2026, Number 2
<< Back Next >>
Rev Mex Traspl 2026; 15 (2)
Six-year experience in the detection of BK virus infection by viruria in patients with acute renal graft dysfunction
Toledo-Sotelo JI, Rodríguez-Villanueva FL, Ortega-Rodríguez R, Rodríguez-Garduño LS, Espinoza-Pérez R, Benítez-Arvizu G, Cancino-López JD, Delgado-Colín G, Martínez-Mendoza ME, Bautista-Olayo R, Aranda-Osorio JR, H HJC
Language: Spanish
References: 22
Page: 61-67
PDF size: 832.12 Kb.
ABSTRACT
Introduction: infections continue to be one of the main complications in kidney transplantation (KT) and are directly related to the duration of the KT and a cause of morbidity and mortality. The objective is to show the incidence of BK virus cases due to viruria.
Material and methods: a descriptive study was conducted of viruria studies in patients within the acute graft dysfunction (AGD) protocol. Patients were included from February 2019 to December 2024, with those with 107 copies considered positive. Descriptive statistics were performed with frequencies and percentages for qualitative variables and categorization of results. The SPSS version 26 statistical package was used.
Results: 521 viruria tests were performed on patients enrolled in the ICD protocol. Twenty-two patients (4.22%) were positive, 421 patients (80.81%) were not detected, and 78 patients (14.97%) were detected without a positive criterion, ranging from 100 to fewer than 10 million copies.
Conclusions: BK virus infection detected by viruria represented 4.22% of the total transplant patients studied by ICD. This type of testing allows for early detection and the implementation of measures that improve the prognosis for graft function. Hospitals that perform this type of testing must be equipped with the appropriate equipment and specialized personnel, as well as the knowledge of the associated risk factors in each case. Decoy cell cytology can be an alternative for those who do not have viruria and/or viremia at their centers.
REFERENCES
Gardner SD, Field AM, Coleman DV, Hulme B. New human papovavirus (B.K.) isolated from urine after renal transplantation. Lancet. 1971; 1 (7712): 1253-1257. doi: 10.1016/s0140-6736(71)91776-4. Available in: https://es.wikipedia.org/wiki/Virus_BK#cite_note-2
Kant S, Dasgupta A, Bagnasco S, Brennan DC. BK virus nephropathy in kidney transplantation: a state-of-the-art review. Viruses. 2022; 14 (8): 1616. doi: 10.3390/v14081616.
Wadei HM, Rule AD, Lewin M et al. Kidney transplant function and histological clearance of virus following diagnosis of polyomavirus-associated nephropathy (PVAN). Am J Transplant. 2006; 6 (5 Pt 1): 1025-1032. doi: 10.1111/j.1600-6143.2006.01296.x.
Knowles WA, Pipkin P, Andrews N et al. Population-based study of antibody to the human polyomaviruses BKV and JCV and the simian polyomavirus SV40. J Med Virol. 2003; 71 (1): 115-123. doi: 10.1002/jmv.10450.
Prelog M, Egli A, Zlamy M, Hirsch HH. JC and BK polyomavirus-specific immunoglobulin G responses in patients thymectomized in early childhood. J Clin Virol. 2013; 58 (3): 553-558. doi: 10.1016/j.jcv.2013.08.035.
Chong S, Antoni M, Macdonald A, Reeves M, Harber M, Magee CN. BK virus: Current understanding of pathogenicity and clinical disease in transplantation. Rev Med Virol. 2019; 29 (4): e2044. doi: 10.1002/rmv.2044.
Schwarz A, Linnenweber-Held S, Heim A, Framke T, Haller H, Schmitt C. Viral origin, clinical course, and renal outcomes in patients with bk virus infection after living-donor renal transplantation. Transplantation. 2016; 100 (4): 844-853. doi: 10.1097/TP.0000000000001066.
