BK virus genotypes and humoral response in kidney transplant recipients with BKV associated nephropathy

Author:

Gras Julien123ORCID,Nere Marie Laure4,Peraldi Marie Noëlle35,Bonnet‐Madin Lucie2,Salmona Maud34,Taupin Jean Luc36ORCID,Desgrandchamps François37,Verine Jérôme8,Brochot Etienne9,Amara Ali23,Molina Jean Michel123,Delaugerre Constance234

Affiliation:

1. Infectious Disease Department APHP‐Saint‐Louis Hospital Paris France

2. INSERM U944, Biology of Emerging Viruses Team Institut de Recherche Saint Louis, APHP‐Saint‐Louis Hospital Paris France

3. Université Paris Cité Paris France

4. Virology Department APHP‐Saint Louis Hospital Paris France

5. Nephrology and Kidney Transplant Department APHP‐Saint Louis Hospital Paris France

6. Immunology Department APHP‐Saint Louis Hospital Paris France

7. Urology Department APHP‐Saint Louis Hospital Paris France

8. Pathology Department APHP‐Saint Louis Hospital Paris France

9. Virology Department CHU Amiens Amiens France

Abstract

AbstractBackgroundAmong kidney transplant recipients (KTR) with BK virus associated nephropathy (BKVN), BKV genotypes’ evolution and anti‐BKV humoral response are not well established. We aim to analyze BKV replication and genetic evolution following transplantation, and characterize concomitant anti‐BKV‐VP1 humoral response.MethodsWe retrospectively analyzed 32 cases of biopsy‐proven BKVN. Stored plasma and kidney biopsies were tested for BKV viral load, and VP1 sequencing performed on positive samples. BKV–VP1 genotype‐specific neutralizing antibodies (NAbs) titers were determined at transplantation and BKVN.ResultsAt the time of BKVN diagnosis, BKV viral load was 8.2 log10IU/106 cells and 5.4 log10IU/mL in kidney and plasma, respectively. VP1 sequencing identified the same BKV‐subtype in both compartments in 31/32 cases. At the time of transplantation, 8/20 (40%) of biopsies tested positive for BKV detection, whereas concomitant BKV viremia was negative. VP1 sequencing identified a different subtype compared to BKVN in 5/6 of these samples. This was confirmed following transplantation: 8 patients had a BKV+ biopsy before BKV viremia, and VP1 sequencing identified a different subtype compared to BKVN in all of them. After the onset of BKV viremia and prior to BKVN diagnosis, the BKV subtype in BKV+ plasma and kidney biopsy was the same as the one isolated at BKVN. BKV–VP1 NAbs titers were significantly higher at the time of BKVN compared to transplantation (p = .0031), with similar titers across genotypes.ConclusionAltogether, our data suggest that among some KTR with BKVN, the BKV genotype from the donor may not be responsible for BKVN pathogenesis. image

Publisher

Wiley

Subject

Infectious Diseases,Transplantation

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