Outcomes of combination therapy including rituximab for antibody-mediated rejection after lung transplantation

被引:14
|
作者
Yamanashi, Keiji [1 ]
Chen-Yoshikawa, Toyofumi Fengshi [1 ]
Hamaji, Masatsugu [1 ]
Yurugi, Kimiko [2 ]
Tanaka, Satona [1 ]
Yutaka, Yojiro [1 ]
Yamada, Yoshito [1 ]
Nakajima, Daisuke [1 ]
Ohsumi, Akihiro [1 ]
Date, Hiroshi [1 ]
机构
[1] Kyoto Univ, Dept Thorac Surg, Sakyo Ku, 54 Shogoin Kawahara Cho, Kyoto 6068507, Japan
[2] Kyoto Univ, Dept Transfus Med & Cell Therapy, Kyoto, Japan
关键词
Rituximab; Antibody-mediated rejection; Donor-specific antibody; Mean fluorescence intensity; Chronic lung allograft dysfunction; ANTI-CD20; MONOCLONAL-ANTIBODY; B-CELL LYMPHOMA; INTERNATIONAL SOCIETY; HEART; SURVIVAL; REGISTRY; CHOP;
D O I
10.1007/s11748-019-01189-1
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Objectives This study assessed the outcomes of combination therapy including rituximab for antibody-mediated rejection after lung transplantation. Methods Retrospective chart reviews were performed for all patients who received combination therapy including rituximab for post-lung transplantation antibody-mediated rejection between June 2008 and October 2018. Results Among the 196 consecutive patients undergoing lung transplantation during the study period, eight (4.1%) were eligible for this study. Two patients (25.0%) were classified as having clinically definite antibody-mediated rejection and six (75.0%) as having possible antibody-mediated rejection. Prior to treatment, four patients (50.0%) met the definition of chronic lung allograft dysfunction; seven of the eight patients (87.5%) remained alive at 6 months and four (50.0%) at 12 months after antibody-mediated rejection. All patients identified as having chronic lung allograft dysfunction, prior to the treatment, died of allograft failure, or underwent re-transplantation. Decreases in the mean fluorescence intensities of the major donor-specific antibodies were observed in three patients. One patient, diagnosed with clinical antibody-mediated rejection but without pre-treatment chronic lung allograft dysfunction, began treatment relatively soon after lung transplantation, and demonstrated improved respiratory function at the 3-year follow-up. Conclusions Our experience suggests that multimodality therapy that includes rituximab is feasible and may prevent progression of antibody-mediated rejection after lung transplantation in selected patients.
引用
收藏
页码:142 / 149
页数:8
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