AI Article Synopsis

  • Thymoglobulin is an induction agent used in kidney transplantation, and this study compared two dosing regimens (1.0 mg/kg/day vs. 1.5 mg/kg/day) for their effects on T-cell clearances.
  • The higher dose (1.5 mg/kg/day) resulted in significantly lower T-cell counts at 30 days and maintained that reduction at 6 months, indicating a more effective and sustained T-cell clearance compared to the lower dose.
  • Both groups showed similar renal function outcomes over 6 and 24 months, with no acute rejections or major infections, suggesting that the higher thymoglobulin dose may offer better long-term immunological protection for kidney transplant recipients.

Article Abstract

Thymoglobulin is used effectively as an induction agent in kidney transplantation, but the optimal dose is not well established. We evaluated the degree and durability of T-cell clearances with two different thymoglobulin regimens in adult kidney transplant recipients (KTR). Seven KTR received a 3-day thymoglobulin-based induction of 1.0 mg/kg/day while nine received 1.5 mg/kg/day, in addition to maintenance immunosuppression. Lymphocyte subsets were monitored for 6 months. Renal function, infections and malignancies were monitored for 24 months. T-cell subsets were significantly lower by day 30 with the thymoglobulin 1.5 mg/kg/day regimen when compared with the 1.0 mg/kg/day regimen; this trend was sustained at 6-month (CD3(+): 438 +/- 254 vs. 1001 +/- 532 cells/mm(3), P = 0.016). Renal function between the two groups was not significantly different at 6- and 24-months post-transplant. One case of BK Virus viremia in the 1.5 mg/kg/day thymoglobulin group was detected. No acute rejection episodes, cytomegalovirus infections, or malignancies were noted in either group. Thymoglobulin induction was efficacious in both groups, but with a significantly sustained T-cell clearance in the 1.5 mg/kg/day regimen. A more profound T-cell clearance within the first 6 months postinduction therapy may translate into a decreased risk of immunological injury and improved long-term outcome after kidney transplantation.

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Source
http://dx.doi.org/10.1111/j.1432-2277.2006.00270.xDOI Listing

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