File Download
There are no files associated with this item.
Links for fulltext
(May Require Subscription)
- Publisher Website: 10.1126/science.aaq0620
- Scopus: eid_2-s2.0-85055907907
- WOS: WOS:000450460000049
- Find via
Supplementary
- Citations:
- Appears in Collections:
Article: Universal protection against influenza infection by a multidomain antibody to influenza hemagglutinin
Title | Universal protection against influenza infection by a multidomain antibody to influenza hemagglutinin |
---|---|
Authors | Laursen, NSFriesen, RHEZhu, XJongeneelen, MBlokland, SVermond, Jvan Eijgen, ATang, Cvan Diepen, HObmolova, Gvan der Neut Kolfschoten, MZuijdgeest, DStraetemans, RHoffman, RMBNieusma, TPallesen, JTurner, HLBernard, SMWard, ABLuo, JPoon, LMLTretiakova, APWilson, JMLimberis, MPVogels, RBrandenburg, BKolkman, JAWilson, IA |
Issue Date | 2018 |
Publisher | American Association for the Advancement of Science. The Journal's web site is located at http://sciencemag.org |
Citation | Science, 2018, v. 362 n. 6414, p. 598-602 How to Cite? |
Abstract | Broadly neutralizing antibodies against highly variable pathogens have stimulated the design of vaccines and therapeutics. We report the use of diverse camelid single-domain antibodies to influenza virus hemagglutinin to generate multidomain antibodies with impressive breadth and potency. Multidomain antibody MD3606 protects mice against influenza A and B infection when administered intravenously or expressed locally from a recombinant adeno-associated virus vector. Crystal and single-particle electron microscopy structures of these antibodies with hemagglutinins from influenza A and B viruses reveal binding to highly conserved epitopes. Collectively, our findings demonstrate that multidomain antibodies targeting multiple epitopes exhibit enhanced virus cross-reactivity and potency. In combination with adeno-associated virus-mediated gene delivery, they may provide an effective strategy to prevent infection with influenza virus and other highly variable pathogens. |
Persistent Identifier | http://hdl.handle.net/10722/268303 |
ISSN | 2023 Impact Factor: 44.7 2023 SCImago Journal Rankings: 11.902 |
PubMed Central ID | |
ISI Accession Number ID |
DC Field | Value | Language |
---|---|---|
dc.contributor.author | Laursen, NS | - |
dc.contributor.author | Friesen, RHE | - |
dc.contributor.author | Zhu, X | - |
dc.contributor.author | Jongeneelen, M | - |
dc.contributor.author | Blokland, S | - |
dc.contributor.author | Vermond, J | - |
dc.contributor.author | van Eijgen, A | - |
dc.contributor.author | Tang, C | - |
dc.contributor.author | van Diepen, H | - |
dc.contributor.author | Obmolova, G | - |
dc.contributor.author | van der Neut Kolfschoten, M | - |
dc.contributor.author | Zuijdgeest, D | - |
dc.contributor.author | Straetemans, R | - |
dc.contributor.author | Hoffman, RMB | - |
dc.contributor.author | Nieusma, T | - |
dc.contributor.author | Pallesen, J | - |
dc.contributor.author | Turner, HL | - |
dc.contributor.author | Bernard, SM | - |
dc.contributor.author | Ward, AB | - |
dc.contributor.author | Luo, J | - |
dc.contributor.author | Poon, LML | - |
dc.contributor.author | Tretiakova, AP | - |
dc.contributor.author | Wilson, JM | - |
dc.contributor.author | Limberis, MP | - |
dc.contributor.author | Vogels, R | - |
dc.contributor.author | Brandenburg, B | - |
dc.contributor.author | Kolkman, JA | - |
dc.contributor.author | Wilson, IA | - |
dc.date.accessioned | 2019-03-18T04:22:49Z | - |
dc.date.available | 2019-03-18T04:22:49Z | - |
dc.date.issued | 2018 | - |
dc.identifier.citation | Science, 2018, v. 362 n. 6414, p. 598-602 | - |
dc.identifier.issn | 0036-8075 | - |
dc.identifier.uri | http://hdl.handle.net/10722/268303 | - |
dc.description.abstract | Broadly neutralizing antibodies against highly variable pathogens have stimulated the design of vaccines and therapeutics. We report the use of diverse camelid single-domain antibodies to influenza virus hemagglutinin to generate multidomain antibodies with impressive breadth and potency. Multidomain antibody MD3606 protects mice against influenza A and B infection when administered intravenously or expressed locally from a recombinant adeno-associated virus vector. Crystal and single-particle electron microscopy structures of these antibodies with hemagglutinins from influenza A and B viruses reveal binding to highly conserved epitopes. Collectively, our findings demonstrate that multidomain antibodies targeting multiple epitopes exhibit enhanced virus cross-reactivity and potency. In combination with adeno-associated virus-mediated gene delivery, they may provide an effective strategy to prevent infection with influenza virus and other highly variable pathogens. | - |
dc.language | eng | - |
dc.publisher | American Association for the Advancement of Science. The Journal's web site is located at http://sciencemag.org | - |
dc.relation.ispartof | Science | - |
dc.rights | Science. Copyright © American Association for the Advancement of Science. | - |
dc.rights | This is the author’s version of the work. It is posted here by permission of the AAAS for personal use, not for redistribution. The definitive version was published in [Science Journal Title] on [Volume number and date], DOI: [insert DOI number]. | - |
dc.title | Universal protection against influenza infection by a multidomain antibody to influenza hemagglutinin | - |
dc.type | Article | - |
dc.identifier.email | Poon, LML: llmpoon@hkucc.hku.hk | - |
dc.identifier.authority | Poon, LML=rp00484 | - |
dc.description.nature | link_to_OA_fulltext | - |
dc.identifier.doi | 10.1126/science.aaq0620 | - |
dc.identifier.pmcid | PMC6241527 | - |
dc.identifier.scopus | eid_2-s2.0-85055907907 | - |
dc.identifier.hkuros | 297098 | - |
dc.identifier.volume | 362 | - |
dc.identifier.issue | 6414 | - |
dc.identifier.spage | 598 | - |
dc.identifier.epage | 602 | - |
dc.identifier.isi | WOS:000450460000049 | - |
dc.publisher.place | United States | - |
dc.identifier.f1000 | 734323560 | - |
dc.identifier.issnl | 0036-8075 | - |