Human monoclonal antibodies as candidate therapeutics against emerging viruses
Identifieur interne : 000E22 ( Main/Exploration ); précédent : 000E21; suivant : 000E23Human monoclonal antibodies as candidate therapeutics against emerging viruses
Auteurs : Yujia Jin [République populaire de Chine] ; Cheng Lei [République populaire de Chine] ; Dan Hu [République populaire de Chine] ; Dimiter S. Dimitrov [États-Unis] ; Tianlei Ying [République populaire de Chine]Source :
- Frontiers of Medicine [ 2095-0217 ] ; 2017.
Descripteurs français
- KwdFr :
- Anticorps monoclonaux (pharmacologie), Antiviraux (pharmacologie), Découverte de médicament (tendances), Humains, Maladies transmissibles émergentes (traitement médicamenteux), Maladies transmissibles émergentes (virologie), Maladies virales (immunologie), Maladies virales (traitement médicamenteux), Phénomènes physiologiques viraux (), Phénomènes physiologiques viraux (immunologie).
- MESH :
- immunologie : Maladies virales, Phénomènes physiologiques viraux.
- pharmacologie : Anticorps monoclonaux, Antiviraux.
- tendances : Découverte de médicament.
- traitement médicamenteux : Maladies transmissibles émergentes, Maladies virales.
- virologie : Maladies transmissibles émergentes.
- Humains, Phénomènes physiologiques viraux.
English descriptors
- KwdEn :
- Antibodies, Monoclonal (pharmacology), Antiviral Agents (pharmacology), Communicable Diseases, Emerging (drug therapy), Communicable Diseases, Emerging (virology), Drug Discovery (trends), Humans, Virus Diseases (drug therapy), Virus Diseases (immunology), Virus Physiological Phenomena (drug effects), Virus Physiological Phenomena (immunology).
- MESH :
- chemical , pharmacology : Antibodies, Monoclonal, Antiviral Agents.
- drug effects : Virus Physiological Phenomena.
- drug therapy : Communicable Diseases, Emerging, Virus Diseases.
- immunology : Virus Diseases, Virus Physiological Phenomena.
- trends : Drug Discovery.
- virology : Communicable Diseases, Emerging.
- Humans.
Abstract
The emergence of new pathogens, such as severe acute respiratory syndrome coronavirus (SARS-CoV), Middle East respiratory syndrome coronavirus (MERS-CoV), and Ebola virus, poses serious challenges to global public health and highlights the urgent need for novel antiviral approaches. Monoclonal antibodies (mAbs) have been successfully used to treat various diseases, particularly cancer and immunological disorders. Antigen-specific mAbs have been isolated using several different approaches, including hybridoma, transgenic mice, phage display, yeast display, and single B-cell isolation. Consequently, an increasing number of mAbs, which exhibit high potency against emerging viruses
Url:
DOI: 10.1007/s11684-017-0596-6
PubMed: 29159596
PubMed Central: 7088856
Affiliations:
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Le document en format XML
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Monoclonal antibodies (mAbs) have been successfully used to treat various diseases, particularly cancer and immunological disorders. Antigen-specific mAbs have been isolated using several different approaches, including hybridoma, transgenic mice, phage display, yeast display, and single B-cell isolation. Consequently, an increasing number of mAbs, which exhibit high potency against emerging viruses <italic>in vitro</italic> and in animal models of infection, have been developed. In this paper, we summarize historical trends and recent developments in mAb discovery, compare the advantages and disadvantages of various approaches to mAb production, and discuss the potential use of such strategies for the development of antivirals against emerging diseases. We also review the application of recently developed human mAbs against SARS-CoV, MERS-CoV, and Ebola virus and discuss prospects for the development of mAbs as therapeutic agents against emerging viral diseases.</p></div></front><back><div1 type="bibliography"><listBibl><biblStruct><analytic><author><name sortKey="Drosten, C" uniqKey="Drosten C">C Drosten</name></author><author><name sortKey="Gunther, S" uniqKey="Gunther S">S Günther</name></author><author><name sortKey="Preiser, W" uniqKey="Preiser W">W Preiser</name></author><author><name sortKey="Van Der Werf, S" uniqKey="Van Der Werf S">S van der Werf</name></author><author><name sortKey="Brodt, Hr" uniqKey="Brodt H">HR Brodt</name></author><author><name sortKey="Becker, S" uniqKey="Becker S">S Becker</name></author><author><name sortKey="Rabenau, H" uniqKey="Rabenau H">H Rabenau</name></author><author><name sortKey="Panning, M" uniqKey="Panning M">M Panning</name></author><author><name sortKey="Kolesnikova, L" 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Ying</name></author></analytic></biblStruct></listBibl></div1></back></TEI><affiliations><list><country><li>République populaire de Chine</li><li>États-Unis</li></country><region><li>Maryland</li></region></list><tree><country name="République populaire de Chine"><noRegion><name sortKey="Jin, Yujia" sort="Jin, Yujia" uniqKey="Jin Y" first="Yujia" last="Jin">Yujia Jin</name></noRegion><name sortKey="Hu, Dan" sort="Hu, Dan" uniqKey="Hu D" first="Dan" last="Hu">Dan Hu</name><name sortKey="Lei, Cheng" sort="Lei, Cheng" uniqKey="Lei C" first="Cheng" last="Lei">Cheng Lei</name><name sortKey="Ying, Tianlei" sort="Ying, Tianlei" uniqKey="Ying T" first="Tianlei" last="Ying">Tianlei Ying</name></country><country name="États-Unis"><region name="Maryland"><name sortKey="Dimitrov, Dimiter S" sort="Dimitrov, Dimiter S" uniqKey="Dimitrov D" first="Dimiter S." last="Dimitrov">Dimiter S. 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