Desensitization Using Bortezomib and High-dose Immunoglobulin Increases Rate of Deceased Donor Kidney Transplantation

被引:43
作者
Jeong, Jong Cheol [1 ]
Jambaldorj, Enkthuya [2 ]
Kwon, Hyuk Yong [3 ]
Kim, Myung-Gyu [4 ]
Im, Hye Jin [5 ]
Jeon, Hee Jung [6 ]
In, Ji Won [7 ]
Han, Miyeun [8 ]
Koo, Tai Yeon [5 ]
Chung, Junho [9 ]
Song, Eun Young [7 ]
Ahn, Curie [2 ,5 ,8 ]
Yang, Jaeseok [2 ,5 ]
机构
[1] Ajou Univ, Sch Med, Dept Nephrol, Suwon 441749, South Korea
[2] Seoul Natl Univ Hosp, Transplantat Res Inst, Seoul 110744, South Korea
[3] BHS Han Seo Hosp, Dept Internal Med, Pusan, South Korea
[4] Korea Univ, Anam Hosp, Dept Internal Med, Div Nephrol, Seoul, South Korea
[5] Seoul Natl Univ Hosp, Transplantat Ctr, Seoul 110744, South Korea
[6] Hallym Univ, Kangdong Sacred Heart Hosp, Dept Internal Med, Seoul, South Korea
[7] Seoul Natl Univ, Coll Med, Dept Lab Med, Seoul 110744, South Korea
[8] Seoul Natl Univ, Coll Med, Dept Internal Med, Seoul 110744, South Korea
[9] Seoul Natl Univ, Coll Med, Dept Biochem & Mol Biol, Seoul 110744, South Korea
关键词
INTRAVENOUS IMMUNOGLOBULIN; PROTEASOME INHIBITION; SENSITIZED PATIENTS; PLASMA-CELLS; RITUXIMAB; ANTIBODY; OUTCOMES; NEPHROPATHY; RECIPIENTS; RISK;
D O I
10.1097/MD.0000000000002635
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Combination therapy of intravenous immunoglobulin (IVIG) and rituximab showed a good transplant rate in highly sensitized wait-listed patients for deceased donor kidney transplantation (DDKT), but carried the risk of antibody-mediated rejection. The authors investigated the impact of a new combination therapy of bortezomib, IVIG, and rituximab on transplantation rate. This study was a prospective, open-labeled clinical trial. The desensitization regimen consisted of 2 doses of IVIG (2 g/kg), a single dose of rituximab (375 mg/m(2)), and 4 doses of bortezomib (1.3 mg/m(2)). The transplant rate was analyzed. Anti-Human leukocyte antigen (HLA) DRB antibodies were determined by a Luminex solid-phase bead assay at baseline and after 2, 3, and 6 months in the desensitized patients. There were 19 highly sensitized patients who received desensitization and 17 patients in the control group. Baseline values of class I and II panel reactive antibody (%, peak mean fluorescence intensity) were 83 +/- 16.0 (14952 +/- 5820) and 63 +/- 36.0 (10321 +/- 7421), respectively. Deceased donor kidney transplantation was successfully performed in 8 patients (42.1%) in the desensitization group versus 4 (23.5%) in the control group. Multivariate time-varying covariate Cox regression analysis showed that desensitization increased the probability of DDKT (hazard ratio, 46.895; 95% confidence interval, 3.468-634.132; P = 0.004). Desensitization decreased mean fluorescence intensity values of class I panel reactive antibody by 15.5% (20.8%) at 2 months. In addition, a liberal mismatch strategy in post hoc analysis increased the benefit of desensitization in donor-specific antibody reduction. Desensitization was well tolerated, and acute rejection occurred only in the control group. In conclusion, a desensitization protocol using bortezomib, high-dose IVIG, and rituximab increased the DDKT rate in highly sensitized, wait-listed patients.
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页码:1 / 10
页数:10
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