» Articles » PMID: 26167458

Modern Approaches to Incompatible Kidney Transplantation

Overview
Journal World J Nephrol
Specialty Nephrology
Date 2015 Jul 14
PMID 26167458
Citations 7
Authors
Affiliations
Soon will be listed here.
Abstract

The presence of human-leukocyte antigen (HLA)-antibodies and blood group incompatibility remain a large barrier to kidney transplantation leading to increased morbidity and mortality on the transplant waiting list. Over the last decade a number of new approaches were developed to overcome these barriers. Intravenous immunoglobulin (IVIG) remains the backbone of HLA desensitization therapy and has been shown in a prospective, randomized, placebo controlled trial to improve transplantation rates. Excellent outcomes with the addition of rituximab (anti-B cell) to IVIG based desensitization have been achieved. There is limited experience with bortezomib (anti-plasma cell) and eculizumab (complement inhibition) for desensitization. However, these agents may be good adjuncts for patients who are broadly sensitized with strong, complement-fixing HLA antibodies. Excellent short and long-term outcomes have been achieved in ABO incompatible transplantation with the combination of antibody removal, B cell depletion, and pre-transplant immunosuppression. Kidney paired donation has emerged as a reasonable alternative for programs who cannot provide desensitization or in conjunction with desensitization. Future therapies directed toward cytokines that alter B cell proliferation are under investigation.

Citing Articles

Current Perspectives in ABO-Incompatible Kidney Transplant.

Maritati F, Bini C, Cuna V, Tondolo F, Lerario S, Grandinetti V J Inflamm Res. 2022; 15:3095-3103.

PMID: 35642217 PMC: 9148605. DOI: 10.2147/JIR.S360460.


Living kidney donation in a developing country.

Dayal C, Davies M, Diana N, Meyers A PLoS One. 2022; 17(5):e0268183.

PMID: 35536829 PMC: 9089923. DOI: 10.1371/journal.pone.0268183.


Tailored immunosuppression after kidney transplantation - a single center real-life experience.

Good-Weber M, Roos M, Mueller T, Rusi B, Fehr T BMC Nephrol. 2020; 21(1):501.

PMID: 33228545 PMC: 7686677. DOI: 10.1186/s12882-020-02137-5.


Quantifying infection risks in incompatible living donor kidney transplant recipients.

Avery R, Motter J, Jackson K, Montgomery R, Massie A, Kraus E Am J Transplant. 2020; 21(4):1564-1575.

PMID: 32949093 PMC: 7972996. DOI: 10.1111/ajt.16316.


Effect of Immunosuppressive Therapy on the Occurrence of Atypical Hemolytic Uremic Syndrome in Renal Transplant Recipients.

Raina R, Chauvin A, Fox K, Kesav N, Ascha M, Vachharajani T Ann Transplant. 2018; 23:631-638.

PMID: 30190449 PMC: 6248048. DOI: 10.12659/AOT.909781.


References
1.
Montgomery R, Locke J . ABO-incompatible transplantation: less may be more. Transplantation. 2008; 84(12 Suppl):S8-9. DOI: 10.1097/01.tp.0000296032.12974.bb. View

2.
Tanabe K . Japanese experience of ABO-incompatible living kidney transplantation. Transplantation. 2008; 84(12 Suppl):S4-7. DOI: 10.1097/01.tp.0000296008.08452.4c. View

3.
Raghavan R, Jeroudi A, Achkar K, Suki W, Gaber A, Knight R . Bortezomib in kidney transplant desensitization: a case report. Clin Transpl. 2010; :339-42. View

4.
Vo A, Lukovsky M, Toyoda M, Wang J, Reinsmoen N, Lai C . Rituximab and intravenous immune globulin for desensitization during renal transplantation. N Engl J Med. 2008; 359(3):242-51. DOI: 10.1056/NEJMoa0707894. View

5.
Montgomery R, Locke J, King K, Segev D, Warren D, Kraus E . ABO incompatible renal transplantation: a paradigm ready for broad implementation. Transplantation. 2009; 87(8):1246-55. DOI: 10.1097/TP.0b013e31819f2024. View