Immunologic Predisposition of HIV Patients to Develop Methicillin-Resistant Staphylococcus Aureus (MRSA) Colonization and Infection (MRSA-2)
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Purpose
The purpose of this study is to investigate the role of T helper 17 cells (Th17) in the pathogenesis of MRSA infections.
| Condition |
|---|
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HIV Infections Staphylococcal Infections |
| Study Type: | Observational |
| Study Design: | Observational Model: Cohort Time Perspective: Cross-Sectional |
| Official Title: | Immunologic Predisposition of HIV Patients to Develop Methicillin-Resistant Staphylococcus Aureus (MRSA) Colonization and Infection |
- To compare distribution of Th17 cells and their functionality, in the peripheral blood of HIV-positive patients who are infected with MRSA with that of HIV-positive patients who are not colonized or infected with Staphylococcus aureus. [ Time Frame: 1 year ] [ Designated as safety issue: No ]
- Compare distribution of Th17 cells in the peripheral blood of groups of HIV-positive and HIV-negative participants who are colonized with MRSA as well as those who have a MRSA infection. [ Time Frame: 1 year ] [ Designated as safety issue: No ]
- Examine distribution of T cells, B cells, macrophages, dendritic cells, neutrophils, defensins, and IL-17 in T cell subsets in the skin [ Time Frame: 1 year ] [ Designated as safety issue: No ]
- Compare Th17 cells in peripheral blood of HIV-negative participants with MRSA infection with that of HIV-negative subjects not colonized of infected with Staph aureus. [ Time Frame: 1 year ] [ Designated as safety issue: No ]
- Collect information on factors that may play a role in development of MRSA colonization/infection. Includes demographic, hygienic, exercise-related, and sexual factors which may contribute to MRSA. [ Time Frame: 1 year ] [ Designated as safety issue: No ]
Biospecimen Retention: Samples With DNA
Skin biopsy will be obtained.
| Estimated Enrollment: | 60 |
| Study Start Date: | March 2009 |
| Estimated Study Completion Date: | December 2014 |
| Primary Completion Date: | November 2010 (Final data collection date for primary outcome measure) |
| Groups/Cohorts |
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1
HIV-positive and MRSA negative
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2
HIV-positive and MRSA infected (skin/soft tissue)
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3
HIV-positive and MRSA colonized
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4
HIV-negative and MRSA negative
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5
HIV-negative and MRSA infected (skin/soft tissue)
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6
HIV-negative and MRSA colonized
|
Eligibility| Ages Eligible for Study: | 18 Years and older |
| Genders Eligible for Study: | Both |
| Accepts Healthy Volunteers: | Yes |
| Sampling Method: | Non-Probability Sample |
HIV-positive and negative patients with a recent screen for MRSA colonization or a history of MRSA infection will be asked to participate. Participants will be recruited by providers within the infectious disease clinics at the sites. In addtion, MRSA isolates will be monitored at the central laboratory and providers of patients with MRSA will be notified and asked to notify their patients of the opportunity to participate in this study.
All participant inclusion criteria:
- Greater or equal to 18 years of age
- Willingness to undergo blood draw. Skin biopsy will be requested, but is optional
-AND-
HIV-positive and MRSA-negative Group:
- Documented positive HIV test result
- Negative colonization swabs for S. aureus within 14 days of enrollment
- No evidence of skin/soft tissue infection
HIV-positive and MRSA-Colonization Group:
- Documented positive HIV test result
- History of of colonization with MRSA w/in 14 days of study enrollment
HIV-positive and MRSA Infection Group:
- Documented positive HIV test result
- Skin/soft tissue infection with a positive wound culture showing MRSA within 7 days of enrollment
- MRSA infection is not associated with an intravenous catheter or other nosocomial procedure
HIV Negative groups:
- Same criteria used for the HIV-negative groups as listed above.
- No history of HIV infection.
- Willing to undergo an HIV blood test, which must have a negative result.
Exclusion Criteria:
- Women with positive urine pregnancy test within 7 days of study enrollment
- Women who are within 6 months of being postpartum or who are currently breastfeeding
- Subjects unable or unwilling to complete questionnaires and blood draw.
Contacts and Locations| United States, California | |
| Naval Medical Center San Diego | |
| San Diego, California, United States, 92134 | |
| United States, Maryland | |
| Walter Reed National Military Medical Center | |
| Bethesda, Maryland, United States, 20889 | |
| Principal Investigator: | Nancy Crum-Cianflone, MD, MPH | NMCSD |
More Information
No publications provided
| Responsible Party: | Dr. Nancy Crum-Cianflone, Research Physician, Uniformed Services University of the Health Sciences |
| ClinicalTrials.gov Identifier: | NCT00859677 History of Changes |
| Other Study ID Numbers: | IDCRP -023 |
| Study First Received: | March 10, 2009 |
| Last Updated: | January 24, 2013 |
| Health Authority: | United States: Institutional Review Board |
Keywords provided by Uniformed Services University of the Health Sciences:
|
HIV Methicillin-resistant Staphylococcus aureus (MRSA) HIV and Staphylococcus aureus infection |
Additional relevant MeSH terms:
|
HIV Infections Acquired Immunodeficiency Syndrome Disease Susceptibility Genetic Predisposition to Disease Staphylococcal Infections Lentivirus Infections Retroviridae Infections RNA Virus Infections Virus Diseases Sexually Transmitted Diseases, Viral Sexually Transmitted Diseases Immunologic Deficiency Syndromes |
Immune System Diseases Slow Virus Diseases Disease Attributes Pathologic Processes Gram-Positive Bacterial Infections Bacterial Infections Methicillin Anti-Bacterial Agents Anti-Infective Agents Therapeutic Uses Pharmacologic Actions |
ClinicalTrials.gov processed this record on May 21, 2013