktoriya Geisbert, Joan B Fenton, Karla A Deer, Daniel J Cross, Robert W Branco, Luis M Garry, Robert F Rowland, Megan M Fullah, Mohamed Agans, Krystle N Momoh, Mambu Grant, Donald S Khan, Sheik Humarr Robinson, James E Goba, Augustine Boisen, Mathew L Mire, Chad E Geisbert, Thomas W |
AuthorAffiliation | 9 Tulane Center of Excellence, Global Viral Network, Tulane University, New Orleans, Louisiana, USA 7 Sections of Infectious Disease, Departments of Pediatrics and Internal Medicine, School of Medicine, Tulane University, New Orleans, Louisiana, USA 4 Viral Hemorrhagic Fever Program, Kenema Government Hospital, Kenema, Sierra Leone 5 Ministry of Health and Sanitation, Freetown, Sierra Leone 8 Department of Microbiology and Immunology, Tulane University, New Orleans, Louisiana, USA 3 Zalgen Labs, Germantown, Maryland, USA 1 Department of Microbiology and Immunology, University of Texas Medical Branch at Galveston, Galveston, Texas, USA 2 Galveston National Laboratory, University of Texas Medical Branch at Galveston, Galveston, Texas, USA 6 Polytechnic College, Kenema, Sierra Leone |
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Author_xml | – sequence: 1 givenname: Chad E orcidid: 0000-0001-7596-1808 surname: Mire fullname: Mire, Chad E organization: Department of Microbiology and Immunology, University of Texas Medical Branch at Galveston, Galveston National Laboratory, University of Texas Medical Branch at Galveston – sequence: 2 givenname: Robert W surname: Cross fullname: Cross, Robert W organization: Department of Microbiology and Immunology, University of Texas Medical Branch at Galveston, Galveston National Laboratory, University of Texas Medical Branch at Galveston – sequence: 3 givenname: Joan B surname: Geisbert fullname: Geisbert, Joan B organization: Department of Microbiology and Immunology, University of Texas Medical Branch at Galveston, Galveston National Laboratory, University of Texas Medical Branch at Galveston – sequence: 4 givenname: Viktoriya surname: Borisevich fullname: Borisevich, Viktoriya organization: Department of Microbiology and Immunology, University of Texas Medical Branch at Galveston, Galveston National Laboratory, University of Texas Medical Branch at Galveston – sequence: 5 givenname: Krystle N orcidid: 0000-0002-7319-6935 surname: Agans fullname: Agans, Krystle N organization: Department of Microbiology and Immunology, University of Texas Medical Branch at Galveston, Galveston National Laboratory, University of Texas Medical Branch at Galveston – sequence: 6 givenname: Daniel J surname: Deer fullname: Deer, Daniel J organization: Department of Microbiology and Immunology, University of Texas Medical Branch at Galveston, Galveston National Laboratory, University of Texas Medical Branch at Galveston – sequence: 7 givenname: Megan L surname: Heinrich fullname: Heinrich, Megan L organization: Zalgen Labs – sequence: 8 givenname: Megan M surname: Rowland fullname: Rowland, Megan M organization: Zalgen Labs – sequence: 9 givenname: Augustine surname: Goba fullname: Goba, Augustine organization: Viral Hemorrhagic Fever Program, Kenema Government Hospital, Ministry of Health and Sanitation – sequence: 10 givenname: Mambu surname: Momoh fullname: Momoh, Mambu organization: Viral Hemorrhagic Fever Program, Kenema Government Hospital, Ministry of Health and Sanitation, Polytechnic College – sequence: 11 givenname: Mathew L surname: Boisen fullname: Boisen, Mathew L organization: Zalgen Labs – sequence: 12 givenname: Donald S surname: Grant fullname: Grant, Donald S organization: Viral Hemorrhagic Fever Program, Kenema Government Hospital, Ministry of Health and Sanitation – sequence: 13 givenname: Mohamed surname: Fullah fullname: Fullah, Mohamed organization: Viral Hemorrhagic Fever Program, Kenema Government Hospital, Ministry of Health and Sanitation – sequence: 14 givenname: Sheik Humarr surname: Khan fullname: Khan, Sheik Humarr organization: Viral Hemorrhagic Fever Program, Kenema Government Hospital, Ministry of Health and Sanitation – sequence: 15 givenname: Karla A surname: Fenton fullname: Fenton, Karla A organization: Department of Microbiology and Immunology, University of Texas Medical Branch at Galveston, Galveston National Laboratory, University of Texas Medical Branch at Galveston – sequence: 16 givenname: James E surname: Robinson fullname: Robinson, James E organization: Departments of Pediatrics and Internal Medicine, Sections of Infectious Disease, School of Medicine, Tulane University – sequence: 17 givenname: Luis M surname: Branco fullname: Branco, Luis M organization: Zalgen Labs – sequence: 18 givenname: Robert F surname: Garry fullname: Garry, Robert F email: rfgarry@tulane.edu organization: Zalgen Labs, Department of Microbiology and Immunology, Tulane University, Tulane Center of Excellence, Global Viral Network, Tulane University – sequence: 19 givenname: Thomas W surname: Geisbert fullname: Geisbert, Thomas W email: twgeisbe@utmb.edu organization: Department of Microbiology and Immunology, University of Texas Medical Branch at Galveston, Galveston National Laboratory, University of Texas Medical Branch at Galveston |
BackLink | https://www.ncbi.nlm.nih.gov/pubmed/28869611$$D View this record in MEDLINE/PubMed |
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Snippet | Thomas Geisbert and colleagues show that a cocktail of monoclonal antibodies protects cynomolgus monkeys from lethal Lassa fever virus infection, including... There are no approved treatments for Lassa fever, which is endemic to the same regions of West Africa that were recently devastated by Ebola. Here we show that... |
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SubjectTerms | 13/1 13/51 631/326/596/1961 692/699/255/2514 Animals Antibodies Antibodies, Monoclonal - therapeutic use Antibodies, Neutralizing - therapeutic use Antibodies, Viral - therapeutic use Biomedicine brief-communication Cancer Research Care and treatment Cross Reactions Drug dosages Drug therapy Enzyme-Linked Immunosorbent Assay Fatalities Fever Glycoproteins Health aspects Humans Immune Evasion - genetics Immunohistochemistry Immunology Immunotherapy Infectious Diseases Lassa fever Lassa Fever - prevention & control Lassa virus - genetics Macaca fascicularis Medicine Metabolic Diseases Molecular Medicine Monoclonal antibodies Neurosciences Plasma Primates Random Allocation RNA, Viral - blood Survival Rate Vaccines Viral diseases Viral Load Viruses |
Title | Human-monoclonal-antibody therapy protects nonhuman primates against advanced Lassa fever |
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