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1 nd in the polyomaviruses simian virus 40 and BK virus.
2 ation is believed to be primarily due to the BK virus.
3 mavirus family and is closely related to the BK virus.
4 ine of a kidney transplant patient and named BK virus.
5 s to investigate the immunologic response to BK virus.
6 und to exhibit elevated titers to the JC and BK viruses.
7 ed for replication of mouse polyomavirus and BK virus, a human polyomavirus associated with allograft
8 n blood and urine for JC virus reactivation; BK virus, a JC virus-related polyomavirus, was used as a
13 also inhibited large T antigen expression by BK virus and JC virus, two important, pathogenic human p
16 gens, including cytomegalovirus, adenovirus, BK virus, and Epstein-Barr virus in the absence of acute
17 cidence of viral infection (cytomegalovirus, BK virus, and Epstein-Barr virus) and posttransplant lym
18 cussed in relation to human cytomegalovirus, BK virus, and Epstein-Barr virus, while the importance o
20 s of cytomegalovirus disease, herpes zoster, BK virus, and nephropathy, which led to the discontinuat
22 ipheral B cell subsets and revealed the anti-BK virus antibody repertoire as clonally complex with re
23 stimulation by overlapping peptide pools of BK virus antigen to determine frequency of CD8+ and CD4+
24 fic T-cell investigational therapy targeting BK virus, as well as five other opportunistic viruses: a
27 lantation after losing their renal grafts to BK virus-associated nephropathy (BKAN) are described.
32 BK virus infection are at risk of developing BK virus-associated nephropathy, allograft rejection, an
34 d 369 renal transplant recipients tested for BK virus at serial time points after transplantation.
39 cially produced secondary standards for both BK virus (BKV) and CMV, using digital polymerase chain r
40 ey, liver, and pancreas transplant patients, BK virus (BKV) and JC virus (JCV) DNAemia were observed
46 erassay variability in the quantification of BK virus (BKV) DNA precludes establishing broadly applic
48 was assayed in urine, and JC virus (JCV) and BK virus (BKV) DNAs were assayed in urine and PBMCs.
53 d monitoring of Epstein-Barr virus (EBV) and BK virus (BKV) in solid organ and hematopoietic stem cel
54 tology for the detection and the role of the BK virus (BKV) in the carcinogenesis of urothelial carci
57 here are limited data on the epidemiology of BK virus (BKV) infection after alemtuzumab induction.
58 CoV-2 Omicron variant in 2022, against prior BK virus (BKV) infection and uninfected (without SARS-Co
63 ssion is a widely recognized risk factor for BK virus (BKV) infection, particularly with the combinat
84 In the case of the human polyomaviruses, BK virus (BKV) replication occurs in the tubular epithel
86 JC virus (JCV) viruria is more common than BK virus (BKV) viruria in healthy individuals but in kid
87 ison of antibody titers to JC virus (JCV) or BK virus (BKV) was made by hemagglutination inhibition (
90 megalovirus (CMV), Epstein-Barr virus (EBV), BK virus (BKV), adenovirus (ADV), and human herpesvirus
92 human polyomaviruses (HPyV)-JC virus (JCV), BK virus (BKV), human polyomavirus 6 (HPyV6), and Merkel
95 mavirus (HPV), Epstein-Barr virus (EBV), and BK Virus (BKV), suggesting the involvement of these viru
96 the human polyomaviruses JC virus (JCV) and BK virus (BKV), the first step to a successful infection
97 the membrane receptor and entry pathway for BK virus (BKV), which can cause severe disease in immuno
98 to the hypothesis that a human virus such as BK virus (BKV), which establishes a persistent subclinic
101 the VP1 polypeptide of a human polyomavirus, BK virus (BKV), which is associated with polyomavirus-as
104 uated the relationship of pretransplantation BK virus (BKV)-specific donor and recipient serostatus t
109 ed the frequent detection of polyomaviruses (BK virus [BKV] or simian virus 40 [SV40]) in 46% of stoo
110 anded DNA (dsDNA) viruses (adenovirus [ADV], BK virus [BKV], cytomegalovirus [CMV], Epstein-Barr viru
111 ntibiotics have antiviral properties against BK virus but efficacy at preventing this infection has n
112 of polyomavirus nephropathy (PVN) is due to BK virus, but rare cases result from JC virus reactivati
113 Some infections, such as cytomegalovirus and BK virus, can promote inflammatory gene expression that
115 in two separate pairs of samples containing BK virus collected from the same individual up to 302 da
117 a broad range of viral infections including BK virus, cytomegalovirus, adenovirus, human herpesvirus
121 It is concluded that quantitative PCR for BK virus DNA in serum is useful both for identifying tra
123 me polymerase chain reaction (PCR) assay for BK virus DNA, a retrospective analysis was done of seque
125 by progressive decrease in the median plasma BK virus-DNA load, and undetectable levels at the last f
128 immunocompromised individuals, JC virus and BK virus, encode miRNAs with the same function as that o
129 s known to have potent inhibitory effects on BK virus gene expression, both at the level of transcrip
131 Finally, we found persistently elevated anti-BK virus IgG titers and a specific anti-BKPyV T cell res
135 avenous bolus steroids to five patients with BK virus in the plasma (BKP) (group 1) and also tried ot
138 blood and urine (by PCR) remain negative for BK virus, indicating the absence of virus reactivation.