Hirsch HH, Knowles W, Dickenmann M et al. Prospective study of polyomavirus type BK replication and nephropathy in renal-transplant recipients. N Engl J Med. 2002; 347 (7): 488-496. doi: 10.1056/NEJMoa020439.
Babel N, Fendt J, Karaivanov S et al. Sustained BK viruria as an early marker for the development of BKV-associated nephropathy: analysis of 4128 urine and serum samples. Transplantation. 2009; 88 (1): 89-95.
Maung MT, Chong CH, von Huben A et al. Serum and urine nucleic acid screening tests for BK polyomavirus-associated nephropathy in kidney and kidney-pancreas transplant recipients. Cochrane Database Syst Rev. 2024; 11 (11): CD014839. doi: 10.1002/14651858.CD014839.pub2
Nankivell BJ. The accuracy of blood nucleic acid testing to predict bk polyomavirus nephropathy varies by clinical context. Transplant Direct. 2025; 11 (10): e1845. doi: 10.1097/TXD.0000000000001845.
Nankivell BJ, Renthawa J, Sharma RN, Kable K, O'Connell PJ, Chapman JR. BK virus nephropathy: histological evolution by sequential pathology. Am J Transplant. 2017; 17 (8): 2065-2077. doi: 10.1111/ajt.14292.
Kotton CN, Kamar N, Wojciechowski D et al. The second international consensus guidelines on the management of BK polyomavirus in kidney transplantation. Transplantation. 2024; 108 (9): 1834-1866. doi: 10.1097/TP.0000000000004976.
ELITech Group S.p.A. Manual de Instrucciones: ELITe InGenius, software versión 1.3 (Ref. SCH-Mint030_08_es). 2022. Available in: https://www.elitechgroup.com/documentation/wp-content/uploads/sites/30/2022/12/SCH-mINT030_08_es_compressed.pdf
Hodowanec AC, Simon DM. BK virus screening and management practices in US kidney transplant programs: a survey. Transpl Int. 2015; 28: 1339-1341. doi: 10.1111/tri.12602.
Zakaria ZE, Elokely AM, Ghorab AA, et al. Screening for BK Viremia/Viruria and the Impact of Management of BK Virus Nephropathy in Renal Transplant Recipients. Exp Clin Transplant. 2019;17(Suppl 1):83-91. doi:10.6002/ect.MESOT2018.O17.
Kraivisitkul N, Noppakun K, Sakuludomkan C et al. The association between serum tacrolimus concentrations and BK viruria in kidney transplant recipients. Sci Rep. 2025; 15 (1): 2872. doi: 10.1038/s41598-025-86465-2.
Eder M, Kainz A, Omic H et al. A systematic literature review and meta-analysis evaluated modifiable risk factors for the development of BK polyoma virus-associated complications. Kidney Int. 2025; 108 (4): 669-685. doi: 10.1016/j.kint.2025.06.014.
Burek KM, Ivkovic V, Kovacevic Vojtusek I, Zunec R. The role of HLA and KIR Immunogenetics in BK virus infection after kidney transplantation. Viruses. 2020; 12 (12): 1417. doi: 10.3390/v12121417.
Bohl DL, Storch GA, Ryschkewitsch C et al. Donor origin of BK virus in renal transplantation and role of HLA C7 in susceptibility to sustained BK viremia. Am J Transplant. 2005; 5 (9): 2213-2221. doi: 10.1111/j.1600-6143.2005.01000.x.
Kavuzlu M, Bastürk B, Atac FB, Aliskan HE, Kantaroglu B. Investigation of the relationship between BK virus and human leukocyte antigens in kidney transplant recipients. Exp Clin Transplant. 2020; 18 (Suppl 1): 51-54. doi: 10.6002/ect.TOND-TDTD2019.O24.
Liu Y, Kong C, Hu H et al. Risk factors for BK virus infection in DCD donor kidney transplant recipients. Front Med (Lausanne). 2023; 10: 1181743. doi: 10.3389/fmed.2023.1181743.