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Expression of Mif Alleles in Individuals With Leishmaniasis
This study is currently recruiting participants.
Verified by Yale University, June 2009
First Received: November 16, 2006   Last Updated: June 10, 2009   History of Changes
Sponsors and Collaborators: Yale University
National Institute of Allergy and Infectious Diseases (NIAID)
Information provided by: Yale University
ClinicalTrials.gov Identifier: NCT00401349
  Purpose

CIDEIM, Centro Internacional de Entrenamiento e Investigaciones Medicas, is conducting a research study about the disease Cutaneous Leishmaniasis, which is caused by the Leishmania parasite and causes skin sores. Researchers hope to find out how the human body defends against Leishmania. A total of 472 individuals, ages 7 to 70 years, belonging to one of the following groups will be included in this study: recurring disease, chronic disease, disease with no sign or symptoms (asymptomatic), and healthy individuals. Study procedures will include a questionnaire and buccal swab (swabbing of the inside of the cheek with a cotton or wooden applicator). In addition, asymptomatic and healthy individuals will provide a blood sample. Study participation will be up to 1.5 hours.


Condition
Leishmaniasis

Study Type: Observational
Study Design: Prospective
Official Title:

Intervenable Host- Leishmania (Vianna) Interactions - Project 3: Immune and Inflammatory Responses in L.

(Viannia) Infection Aim 2: Expression of Mif Alleles in Individuals With Recurrent Leishmaniasis, Chronic Leishmaniasis and Asymptomatic Infection


Resource links provided by NLM:


Further study details as provided by Yale University:

Biospecimen Retention:   Samples With DNA

Biospecimen Description:

DNA samples from bucal swabs are being retained for genetic analyses of MIF alleles and possibly other genes associated with disease (leishmaniasis) resistance/susceptibility.


Estimated Enrollment: 472
Study Start Date: December 2006
Estimated Study Completion Date: September 2010
Detailed Description:

The purpose of this study is to define the proportion of low and high expression Mif alleles in individuals with recurrent or chronic Cutaneous Leishmaniasis and compare it with that of individuals with asymptomatic infection and healthy donors (controls), in order to determine if these alleles are associated with outcome of infection.

This study is part 2 of a project that includes DMID protocols 05-0139 and 06-0010. Specific objectives are to:

determine the proportion of low expression (5-CATT) Mif alleles in individuals with recurrent or chronic cutaneous leishmaniasis, healthy donors (controls), and individuals with asymptomatic infection; determine the proportion of high expression (6,7,8-CATT) Mif alleles in individuals with recurrent or chronic cutaneous leishmaniasis, healthy donors (controls), and individuals with asymptomatic infection; and determine the Mif Genotype repertoire and frequency distribution in the endemic population of study. This study will be conducted in 472 participants who will be enrolled into one of the following 4 groups: recurrent disease, chronic disease, asymptomatic infection, and healthy donors (controls). Patients (males and females) aged between 7-70 years with chronic or recurrent cutaneous leishmaniasis (historic or active) diagnosed in either Cali (CIDEIM) and Tumaco (San Andrés Hospital) on the Colombian Pacific Coast will be invited to participate in the study. Asymptomatic and healthy donors (controls) will also be enrolled. Pregnant women will not be enrolled. Consent and samples will be obtained during a single study visit of up to 1.5 hours. No further follow-up visits are planned for this study. Genetic material extracted and amplified from buccal swabs will be used to determine the proportion of low and high expression Mif alleles of each group. Expression in recurrent and chronic participants will be compared to that of asymptomatic participants and healthy donors (controls) in order to determine if expression frequencies are related to the outcome of infection. Blood samples obtained from asymptomatic and healthy donors will undergo in vitro blastogenesis testing to confirm asymptomatic/healthy donor status. Study outcome measures are: frequency of low expression (5-CATT) Mif alleles in participants with recurrent or chronic disease, individuals with asymptomatic infection and healthy donors (controls); frequency of high expression (6,7,8-CATT) Mif alleles in participants with recurrent or chronic disease individuals with asymptomatic infection and healthy donors (controls); and Mif Genotype repertoire and frequency distribution in the endemic population in the study site.

  Eligibility

Ages Eligible for Study:   7 Years to 70 Years
Genders Eligible for Study:   Both
Accepts Healthy Volunteers:   Yes
Sampling Method:   Non-Probability Sample
Study Population
  1. Active or historical cases of recurrent cutaneous leishmaniasis
  2. Active or historical cases of chronic or recurrent cutaneous leishmaniasis
  3. Endemic area controls - Resident of endemic area with no history or evidence of active or prior dermal leishmaniasis
  4. Healthy donors (non-exposed to leishmaniasis)
Criteria

Inclusion Criteria:

Active or historical cases of recurrent cutaneous leishmaniasis

  • Age 7-70 years
  • History of parasitologically confirmed (at time of diagnosis) recurrent leishmaniasis
  • Voluntary participation in the study
  • Written and signed Informed consent/assent forms

Active or historical cases of chronic cutaneous leishmaniasis

  • Age 7-70 years
  • History of parasitologically confirmed (at time of diagnosis) chronic leishmaniasis
  • Voluntary participation in the study
  • Written and signed Informed consent/assent forms

Asymptomatic infection

  • Age 7-70 years
  • Resident of endemic area
  • No history or evidence of active or prior dermal leishmaniasis
  • Voluntary participation in the study
  • Written and signed Informed consent/assent forms

Healthy donors

  • Age 7-70 years
  • No history or evidence of exposure to transmission of leishmaniasis
  • Voluntary participation in the study
  • Written and signed Informed consent/assent forms

Exclusion Criteria:

Pregnancy

  Contacts and Locations
Please refer to this study by its ClinicalTrials.gov identifier: NCT00401349

Contacts
Contact: Diane McMahon-Pratt (203) 785-4481

Locations
Colombia
Centro Internacional de Entrenamiento e Investigaciones Medicas, CIDEIM Recruiting
Cali, Colombia
Sponsors and Collaborators
Yale University
  More Information

No publications provided

Responsible Party: Yale University ( Dr. Diane McMahon-Pratt )
Study ID Numbers: 06-0009
Study First Received: November 16, 2006
Last Updated: June 10, 2009
ClinicalTrials.gov Identifier: NCT00401349     History of Changes
Health Authority: United States: Institutional Review Board

Keywords provided by Yale University:
Leishmania
Mif Alleles
Colombia
children

Study placed in the following topic categories:
Leishmaniasis
Protozoan Infections
Skin Diseases, Infectious
Skin Diseases
Parasitic Diseases
Recurrence

Additional relevant MeSH terms:
Leishmaniasis
Protozoan Infections
Skin Diseases, Infectious
Skin Diseases
Skin Diseases, Parasitic
Parasitic Diseases
Sarcomastigophora Infections
Mastigophora Infections

ClinicalTrials.gov processed this record on September 03, 2009