Thymoglobulin‐Associated Cd4+ T‐Cell Depletion and Infection Risk in HIV‐Infected Renal Transplant Recipients

HIV‐infected patients are increasingly referred for kidney transplantation, and may be at an increased risk for rejection. Treatment for rejection frequently includes thymoglobulin. We studied thymoglobulin's effect on CD4+ T‐cell count, risk of infection and rejection reversal in 20 consecutiv...

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Published inAmerican journal of transplantation Vol. 6; no. 4; pp. 753 - 760
Main Authors Carter, J.T., Melcher, M.L., Carlson, L.L., Roland, M.E., Stock, P.G.
Format Journal Article
LanguageEnglish
Published Oxford UK Blackwell Publishing Ltd 01.04.2006
Blackwell
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Summary:HIV‐infected patients are increasingly referred for kidney transplantation, and may be at an increased risk for rejection. Treatment for rejection frequently includes thymoglobulin. We studied thymoglobulin's effect on CD4+ T‐cell count, risk of infection and rejection reversal in 20 consecutive HIV‐infected kidney recipients. All patients used antiretroviral therapy and opportunistic infection prophylaxis. Maintenance immunosuppression consisted of prednisone, mycophenolate mofetil and cyclosporine. Eleven patients received thymoglobulin (7 for rejection and 4 for delayed/slow graft function) while 9 did not. These two groups were similar in age, gender, race, donor characteristics and immunosuppression. Mean CD4+ T‐cell counts remained stable in patients who did not receive thymoglobulin, but became profoundly suppressed in those who did, decreasing from 475 ± 192 to 9 ± 10 cells/μL (p < 0.001). Recovery time ranged from 3 weeks to 2 years despite effective HIV suppression. Although opportunistic infections were successfully suppressed, low CD4+ T‐cell count was associated with increased risk of serious infections requiring hospitalization. Rejection reversed in 6 of 7 patients receiving thymoglobulin. We conclude that thymoglobulin reverses acute rejection in HIV‐infected kidney recipients, but produces profound and long‐lasting suppression of the CD4+ T‐cell count associated with increased risk of infections requiring hospitalization.
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ISSN:1600-6135
1600-6143
DOI:10.1111/j.1600-6143.2006.01238.x