Characterization of Immune Responses Induced by Ebola Virus Glycoprotein (GP) and Truncated GP Isoform DNA Vaccines and Protection Against Lethal Ebola Virus Challenge in Mice
In addition to its surface glycoprotein (GP), Ebola virus directs the production of large quantities of a truncated glycoprotein isoform (sGP) that is secreted into the extracellular space. We recently reported that sGP actively diverts host antibody responses against the epitopes that it shares wit...
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| Veröffentlicht in: | The Journal of infectious diseases Jg. 212 Suppl 2; S. S398 |
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| Abstract | In addition to its surface glycoprotein (GP), Ebola virus directs the production of large quantities of a truncated glycoprotein isoform (sGP) that is secreted into the extracellular space. We recently reported that sGP actively diverts host antibody responses against the epitopes that it shares with GP and thereby allows itself to absorb anti-GP antibodies, a phenomenon we termed "antigenic subversion." To investigate the effect of antigenic subversion by sGP on protection against virus infection, we compared immune responses induced by different prime-boost immunization regimens with GP and sGP DNA vaccines in mice and their efficacy against lethal Ebola virus challenge. Similar levels of anti-GP antibodies were induced by 2 immunizations with sGP and GP DNA vaccines. However, 2 immunizations with GP but not sGP DNA vaccine fully protected mice from lethal challenge. Boosting with sGP or GP DNA vaccine in mice that had been primed by GP or sGP DNA vaccine augmented the levels of anti-GP antibody responses and further improved protective efficacy against Ebola virus infection. These results show that both the quality and the levels of anti-GP antibody responses affect the efficacy of protection against Ebola virus infection. |
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| AbstractList | In addition to its surface glycoprotein (GP), Ebola virus directs the production of large quantities of a truncated glycoprotein isoform (sGP) that is secreted into the extracellular space. We recently reported that sGP actively diverts host antibody responses against the epitopes that it shares with GP and thereby allows itself to absorb anti-GP antibodies, a phenomenon we termed "antigenic subversion." To investigate the effect of antigenic subversion by sGP on protection against virus infection, we compared immune responses induced by different prime-boost immunization regimens with GP and sGP DNA vaccines in mice and their efficacy against lethal Ebola virus challenge. Similar levels of anti-GP antibodies were induced by 2 immunizations with sGP and GP DNA vaccines. However, 2 immunizations with GP but not sGP DNA vaccine fully protected mice from lethal challenge. Boosting with sGP or GP DNA vaccine in mice that had been primed by GP or sGP DNA vaccine augmented the levels of anti-GP antibody responses and further improved protective efficacy against Ebola virus infection. These results show that both the quality and the levels of anti-GP antibody responses affect the efficacy of protection against Ebola virus infection.In addition to its surface glycoprotein (GP), Ebola virus directs the production of large quantities of a truncated glycoprotein isoform (sGP) that is secreted into the extracellular space. We recently reported that sGP actively diverts host antibody responses against the epitopes that it shares with GP and thereby allows itself to absorb anti-GP antibodies, a phenomenon we termed "antigenic subversion." To investigate the effect of antigenic subversion by sGP on protection against virus infection, we compared immune responses induced by different prime-boost immunization regimens with GP and sGP DNA vaccines in mice and their efficacy against lethal Ebola virus challenge. Similar levels of anti-GP antibodies were induced by 2 immunizations with sGP and GP DNA vaccines. However, 2 immunizations with GP but not sGP DNA vaccine fully protected mice from lethal challenge. Boosting with sGP or GP DNA vaccine in mice that had been primed by GP or sGP DNA vaccine augmented the levels of anti-GP antibody responses and further improved protective efficacy against Ebola virus infection. These results show that both the quality and the levels of anti-GP antibody responses affect the efficacy of protection against Ebola virus infection. In addition to its surface glycoprotein (GP), Ebola virus directs the production of large quantities of a truncated glycoprotein isoform (sGP) that is secreted into the extracellular space. We recently reported that sGP actively diverts host antibody responses against the epitopes that it shares with GP and thereby allows itself to absorb anti-GP antibodies, a phenomenon we termed "antigenic subversion." To investigate the effect of antigenic subversion by sGP on protection against virus infection, we compared immune responses induced by different prime-boost immunization regimens with GP and sGP DNA vaccines in mice and their efficacy against lethal Ebola virus challenge. Similar levels of anti-GP antibodies were induced by 2 immunizations with sGP and GP DNA vaccines. However, 2 immunizations with GP but not sGP DNA vaccine fully protected mice from lethal challenge. Boosting with sGP or GP DNA vaccine in mice that had been primed by GP or sGP DNA vaccine augmented the levels of anti-GP antibody responses and further improved protective efficacy against Ebola virus infection. These results show that both the quality and the levels of anti-GP antibody responses affect the efficacy of protection against Ebola virus infection. |
| Author | Compans, Richard W Li, Wenfang Patterson, Jean L Ticer, Anysha Yang, Chinglai Carrion, Jr, Ricardo Nunneley, Jerritt Ye, Ling Mohan, Gopi S Staples, Hilary |
| Author_xml | – sequence: 1 givenname: Wenfang surname: Li fullname: Li, Wenfang organization: Department of Microbiology and Immunology Emory Vaccine Center, Emory University, Atlanta, Georgia – sequence: 2 givenname: Ling surname: Ye fullname: Ye, Ling organization: Department of Microbiology and Immunology Emory Vaccine Center, Emory University, Atlanta, Georgia – sequence: 3 givenname: Ricardo surname: Carrion, Jr fullname: Carrion, Jr, Ricardo organization: Department of Virology and Immunology, Texas Biomedical Research Institute, San Antonio – sequence: 4 givenname: Gopi S surname: Mohan fullname: Mohan, Gopi S organization: Department of Microbiology and Immunology Emory Vaccine Center, Emory University, Atlanta, Georgia – sequence: 5 givenname: Jerritt surname: Nunneley fullname: Nunneley, Jerritt organization: Department of Virology and Immunology, Texas Biomedical Research Institute, San Antonio – sequence: 6 givenname: Hilary surname: Staples fullname: Staples, Hilary organization: Department of Virology and Immunology, Texas Biomedical Research Institute, San Antonio – sequence: 7 givenname: Anysha surname: Ticer fullname: Ticer, Anysha organization: Department of Virology and Immunology, Texas Biomedical Research Institute, San Antonio – sequence: 8 givenname: Jean L surname: Patterson fullname: Patterson, Jean L organization: Department of Virology and Immunology, Texas Biomedical Research Institute, San Antonio – sequence: 9 givenname: Richard W surname: Compans fullname: Compans, Richard W organization: Department of Microbiology and Immunology Emory Vaccine Center, Emory University, Atlanta, Georgia – sequence: 10 givenname: Chinglai surname: Yang fullname: Yang, Chinglai organization: Department of Microbiology and Immunology Emory Vaccine Center, Emory University, Atlanta, Georgia |
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| SubjectTerms | Animals Antibodies, Viral - immunology Antibody Formation - immunology Ebola Vaccines - immunology Ebolavirus - immunology Female Glycoproteins - immunology HEK293 Cells Hemorrhagic Fever, Ebola - immunology Hemorrhagic Fever, Ebola - virology Humans Immunization, Secondary - methods Mice Mice, Inbred BALB C Protein Isoforms - immunology Vaccination - methods Vaccines, DNA - immunology Viral Proteins - immunology |
| Title | Characterization of Immune Responses Induced by Ebola Virus Glycoprotein (GP) and Truncated GP Isoform DNA Vaccines and Protection Against Lethal Ebola Virus Challenge in Mice |
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