Purpose: The purpose of this study was to determine whether thymic transplantation in addition to highly active antiretroviral therapy (HAART) would lead to restoration of T cell function in HIV infection. Methods: Eight treatment-naive HIV-infected patients were enrolled who had CD4+ T cell counts between 200 and 500/mm3. After 3 weeks of HAART, the patients were randomized into two groups: 4 patients received cultured allogeneic postnatal thymic tissue at day 42 of HAART and the other 4 were controls. Following 1 week of HAART, patients were immunized every 6 months with the neoantigen keyhole limpet hemocyanin (KLH) and the recall antigen tetanus toxoid (TT). Results: HIV plasma RNA levels of 16,625 copies /ml (median) decreased to <100 copies/ml within 12 weeks of therapy in all but one patient. The median increase in CD4+ T cell count over the first 399 days of HAART was 175/mm3. The T cell proliferative responses to Candida antigen and TT normalized in all patients. T cell proliferative responses to KLH developed in 3 of 4 transplant recipients and in 1 of 2 controls (the 2 other controls dropped out) after the secondary immunization. All 4 thymic grafts were rejected. Summary: Four of 6 patients developed T cell proliferative responses to neoantigens over the first 600 days of HAART. Transplanted thymus tissue was rejected. There was with no clear difference in restoration of T cell function in the transplant recipients compared to the controls. Novel immune reconstitution strategies may be needed in those patients on HAART with suboptimal immune restoration. Future plans: We have begun a substudy to evaluate whether rejection of thymus grafts can be prevented by use of a course of immunosuppression prior to thymic transplantation in patients with very low CD4 T cell counts despite over one year of HAART. Significance: It is important to determine how to restore immune function in patients with low T cell counts despite HAART. HIV-infected patients in this category remain at risk for life threatening infections.

Agency
National Institute of Health (NIH)
Institute
National Center for Research Resources (NCRR)
Type
General Clinical Research Centers Program (M01)
Project #
3M01RR000030-39S4
Application #
6425040
Study Section
Project Start
1999-12-01
Project End
2000-11-30
Budget Start
Budget End
Support Year
39
Fiscal Year
2000
Total Cost
Indirect Cost
Name
Duke University
Department
Type
DUNS #
071723621
City
Durham
State
NC
Country
United States
Zip Code
27705
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