Phase
Condition
Hiv Infections
Primary Immunodeficiency Disorders
Treatment
N/AClinical Study ID
Ages 1-90 All Genders Accepts Healthy Volunteers
Study Summary
Eligibility Criteria
Inclusion
- INCLUSION CRITERIA:
Subjects must meet one of the following 4 criteria:
Patients (age 0-90 years) with a clinical diagnosis of a form of PID (either known or unknown). PID is defined by laboratory and/or clinicalfindings on two or more occasions that are consistent with a defect ininnate or adaptive immunity. Specific PIDs are defined by theInternational Union of Immunological Societies guidelines. These subjectsmust also be willing to undergo genetic testing and to allow theirbiospecimens to be modified into iPS cells. Women of childbearingpotential, or who are pregnant or lactating, may be eligible. The volumeof blood collected for research purposes will be reduced, and no skinbiopsies will be performed for research purposes in consideration of theirsafety.
Infants identified at birth with positive newborn screening for SCID andconfirmed to have T-cell lymphocytopenia. These subjects must be willingto undergo genetic testing.
Biological relatives (age 0-90 years) of a subject who meets criterion 1aor 1b but who do not have a PID themselves. All relatives must be willingto undergo genetic testing. Women of childbearing potential, or who arepregnant or lactating, may be eligible. The volume of blood collected forresearch purposes will be reduced in consideration of their safety.
Healthy volunteers (age 18-75 years) who are not related to another studysubject, who do not have a PID, whose weight is greater than 110 pounds,do not have a history of any heart, lung, or kidney disease, or bleedingdisorders, do not have a history of viral hepatitis (B or C), and have anegative HIV screening test.
All subjects must be willing to allow their samples to be stored for futureresearch.
Exclusion
EXCLUSION CRITERIA:
Subjects with secondary causes of immunodeficiency are excluded from this study.Secondary causes of immunodeficiency include HIV infection and immunodeficiency thatis deemed to be secondary to chronic use of immunosuppressive medications orchemotherapeutic agents.
Any condition that, in the opinion of the investigator, contraindicatesparticipation in this study.
Study Design
Study Description
Connect with a study center
Children's National Health System (CNHS)
Washington, District of Columbia 20010
United StatesSite Not Available
Children's National Health System (CNHS)
Washington D.C., District of Columbia 20010
United StatesActive - Recruiting
Children's National Health System (CNHS)
Washington D.C. 4140963, District of Columbia 4138106 20010
United StatesSite Not Available
National Institutes of Health Clinical Center
Bethesda, Maryland 20892
United StatesActive - Recruiting
National Institutes of Health Clinical Center
Bethesda 4348599, Maryland 4361885 20892
United StatesSite Not Available

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