Efficient In Vitro and In Vivo Activity of Glyco-Engineered Plant-Produced Rabies Monoclonal Antibodies E559 and 62-71-3
Rabies is a neglected zoonotic disease that has no effective treatment after onset of illness. However the disease can be prevented effectively by prompt administration of post exposure prophylaxis which includes administration of passive immunizing antibodies (Rabies Immune Globulin, RIG). Currentl...
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creator | Tsekoa, Tsepo Lebiletsa Lotter-Stark, Therese Buthelezi, Sindisiwe Chakauya, Ereck Stoychev, Stoyan H Sabeta, Claude Shumba, Wonderful Phahladira, Baby Hume, Steve Morton, Josh Rupprecht, Charles E Steinkellner, Herta Pauly, Michael Zeitlin, Larry Whaley, Kevin Chikwamba, Rachel |
description | Rabies is a neglected zoonotic disease that has no effective treatment after onset of illness. However the disease can be prevented effectively by prompt administration of post exposure prophylaxis which includes administration of passive immunizing antibodies (Rabies Immune Globulin, RIG). Currently, human RIG suffers from many restrictions including limited availability, batch-to batch inconsistencies and potential for contamination with blood-borne pathogens. Anti-rabies monoclonal antibodies (mAbs) have been identified as a promising alternative to RIG. Here, we applied a plant-based transient expression system to achieve rapid, high level production and efficacy of the two highly potent anti-rabies mAbs E559 and 62-71-3. Expression levels of up to 490 mg/kg of recombinant mAbs were obtained in Nicotiana benthamiana glycosylation mutants by using a viral based transient expression system. The plant-made E559 and 62-71-3, carrying human-type fucose-free N-glycans, assembled properly and were structurally sound as determined by mass spectrometry and calorimetric density measurements. Both mAbs efficiently neutralised diverse rabies virus variants in vitro. Importantly, E559 and 62-71-3 exhibited enhanced protection against rabies virus compared to human RIG in a hamster model post-exposure challenge trial. Collectively, our results provide the basis for the development of a multi-mAb based alternative to RIG. |
doi_str_mv | 10.1371/journal.pone.0159313 |
format | Article |
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However the disease can be prevented effectively by prompt administration of post exposure prophylaxis which includes administration of passive immunizing antibodies (Rabies Immune Globulin, RIG). Currently, human RIG suffers from many restrictions including limited availability, batch-to batch inconsistencies and potential for contamination with blood-borne pathogens. Anti-rabies monoclonal antibodies (mAbs) have been identified as a promising alternative to RIG. Here, we applied a plant-based transient expression system to achieve rapid, high level production and efficacy of the two highly potent anti-rabies mAbs E559 and 62-71-3. Expression levels of up to 490 mg/kg of recombinant mAbs were obtained in Nicotiana benthamiana glycosylation mutants by using a viral based transient expression system. The plant-made E559 and 62-71-3, carrying human-type fucose-free N-glycans, assembled properly and were structurally sound as determined by mass spectrometry and calorimetric density measurements. Both mAbs efficiently neutralised diverse rabies virus variants in vitro. Importantly, E559 and 62-71-3 exhibited enhanced protection against rabies virus compared to human RIG in a hamster model post-exposure challenge trial. Collectively, our results provide the basis for the development of a multi-mAb based alternative to RIG.