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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Veröffentlicht in:PloS one 2016-07, Vol.11 (7), p.e0159313
Hauptverfasser: 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
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container_issue 7
container_start_page e0159313
container_title PloS one
container_volume 11
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
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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. 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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. 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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 &amp; dosage</subject><subject>Antibodies, Monoclonal - biosynthesis</subject><subject>Antibodies, Monoclonal - genetics</subject><subject>Antibodies, Viral - administration &amp; 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 &amp; 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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 &amp; dosage</topic><topic>Antibodies, Monoclonal - biosynthesis</topic><topic>Antibodies, Monoclonal - genetics</topic><topic>Antibodies, Viral - administration &amp; 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 Tests</topic><topic>Nicotiana - genetics</topic><topic>Nicotiana - metabolism</topic><topic>Nicotiana benthamiana</topic><topic>People and places</topic><topic>Plants, Genetically Modified</topic><topic>Polysaccharides</topic><topic>Prophylaxis</topic><topic>Rabies</topic><topic>Rabies - immunology</topic><topic>Rabies - mortality</topic><topic>Rabies - prevention &amp; 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Medical Complete (Alumni)</collection><collection>Materials Science Database</collection><collection>Nursing &amp; Allied Health Database (Alumni Edition)</collection><collection>Meteorological &amp; Geoastrophysical Abstracts - Academic</collection><collection>ProQuest Engineering Collection</collection><collection>ProQuest Biological Science Collection</collection><collection>Agricultural Science Database</collection><collection>Health &amp; Medical Collection (Alumni Edition)</collection><collection>Medical Database</collection><collection>Algology Mycology and Protozoology Abstracts (Microbiology C)</collection><collection>Biological Science Database</collection><collection>Engineering Database</collection><collection>Nursing &amp; Allied Health Premium</collection><collection>Advanced Technologies &amp; Aerospace Database</collection><collection>ProQuest Advanced Technologies &amp; Aerospace Collection</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>Environmental Science 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>
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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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