Chitosan Interferon-γ Nanogene Therapy for Lung Disease: Modulation of T-Cell and Dendritic Cell Immune Responses

<p/> <p>The use of chitosan nanoparticles as carriers for expression plasmids represents a major improvement in gene expression technology. We demonstrated previously that treatment with chitosan interferon-γ (IFN-γ) plasmid deoxyribonucleic acid (DNA) nanoparticles (chitosan interferon-...

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Main Authors: Kong Xiaoyuan, Hellermann Gary R, Zhang Weidong, Jena Prasanna, Kumar Mukesh, Behera Aruna, Behera Sumita, Lockey Richard, Mohapatra Shyam S
Format: Article
Language:English
Published: BMC 2008-09-01
Series:Allergy, Asthma & Clinical Immunology
Subjects:
Online Access:http://www.aacijournal.com/content/4/3/95
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author Kong Xiaoyuan
Hellermann Gary R
Zhang Weidong
Jena Prasanna
Kumar Mukesh
Behera Aruna
Behera Sumita
Lockey Richard
Mohapatra Shyam S
author_facet Kong Xiaoyuan
Hellermann Gary R
Zhang Weidong
Jena Prasanna
Kumar Mukesh
Behera Aruna
Behera Sumita
Lockey Richard
Mohapatra Shyam S
author_sort Kong Xiaoyuan
collection DOAJ
description <p/> <p>The use of chitosan nanoparticles as carriers for expression plasmids represents a major improvement in gene expression technology. We demonstrated previously that treatment with chitosan interferon-γ (IFN-γ) plasmid deoxyribonucleic acid (DNA) nanoparticles (chitosan interferon-γ nanogene [CIN]) led to in situ production of IFN-γ and a reduction in inflammation and airway reactivity in mice, but the mechanism underlying the immunomodulatory effects of CIN remains unclear. In this report, the effect of CIN treatment on the immune responses of CD8<sup>+ </sup>T cells and dendritic cells was examined in a BALB/c mouse model of ovalbumin (OVA)-induced allergic asthma. OT1 mice (OVA-T cell receptor [TCR] transgenic) were also used to test the effects of CIN on OVA-specific CD8<sup>+ </sup>T cells. CIN treatment caused a reduction in IFN-γ production in a subpopulation of OVA-specific CD8<sup>+ </sup>T cells cultured in vitro in the presence of OVA. CIN also reduced apoptosis of the CD8<sup>+ </sup>T cells. Examination of dendritic cells from lung and lymph nodes indicated that CIN treatment decreased their antigen-presenting activity, as evident from the reduction in CD80 and CD86 expression. Furthermore, CIN treatment significantly decreased the number of CD11c<sup>+</sup>b<sup>+ </sup>dendritic cells in lymph nodes, suggesting that endogenous IFN-γ expression may immunomodulate dendritic cell migration and activation. CIN therapy results in a reduction in proinflammatory CD8<sup>+ </sup>T cells and decreases the number and antigen-presenting activity of dendritic cells.</p>
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spelling doaj.art-7ba1e100b3424fe2afb3355c88d0ed132022-12-22T03:10:18ZengBMCAllergy, Asthma & Clinical Immunology1710-14841710-14922008-09-01439510510.1186/1710-1492-4-3-95Chitosan Interferon-γ Nanogene Therapy for Lung Disease: Modulation of T-Cell and Dendritic Cell Immune ResponsesKong XiaoyuanHellermann Gary RZhang WeidongJena PrasannaKumar MukeshBehera ArunaBehera SumitaLockey RichardMohapatra Shyam S<p/> <p>The use of chitosan nanoparticles as carriers for expression plasmids represents a major improvement in gene expression technology. We demonstrated previously that treatment with chitosan interferon-γ (IFN-γ) plasmid deoxyribonucleic acid (DNA) nanoparticles (chitosan interferon-γ nanogene [CIN]) led to in situ production of IFN-γ and a reduction in inflammation and airway reactivity in mice, but the mechanism underlying the immunomodulatory effects of CIN remains unclear. In this report, the effect of CIN treatment on the immune responses of CD8<sup>+ </sup>T cells and dendritic cells was examined in a BALB/c mouse model of ovalbumin (OVA)-induced allergic asthma. OT1 mice (OVA-T cell receptor [TCR] transgenic) were also used to test the effects of CIN on OVA-specific CD8<sup>+ </sup>T cells. CIN treatment caused a reduction in IFN-γ production in a subpopulation of OVA-specific CD8<sup>+ </sup>T cells cultured in vitro in the presence of OVA. CIN also reduced apoptosis of the CD8<sup>+ </sup>T cells. Examination of dendritic cells from lung and lymph nodes indicated that CIN treatment decreased their antigen-presenting activity, as evident from the reduction in CD80 and CD86 expression. Furthermore, CIN treatment significantly decreased the number of CD11c<sup>+</sup>b<sup>+ </sup>dendritic cells in lymph nodes, suggesting that endogenous IFN-γ expression may immunomodulate dendritic cell migration and activation. CIN therapy results in a reduction in proinflammatory CD8<sup>+ </sup>T cells and decreases the number and antigen-presenting activity of dendritic cells.</p>http://www.aacijournal.com/content/4/3/95allergyasthmainterferon
spellingShingle Kong Xiaoyuan
Hellermann Gary R
Zhang Weidong
Jena Prasanna
Kumar Mukesh
Behera Aruna
Behera Sumita
Lockey Richard
Mohapatra Shyam S
Chitosan Interferon-γ Nanogene Therapy for Lung Disease: Modulation of T-Cell and Dendritic Cell Immune Responses
Allergy, Asthma & Clinical Immunology
allergy
asthma
interferon
title Chitosan Interferon-γ Nanogene Therapy for Lung Disease: Modulation of T-Cell and Dendritic Cell Immune Responses
title_full Chitosan Interferon-γ Nanogene Therapy for Lung Disease: Modulation of T-Cell and Dendritic Cell Immune Responses
title_fullStr Chitosan Interferon-γ Nanogene Therapy for Lung Disease: Modulation of T-Cell and Dendritic Cell Immune Responses
title_full_unstemmed Chitosan Interferon-γ Nanogene Therapy for Lung Disease: Modulation of T-Cell and Dendritic Cell Immune Responses
title_short Chitosan Interferon-γ Nanogene Therapy for Lung Disease: Modulation of T-Cell and Dendritic Cell Immune Responses
title_sort chitosan interferon γ nanogene therapy for lung disease modulation of t cell and dendritic cell immune responses
topic allergy
asthma
interferon
url http://www.aacijournal.com/content/4/3/95
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