The effect of rabbit anti-thymocyte globulin induction therapy on regulatory T cells in kidney transplant patients
The effect of rabbit anti-thymocyte globulin induction therapy on regulatory T cells in kidney transplant patients
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DOI：
10.1093/ndt/gfn778
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发表时间：
2009-05-01
影响因子：
6.1
通讯作者：
Baan, Carla C.
中科院分区：
文献类型：
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作者：
Sewgobind, Varsha D. K. D.;Kho, Marcia M. L.;Baan, Carla C.
Background. Prevention of alloreactivity by rabbit anti-thymocyte globulins (rATG) may not only result from immunodepletion but also from the induction of T cells that control allogeneic immune responses. In the present prospective and controlled study, we investigated the effect of rATG on the frequency, function and phenotype of peripheral immunoregulatory CD4(+) T cells in kidney transplant (KTx) patients.Methods. After transplantation, 16 patients received ATG-induction therapy and triple therapy consisting of tacrolimus, MMF and steroids. The control group (n = 18) received triple therapy only. By flow cytometry, T cells were analysed for CD25, FoxP3, CD127, CD45RO and CCR7. To study their suppressive capacities, CD25(bright) T cells were co-cultured with CD25(-/dim) effector T cells (Teff) in mixed lymphocyte reactions (MLR), stimulated with donor and third party (3P) antigens.Results. Pre-transplant levels of FoxP3(+)CD127(-/low) T cells were 6% of CD4(+) T cells. One week post-ATG treatment, no measurable numbers of regulatory T cells were present (P < 0.01). After 4 weeks, the cell numbers of CD4(+)FoxP3(+)CD127(-/low) T cells slowly reappeared and thereafter remained low (P < 0.01). At 14 weeks, a significant shift towards the CD45RO(+)CCR7(+) (central memory) phenotype within CD4(+)FoxP3(+) T cells was observed (P < 0.01). At 26 weeks, the proliferative alloresponses of the PBMC and CD25(-/dim) Teff profoundly decreased compared to pre-transplant (P = 0.01 and P = 0.02 respectively), while the regulatory capacity of the CD25(bright) T cells, of which 90% consisted of FoxP3(+)CD127(-/low) T cells, remained unaffected. The CD25(bright) T cells suppressed the anti-donor (94%) and 3P responses (93%).Conclusion. Our findings show that rATG therapy does not spare peripheral immunoregulatory T cells in vivo, but after regeneration preserves their suppressive activity.
