The primary objective of this study is to evaluate the safety of solid organ transplantation using HIV-positive deceased donors (liver, kidney) and HIV-positive living donors (liver) in HIV-positive recipients. HIV-positive individuals who agree to accept and receive a solid organ transplant from and HIV-positive donor will be followed to determine the safety and efficacy of this practice.
This is a prospective observational study of solid organ transplantation utilizing HIV-positive donors in HIV-positive recipients. Stable HIV-infected adults in need of a solid organ transplant (kidney, liver) who meet standard and study specified HIV criteria for organ transplantation will be offered enrollment in the study. Deceased donors (kidney, liver) and living donors (liver) will be utilized in this protocol. No living kidney donors will be enrolled. This study will evaluate overall survival and graft survival. In addition the study will assess potential complications of organ transplant using HIV+ donor organs, including but not limited to: HIV disease progression, development of antiretroviral resistance mutations, incidence of opportunistic infections, incidence of transplant complications, impacts of liver regeneration, incidence of viral-related malignancies, and incidence of HIV-superinfection.
Study Type
OBSERVATIONAL
Enrollment
10
University of Minnesota Medical Center
Minneapolis, Minnesota, United States
Patient Survival
Patient survival at one year.
Time frame: One Year
Graft Survival
Time frame: Months 3, 6, 9, Years 1, 2, 3
Incidence and Severity of Graft Rejection
Time frame: Through study completion, up to three years
HIV Disease Progression
Time frame: Through study completion, up to three years
Development of antiretroviral resistance mutations and/or X4 tropic virus in blood and allograft
Time frame: Through study completion, up to three years
Incidence of bacterial, fungal, viral and other opportunistic infections
Time frame: Through study completion, up to three years
Incidence of other transplant complications (surgical and vascular)
Time frame: Through study completion, up to three years
Liver transplant recipients: Impact on liver regeneration
Time frame: Through study completion, up to three years
Analysis of recurrent HIV associated nephropathy among kidney transplant recipients
Time frame: Through study completion, up to three years
Incidence of other viral-related malignancies (HPV, EBV, HBV, HCV)
Time frame: Through study completion, up to three years
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Incidence of systemic HIV-superinfection in blood
Time frame: Through study completion, up to three years
Incidence of tissue specific HIV-superinfection
Time frame: Through study completion, up to three years