Potent induction immunotherapy promotes long-term insulin independence after islet transplantation in type 1 diabetes.
Potent induction immunotherapy promotes long-term insulin independence after islet transplantation in type 1 diabetes.
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DOI:
10.1111/j.1600-6143.2011.03977.x
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发表时间:
2012-06
期刊:
影响因子:
--
通讯作者:
Hering BJ
中科院分区:
文献类型:
--
作者:
Bellin MD;Barton FB;Heitman A;Harmon JV;Kandaswamy R;Balamurugan AN;Sutherland DE;Alejandro R;Hering BJ
The seemingly inexorable decline in insulin independence after islet transplant alone (ITA) has raised concern about its clinical utility. We hypothesized that induction immunosuppression therapy determines durability of insulin independence. We analyzed the proportion of insulin independent patients following final islet infusion in four groups of ITA recipients according to induction immunotherapy: University of Minnesota recipients given FcR nonbinding anti-CD3 antibody alone or T cell depleting antibodies (TCDAb) and TNF-α inhibition (TNF-α-i) (Group 1;n=29); recipients reported to the Collaborative Islet Transplant Registry (CITR) given TCDAb+TNF-α-i (Group 2; n=20); CITR recipients given TCDAb without TNF-α-i (Group 3;n=43); and CITR recipients given IL-2 receptor antibodies (IL-2RAb) alone (Group 4,n=177). Results were compared with outcomes in pancreas transplant alone (PTA) recipients reported to the Scientific Registry of Transplant Recipients (Group 5;n=677). 5-yr insulin independence rates in Group 1 (50%) and Group 2 (50%) were comparable to outcomes in PTA (Group 5: 52%; p>>0.05) but significantly higher than in Group 3 (0%; p=0.001) and Group 4 (20%; p=0.02). Induction immunosuppression was significantly associated with 5-year insulin independence (p=0.03), regardless of maintenance immunosuppression or other factors. These findings support potential for long-term insulin independence after ITA using potent induction therapy, with anti-CD3 Ab or TCDAb+TNF-α-i.
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DOI:
10.1016/j.clim.2009.04.007
发表时间:
2009-08
期刊:
Clinical immunology (Orlando, Fla.)
影响因子:
--
作者:
Herold KC;Gitelman S;Greenbaum C;Puck J;Hagopian W;Gottlieb P;Sayre P;Bianchine P;Wong E;Seyfert-Margolis V;Bourcier K;Bluestone JA;Immune Tolerance Network ITN007AI Study Group
通讯作者:
Immune Tolerance Network ITN007AI Study Group
影响因子:
8.8
作者:
Bellin, M. D.;Kandaswamy, R.;Hering, B. J.
通讯作者:
Hering, B. J.
DOI:
10.1073/pnas.89.8.3434
发表时间:
1992-04-15
影响因子:
11.1
作者:
MAKI, T;ICHIKAWA, T;PORTER, J
通讯作者:
PORTER, J
影响因子:
7.7
作者:
Robertson RP
通讯作者:
Robertson RP
DOI:
10.1111/j.1600-6143.2009.02921.x
发表时间:
2010-01
期刊:
American journal of transplantation : official journal of the American Society of Transplantation and the American Society of Transplant Surgeons
影响因子:
--
作者:
Ishii D;Schenk AD;Baba S;Fairchild RL
通讯作者:
Fairchild RL