ICIVET-LITORAL   24728
INSTITUTO DE CIENCIAS VETERINARIAS DEL LITORAL
Unidad Ejecutora - UE
artículos
Título:
Preclinical studies of NEAST (Neutralizing Equine Anti-Shiga Toxin): A potential treatment for prevention of STEC-HUS
Autor/es:
YANINA HIRIART; CONSTANZA LAUCHÉ; MARIANA COLONNA ; SANTIAGO SANGUINETI; LUCAS BUTAKÁ; ANDREA L. BERENGENO; FERNANDO GOLDBAUM ; ROMINA PARDO; LUCIANA MUÑOZ; HUGO H. ORTEGA; VANESA ZYLBERMAN
Revista:
International Journal of Drug Development and Research
Editorial:
iMedPub LTD
Referencias:
Lugar: Londres; Año: 2019 vol. 11 p. 15 - 24
ISSN:
0975-9344
Resumen:
Abstract: STEC-HUS is a clinical syndrome characterized by the triad of thrombotic microangiopathy, thrombocytopenia and acute kidney injury. Despite of the magnitude of the social and economic problems caused by STEC infections, there are currently no specific therapeutic options on the market. HUS is a toxemic disorder and the therapeutic effect of the early intervention with the anti-toxin neutralizing antibodies has been supported in several animal models. We have designed novel protein nanoparticles with very strong immunogenic capacity by inserting Stx1B and Stx2B subunits of the Shiga toxin to Brucella abortus Lumazine Synthase (BLS). The chimeric BLS- StxBs particles elicited strong neutralizing antibodies against Shiga toxins in horses. Based on these responses, we produced NEAST (Neutralizing Equine Anti-Shiga Toxin), composed of purifiedF(ab?)2 fragments. In this report, we present the preclinical analysis of this new treatment. As a general conclusion, NEAST shows a very strong neutralizing capacity against 8 Shoga toxin variants in preclinical models of STEC-HUS. NEAST is also able to neutralize pathologic effects after previous exposure to Shiga toxin, defining a potential therapeutic window. Besides, NEAST shows an excellent pharmacokinetics and safety profile in animal models. Overall, these results indicate that NEAST is a very good drug candidate for preventing the onset of HUS in STEC-infected patients and validate the conduction of a first in human clinical study at the Hospital Italiano de Buenos Aires in order to evaluate its safety and pharmacokinetic profiles in healthy adult volunteers.