BK virus (BKV) is one of the most common pathogens in
post-transplantation
infections. For kidney transplantation, BKV infection results in the
impairment of allograft function and thus increases the risk of allograft
loss. However, clinical evaluation of the prognosis of BKV-associated
allograft impairment is difficult. In the present study, differential
plasma proteins were screened using proteomic methods from ten patients
with a transition from BKV-negative to BKV activation. We identified
12 differentially expressed proteins, and S100A8 and S100A9 were the
top two upregulated proteins. Data from a cross-sectional study with
66 BKV-negative and 66 BKV-positive recipients of renal transplantation
indicated that plasma S100A8/A9 was upregulated in BKV-infected recipients.
Plasma S100A8/A9 positively correlated with the 1 month creatinine
increase (ρ = 0.499, P = 0.021) and negatively
correlated with the 1 month estimated glomerular filtration rate change
(ρ = −0.618, P = 0.003) in recipients
with BK viremia. Using least absolute shrinkage and selection operator
regression models, we found that S100A8/A9 was an independent risk
factor for the decrease in allograft function after BKV infection.
In conclusion, S100A8/A9 is a potential host biomarker for the clinical
evaluation of BKV-associated allograft function impairment in kidney
transplantation.