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

Authors
Jeong, Jong CheolJambaldorj, EnkthuyaKwon, Hyuk YongKim, Myung-GyuIm, Hye JinJeon, Hee JungIn, Ji WonHan, MiyeunKoo, Tai YeonChung, JunhoSong, Eun YoungAhn, CurieYang, Jaeseok
Issue Date
2월-2016
Publisher
LIPPINCOTT WILLIAMS & WILKINS
Citation
MEDICINE, v.95, no.5, pp.1 - 10
Indexed
SCIE
SCOPUS
Journal Title
MEDICINE
Volume
95
Number
5
Start Page
1
End Page
10
URI
https://scholar.korea.ac.kr/handle/2021.sw.korea/89613
DOI
10.1097/MD.0000000000002635
ISSN
0025-7974
Abstract
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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