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
- Manuel Okatami Perera Lecoin, Mecanismos de acción de compuestos antivirales aislados en plantas , VITAE Academia Biomédica Digital: Vol. 2 Núm. 31: Abril-Junio 2007
- Susana González Rico, Drogas Oligonucleotídicas: nuevas armas de la biología molecular contra los agentes infecciosos , VITAE Academia Biomédica Digital: Vol. 3 Núm. 16: Julio-Septiembre 2003
- Luisa Massarani, SciDev.Net en América Latina: Información sobre ciencia, tecnología y desarrollo vía Internet , VITAE Academia Biomédica Digital: Vol. 3 Núm. 16: Julio-Septiembre 2003
- Carlos Sardiñas, El riesgo de infección por VIH en cirugía , VITAE Academia Biomédica Digital: Vol. 1 Núm. 1: Junio-Agosto 1999
- Carlos Sardiñas, José Manuel Pestana, Luis Rodríguez Nissi, Cardiloma acuminado gigante perianal (Tumor de Buschke Lowenstein) , VITAE Academia Biomédica Digital: Vol. 1 Núm. 1: Junio-Agosto 1999
- Ramón Andrade, José Manuel Landaeta, Jenny Montes de Oca, Marcel Jesús Marcano-Lozada, Infecciones bacterianas asociadas al VIH/SIDA , VITAE Academia Biomédica Digital: Vol. 4 Núm. 17: Octubre-Diciembre 2003
- Alipio A. Hernández F., Ghislaine Céspedes C., Jorge I. Rivas S., Vacuolización neuronal y cambio espongiforme en la corteza cerebelosa de un perro Pastor Alemán joven , VITAE Academia Biomédica Digital: Vol. 1 Núm. 73: Enero-Marzo 2018
- Jorge García Tamayo, Cathy Hernández, Adriana María Morales Araujo, Inmunohistoquímica en tumores de partes blandas , VITAE Academia Biomédica Digital: Vol. 4 Núm. 17: Octubre-Diciembre 2003
- Anubis M. Suárez S., Abordaje médico terapéutico de un caso probable de influenza A (H1N1) , VITAE Academia Biomédica Digital: Vol. 2 Núm. 46: Abril-Junio 2011
- Leopoldo Córdova, Enrique Blanco, José Suárez, Roque Aouad, Laura Naranjo, Angela Picciuto, Neumonías , VITAE Academia Biomédica Digital: Vol. 2 Núm. 3: Febrero-Abril 2000
También puede Iniciar una búsqueda de similitud avanzada para este artículo.

