Use of an immune function assay to monitor immunosuppression for treatment of post-transplant lymphoproliferative disorder

被引:23
作者
Gautam, A
Morrissey, PE
Brem, AS
Fischer, SA
Gohh, RY
Yango, AF
Monaco, AP
机构
[1] Rhode Isl Hosp, Div Organ Transplantat, Providence, RI 02903 USA
[2] Brown Med Sch, Dept Surg, Providence, RI USA
[3] Brown Med Sch, Dept Pediat, Providence, RI USA
[4] Brown Med Sch, Dept Med, Div Nephrol, Providence, RI USA
[5] Brown Med Sch, Dept Med, Div Infect Dis, Providence, RI USA
关键词
lymphoproliferative disorders; Epstein-Barr virus infections; kidney transplantation; immunologic monitoring;
D O I
10.1111/j.1399-3046.2006.00510.x
中图分类号
R72 [儿科学];
学科分类号
100202 ;
摘要
The first-line treatment for PTLD is reduction in immunosuppression, allowing partial reconstitution of cell-mediated immunity. However, there is a risk of inducing acute allograft rejection during clinical resolution of PTLD. A recently available assay, Immuknow(TM), measures the cell-mediated immune response and could be used to monitor reduction of immunosuppression. We report a case of PTLD occurring in a pediatric kidney transplant recipient where the reduction in immunosuppression was serially followed using this assay and quantitative EBV-PCR. A rapid reduction to minimal immunosuppression was followed by resolution of PTLD. Later, when the cell-mediated immune response increased, with negative viral load, immunosuppression was gradually increased utilizing the assay to adjust dosing. Presently, there are no signs of PTLD and renal function remains normal.
引用
收藏
页码:613 / 616
页数:4
相关论文
共 6 条
[1]   Post-transplant infections now exceed acute rejection as cause for hospitalization: A report of the NAPRTCS [J].
Dharnidharka, VR ;
Stablein, DM ;
Harmon, WE .
AMERICAN JOURNAL OF TRANSPLANTATION, 2004, 4 (03) :384-389
[2]   Establishing pediatric immune response zones using the Cylex® ImmuKnow™ assay [J].
Hooper, E ;
Hawkins, DM ;
Kowalski, RJ ;
Post, DR ;
Britz, JA ;
Brooks, KC ;
Turman, MA .
CLINICAL TRANSPLANTATION, 2005, 19 (06) :834-839
[3]   Immune cell function testing: an adjunct to therapeutic drug monitoring in transplant patient management [J].
Kowalski, R ;
Post, D ;
Schneider, MC ;
Britz, J ;
Thomas, J ;
Deierhoi, M ;
Lobashevsky, A ;
Redfield, R ;
Schweitzer, E ;
Heredia, A ;
Reardon, E ;
Davis, C ;
Bentlejewski, C ;
Fung, J ;
Shapiro, R ;
Zeevi, A .
CLINICAL TRANSPLANTATION, 2003, 17 (02) :77-88
[4]   Quantitative EBV viral loads and immunosuppression alterations can decrease PTLD incidence in pediatric liver transplant recipients [J].
Lee, TC ;
Savoldo, B ;
Rooney, CM ;
Heslop, HE ;
Gee, AP ;
Caldwell, Y ;
Barshes, NR ;
Scott, JD ;
Bristow, LJ ;
O'Mahony, CA ;
Goss, JA .
AMERICAN JOURNAL OF TRANSPLANTATION, 2005, 5 (09) :2222-2228
[5]   Epstein-Barr virus-induced, posttransplant lymphoproliferative disorders [J].
Paya, CV ;
Fung, JJ ;
Nalesnik, MA ;
Kieff, E ;
Green, M ;
Gores, G ;
Habermann, TM ;
Wiesner, RH ;
Swinnen, LJ ;
Woodle, ES ;
Bromberg, JS .
TRANSPLANTATION, 1999, 68 (10) :1517-1525
[6]   Preventing acute and chronic rejection after diagnosis of post-transplantation lymphoproliferative disorder [J].
Sindhi, R ;
Webber, SA .
PEDIATRIC TRANSPLANTATION, 2003, 7 (05) :339-341