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February 14, 2024 - Press notes

A new antibody manages to block all variants of SARS-CoV-2 in preclinical models

It is a monoclonal antibody with both prophylactic and therapeutic action, isolated from blood samples of a patient infected with SARS-CoV-2 during the first wave of the pandemic.

The antibody has been designed and developed by researchers from the Hospital del Mar Research Institute, the IrsiCaixa AIDS Research Institute, the National Center for Biotechnology, and the Center for Genomic Regulation.

This new treatment has been patented pending commercial development. The results of the work have been published in Nature Communications journal.

Barcelona, February 14, 2024. A study by the Hospital del Mar Research Institute, the IrsiCaixa AIDS Research Institute -a center jointly promoted by the "la Caixa" Foundation and the Department of Health of the Government of Catalonia-, the National Centre for Biotechnology, belonging to the Spanish National Research Council  (CNB-CSIC), and the Protein Technologies Unit of the Center for Genomic Regulation (CRG) has led to the development of a new antibody that is active against all existing variants of SARS-CoV-2, including the Omicron subvariants currently circulating. It is a monoclonal antibody, a protein from the immune system developed in the laboratory, called 17T2. The work, in which a scientific team from the CIBER of Infectious Diseases (CIBERINFEC) also participated, has just been published by the journal Nature Communications.

Image obtained by cryo-electron microscopy of the Spike protein of the SARS-CoV-2 virus (in gray) with the new antibody attached (heavy chain in blue and light chain in violet). Andrea Modrego, CNB-CSIC

The isolation of the new antibody has been possible thanks to blood samples from a patient infected with SARS-CoV-2 in March 2020, during the first wave of the pandemic. From these samples, some B lymphocytes were selected, the blood cells responsible for producing antibodies. Specifically, those generating specific antibodies against the spike protein, which allows the virus to infect human cells, multiply, and trigger COVID-19, were chosen.

Dr. Giuliana Magri

 Julià Blanco, co-leader of the study and IGTP researcher at IrsiCaixa

The researchers reproduced these antibodies in the laboratory using genetic engineering techniques. Once this was achieved, they evaluated their neutralizing activity in vitro, that is, their ability to bind to the virus and block it, against the different variants of SARS-CoV-2 existing up to that point. Thus, they were able to select the antibody that managed to neutralize all of them, including XBB.1.16 and BA.2.86, from which the most concerning variants currently derive. As Giuliana Magri, the study's leader and researcher at the Hospital del Mar Research Institute during its execution, points out, "our antibody maintains neutralizing activity against all variants of SARS-CoV-2." At the same time, Benjamin Trinité, one of the study's first authors and senior researcher at IrsiCaixa, highlights the importance of the results and mentions that "the latest virus variants have incorporated dozens of mutations that hinder the work of previously developed antibodies, as they cannot bind as effectively. Having a treatment that is effective even as new variants of SARS-CoV-2 appear can change the rules of the game in combating the infection."

Also prophylactic capacity

The study analyzed in a mouse model the therapeutic capacity of the antibody, but also the prophylactic, that is, preventive, activity of the new treatment, certifying its ability to significantly reduce lung lesions and viral load. In this sense, Magri emphasizes that the study "demonstrates that the developed antibody shows prophylactic activity and not only therapeutic, a fact that identifies it as a potential candidate for preventive clinical interventions and treatment of the infection."

Finally, the team carried out a detailed analysis of the antibody's structure bound to the spike protein, in order to understand its functioning and how it manages to maintain neutralizing activity, despite the mutations accumulated by the SARS-CoV-2 virus. This structural study, carried out at the CNB-CSIC by Rocío Arranz's team, co-leader of the study, allows stating that "this antibody has the ability to bind to a wide area of the virus spike, which gives it the ability to neutralize all variants and prevent new mutations from evading this neutralization. This suggests that, in this interaction area, there is a conserved region in the spike, which could be essential for the virus's ability to infect human cells."

Before its development for use in patients, a clinical trial in humans will have to be carried out. For now, there is an active European patent associated with this project.

"Having antibodies like 17T2 is key to protecting immunocompromised individuals and those at high risk of developing severe COVID-19. The results obtained show us that it is possible to design tools capable of blocking all variants of the same virus. In fact, it opens the way to the design of pan-coronavirus antibodies and/or vaccines, that is, with the ability to combat different types of coronaviruses", concludes Julià Blanco, co-leader of the study and IGTP researcher at IrsiCaixa.

This research project has received support from the COVID-19 call for proposals from the Government of Catalonia, as well as from the Miguel Servet research program, and has been partially funded by the #YoMeCorono fundraising campaign and the Glòria Soler Foundation.

Reference article

de Campos-Mata, L., Trinité, B., Modrego, A. et al. A monoclonal antibody targeting a large surface of the receptor binding motif shows pan-neutralizing SARS-CoV-2 activity. Nat Commun 15, 1051 (2024). https://doi.org/10.1038/s41467-024-45171-9