Lung Disease and Its Affect on the Work of White Blood Cells in the Lungs
Status: | Recruiting |
---|---|
Conditions: | Pulmonary |
Therapuetic Areas: | Pulmonary / Respiratory Diseases |
Healthy: | No |
Age Range: | 18 - Any |
Updated: | 8/26/2018 |
Start Date: | September 2007 |
End Date: | November 2019 |
Contact: | Jesse West, RN |
Email: | jesse.west@medicine.ufl.edu |
Phone: | 352-273-8666 |
The Role of Conformational Diseases on Macrophage Function
The purpose of this study is to look at how Alpha-1-antitrypsin (AAT) deficiency and Cystic
Fibrosis (CF) affect white blood cells in the lungs, called macrophages, and their ability to
work.
Fibrosis (CF) affect white blood cells in the lungs, called macrophages, and their ability to
work.
AAT deficiency is a genetic disorder that affects around 100,000 people in the USA, including
1-3% of all people diagnosed with chronic obstructive pulmonary disease (COPD). In AAT
deficient people diagnosed with COPD, it was originally believed the cause of the disease was
due to a lack of supply of alpha-1 antitrypsin. However, early information gathered in our
laboratory suggests another cause of the development of COPD and the progressing of the
disease may be due to a malfunction in macrophages.
CF is also a genetic disorder which affects 1/300 births among the Caucasian population. One
of the main symptoms of CF is inflammation of the lung tissue. Lung macrophages play a major
role in lung inflammation as well as in helping to resolve the inflammation.
Inflammation is an important defense of the body. It is the body's response to infection
causing germs and things that may cause irritation, as well as, a way for the body to repair
damaged tissue.
We suggest that the effects of AAT deficiency and CF decreases the inflammation response in
the lungs and also restricts the ability of macrophages to correct that inflammation once it
occurs.
1-3% of all people diagnosed with chronic obstructive pulmonary disease (COPD). In AAT
deficient people diagnosed with COPD, it was originally believed the cause of the disease was
due to a lack of supply of alpha-1 antitrypsin. However, early information gathered in our
laboratory suggests another cause of the development of COPD and the progressing of the
disease may be due to a malfunction in macrophages.
CF is also a genetic disorder which affects 1/300 births among the Caucasian population. One
of the main symptoms of CF is inflammation of the lung tissue. Lung macrophages play a major
role in lung inflammation as well as in helping to resolve the inflammation.
Inflammation is an important defense of the body. It is the body's response to infection
causing germs and things that may cause irritation, as well as, a way for the body to repair
damaged tissue.
We suggest that the effects of AAT deficiency and CF decreases the inflammation response in
the lungs and also restricts the ability of macrophages to correct that inflammation once it
occurs.
Inclusion Criteria:
- Signed informed consent
- Male or female 18 years of age or older
- Negative pregnancy test for women of childbearing potential
- Hemoglobin >12.5 g/dl measured on the day of participation
- Negative urine nicotine test
Exclusion Criteria:
- Pregnancy or breastfeeding
- Weight < 50 kg
- History of anemia requiring blood transfusions, erythropoietin supplementation, or
iron supplementation within the past 36 months
- Known hemoglobin <12.5 g/dl within the past 90 days
- Systolic blood pressure > 180 mmHg and/or diastolic blood pressure >100 mmHg
- Poor venous access
- Large volume blood donation (>200 ml or 7 ounces) within the previous 56 days (e.g.
blood donation for the purposes of blood banking)
- Clinically significant cardiac, hemostatic or neurological impairment or any other
significant medical condition that, in the opinion of the investigator would affect
subject safety (e.g., recent myocardial infarction, history of prolonged bleeding
time, cerebral vascular accident, advanced cancer or uncontrolled medical condition)
- Psychiatric or cognitive disturbance or illness that would affect subject safety
- Current smoker
We found this trial at
1
site
Gainesville, Florida 32610
Principal Investigator: Mark Brantly, MD
Phone: 352-273-8666
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