Neutralization Serotyping of BK Polyomavirus Infection in Kidney Transplant Recipients

被引:76
|
作者
Pastrana, Diana V. [1 ]
Brennan, Daniel C. [2 ]
Cuburu, Nicolas [1 ]
Storch, Gregory A. [2 ]
Viscidi, Raphael P. [3 ]
Randhawa, Parmjeet S. [4 ]
Buck, Christopher B. [1 ]
机构
[1] NCI, Cellular Oncol Lab, Bethesda, MD 20892 USA
[2] Washington Univ, Sch Med, St Louis, MO USA
[3] Johns Hopkins Med Ctr, Dept Pediat, Baltimore, MD USA
[4] Univ Pittsburgh, Dept Pathol, Med Ctr, Pittsburgh, PA USA
关键词
VIRUS-LIKE PARTICLES; INTRAVENOUS IMMUNOGLOBULIN; RENAL-TRANSPLANTATION; HEMORRHAGIC CYSTITIS; IDENTIFICATION; NEPHROPATHY; ANTIBODY; ORIGIN; CYCLOSPORINE; REPLICATION;
D O I
10.1371/journal.ppat.1002650
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
BK polyomavirus (BKV or BKPyV) associated nephropathy affects up to 10% of kidney transplant recipients (KTRs). BKV isolates are categorized into four genotypes. It is currently unclear whether the four genotypes are also serotypes. To address this issue, we developed high-throughput serological assays based on antibody-mediated neutralization of BKV genotype I and IV reporter vectors (pseudoviruses). Neutralization-based testing of sera from mice immunized with BKV-I or BKV-IV virus-like particles (VLPs) or sera from naturally infected human subjects revealed that BKV-I specific serum antibodies are poorly neutralizing against BKV-IV and vice versa. The fact that BKV-I and BKV-IV are distinct serotypes was less evident in traditional VLP-based ELISAs. BKV-I and BKV-IV neutralization assays were used to examine BKV type-specific neutralizing antibody responses in KTRs at various time points after transplantation. At study entry, sera from 5% and 49% of KTRs showed no detectable neutralizing activity for BKV-I or BKV-IV neutralization, respectively. By one year after transplantation, all KTRs were neutralization seropositive for BKV-I, and 43% of the initially BKV-IV seronegative subjects showed evidence of acute seroconversion for BKV-IV neutralization. The results suggest a model in which BKV-IV-specific seroconversion reflects a de novo BKV-IV infection in KTRs who initially lack protective antibody responses capable of neutralizing genotype IV BKVs. If this model is correct, it suggests that pre-vaccinating prospective KTRs with a multivalent VLP-based vaccine against all BKV serotypes, or administration of BKV-neutralizing antibodies, might offer protection against graft loss or dysfunction due to BKV associated nephropathy.
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页数:11
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