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CompletedNCT01224223Updated Jun 28, 2012

Myeloid Suppressors in Inflammation

An observational study in Asthma, sponsored by University of South Florida. Completed at 1 site in United States. Open to participants aged 18 Years to 60 Years. Per ClinicalTrials.gov, last updated 2012-06-28.

Sponsored by University of South Florida · Observational

Study type
Observational
Time perspective
Prospective
Enrollment
20
Ages
18 Years to 60 Years
Sex
All
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Study summary

Myeloid-derived suppressor cells (MDSC) have been studied for their ability to suppress T cell responses in vivo and in vitro. As a result, MDSC can regulate cellular responses to chronic inflammatory conditions such as cancer, leading to the induction of tolerance and, ultimately, tumor escape from immune surveillance.

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Conditions studied

  • Asthma

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Keywords

  • asthma
03

In context

Inflammation

3,439 studies on the registry are indexed under Inflammation; 629 are open to participants now.

This study's enrollment of 20 is below the median of 95 across 895 observational studies indexed under Inflammation.

Browse Inflammation studies →

Lead sponsor

University of South Florida is the lead sponsor of 333 studies on the registry; 63 are open to participants now.

Of its 17 completed or terminated interventional studies of FDA-regulated products, 4 (24%) have results posted.

Counted across the registry records on this site, refreshed daily.

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Who can participate

Ages eligible
18 Years to 60 Years
Sexes eligible
All
Accepts healthy volunteers
No
Sampling method
Probability sample

Study population

Ages eligible for study: 18 to 60 years Genders eligible for study: male and female Signed and dated written informed consent is obtained prior to study blood draw.

Subjects being actively treated for chronic moderate to severe asthma based on National Heart Lung and Blood Institute guidelines (figure 1). Subjects must carry the diagnosis of asthma (made by a physician) for a minimum of six months.

Subjects within the first seven days of an acute asthma exacerbation, as determined by the referring physician.Able to give informed consent.

Inclusion criteria

  1. Ages eligible for study: 18 to 60 years
  2. Genders eligible for study: male and female
  3. Signed and dated written informed consent is obtained prior to study blood draw.
  4. Subjects being actively treated for chronic moderate to severe asthma based on National Heart Lung and Blood Institute guidelines (figure 1). Subjects must carry the diagnosis of asthma (made by a physician) for a minimum of six months.
  5. Subjects within the first seven days of an acute asthma exacerbation, as determined by the referring physician.
  6. Able to give informed consent.

Exclusion criteria

Exclusion Criteria:

  1. Use of systemic corticosteroids within the previous two weeks.
  2. Pregnant and/or lactating females.
  3. Current tobacco use.
  4. Severe psychiatric illness.
  5. Current illicit substance abuse or dependence and/or abuse of alcohol.
  6. Current use of anti-microbial medications.
  7. Primary or secondary immunodeficiency.
  8. Any clinically significant uncontrolled medical condition that would put the patient's safety at risk.
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Study design

Time perspective
Prospective
Enrollment
20 participants (actual)

Groups and cohorts

  • acute asthma exaecerbtion patients

    Patients experiencing acute exacerbation of their asthma

  • chronic asthma group

    Two groups are being enrolled. The first group is chronic asthma patients with FEV1 below 80% and FEV1/FVC ratio reduced by 5%

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What researchers measure

Primary outcomes

  1. To identify and characterize specific cell types (human dendritic cells, myeloid-derived suppressor cells and T lymphocytes) that are present in acute and chronic asthma.

    Time frame: one year from start of study

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Study locations

1 site
  • USF Asthma, Allergy and Immunology CRU
    Tampa, Florida 33613, United States
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Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Jun 28, 2012, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
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Registry details

Key details

Study ID
NCT01224223
Lead sponsor
University of South Florida
Responsible party
Richard Lockey (principal investigator, University of South Florida) — Principal investigator
First posted
Oct 19, 2010
Start date
Oct 2010
Primary completion
Jan 2012
Completion
Jan 2012
Last update
Jun 28, 2012

Study contacts

Richard Lockey, MD
principal investigator · USF Asthma, Allergy and Immunology CRU

Oversight

Data monitoring committee
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is completed, as verified in Oct 2010. You cannot join it, but the record below documents what was studied.

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