Immune responses modulation by curcumin and allergen encapsulated into PLGA nanoparticles in mice model of rhinitis allergic through sublingual immunotherapy.


Journal

International immunopharmacology
ISSN: 1878-1705
Titre abrégé: Int Immunopharmacol
Pays: Netherlands
ID NLM: 100965259

Informations de publication

Date de publication:
Jul 2020
Historique:
received: 01 02 2020
revised: 11 04 2020
accepted: 16 04 2020
pubmed: 4 5 2020
medline: 11 3 2021
entrez: 4 5 2020
Statut: ppublish

Résumé

The purpose of this study was the combination of curcumin and ovalbumin in free form or encapsulated into PLGA NPs (polylactic co-glycolic acid nanoparticles) to enhance their sublingual immunotherapy (SLIT) efficiency in mouse model of rhinitis allergic. PLGA NPs containing curcumin (CUR), ovalbumin (OVA) or both were prepared by emulsion-solvent evaporation method and characterized. After sensitization of BALB/C mice with ovalbumin, SLIT with free or encapsulated formulations was carried out and immunological profiles were evaluated. SLIT treatment with all synthesized PLGA formulations lead to significantly decreased total IgE. The combination immunotherapy in the present of free form of curcumin or ovalbumin with encapsulated forms of the another substance (P.OVA-CUR 10 and P.CUR 5-OVA), showed the highest level of IFN-γ:IL-4 compared to other target groups. On the other hands, a significant increasment was observed in this ratio between these optimal groups and treated group with subcutaneous administration of OVA as the most commonly used method for immunotherapy. The study of nasal lavage fluid (NALF) showed significant decreased levels of total and eosinophil cell count in the traeted nano-formulation groups. The histopathological results of NAL were also like normal with no cellular infiltration and no inflammation in the optimal formulations. Therefore, using curcumin and nanoparticles with allergen can be considerd as potential immune modulatory agents.

Identifiants

pubmed: 32361190
pii: S1567-5769(20)30293-9
doi: 10.1016/j.intimp.2020.106525
pii:
doi:

Substances chimiques

Allergens 0
IFNG protein, mouse 0
Il4 protein, mouse 0
Polylactic Acid-Polyglycolic Acid Copolymer 1SIA8062RS
Interleukin-4 207137-56-2
Immunoglobulin E 37341-29-0
Interferon-gamma 82115-62-6
Ovalbumin 9006-59-1
Curcumin IT942ZTH98

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

106525

Informations de copyright

Copyright © 2020 Elsevier B.V. All rights reserved.

Déclaration de conflit d'intérêts

Declaration of Competing Interest The author declare that there is no conflict of interest.

Auteurs

Sanaz Shahgordi (S)

Department of Immunology, School of Medicine, Golestan University of Medical Sciences, Gorgan, Iran; Nanotechnology Research Center, Pharmaceutical Technology Institute, Mashhad University of Medical Sciences, Mashhad, Iran.

Mojtaba Sankian (M)

Immunology Research Center, Pharmaceutical Technology Institute, Mashhad University of Medical Sciences, Mashhad, Iran.

Yaghoub Yazdani (Y)

Infectious Diseases Research Center, Golestan University of Medical Sciences, Gorgan, Iran.

Kazem Mashayekhi (K)

Immunology Research Center, Department of Immunology, Medical School, Mashhad University of Medical Sciences, Mashhad, Iran.

Seyed Hasan Ayati (S)

Immunology Research Center, Department of Immunology, Medical School, Mashhad University of Medical Sciences, Mashhad, Iran.

Mahvash Sadeghi (M)

Immunology Research Center, Department of Immunology, Medical School, Mashhad University of Medical Sciences, Mashhad, Iran.

Mohsen Saeidi (M)

Stem Cell Research Center, Golestan University of Medical Sciences, Gorgan, Iran. Electronic address: dr.saeedi@goums.ac.ir.

Maryam Hashemi (M)

Nanotechnology Research Center, Pharmaceutical Technology Institute, Mashhad University of Medical Sciences, Mashhad, Iran; Department of Pharmaceutical Biotechnology, School of Pharmacy, Mashhad, University of Medical Sciences, Mashhad, Iran. Electronic address: hashemim@mums.ac.ir.

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Classifications MeSH