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Table 2 Pre/post-transplant HBV serology and post-transplant complications in the two groups

From: Pre-transplant donor HBV DNA+ and male recipient are independent risk factors for treatment failure in HBsAg+ donors to HBsAg- kidney transplant recipients

 

D(HBsAg+)/R(HBsAg-) group

(n = 83)

D(HBcAb+)/R(HBcAb-) group

(n = 83)

P value

Donors’ pre-transplant HBV serology

 HBsAg+

83 (100%)

0

< 0.001

 HBsAb+

3 (3.6%)

58 (69.9%)

< 0.001

 HBeAg+

0

0

/

 HBeAb+

78 (94.0%)

35 (42.2%)

< 0.001

 HBcAb+

82 (98.8%)

83 (100%)

1.000

 HBV DNA+

24 (28.9%)

Unknowna

/

Recipients’ pre-transplant HBV serology

 HBsAg+

0

0

/

 HBsAb+

63 (75.9%)

63 (75.9%)

1.000

  HBsAb titer > 100

32 (38.6%)

32 (38.6%)

1.000

 HBeAg+

0

0

/

 HBeAb+

34 (41.0%)

0

< 0.001

 HBcAb+

58 (69.9%)

0

< 0.001

 HBV DNA+

0

Unknowna

/

Recipients’ most recent HBV serology

 HBV DNA - → +

2b (2.4%)

0

0.477

 HBsAg - → +

2b (2.4%)

0

0.477

 HBeAg - → +

1 (1.2%)

0

1.000

 HBeAb - → +

4 (4.8%)

0

0.129

 HBeAb + → -

4 (4.8%)

0

0.129

 HBcAb - → +

7 (8.4%)

2 (2.4%)

0.170

 HBsAb titer downgrade

1 (1.2%)

11 (13.3%)

0.012

 HBsAb titer upgrade

13 (15.7%)

2 (2.4%)

0.013

Recipients’ post-transplant complications

 Treatment failure

18 (21.7%)

9 (10.8%)

< 0.001

 Delayed graft function

2 (2.4%)

0

0.477

 Rejection

12 (14.5%)

12 (14.5%)

1.000

 Infection

34 (41.0%)

22 (26.5%)

0.071

 Graft loss

4 (4.8%)

4 (4.8%)

1.000

 Recipient death

5 (6.0%)

1 (1.2%)

0.216

 Abnormal liver function

29 (34.9%)

32 (38.6%)

0.650

  Active liver injury

8 (9.6%)

2 (2.4%)

0.048

 Malignancy

0

0

/

  1. aWe did not test the pre-transplant HBV DNA levels of the donors or recipients in the D(HBcAb+)/R(HBcAb-) group
  2. b Two recipients in the D(HBsAg+)/R(HBsAg-) group developed post-transplant HBV DNA+ accompanied with HBsAg+. The first recipient: 32-year-old male, pre-transplant donor/recipient HBV serology was HBV DNA −/−, HBsAg +/−, HBsAb −/−, HBeAg −/−, HBeAb +/−, HBcAb +/−. His prophylaxis was lamivudine alone for 1.5 months. The recipient experienced a temporary rise of ALT, up to 163 IU/L 1 year after transplantation. Then he was lost to follow-up during post-transplant years 1.5–5.5. He was found to have HBV DNA+ (5.02 × 104 IU/ml), HBsAg+, HBeAb+, and HBcAb+, ALT 55 IU/L when admitted due to pulmonary infection 5.5 years after transplantation. He received long-term entecavir monotherapy until he died of pulmonary infection 7 years after transplantation. The second recipient: 24-year-old male, pre-transplant donor/recipient HBV serology was HBV DNA + (1.14 × 103 IU/mL)/−, HBsAg +/−, HBsAb −/−, HBeAg −/−, HBeAb +/−, HBcAb +/−. His prophylaxis was HBIG 2000 IU and lamivudine for 2 months. He received a total of 1500 mg Intravenous methylprednisolone to treat acute rejection 5 months after transplantation. He became HBV DNA+ (> 5.00 × 107 IU/mL), HBsAg+, and HBcAb+ 6 months after transplantation. His total bilirubin level rapidly increased from 26 μmol/L at month 6 to 489 μmol/L at month 8 when he died of liver failure and pulmonary infection