139 ctors significantly associated with PML were BK virus infection (22.2% vs. 1.1%), pretransplant trans
141 with clinical consequences quite similar to BK virus infection in humans, including renal dysfunctio
142 tion must be paid to the higher incidence of BK virus infection in recipients of ABO-incompatible gra
146 s of cytomegalovirus infection, two cases of BK virus infection, and one case of Epstein-Barr virus i
155 opoietic cell transplantation (HCT), polyoma-BK virus is associated with hemorrhagic cystitis and als
156 A monoclonal antibody directed against the BK virus large T-antigen (clone BK.T-1) has previously b
158 ingle-chain variable fragment complexed with BK virus-like particles revealed the quaternary nature o
160 renal transplantation, and we correlated the BK virus load with clinical course and with the presence
161 eveloped a real-time PCR assay to quantitate BK virus loads in the setting of renal transplantation,
163 s, and kidney and lung outcomes of BKPyV and BK virus native kidney nephropathy (BKVN) in lung transp
165 immunosuppressive agents as risk factors for BK virus nephropathy (BKN) has not been well studied.
166 titial fibrosis and tubular atrophy (14.4%); BK virus nephropathy (BKVAN) 9.9%; and acute tubular nec
178 dentifying transplant recipients at risk for BK virus nephropathy and for monitoring the response to
179 cipients with histopathologically documented BK virus nephropathy and from samples (n=76) from 16 tra
185 toxicity, chronic allograft nephropathy, and BK virus nephropathy, as well as donor and recipient fac
186 iciency was not associated with CMV disease, BK virus nephropathy, or kidney allograft function at 1
190 , we summarize accumulated knowledge on anti-BK virus neutralizing antibodies as well as their clinic
192 by addition of SV40 VLPs but not by VLPs for BK virus or JC virus, which are related human polyomavir
194 e incorporated site-specifically into a SV40/BK virus origin-based shuttle vector and replicated in x
196 ntrols and viremic KTR were stimulated using BK virus peptide libraries loaded or not on monocytes-de
201 f graft-versus-host disease, whereas CMV and BK virus reactivation did not predict clinical outcomes.
202 omavirus-associated nephropathy (PVAN) after BK virus reactivation in kidney transplant recipients (K
205 kidney recipients had a higher incidence of BK virus replication (P = 0.04) and nephropathy (P = 0.0
207 ide insight into the mechanism of control of BK virus replication and may allow for future patient ri
212 iant culture system, we show that autologous BK virus-specific T cell lines can be reliably generated
213 that use of partly HLA-matched donor-derived BK virus-specific T cells for immunotherapy in progressi
215 an increase in the circulating frequency of BK virus-specific T cells, and the presence and persiste
218 ding to MPtV, bovine polyomavirus, Sa12, and BK virus, suggesting a combination of vertical and horiz
223 ts were screened for T-cell immunity to this BK virus VP1 epitope by in vitro stimulation of their pe
227 eings (simian virus 40 [SV40], JC virus, and BK virus) was associated with non-Hodgkin lymphoma.
228 VP1, an effective marker for diagnosing the BK virus, was amplified on an on-chip device in less tha
229 ge T antigen and major capsid protein VP1 of BK virus with high sequence homology to JC virus counter