Risk Stratification for Hepatitis B Virus Reactivation in Kidney Transplant Recipients With Resolved HBV Infection
Hsin-Ju Tsai1,2,3, Ming-Ju Wu3,4,5,6,7, Cheng-Hsu Chen3,4,8, Sheng-Shun Yang2,3,5,6,7, Yi-Hsiang Huang9,10, Yan-Zin Chang1,11, Horng-Rong Chang1,5,12* and 
Teng-Yu Lee2,5*- 1Institute of Medicine, Chung Shan Medical University, Taichung, Taiwan
- 2Division of Gastroenterology and Hepatology, Department of Internal Medicine, Taichung Veterans General Hospital, Taichung, Taiwan
- 3Department of Post-Baccalaureate Medicine, College of Medicine, National Chung Hsing University, Taichung, Taiwan
- 4Division of Nephrology, Department of Internal Medicine, Taichung Veterans General Hospital, Taichung, Taiwan
- 5School of Medicine, Chung Shan Medical University, Taichung, Taiwan
- 6Ph.D. Program in Translational Medicine, National Chung Hsing University, Taichung, Taiwan
- 7Institute of Biomedical Sciences, National Chung Hsing University, Taichung, Taiwan
- 8Department of Life Science, Tunghai University, Taichung, Taiwan
- 9Division of Gastroenterology and Hepatology, Department of Medicine, Taipei Veterans General Hospital, Taipei, Taiwan
- 10Institute of Clinical Medicine, National Yang Ming Chiao Tung University, Taipei, Taiwan
- 11Department of Clinical Laboratory, Drug Testing Center, Chung Shan Medical University Hospital, Taichung, Taiwan
- 12Division of Nephrology, Department of Internal Medicine, Chung Shan Medical University Hospital, Taichung, Taiwan
The prophylaxis strategy for hepatitis B virus (HBV) reactivation in kidney transplant recipients (KTRs) with resolved HBV infection remains unclear. In this hospital-based retrospective cohort study, consecutive KTRs with resolved HBV infection were screened from the years 2000 through 2020. After excluding confounding conditions, 212 and 45 patients were respectively recruited into Anti-HBs positive and Anti-HBs negative groups. Cumulative incidences of, and subdistribution hazard ratios (SHRs) for HBV reactivation were analyzed after adjusting the competing risk. During a median 8.3 (mean 8.4 ± 4.9) years of follow-up, the 10-year cumulative incidence of HBV reactivation was significantly higher in Anti-HBs negative group when compared to that in Anti-HBs positive group (15.2%, 95% CI: 3.6–26.7 vs. 1.3%, 95% CI: 0.0–3.0; p < 0.001). In multivariable regression analysis, absence of anti-HBs (SHR 14.2, 95% CI: 3.09–65.2; p < 0.001) and use of high-dose steroids, i.e., steroid dose ≥20 mg/day of prednisolone equivalent over 4 weeks (SHR 8.96, 95% CI: 1.05–76.2; p = 0.045) were independent risk factors related to HBV reactivation. Accordingly, the 10-year cumulative incidence of HBV reactivation occurring in patients with two, one and zero risk factors was 42.7% (95% CI: 0.0–87.1), 7.9% (95% CI: 1.2–14.7) and 0%, respectively (p < 0.001). In conclusion, the strategy of HBV antiviral prophylaxis may be defined according to the risk stratification.
GRAPHICAL ABSTRACT
Introduction
Kidney diseases are the leading cause of solid organ transplantation globally, with more than 100,000 patients receiving a kidney transplant per year (1). Although hepatitis B virus (HBV) infection may not directly involve the pathogenesis of kidney diseases, hepatitis B progression can be the major cause of either patient morbidity or mortality after kidney transplantation (2). In kidney transplant patients with chronic HBV infection, immunosuppressive therapy can result in rapid liver fibrosis progression, and patients may in turn die of liver-related complications (2, 3). In patients with resolved HBV infection, i.e., those with positive antibody to hepatitis B core antigen (anti-HBc) but negative hepatitis B surface antigen (HBsAg) in the blood, although the risk of hepatitis B progression is much lower than that in HBsAg-positive patients, HBV may still exist somewhere in the body; e.g., in the nucleus of hepatic cells (4). While the host immune system is suppressed, HBV replication may be reactivated, i.e., the reappearance of HBsAg and HBV deoxyribonucleic acid (DNA) in blood (5). Previous studies have reported that immunosuppressive chemotherapy could induce both severe hepatitis B flare and death in patients with resolved HBV infection (6–8), where nucleos(t)ide analogue (NA) therapy can be considered for patients in the high-risk stratification.
