UF researchers probe why lung defenses fail in two genetic diseases
NCT ID NCT01851642
First seen Jun 26, 2026 · Last updated Jun 27, 2026 · Updated 1 time
Summary
This study from the University of Florida is looking at how two genetic lung conditions—Alpha-1 antitrypsin deficiency and cystic fibrosis—affect immune cells called macrophages. Researchers will collect blood and measure lung function in 220 adults to see how well these cells work. The goal is to better understand the disease process, not to test a new treatment.
What this could mean
Our plain-language read of the trial. This is informational only — not medical advice or a prediction.
- What this could lead to
- If successful, this research could reveal why lung immune cells work poorly in these diseases, pointing toward new treatment targets.
- What could go wrong
- This is an observational study, not a treatment trial. It will not directly improve health, and results may not lead to therapies for years.
This is an AI summary of the original study and may miss details. Read our disclaimer.
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Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
Contacts and locations
Locations
-
Shands at the University of Florida
RECRUITINGGainesville, Florida, 32610, United States
More trials for these conditions
Other studies related to the condition(s) this trial covers.
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- Could modern CF drugs make daily inhaled treatments obsolete?
- New study investigates hidden heart risks in cystic fibrosis patients on modern drugs
- Blood pressure drug may help preserve insulin in cystic fibrosis
- Hidden toll: depression and anxiety in kids with cystic fibrosis