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Polyclonal F(ab’)(2) fragments of equine antibodies raised against the spike protein neutralize SARS-CoV-2 variants with high potency

We used the recombinant trimeric spike (S) glycoprotein in the prefusion conformation to immunize horses for the production of hyperimmune globulins against SARS-CoV-2. Serum antibody titers measured by ELISA were above 1:10(6), and the neutralizing antibody titer against authentic virus (WT) was 1:...

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Detalles Bibliográficos
Autores principales: Cunha, Luis Eduardo R., Stolet, Adilson A., Strauch, Marcelo A., Pereira, Victor A.R., Dumard, Carlos H., Gomes, Andre M.O., Monteiro, Fábio L., Higa, Luiza M., Souza, Patrícia N.C., Fonseca, Juliana G., Pontes, Francisco E., Meirelles, Leonardo G.R., Albuquerque, José W.M., Sacramento, Carolina Q., Fintelman-Rodrigues, Natalia, Lima, Tulio M., Alvim, Renata G.F., Marsili, Federico F., Caldeira, Marcella Moreira, Zingali, Russolina B., de Oliveira, Guilherme A.P., Souza, Thiago M.L., Silva, Alexandre S., Muller, Rodrigo, Rodrigues, Daniela del Rosário Flores, Jesus da Costa, Luciana, Alves, Arthur Daniel R., Pinto, Marcelo Alves, Oliveira, Andréa C., Guedes, Herbert L.M., Tanuri, Amilcar, Castilho, Leda R., Silva, Jerson L.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8539203/
https://www.ncbi.nlm.nih.gov/pubmed/34723156
http://dx.doi.org/10.1016/j.isci.2021.103315
Descripción
Sumario:We used the recombinant trimeric spike (S) glycoprotein in the prefusion conformation to immunize horses for the production of hyperimmune globulins against SARS-CoV-2. Serum antibody titers measured by ELISA were above 1:10(6), and the neutralizing antibody titer against authentic virus (WT) was 1:14,604 (average PRNT(90)). Plasma from immunized animals was pepsin digested to remove the Fc portion and purified, yielding an F(ab’)(2) preparation with PRNT(90) titers 150-fold higher than the neutralizing titers in human convalescent plasma. Challenge studies were carried out in hamsters and showed the in vivo ability of equine F(ab’)(2) to reduce viral load in the pulmonary tissues and significant clinical improvement determined by weight gain. The neutralization curve by F(ab’)(2) was similar against the WT and P.2 variants, but displaced to higher concentrations by 0.39 log units against the P.1 (Gamma) variant. These results support the possibility of using equine F(ab’)(2) preparation for the clinical treatment of COVID patients.