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Center-Defined Unacceptable HLA Antigens Facilitate Transplants for Sensitized Patients in a Multi-Center Kidney Exchange Program
被引:48
作者:

Baxter-Lowe, L. A.
论文数: 0 引用数: 0
h-index: 0
机构:
Childrens Hosp Los Angeles, HLA Lab, Los Angeles, CA 90027 USA Childrens Hosp Los Angeles, HLA Lab, Los Angeles, CA 90027 USA

Cecka, M.
论文数: 0 引用数: 0
h-index: 0
机构:
Univ Calif Los Angeles, UCLA Immunogenet Ctr, Los Angeles, CA USA Childrens Hosp Los Angeles, HLA Lab, Los Angeles, CA 90027 USA

Kamoun, M.
论文数: 0 引用数: 0
h-index: 0
机构:
Univ Penn, Dept Pathol & Lab Med, Philadelphia, PA USA Childrens Hosp Los Angeles, HLA Lab, Los Angeles, CA 90027 USA

Sinacore, J.
论文数: 0 引用数: 0
h-index: 0
机构:
Natl Kidney Registry, Babylon, NY USA Childrens Hosp Los Angeles, HLA Lab, Los Angeles, CA 90027 USA

Melcher, M. L.
论文数: 0 引用数: 0
h-index: 0
机构:
Stanford Univ, Dept Surg, Stanford, CA 94305 USA Childrens Hosp Los Angeles, HLA Lab, Los Angeles, CA 90027 USA
机构:
[1] Childrens Hosp Los Angeles, HLA Lab, Los Angeles, CA 90027 USA
[2] Univ Calif Los Angeles, UCLA Immunogenet Ctr, Los Angeles, CA USA
[3] Univ Penn, Dept Pathol & Lab Med, Philadelphia, PA USA
[4] Natl Kidney Registry, Babylon, NY USA
[5] Stanford Univ, Dept Surg, Stanford, CA 94305 USA
关键词:
HLA antibodies;
kidney paired donation (KPD);
virtual crossmatch;
PAIRED DONATION;
ANTIBODIES;
RECIPIENTS;
CHAIN;
DESENSITIZATION;
PREDICTION;
EXPERIENCE;
STRENGTH;
D O I:
10.1111/ajt.12734
中图分类号:
R61 [外科手术学];
学科分类号:
摘要:
Multi-center kidney paired donation (KPD) is an exciting new transplant option that has not yet approached its full potential. One barrier to progress is accurate virtual crossmatching for KPD waitlists with many highly sensitized patients. Virtual crossmatch results from a large multi-center consortium, the National Kidney Registry (NKR), were analyzed to determine the effectiveness of flexible center-specific criteria for virtual crossmatching. Approximately two-thirds of the patients on the NKR waitlist are highly sensitized (>80% CPRA). These patients have antibodies against HLA-A (63%), HLA-B (66%), HLA-C (41%), HLA-DRB1 (60%), HLA-DRB3/4/5 (18-22%), HLA-DQB1 (54%) and HLA-DPB1 (26%). With donors typed for these loci before activation, 91% of virtual crossmatches accurately predicted an acceptable cell-based donor crossmatch. Failed virtual crossmatches were attributed to equivocal virtual crossmatches (46%), changes in HLA antibodies (21%), antibodies against HLA-DQA (6%), transcription errors (6%), suspected non-HLA antibodies (5%), allele-specific antibodies (1%) and unknown causes (15%). Some failed crossmatches could be prevented by modifiable factors such as more frequent assessment of HLA antibodies, DQA1 typing of donors and auditing data entry. Importantly, when transplant centers have flexibility to define crossmatch criteria, it is currently feasible to use virtual crossmatching for highly sensitized patients to reliably predict acceptable cell-based crossmatches.
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页码:1592 / 1598
页数:7
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