2021
DOI: 10.1016/j.intimp.2021.108200
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Monoclonal antibodies for the treatment of COVID-19 patients: An umbrella to overcome the storm?

Abstract: The world is facing up the most considerable vaccination effort in history to end the Coronavirus disease 2019 (COVID-19) pandemic. Several monoclonal antibodies (mAbs) direct against the Receptor binding domain of the S protein of severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) received an Emergency Use Authorization for outpatient management of mild to moderate manifestation from COVID-19. MAbs could prevent the transmission SARS-CoV-2 infection and protect individuals from progression to severe… Show more

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Cited by 20 publications
(7 citation statements)
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“…Typically, it is better if individuals are vaccinated prior to being infected, but the virus typically moves faster than the vaccination pace. In this regard, and given the impossibility of preventing infection, symptoms should be reduced to certain levels [ 94 ], and mAb’s is a pioneer in this aspect [ 93 , 95 ]. Despite the suitability of mAb’s as treatment, if its distribution effort is not as quick as the virus spread, many people’s health would worsen and severely influence patients’ quality of life, even the economy [ 96 ].…”
Section: Proposed Methodologymentioning
confidence: 99%
“…Typically, it is better if individuals are vaccinated prior to being infected, but the virus typically moves faster than the vaccination pace. In this regard, and given the impossibility of preventing infection, symptoms should be reduced to certain levels [ 94 ], and mAb’s is a pioneer in this aspect [ 93 , 95 ]. Despite the suitability of mAb’s as treatment, if its distribution effort is not as quick as the virus spread, many people’s health would worsen and severely influence patients’ quality of life, even the economy [ 96 ].…”
Section: Proposed Methodologymentioning
confidence: 99%
“…There are no FDA-approve treatments for outpatients with newly diagnosed COVID-19. Monoclonal antibody therapy has demonstrated notable safety and efficacy for those at high-risk of hospitalization, but therapeutic options for low- and moderate-risk outpatients are lacking [ 36 ]. Moreover, the resources associated with antibody infusion limit its use in many locations.…”
Section: Immunomodulators For Outpatientsmentioning
confidence: 99%
“…Monoclonal antibodies are being studied to evaluate their efficacy in treating and preventing COVID-19. To date, FDA authorized EUA for many investigational mAbs both for pre-exposure prophylaxis and managing post-exposure mild-to-moderate COVID-19 based on their clinical trial potency against a virus strain (Mornese Pinna et al, 2021). These include casirivimab and imedevimab, bamlanivimab and etesevimab, sotrovimab, tocilizumab, and bebtelovimab (Mornese Pinna et al, 2021).…”
Section: Monoclonal Antibodiesmentioning
confidence: 99%
“…Due to the increased frequency of omicron sub-variants BA.2, BA.4, and BA.5 in U.S. HHS regions, casirivimab and imedevimab, bamlanivimab and etesevimab, and sotrovimab are no longer authorized for post-exposure prevention of COVID-19 until further notice by the FDA. Tixagevimab together with cilgavimab is being used for pre-exposure prophylaxis and is found to be potent enough against new sub-variants (Mornese Pinna et al, 2021).…”
Section: Monoclonal Antibodiesmentioning
confidence: 99%