With a high risk of HBV reactivation and liver-related mortality in kidney transplant recipients (KTRs) with chronic HBV infection, i.e., positive HBsAg, life-long prophylactic NA therapy has been recommended in the practice guidelines (9–11). However, with a relatively lower risk of HBV reactivation, ranging from 2% to 9.6% in KTRs with resolved HBV infection (12–18), current guidelines only suggest regular follow-ups, rather than long-term NA therapy prophylaxis (10, 11). However, several clinical studies have observed that the risk of HBV reactivation may be particularly higher in patients with resolved HBV infection, but without antibody to HBsAg (anti-HBs) (6, 19). Although the absence of anti-HBs could be a risk factor for HBV reactivation in KTRs with resolved HBV infection, the role in which other risk factors may play remains largely unknown (12–18).
In previous studies of patients with resolved HBV infection, immunosuppressants could be seen as being strongly related to HBV reactivation (7, 20), however their role in KTRs has not yet been systemically investigated. For example, corticosteroids are commonly used as the backbone of immunosuppression therapy, with a dose ranging from an ultra-high dose of pulse therapy or a high dose of rejection therapy, to low-dose maintenance therapy (21); however, the association between steroid dosages and the risk of HBV reactivation remains unclear. For patients at a high risk of HBV reactivation, severe liver complications may be avoided or prevented. We therefore aimed to conduct a long-term cohort study to assess the timing and severity of HBV reactivation in KTRs with resolved HBV infection, as well as comprehensively analyze any possible risk factors which may be of concern.
Patients and Methods
Study Design
This retrospective cohort study was conducted at Taichung Veterans General Hospital (VGHTC), a tertiary medical center in central Taiwan. Any end-stage renal disease patient who had received kidney transplantation at VGHTC between 1st January 2000 and 31st December 2020 was recruited. The study subjects were followed up for clinical outcomes until 31st December of 2021. The medical records of the study subjects were retrieved for analysis. This study was approved by the Institutional Review Board of VGHTC (CE21059B).
Study Subjects
The patient selection process is shown in Figure 1. The inclusion criteria were as follows: 1) KTRs and 2) positive anti-HBc. The exclusion criteria were as follows: 1) positive HBsAg, 2) receiving long-term prophylactic NA therapy, 3) kidney graft failure within 3 months after transplantation, and 4) incomplete essential data. The study subjects were followed up for 10 years or until the dates of 1) HBV reactivation, 2) kidney graft failure, 3) patient mortality, 4) receiving of chemotherapy for a newly diagnosed malignancy, 5) loss follow-up, or 6) 31st December of 2020. According to the positivity of serum anti-HBs before kidney transplantation, patients were recruited into anti-HBs positive or anti-HBs negative group.
FIGURE 1
FIGURE 1. Selection of study subjects. Anti-HBc, antibody to hepatitis B core antigen; anti-HBs, antibody to HBsAg; HBV, hepatitis B virus; HBsAg, hepatitis B surface antigen; NA, nucleos(t)ide analogue.
HBV Reactivation and Hepatitis Flare
The primary endpoint was HBV reactivation, which was defined as HBsAg reverse seroconversion from HBsAg-negative to HBsAg-positive (10). According to the clinical practice routines in our hospital, periodical surveillance for HBV reactivation was performed after kidney transplantation, i.e., serum ALT every 3 months and serum HBsAg every 6–12 months. In addition, serum HBsAg and HBV DNA would be additionally checked if serum ALT was increased for at least twice the baseline level or above the upper limit of normal (ULN). The secondary endpoints included HBV-associated hepatitis in combination with HBV reactivation and hepatitis flare. Hepatitis flare is defined as alanine aminotransferase (ALT) increase >3 times baseline and >100 U/L (10). Other endpoint, including severe flare, was defined as hepatitis B flare (HBV DNA level >2,000 IU/mL and ALT > 5x the ULN) with jaundice (total bilirubin ≥2 mg/dL), and/or coagulopathy (prothrombin time prolongation ≥3 s) (22). The ULN of ALT was defined according to the updated American Association for the Study of Liver Diseases criteria (>25 U/L for females and >35 U/L for males) (10).
