COVID-19 update: The race to therapeutic development
Publicado: 2021-01-17
Julianne D. Twomey
Shen Luo
Alexis Q. Dean
William P. Bozza
Ancy Nalli
Baolin Zhang
Resumen
The COVID-19 pandemic, caused by severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2), represents
an unprecedented challenge to global public health. At the time of this review, COVID-19 has been diagnosed in
over 40 million cases and associated with 1.1 million deaths worldwide. Current management strategies for
COVID-19 are largely supportive, and while there are more than 2000 interventional clinical trials registered
with the U.S. National Library of Medicine (clinicaltrials.gov), results that can clarify benefits and risks of
candidate therapies are only gradually becoming available. We herein describe recent advances in understanding
SARS-CoV-2 pathobiology and potential therapeutic targets that are involved in viral entry into host cells, viral
spread in the body, and the subsequent COVID-19 progression. We highlight two major lines of therapeutic
strategies for COVID-19 treatment: 1) repurposing the existing drugs for use in COVID-19 patients, such as
antiviral medications (e.g., remdesivir) and immunomodulators (e.g., dexamethasone) which were previously
approved for other disease conditions, and 2) novel biological products that are designed to target specific
molecules that are involved in SARS-CoV-2 viral entry, including neutralizing antibodies against the spike
protein of SARS-CoV-2, such as REGN-COV2 (an antibody cocktail), as well as recombinant human soluble ACE2
protein to counteract SARS-CoV-2 binding to the transmembrane ACE2 receptor in target cells. Finally, we
discuss potential drug resistance mechanisms and provide thoughts regarding clinical trial design to address the
diversity in COVID-19 clinical manifestation. Of note, preventive vaccines, cell and gene therapies are not within
the scope of the current review.
Detalles del artículo
Artículos similares
- Juan Carlos Valls Puig, La caída del halcón negro y el nuevo manejo del paciente con heridas , VITAE Academia Biomédica Digital: Vol. 4 Núm. 80: Octubre-Diciembre 2019
- Miguel Antonio Alfonzo Díaz, Las Células T memoria. , VITAE Academia Biomédica Digital: Vol. 4 Núm. 21: Octubre-Diciembre 2004
- Héctor Hueso, Micosis asociadas al SIDA , VITAE Academia Biomédica Digital: Vol. 3 Núm. 8: Junio-Agosto 2001
- Irene Pérez Schael, Belén Salinas, Vacuna de Rotavirus , VITAE Academia Biomédica Digital: Vol. 4 Núm. 21: Octubre-Diciembre 2004
- Carlos M. Fernández Andreu , Epidemiología de la histoplasmosis en Cuba , VITAE Academia Biomédica Digital: Vol. 4 Núm. 9: Octubre-Diciembre 2001
- E. Valderrama, G. Bracho V, A. Hernández, L. Taylor, D. Tamayo, J.R. Tovar, Linfoma no Hodgkin de células grandes inmunofenotipo T/NK extraganglionar de tipo nasal (granuloma letal de la línea media) A propósito de un caso , VITAE Academia Biomédica Digital: Vol. 4 Núm. 56: Octubre-Diciembre 2013
- Miguel A. Grassini, Hepatitis autoinmune , VITAE Academia Biomédica Digital: Vol. 4 Núm. 9: Octubre-Diciembre 2001
- Julman R. Cermeño Vivas , Pneumocystis carinii y neumocistosis , VITAE Academia Biomédica Digital: Vol. 1 Núm. 10: Enero-Marzo 2002
- Silvia Pilar González Rodríguez, Ángel Garcia-Iglesias, Silvia García Valle, Alexandra Henríquez Linares, Luz Maria Jiménez Losa, Ana Villalba Yarza, Juan Luis Lanchares Pérez, Estudio comparativo de los tratamientos tópicos para las lesiones vulvares por el virus del papiloma humano. , VITAE Academia Biomédica Digital: Vol. 3 Núm. 24: Julio-Septiembre 2005
- 9th Conference on Retroviruses and Opportunistic Infections. , VITAE Academia Biomédica Digital: Vol. 2 Núm. 11: Abril-Julio 2002
También puede Iniciar una búsqueda de similitud avanzada para este artículo.