</description><identifier>ISSN: 1932-6203</identifier><identifier>EISSN: 1932-6203</identifier><identifier>DOI: 10.1371/journal.pone.0159313</identifier><identifier>PMID: 27427976</identifier><language>eng</language><publisher>United States: Public Library of Science</publisher><subject><![CDATA[Agrobacterium tumefaciens - genetics ; Agrobacterium tumefaciens - metabolism ; Animals ; Antibodies, Monoclonal - administration & dosage ; Antibodies, Monoclonal - biosynthesis ; Antibodies, Monoclonal - genetics ; Antibodies, Viral - administration & dosage ; Antibodies, Viral - biosynthesis ; Antibodies, Viral - genetics ; Biology and life sciences ; Cancer ; Cloning, Molecular ; Contamination ; Councils ; Dosage and administration ; Exposure ; Female ; Fucose ; Gene Expression ; Genetic Vectors - chemistry ; Genetic Vectors - metabolism ; Globulins ; Glycosylation ; Immunization ; Immunization, Passive ; Immunoglobulins ; Lyssavirus ; Mass spectrometry ; Mass spectroscopy ; Medical treatment ; Medicine and Health Sciences ; Mesocricetus ; Methods ; Monoclonal antibodies ; Mutants ; N-glycans ; Neutralization Tests ; Nicotiana - genetics ; Nicotiana - metabolism ; Nicotiana benthamiana ; People and places ; Plants, Genetically Modified ; Polysaccharides ; Prophylaxis ; Rabies ; Rabies - immunology ; Rabies - mortality ; Rabies - prevention & control ; Rabies - virology ; Rabies vaccines ; Rabies Vaccines - administration & dosage ; Rabies Vaccines - biosynthesis ; Rabies virus ; Rabies virus - drug effects ; Rabies virus - growth & development ; Rabies virus - immunology ; Rabies virus - pathogenicity ; Recombinant Proteins - administration & dosage ; Recombinant Proteins - biosynthesis ; Recombinant Proteins - genetics ; Survival Analysis ; Vectors (Biology) ; Viruses ; Zoonoses]]></subject><ispartof>PloS one, 2016-07, Vol.11 (7), p.e0159313</ispartof><rights>COPYRIGHT 2016 Public Library of Science</rights><rights>2016 Tsekoa et al. This is an open access article distributed under the terms of the Creative Commons Attribution License: http://creativecommons.org/licenses/by/4.0/ (the “License”), which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.</rights><rights>2016 Tsekoa et al 2016 Tsekoa et al</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c791t-da35cf9d2119f767993b9efa65bc1203f42485f1d1b93a1c2ee18da555e671013</citedby><cites>FETCH-LOGICAL-c791t-da35cf9d2119f767993b9efa65bc1203f42485f1d1b93a1c2ee18da555e671013</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC4948892/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC4948892/$$EHTML$$P50$$Gpubmedcentral$$Hfree_for_read</linktohtml><link.rule.ids>230,314,723,776,780,860,881,2096,2915,23845,27901,27902,53766,53768,79342,79343</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/27427976$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Tsekoa, Tsepo Lebiletsa</creatorcontrib><creatorcontrib>Lotter-Stark, Therese</creatorcontrib><creatorcontrib>Buthelezi, Sindisiwe</creatorcontrib><creatorcontrib>Chakauya, Ereck</creatorcontrib><creatorcontrib>Stoychev, Stoyan H</creatorcontrib><creatorcontrib>Sabeta, Claude</creatorcontrib><creatorcontrib>Shumba, Wonderful</creatorcontrib><creatorcontrib>Phahladira, Baby</creatorcontrib><creatorcontrib>Hume, Steve</creatorcontrib><creatorcontrib>Morton, Josh</creatorcontrib><creatorcontrib>Rupprecht, Charles E</creatorcontrib><creatorcontrib>Steinkellner, Herta</creatorcontrib><creatorcontrib>Pauly, Michael</creatorcontrib><creatorcontrib>Zeitlin, Larry</creatorcontrib><creatorcontrib>Whaley, Kevin</creatorcontrib><creatorcontrib>Chikwamba, Rachel</creatorcontrib><title>Efficient In Vitro and In Vivo Activity of Glyco-Engineered Plant-Produced Rabies Monoclonal Antibodies E559 and 62-71-3</title><title>PloS one</title><addtitle>PLoS One</addtitle><description>Rabies is a neglected zoonotic disease that has no effective treatment after onset of illness. However the disease can be prevented effectively by prompt administration of post exposure prophylaxis which includes administration of passive immunizing