Development of Glycyrrhizinic Acid-Based Lipid Nanoparticle (LNP-GA) as An Adjuvant That Improves the Immune Response to Porcine Epidemic Diarrhea Virus Spike Recombinant Protein

Author:

García-Cambrón José Bryan1ORCID,Cerriteño-Sánchez José Luis2,Lara-Romero Rocío3,Quintanar-Guerrero David4ORCID,Blancas-Flores Gerardo5ORCID,Sánchez-Gaytán Brenda L.6,Herrera-Camacho Irma7ORCID,Cuevas-Romero Julieta Sandra2

Affiliation:

1. Programa de Doctorado en Biología Experimental, Universidad Autónoma Metropolitana, Iztapalapa, Ciudad de México 09089, Mexico

2. Instituto Nacional de Investigaciones Forestales Agrícolas y Pecuarias, Centro Nacional de Investigación Disciplinaria en Salud Animal e Inocuidad, Cuajimalpa, Ciudad de México 05110, Mexico

3. Programa de Estancia Posdoctoral, Facultad de Medicina Veterinaria y Zootecnia, Universidad Nacional Autónoma de México, Ciudad de México 04510, Mexico

4. División de Estudios de Posgrado (Tecnología Farmacéutica), Facultad de Estudios Superiores, Universidad Nacional Autónoma de México, Cuautitlán Izcalli, Estado de México 54740, Mexico

5. Laboratorio de Farmacología, División de Ciencias Biológicas y de la Salud, Universidad Autónoma Metropolitana, Iztapalapa, Ciudad de México 09089, Mexico

6. Centro de Química ICUAP, Laboratorio de Bioinorgánica Aplicada, Benemérita Universidad Autónoma de Puebla, Puebla 72592, Mexico

7. Centro de Química ICUAP, Laboratorio de Bioquímica y Biología Molecular, Edificio IC7, Benemérita Universidad Autónoma de Puebla, Puebla 72592, Mexico

Abstract

Porcine epidemic diarrhea virus (PEDV) has affected the pork industry worldwide and during outbreaks the mortality of piglets has reached 100%. Lipid nanocarriers are commonly used in the development of immunostimulatory particles due to their biocompatibility and slow-release delivery properties. In this study, we developed a lipid nanoparticle (LNP) complex based on glycyrrhizinic acid (GA) and tested its efficacy as an adjuvant in mice immunized with the recombinant N-terminal domain (NTD) of porcine epidemic diarrhea virus (PEDV) spike (S) protein (rNTD-S). The dispersion stability analysis (Z-potential −27.6 mV) confirmed the size and charge stability of the LNP-GA, demonstrating that the particles were homogeneously dispersed and strongly anionic, which favors nanoparticles binding with the rNTD-S protein, which showed a slightly positive charge (2.11 mV) by in silico analysis. TEM image of LNP-GA revealed nanostructures with a spherical-bilayer lipid vesicle (~100 nm). The immunogenicity of the LNP-GA-rNTD-S complex induced an efficient humoral response 14 days after the first immunization (p < 0.05) as well as an influence on the cellular immune response by decreasing serum TNF-α and IL-1β concentrations, which was associated with an anti-inflammatory effect.

Funder

CENID-SAI/INIFAP, Ciudad de México, Mexico

Publisher

MDPI AG

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