Cited by 107Monoclonal and Polyclonal Antibodies ResearchSARS-CoV-2 and COVID-19 ResearchVirology and Viral Diseases

Monoclonal antibodies for prophylactic and therapeutic use against viral infections

Open access
Both, Leonard, Banyard, Ashley C., van Dolleweerd, Craig, Wright, Edward, Ma, Julian K.-C., Fooks, Anthony R.·2013·Vaccine

Abstract

Neutralizing antibodies play an essential part in antiviral immunity and are instrumental in preventing or modulating viral diseases. Polyclonal antibody preparations are increasingly being replaced by highly potent monoclonal antibodies (mAbs). Cocktails of mAbs and bispecific constructs can be used to simultaneously target multiple viral epitopes and to overcome issues of neutralization escape. Advances in antibody engineering have led to a large array of novel mAb formats, while deeper insight into the biology of several viruses and increasing knowledge of their neutralizing epitopes has extended the list of potential targets. In addition, progress in developing inexpensive production platforms will make antiviral mAbs more widely available and affordable.

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Registry

Crossref · 10.1016/j.vaccine.2013.01.025

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  • It is possible to generate protective mAbs against many viruses and microorganisms.

    “there is ample evidence that it is possible to generate protective mAbs against many viruses and microorganisms (Teitelbaum et al, 1998; Nosanchuk et al, 2003; Both et al, 2013).”

    From mRNA mediates passive vaccination against infectious agents, toxins, and tumors (2017) · cites this paper as Both et al, 2013

    The Development of monoclonal antibodies section reports that many antiviral mAbs have been developed, and the Antiviral immunity section describes protection in mAb-treated mice. The paper supports the claim for viruses, but the passages do not establish it for other microorganisms (searched: bacteria, fungi, parasites, and nonviral pathogens). No page numbers are available in our copy. (LLM, conf=0.87)

    Experimental — accuracy not yet measured

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Authors
Both, L., Banyard, A. C., van Dolleweerd, C., Wright, E., Ma, J. K.-C., & Fooks, A. R.
Affiliations
  • University of London (GB)
  • Animal and Plant Health Agency (GB)
  • University of Westminster (GB)
  • University of Liverpool (GB)
Corresponding author
Fooks, Anthony R.
Venue
Vaccine
Publisher
Elsevier BV
Published
2013-03
Volume
31
Issue
12
Pages
1553-1559
ISSN
0264-410X (ISSN-L)
OpenAlex
W2157171051
Cited by
107
References
103
Citations by year
2026: 5 · 2025: 7 · 2024: 8 · 2023: 9 · 2022: 10 · 2021: 11 · 2020: 10 · 2019: 3 · 2018: 8 · 2017: 9 · 2016: 7 · 2015: 9 · 2014: 8 · 2013: 3
FWCI
1.28
Type
journal article
Language
en
Open access
Locations
  • Vaccine (publishedVersion, cc-by-nc-nd)
  • PubMed Central (publishedVersion)
  • PubMed (publishedVersion)
  • WestminsterResearch (University of Westminster) (acceptedVersion)
Topics
  • Health Sciences › Medicine › Radiology, Nuclear Medicine and Imaging › Monoclonal and Polyclonal Antibodies Research
  • Health Sciences › Medicine › Infectious Diseases › SARS-CoV-2 and COVID-19 Research
  • Health Sciences › Medicine › Epidemiology › Virology and Viral Diseases
Keywords
monoclonal antibodies, neutralizing antibodies, antiviral immunity, prophylaxis, bispecific antibodies, neutralization escape, antibody engineering, viral epitopes, viral infection
MeSH terms
Antibodies, Monoclonal, Antibodies, Viral, Antibody Specificity, Antiviral Agents, Humans, Immunization, Passive, Virus Diseases, Protein Engineering, Antibodies, Neutralizing

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