This study is NOT currently recruiting participants.
Number
02-I-0080
Sponsoring Institute
National Institute of Allergy and Infectious Diseases (NIAID)
Recruitment Detail
Type: No longer recruiting/follow-up only Gender: Male & Female Min Age: 18 Max Age: N/A
Referral Letter Required
Yes
Population Exclusion(s)
Children
Keywords
Adoptive Immunotherapy; Anti-Retroviral Medications; Treatment Strategies; Natural History
Recruitment Keyword(s)
HIV; Gemini Study
Condition(s)
HIV Disease
Investigational Drug(s)
None
Investigational Device(s)
Intervention(s)
Procedure/Surgery: Blood draw
Supporting Site
National Institute of Allergy and Infectious Diseases
- place subjects from the various identical twin cell transfer/gene therapy studies on a single, more uniform schedule of visits;
- examine the long-term safety of apheresis procedures in non-HIV-infected lymphocyte donor twins;
- examine the long-term safety of lymphocytes in HIV-infected lymphocyte recipient twins.
Identical twins enrolled in NIH protocols 93-I-0110, 94-I-0206, 96-HG-0051, and 97-I-0165 involving the transfer of lymphocytes for the treatment of HIV infection are eligible to continue their research participation under the current protocol, 02-I-0080.
Participants will not undergo any additional research procedures in this study. They will continue to take their antiretroviral therapy and will be followed at least once a year, or more often if medically indicated, with a medical history, physical examination and blood tests for routine studies and to determine the number of lymphocytes in the blood. Recipient twins will also have blood levels of gene-modified lymphocytes checked.
Recipient twins will have some blood stored for RCR (replication competent retrovirus) testing, should it become necessary. A special virus was used to insert genes into the donated lymphocytes and, although the virus was rendered incapable of growing in the body, a theoretical risk exists that the virus could mix with other viruses and possibly begin growing or reproducing. If a participant subsequently develops medical problems, the stored blood samples can be checked for RCR to see if it may be a cause of the problem.
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INCLUSION CRITERIA: Activet participation, in an NIAID/CCMD/NHGRI protocol involving the transfer of unmodified lymphocytes, gene-marked lymphocytes or cells containing potentially therapeutic genes in the treatment of HIV-1 infection (cell donors and recipients were eligible). Ongoing follow-up with a primary medical care provider who manages the subject's HIV-related and/or other medical conditions. Agree to comply with study requirements and clinical policies. Able to provide informed consent. EXCLUSION CRITERIA: A history of gross noncompliance with prior NIAID/CCMD protocol requirements that, in the opinion of the Principal Investigator, is likely to seriously compromise the safety or value of an individual's participation in the present protocol. Refusal to follow Clinical Center policy on partner notification (if HIV-positive). Refusal to permit research blood specimens to be stored (frozen) for potential future studies, including RCR testing will be excluded (participants who have received gene-modified cells may refuse to have specimens stored for research purposes other than RCR). Any medical condition that, in the opinion of the Principal Investigator, would make the subject inappropriate for protocol participation (such as anemia or inadequate venous access). Refusal to allow the NIH research team to exchange pertinent medical information with the subjects primary medical care provider.
Activet participation, in an NIAID/CCMD/NHGRI protocol involving the transfer of unmodified lymphocytes, gene-marked lymphocytes or cells containing potentially therapeutic genes in the treatment of HIV-1 infection (cell donors and recipients were eligible).
Ongoing follow-up with a primary medical care provider who manages the subject's HIV-related and/or other medical conditions.
Agree to comply with study requirements and clinical policies.
Able to provide informed consent.
EXCLUSION CRITERIA:
A history of gross noncompliance with prior NIAID/CCMD protocol requirements that, in the opinion of the Principal Investigator, is likely to seriously compromise the safety or value of an individual's participation in the present protocol.
Refusal to follow Clinical Center policy on partner notification (if HIV-positive).
Refusal to permit research blood specimens to be stored (frozen) for potential future studies, including RCR testing will be excluded (participants who have received gene-modified cells may refuse to have specimens stored for research purposes other than RCR).
Any medical condition that, in the opinion of the Principal Investigator, would make the subject inappropriate for protocol participation (such as anemia or inadequate venous access).
Refusal to allow the NIH research team to exchange pertinent medical information with the subjects primary medical care provider.
Principal Investigator
Referral Contact
For more information: