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The Impact of Microcirculation Inflammation in Predicting Treatment Response for Late Onset Antibody Mediated Rejection

J. Lee,1 J. Lee,1 B. Lim,2 B. Kim,3 M. Ju,1 M. Kim,1 S. Kim,1 Y. Kim,1 H. Jeong,2 K. Park,4 K. Huh.1

1Department of Transplantation Surgery, Yonsei University Health System, Seoul, Republic of Korea
2Department of Pathology, Yonsei University Health System, Seoul, Republic of Korea
3Department of Internal Medicine, Yonsei University Health System, Seoul, Republic of Korea
4Department of Surgery, CHA Bundang Medical Center, Bundang, Republic of Korea.

Meeting: 2015 American Transplant Congress

Abstract number: A109

Keywords: Antibodies, Biopsy, Microcirculation, Rejection

Session Information

Session Name: Poster Session A: Kidney Antibody Mediated Rejection

Session Type: Poster Session

Date: Saturday, May 2, 2015

Session Time: 5:30pm-7:30pm

 Presentation Time: 5:30pm-7:30pm

Location: Exhibit Hall E

Background

There have been marked advances of immunosuppression. However, management of late onset antibody-mediated rejection (AMR) after 6 months is still challenging. Despite important diagnostic and prognostic role of microcirculation inflammation (MI; defined by the addition of glomerulitis score and peritubular capillaritis score) in AMR, there is no data of the impact of MI score in predicting treatment response.

Methods

Late onset AMR was diagnosed using Banff 2007 criteria. We exclude patients with estimated glomerular filtration rates (eGFR; MDRD) less than 15ml/minute/1.73m2 at the time of diagnosis. Patients were categorized by MI score. Responses to therapy were assessed by eGFR at 6 month after treatment compared to eGFR at diagnosis of AMR; complete response if the eGFR improved more than 10%, no response if the eGFR declined over 10%, and partial response if cases fell between the extremes.

Results

A total of 27 patients were treated with AMR between 2011 and 2014. All patients were treated with plasmapheresis. Twenty six recipients (96.3%) received low dose intravenous immunoglobulin and/or rituximab. We divided the patients into three groups according to MI score assessed on the biopsy; MI 0 (n=7), MI 1-2 (n=12), and MI>3 (n=8). Based on our response criteria, 8 patients (3 of MI 0, 3 of MI 1-2, 2 of MI≥3) showed complete response, and 11 patients (4 of MI 0, 5 of MI 1-2, 2 of MI≥3) showed no response (p=0.735).

Conclusion

In late onset AMR after kidney transplantation, MI score could not predict the treatment response.

Treatment response of antibody-mediated rejection according to MI score

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To cite this abstract in AMA style:

Lee J, Lee J, Lim B, Kim B, Ju M, Kim M, Kim S, Kim Y, Jeong H, Park K, Huh K. The Impact of Microcirculation Inflammation in Predicting Treatment Response for Late Onset Antibody Mediated Rejection [abstract]. Am J Transplant. 2015; 15 (suppl 3). https://atcmeetingabstracts.com/abstract/the-impact-of-microcirculation-inflammation-in-predicting-treatment-response-for-late-onset-antibody-mediated-rejection/. Accessed May 19, 2025.

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