CHRONIC OBSTRUCTIVE PULMONARY DISEASE

January 30, 2018 | Author: Anonymous | Category: Science, Health Science, Immunology
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CHRONIC OBSTRUCTIVE PULMONARY DISEASE ZULEYHA OZEN

OVERVIEW ● Introduction ● Information about Chronic Obstructive Pulmonary Disease (COPD)

● Inflammatory Responses ● Paper 1 ● Paper 2 ● What is still unknown? ● Future Studies/Specific Aim

Disease Overview 

Pathophysiology of COPD (Chronic Bronchitis and Emphysema)

-Chronic Bronchitis: Loss of muco-ciliary clearance 

Loss of cilia function

-Emphysema: Destruction of elastin fibers 

Proteases, matrix metalloproteinase 9 (MMP9) cause elastin degradation

Shortness of Breath Cough/Sputum-(Progressive dyspnea) http://www.wgabinecie.pl/artykul/65-pochp-przewlekla-obturacyjna-choroba-pluc/

Current existing medicines 

Bronchodilators



Combination of Bronchodilators and cortisteroids



Vaccines



Pulmonary Rehabilitation



Oxygen Therapy



Change in Lifestyle

http://www.ncbi.nlm.nih.gov/books/NBK26827/figure/A4531/?report=objectonly

https://www.caymanchem.com/app/template/Article.vm/article/2177

Inflammatory and immune cells involved in chronic obstructive pulmonary disease (COPD) Macrophages and epithelial cells: -chemotactic factors -attract inflammatory cells

http://www.nature.com/nri/journal/v8/n3/fig_tab/nri2254_F2.html

TH17 cells and airway inflammation

http://www.nature.com/nri/journal/v8/n3/fig_tab/nri2254_F5.html

Smoke Exposure (n=20/group) Whole body exposed to cigarette smoke (CS) 20 mice exposed to CS of 5 cigarettes

30 min smoke free interval

20 mice exposed to CS of 5 cigarettes

30 min smokefree interval

20 mice exposed to CS of 5 cigarettes

30 min smokefree interval

20 mice exposed to CS of 5 cigarettes

The CS exposure animals were divided into two subgroups:

Control group: exposed to air Sub-acute exposure: Initiated CS at 26-28 weeks old

Mice of each group 30-32 weeks old when the CS & Air exposure ended

Chronic exposure: initiated CS at 6-8 weeks old

Figure 1. Assessing effect of CS exposure on lung inflammation Total number of alveolar inflammatory cells increased in chronic CS exposure •

Sub-acute exposure significantly lower than chronic CS

Figure 2A. Prevalence of Th17 cells in lung tissue

Prevalence of Th17 cells: -ratio of CD4+ IL-17A+ cells to the total amount of CD4+ T lymphocytes

-Th17 prevalence markedly higher in mice with chronic CS and Sub-acute CS

Figure 2B. Peripheral blood mononuclear cells -similarly the prevalence of Th17 cells increased in CS exposure

Figure 2C. Collective analysis of flow cytometry

Figure 3A. Prevalence of T regulatory cells (ratio of CD4+CD25+Foxp3+ cells to the total amount of CD4+ T lymphocytes) in lung tissue

Prevalence of T regulatory cells: -markedly higher in sub-acute exposure -drops in chronic CS exposure

Figure 3B. Peripheral blood mononuclear cells -similarly the prevalence of T regulatory cells decreased in chronic CS exposure

Figure 3C. Collective analysis of flow cytometry

Figure 4. Assessing the ratio of Th17 and Treg in lung tissue and peripheral blood

-In lung tissues, the ratio of Th/Treg is decreased with sub-acute CS exposure -Increases in chronic CS exposure Ratio of Th17/Treg in peripheral blood: -significantly increased in chronic CS exposure

Figure 5. The expression of Foxp3 and ROR gamma t mRNA -Looking at specific transcription factors of both Tsubsets by real time-PCR

-Th17 specific transcription factor ROR gamma t mRNA expression: significantly increased in CS exposed

