Circulating Antibody Free Light Chains and Risk of Posttransplant Lymphoproliferative Disorder

被引:19
作者
Engels, E. A. [1 ]
Preiksaitis, J. [2 ]
Zingone, A. [3 ]
Landgren, O. [3 ]
机构
[1] NCI, Div Canc Epidemiol & Genet, Rockville, MD USA
[2] Univ Alberta, Dept Med, Div Infect Dis, Edmonton, AB, Canada
[3] NCI, Ctr Canc Res, Bethesda, MD 20892 USA
关键词
Epstein-Barr virus; immunology; lymphocyte activation; monoclonal gammopathy of undertermined significance; posttransplant lymphoproliferative disorder; tumor markers; EPSTEIN-BARR-VIRUS; ORGAN TRANSPLANT PATIENTS; MONOCLONAL GAMMOPATHY; RHEUMATOID-ARTHRITIS; SERUM; EBV; IMMUNOGLOBULINS; RECIPIENTS; DIAGNOSIS; LOAD;
D O I
10.1111/j.1600-6143.2011.03954.x
中图分类号
R61 [外科手术学];
学科分类号
摘要
Posttransplant lymphoproliferative disorder (PTLD) is a major complication of solid-organ transplantation. With human immunodeficiency virus infection (an analogous immunosuppressive state), elevated kappa and lambda immunoglobulin free light chains (FLCs) in peripheral blood are associated with increased risk of lymphoma. To assess the role of B-cell dysfunction in PTLD, we measured circulating FLCs among Canadian transplant recipients, including 29 individuals with PTLD and 57 matched transplant recipients who were PTLD-free. Compared with controls, PTLD cases had higher kappa FLCs (median 1.53 vs. 1.07 times upper limit of normal) and lambda FLCs (1.03 vs. 0.68). Using samples obtained on average 3.5 months before PTLD diagnosis, cases were more likely to have polyclonal FLC elevations (i.e. elevated kappa and/or lambda with normal kappa/lambda ratio: odds ratio [OR] 4.2, 95%CI 1.115) or monoclonal elevations (elevated kappa and/or lambda with abnormal ratio: OR 3.0, 95%CI 0.518). Strong FLC-PTLD associations were also observed at diagnosis/selection. Among recipients with EpsteinBarr virus (EBV) DNA measured in blood, EBV DNAemia was associated with FLC abnormalities (ORs 6.2 and 3.2 for monoclonal and polyclonal elevations). FLC elevations are common in transplant recipients and associated with heightened PTLD risk. FLCs likely reflect B-cell dysfunction, perhaps related to EBV-driven lymphoproliferation.
引用
收藏
页码:1268 / 1274
页数:7
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