antibodies (Rabies Immune Globulin, RIG). Currently, human RIG suffers from many restrictions including limited availability, batch-to batch inconsistencies and potential for contamination with blood-borne pathogens. Anti-rabies monoclonal antibodies (mAbs) have been identified as a promising alternative to RIG. Here, we applied a plant-based transient expression system to achieve rapid, high level production and efficacy of the two highly potent anti-rabies mAbs E559 and 62-71-3. Expression levels of up to 490 mg/kg of recombinant mAbs were obtained in Nicotiana benthamiana glycosylation mutants by using a viral based transient expression system. The plant-made E559 and 62-71-3, carrying human-type fucose-free N-glycans, assembled properly and were structurally sound as determined by mass spectrometry and calorimetric density measurements. Both mAbs efficiently neutralised diverse rabies virus variants in vitro. Importantly, E559 and 62-71-3 exhibited enhanced protection against rabies virus compared to human RIG in a hamster model post-exposure challenge trial. Collectively, our results provide the basis for the development of a multi-mAb based alternative to RIG.</description><subject>Agrobacterium tumefaciens - genetics</subject><subject>Agrobacterium tumefaciens - metabolism</subject><subject>Animals</subject><subject>Antibodies, Monoclonal - administration & dosage</subject><subject>Antibodies, Monoclonal - biosynthesis</subject><subject>Antibodies, Monoclonal - genetics</subject><subject>Antibodies, Viral - administration & dosage</subject><subject>Antibodies, Viral - biosynthesis</subject><subject>Antibodies, Viral - genetics</subject><subject>Biology and life sciences</subject><subject>Cancer</subject><subject>Cloning, Molecular</subject><subject>Contamination</subject><subject>Councils</subject><subject>Dosage and administration</subject><subject>Exposure</subject><subject>Female</subject><subject>Fucose</subject><subject>Gene Expression</subject><subject>Genetic Vectors - chemistry</subject><subject>Genetic Vectors - metabolism</subject><subject>Globulins</subject><subject>Glycosylation</subject><subject>Immunization</subject><subject>Immunization, Passive</subject><subject>Immunoglobulins</subject><subject>Lyssavirus</subject><subject>Mass spectrometry</subject><subject>Mass spectroscopy</subject><subject>Medical treatment</subject><subject>Medicine and Health Sciences</subject><subject>Mesocricetus</subject><subject>Methods</subject><subject>Monoclonal antibodies</subject><subject>Mutants</subject><subject>N-glycans</subject><subject>Neutralization Tests</subject><subject>Nicotiana - genetics</subject><subject>Nicotiana - metabolism</subject><subject>Nicotiana benthamiana</subject><subject>People and places</subject><subject>Plants, Genetically Modified</subject><subject>Polysaccharides</subject><subject>Prophylaxis</subject><subject>Rabies</subject><subject>Rabies - immunology</subject><subject>Rabies - mortality</subject><subject>Rabies - prevention & control</subject><subject>Rabies - virology</subject><subject>Rabies vaccines</subject><subject>Rabies Vaccines - administration & dosage</subject><subject>Rabies Vaccines - biosynthesis</subject><subject>Rabies virus</subject><subject>Rabies virus - drug effects</subject><subject>Rabies virus - growth & development</subject><subject>Rabies virus - immunology</subject><subject>Rabies virus - pathogenicity</subject><subject>Recombinant Proteins - administration & dosage</subject><subject>Recombinant Proteins - biosynthesis</subject><subject>Recombinant Proteins - genetics</subject><subject>Survival Analysis</subject><subject>Vectors (Biology)</subject><subject>Viruses</subject><subject>Zoonoses</subject><issn>1932-6203</issn><issn>1932-6203</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2016</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><sourceid>BENPR</sourceid><sourceid>DOA</sourceid><recordid>eNqNk11v0zAUhiMEYmPwDxBEQkJwkRLHX_ENUjWVUWlo04DdWo4_Wlep3cVOtf573I9NDdrF5IvYx895c_zaJ8veg3IEIAXfFr7vnGhHK-_0qASYQQBfZKeAwaogVQlfHs1PsjchLMoSw5qQ19lJRVFFGSWn2f3EGCutdjGfuvzWxs7nwqn9Yu3zsYx2beMm9ya_aDfSFxM3s07rTqv8uhUuFtedV71MyxvRWB3yX9552fpUWz520TZebaMTjNlOmVQFBQV8m70yog363eF7lv39Mflz_rO4vLqYno8vC0kZiIUSEEvDVAUAM5RQxmDDtBEENxKkkxlUoRoboEDDoACy0hrUSmCMNaGgBPAs-7jXXbU-8INpgYO6xIhiTFEipntCebHgq84uRbfhXli-C_huxkUXrWw1B7ikdYMUJAIhA2QtGRM1UZoaWGook9b3w9_6ZqmVTL52oh2IDnecnfOZX3PEUF2zKgl8OQh0_q7XIfKlDVK3yWnt-13dNYW0ws9CMSWsqmhCP_2HPm3EgZqJdFbrjE8lyq0oHyNcE8gQwokaPUGlofTSyvQYjU3xQcLXQUJior6PM9GHwKe_b57PXt0O2c9H7FyLNs6Db_tovQtDEO1B2fkQOm0e7wOUfNtLD27wbS_xQy-ltA_Hd_mY9NA88B8tBRZg</recordid><startdate>20160718</startdate><enddate>20160718</enddate><creator>Tsekoa, 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In Vitro and In Vivo Activity of Glyco-Engineered Plant-Produced Rabies Monoclonal Antibodies E559 and 62-71-3</title><author>Tsekoa, Tsepo Lebiletsa ; Lotter-Stark, Therese ; Buthelezi, Sindisiwe ; Chakauya, Ereck ; Stoychev, Stoyan H ; Sabeta, Claude ; Shumba, Wonderful ; Phahladira, Baby ; Hume, Steve ; Morton, Josh ; Rupprecht, Charles E ; Steinkellner, Herta ; Pauly, Michael ; Zeitlin, Larry ; Whaley, Kevin ; Chikwamba, Rachel</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c791t-da35cf9d2119f767993b9efa65bc1203f42485f1d1b93a1c2ee18da555e671013</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2016</creationdate><topic>Agrobacterium tumefaciens - genetics</topic><topic>Agrobacterium tumefaciens - metabolism</topic><topic>Animals</topic><topic>Antibodies, Monoclonal - administration & dosage</topic><topic>Antibodies, Monoclonal - biosynthesis</topic><topic>Antibodies, Monoclonal - genetics</topic><topic>Antibodies, Viral - administration & dosage</topic><topic>Antibodies, Viral - biosynthesis</topic><topic>Antibodies, Viral - genetics</topic><topic>Biology and life sciences</topic><topic>Cancer</topic><topic>Cloning, Molecular</topic><topic>Contamination</topic><topic>Councils</topic><topic>Dosage and administration</topic><topic>Exposure</topic><topic>Female</topic><topic>Fucose</topic><topic>Gene Expression</topic><topic>Genetic Vectors - chemistry</topic><topic>Genetic Vectors - metabolism</topic><topic>Globulins</topic><topic>Glycosylation</topic><topic>Immunization</topic><topic>Immunization, Passive</topic><topic>Immunoglobulins</topic><topic>Lyssavirus</topic><topic>Mass spectrometry</topic><topic>Mass spectroscopy</topic><topic>Medical treatment</topic><topic>Medicine and Health Sciences</topic><topic>Mesocricetus</topic><topic>Methods</topic><topic>Monoclonal antibodies</topic><topic>Mutants</topic><topic>N-glycans</topic><topic>Neutralization 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Database</collection><collection>Materials Science Collection</collection><collection>Publicly Available Content Database</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central China</collection><collection>Engineering Collection</collection><collection>Environmental Science Collection</collection><collection>Genetics Abstracts</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><collection>DOAJ Directory of Open Access Journals</collection><jtitle>PloS one</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Tsekoa, Tsepo Lebiletsa</au><au>Lotter-Stark, Therese</au><au>Buthelezi, Sindisiwe</au><au>Chakauya, Ereck</au><au>Stoychev, Stoyan H</au><au>Sabeta, Claude</au><au>Shumba, Wonderful</au><au>Phahladira, Baby</au><au>Hume, Steve</au><au>Morton, Josh</au><au>Rupprecht, Charles E</au><au>Steinkellner, Herta</au><au>Pauly, Michael</au><au>Zeitlin, Larry</au><au>Whaley, Kevin</au><au>Chikwamba, Rachel</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Efficient In Vitro and In Vivo Activity of Glyco-Engineered Plant-Produced Rabies