-T regulatory specific transcription factor Foxp3 mRNA expression: significantly decreased in CS exposed

Table 1: levels of IL-17A, IL-6, IL23 and TGF-beta in serum significantly higher in chronic CS exposure -IL-10 sig. lower in chronic CS

Conclusions from paper 1 

There is an obvious imbalance between Th/Treg cells in CS exposed mice



Prevalence of Th17 and Th17 specific transcription factor, ROR gamma t mRNA: increased



Treg cell prevalence and Treg specific transcription factor, Foxp3 mRNA: decreased 



Thus, leading to an imbalance in the ratio of Th/Treg cell profiles

The existing cytokine profile can be further evaluated for specific therapeutic approach

Figure 1. Assessing histology of lung tissues

Fig.1 Histology of Lung Tissues



Mean alveoli were expanded and broken



COPD lung- more inflammatory cells

Figure 2. Expression of transcription factors ROR gamma t and Foxp3

• • •

Fig.2a. Foxp3 relative mRNA expression level significantly lower in COPD patients Fig.2b. RORyt relative mRNA expression level significantly higher in COPD patients Fig.2c. Ratio of Treg/Thelper cells in the level of mRNA lower in COPD patients

Figure 3. Assessing expression of Foxp3 and ROR gamma t protein levels

-Increased protein expression of ROR gamma t in COPD patients -Viceversa, decreased protein expression of Foxp3 compared with smokers and nonsmokers

Figure 4. Immunohistochemistry staining of different proteins All p-values were less than 0.001 -IL-17+, CCR6+ and IL-23R cells increased -Foxp3 cells in alveolar walls decreased

Figure 5. The number of Foxp3+, IL-17+, CCR6+ and IL-23R+ cells in alveolar walls -Foxp3+ and Foxp3+ / IL-17+ cells decreased in cell number in chronic CS exposure -IL-17+, CCR6+ and IL-23R+ cells increased in cell number in chronic CS exposure -Foxp3+ & Foxp3+/IL-17+ cells decreased in alveolar walls of COPD

A: ROR gamma t & Foxp3 mRNA expression: negatively correlated B: Ratio of Foxp3/ROR gamma t mRNA expression negatively correlated with mean alveoli area C: Positive correlation with the ratio of Foxp3/ROR gamma t and FEV1%pred

D: ROR gamma t & Foxp3 protein: negatively correlated E: Ratio of Foxp3/ROR gamma t in level of protein and mean alveoli area F: Positive correlation with the ratio of Foxp3/ROR gamma t in level of protein and FEV1%pred

G: Numbers of Foxp3+/IL-17+ cells: negatively correlated H: Ratio of Foxp3/IL-17+ cells: negatively correlated to the mean alveoli area I: Positive correlation with the ratio of Foxp3+/IL-17+ cells and FEV1%pred

Conclusions from paper 2 

Decreased ratio of Foxp3/ROR gamma t in patients with COPD and normal smokers 



persistent with the aggravation of the disease

Decreased ratio of Foxp3/ROR gamma t important in pathogenesis of COPD 

Immune dysregulation, and participation in lung inflammation: leading to destruction in

the lung 

Pro-inflammatory cytokines and chemokine receptors are also evident in development of the disease



Their association with the transcription factors ROR gamma t and Foxp3 can be further researched for potential therapeutics

What is still unknown ? 

The regulatory cytokine involvement: TGF-beta levels in the progression of the disease is still unknown



Study by Zhou et al. TGF-beta induced Foxp3 leads to inhibition of Th17 cell differentiation



In a dose dependent matter, TGF-beta might be a factor seen in the imbalance between Th/T regulatory cells

Specific Aim 

In the research proposal, my area of focus will be to further analyze the negatively correlated relationship between the T-regulatory and T helper cells with regards to changes in the expression of the specific transcription factors and cytokine TGF-beta

 Implement TGF-beta induced Foxp3 and use of cytokine IL-6 antagonist for therapeutic approach

THANK YOU! QUESTIONS?

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