﻿<?xml version="1.0" encoding="UTF-8"?>
<ArticleSet>
  <Article>
    <Journal>
      <PublisherName>Tabriz University of Medical Sciences</PublisherName>
      <JournalTitle>ImmunoAnalysis</JournalTitle>
      <Issn>2783-2589</Issn>
      <Volume>3</Volume>
      <Issue>1</Issue>
      <PubDate PubStatus="ppublish">
        <Year>2023</Year>
        <Month>03</Month>
        <DAY>27</DAY>
      </PubDate>
    </Journal>
    <ArticleTitle>Immunogenicity of Chitosan-Based Non-invasive Vaccine Strategy Against Mycobacterium tuberculosis</ArticleTitle>
    <FirstPage>2</FirstPage>
    <LastPage>2</LastPage>
    <ELocationID EIdType="doi">10.34172/ia.2023.02</ELocationID>
    <Language>EN</Language>
    <AuthorList>
      <Author>
        <FirstName>Rasoul</FirstName>
        <LastName>Hoseinpour</LastName>
        <Identifier Source="ORCID">https://orcid.org/0000-0002-2717-0355</Identifier>
      </Author>
      <Author>
        <FirstName>Alka</FirstName>
        <LastName>Hasani</LastName>
        <Identifier Source="ORCID">https://orcid.org/0000-0001-6648-0893</Identifier>
      </Author>
      <Author>
        <FirstName>Behzad</FirstName>
        <LastName>Baradaran</LastName>
        <Identifier Source="ORCID">https://orcid.org/0000-0002-8642-6795</Identifier>
      </Author>
      <Author>
        <FirstName>Jalal</FirstName>
        <LastName>Abdolalizadeh</LastName>
        <Identifier Source="ORCID">https://orcid.org/0000-0002-8283-5057</Identifier>
      </Author>
      <Author>
        <FirstName>Roya</FirstName>
        <LastName>Salehi</LastName>
        <Identifier Source="ORCID">https://orcid.org/0000-0001-9284-0055</Identifier>
      </Author>
      <Author>
        <FirstName>Akbar</FirstName>
        <LastName>Hasani</LastName>
        <Identifier Source="ORCID">https://orcid.org/0000-0002-9461-821X</Identifier>
      </Author>
      <Author>
        <FirstName>Hossein</FirstName>
        <LastName>Samadi Kafil</LastName>
        <Identifier Source="ORCID">https://orcid.org/0000-0001-6026-8795</Identifier>
      </Author>
      <Author>
        <FirstName>Edris</FirstName>
        <LastName>Nabizadeh</LastName>
        <Identifier Source="ORCID">https://orcid.org/0000-0002-8192-8382</Identifier>
      </Author>
    </AuthorList>
    <PublicationType>Journal Article</PublicationType>
    <ArticleIdList>
      <ArticleId IdType="doi">10.34172/ia.2023.02</ArticleId>
    </ArticleIdList>
    <History>
      <PubDate PubStatus="received">
        <Year>2023</Year>
        <Month>01</Month>
        <Day>27</Day>
      </PubDate>
      <PubDate PubStatus="accepted">
        <Year>2023</Year>
        <Month>02</Month>
        <Day>19</Day>
      </PubDate>
    </History>
    <Abstract>Background: In spite of Bacillus Calmette-Guerin (BCG) vaccination, still tuberculosis caused by Mycobacterium tuberculosis remains a problematic impediment that requires perspective management. The aim of this study was to evaluate the immunogenicity of chitosan nanoparticles containing recombinant mycobacterial proteins and adjuvant in the Balb/C mice through a non-invasive nasal inhalation delivery route and measure the level of cytokines interferon gamma (IFN-γ), interleukin-4 (IL-4), and IL-17. Methods: Thirty mice in five different groups were vaccinated through inhalation with compounds set in different combinations. Two weeks after the last nasal delivery, IFN-γ, IL-4, and IL-17 were measured in spleen cell culture supernatants. Results: The IFN-γ and IL-17 concentrations were found to increase in the groups that received chitosan nanoparticles containing protein and adjuvant alone or as a BCG booster. Our study showed that the chitosan nanoparticle containing protein and adjuvant induced a Th1 response. However, the groups that first received BCG and then chitosan nanoparticles containing protein and adjuvant had the greatest Th1 response in terms of IFN-γ and IL-17 production in all the groups. Conclusion: Our findings showed that the vaccine designed to be administered through the nasal mucosa well stimulates cellular immunity and enhances the BCG vaccine’s effectiveness.</Abstract>
    <ObjectList>
      <Object Type="keyword">
        <Param Name="value">Nasal mucosa</Param>
      </Object>
      <Object Type="keyword">
        <Param Name="value">Vaccine</Param>
      </Object>
      <Object Type="keyword">
        <Param Name="value">Bacillus Calmette-Guerin</Param>
      </Object>
      <Object Type="keyword">
        <Param Name="value">Chitosan</Param>
      </Object>
      <Object Type="keyword">
        <Param Name="value">Tuberculosis</Param>
      </Object>
      <Object Type="keyword">
        <Param Name="value">Immunogenicity</Param>
      </Object>
    </ObjectList>
  </Article>
</ArticleSet>