Monoclonal Antibodies E559 and 62-71-3</atitle><jtitle>PloS one</jtitle><addtitle>PLoS One</addtitle><date>2016-07-18</date><risdate>2016</risdate><volume>11</volume><issue>7</issue><spage>e0159313</spage><pages>e0159313-</pages><issn>1932-6203</issn><eissn>1932-6203</eissn><abstract>Rabies is a neglected zoonotic disease that has no effective treatment after onset of illness. However the disease can be prevented effectively by prompt administration of post exposure prophylaxis which includes administration of passive immunizing antibodies (Rabies Immune Globulin, RIG). Currently, human RIG suffers from many restrictions including limited availability, batch-to batch inconsistencies and potential for contamination with blood-borne pathogens. Anti-rabies monoclonal antibodies (mAbs) have been identified as a promising alternative to RIG. Here, we applied a plant-based transient expression system to achieve rapid, high level production and efficacy of the two highly potent anti-rabies mAbs E559 and 62-71-3. Expression levels of up to 490 mg/kg of recombinant mAbs were obtained in Nicotiana benthamiana glycosylation mutants by using a viral based transient expression system. The plant-made E559 and 62-71-3, carrying human-type fucose-free N-glycans, assembled properly and were structurally sound as determined by mass spectrometry and calorimetric density measurements. Both mAbs efficiently neutralised diverse rabies virus variants in vitro. Importantly, E559 and 62-71-3 exhibited enhanced protection against rabies virus compared to human RIG in a hamster model post-exposure challenge trial. Collectively, our results provide the basis for the development of a multi-mAb based alternative to RIG.</abstract><cop>United States</cop><pub>Public Library of Science</pub><pmid>27427976</pmid><doi>10.1371/journal.pone.0159313</doi><oa>free_for_read</oa></addata></record> |
fulltext | fulltext |
identifier | ISSN: 1932-6203 |
ispartof | PloS one, 2016-07, Vol.11 (7), p.e0159313 |
issn | 1932-6203 1932-6203 |
language | eng |
recordid | cdi_plos_journals_1805475574 |
source | Public Library of Science (PLoS) Journals Open Access; MEDLINE; DOAJ Directory of Open Access Journals; EZB-FREE-00999 freely available EZB journals; PubMed Central; Free Full-Text Journals in Chemistry |
subjects | Agrobacterium tumefaciens - genetics Agrobacterium tumefaciens - metabolism Animals Antibodies, Monoclonal - administration & dosage Antibodies, Monoclonal - biosynthesis Antibodies, Monoclonal - genetics Antibodies, Viral - administration & dosage Antibodies, Viral - biosynthesis Antibodies, Viral - genetics Biology and life sciences Cancer Cloning, Molecular Contamination Councils Dosage and administration Exposure Female Fucose Gene Expression Genetic Vectors - chemistry Genetic Vectors - metabolism Globulins Glycosylation Immunization Immunization, Passive Immunoglobulins Lyssavirus Mass spectrometry Mass spectroscopy Medical treatment Medicine and Health Sciences Mesocricetus Methods Monoclonal antibodies Mutants N-glycans Neutralization Tests Nicotiana - genetics Nicotiana - metabolism Nicotiana benthamiana People and places Plants, Genetically Modified Polysaccharides Prophylaxis Rabies Rabies - immunology Rabies - mortality Rabies - prevention & control Rabies - virology Rabies vaccines Rabies Vaccines - administration & dosage Rabies Vaccines - biosynthesis Rabies virus Rabies virus - drug effects Rabies virus - growth & development Rabies virus - immunology Rabies virus - pathogenicity Recombinant Proteins - administration & dosage Recombinant Proteins - biosynthesis Recombinant Proteins - genetics Survival Analysis Vectors (Biology) Viruses Zoonoses |
title | Efficient In Vitro and In Vivo Activity of Glyco-Engineered Plant-Produced Rabies Monoclonal Antibodies E559 and 62-71-3 |
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