Risk Factors Assessment
The data including blood type ABO incompatibility and human leukocyte antigens (HLA) mismatch numbers were collected. Hepatitis C virus (HCV) co-infection in patients was defined as those who were hepatitis C antibody positive with a detected HCV viral load in their serum. We retrieved the immunosuppressants used during induction (rituximb, basiliximab, thymoglobulin and others), as well as the standard triple agents in maintenance (calcineurin inhibitor, mycophenolate mofetil and corticosteroids). The calcineurin inhibitors included cyclosporine and tacrolimus. The data on sirolimus or everolimus combination with the triple agents used in maintenance was also captured. Steroid therapy is a part of immunosuppressive regimens used for induction, maintenance and anti-rejection therapy. Detailed information regarding steroid therapy, including dosage and duration, was comprehensively obtained from medical records. We converted dosages of various steroid therapies into equivalent doses of prednisolone based on anti-inflammatory potency (23). The average steroid dose was defined as the total amount of steroid dosage used in maintenance divided by the sum of the days of steroid treatment. Peak steroid dose was defined as the maximal steroid dosage which persisted at least 4 weeks in maintenance. We set up three strata of peak steroid dose using prednisolone equivalents as rates of <10 mg/day, 10–19 mg/day and ≥20 mg/day (24). After kidney transplantation, allograft rejection development would be suspected as patients experienced a rising serum creatinine or worsening proteinuria. Acute rejection was defined by the presence of pathologic evidence seen on a kidney allograft biopsy (21). The data on rejection episodes and treatments were collected.
Statistical Analyses
Continuous variables were expressed in median with interquartile ranges (IQRs), while categorical variables were presented as both number and percentage. Continuous variables were compared by the Mann-Whitney U test, while categorical variables were compared through use of either the Chi-square test or Fisher’s exact test. Cumulative incidence rates of HBV reactivation or hepatitis flare were calculated and compared by using a Fine-Gray method and Kaplan-Meier method, respectively (25). The differences in the full time-to-event distributions among the study groups were compared by a log-rank test. Renal graft failure or patient mortality before HBV reactivation was treated as a competing event. We further performed univariable analysis to identify any potential risk factors for HBV reactivation, with independent risk factors being determined according to the results of multivariable regression analysis. Subdistribution hazard ratios (SHRs) were obtained in Cox proportional hazard models and adjusted on the basis of the subdistribution of the competing risk. The R-package “cmprsk” was used for the purpose of competing risks regression (26). A two-tailed p < 0.05 was considered statistically significant. We managed the data using SAS 9.3 software (SAS Institute, Inc., Cary, NC, USA).
Results
Study Subjects
As shown in Figure 1, after excluding those with confounding conditions, 257 patients were identified for final analysis. According to the positivity of serum anti-HBs, 212 and 45 patients were respectively recruited into anti-HBs positive and anti-HBs negative groups. As shown in Table 1, apart from age, nearly all the baseline patient characteristics do not reveal significant differences between the two study groups. The median age was younger in the anti-HBs positive group than that in the anti-HBs negative group (49.0 vs. 51.5 years). The proportions of other possible risk factors were not significantly different between the two study groups, including gender, HCV co-infection, HBsAg-positive donor, blood type ABO incompatible transplant, HLA mismatch, immunosuppressive regimens, short-term NA prophylaxis during induction, episodes of biopsy proven acute rejection, and treatment for acute rejection. Moreover, we also analyzed the details surrounding steroid use, including average steroid dose and peak steroid dose, which were also similar in the two study groups. The median follow-up duration was 8.3 (IQR, 4.4–11.9) years, with a mean duration of 8.4 ± 4.9 years (Supplementary Figure S1). The median follow-up duration was not significantly different in the two study groups. (anti-HBs positive vs. anti-HBs negative: 8.8 [IQR: 4.3–10.0] vs. 6.8 [IQR, 4.5–8.6] years; p = 0.084).
TABLE 1
TABLE 1. Baseline characteristics of study subjects.
HBV Reactivation and Hepatitis Flare
As shown in Figure 2A, the 10-year cumulative incidence of HBV reactivation was significantly higher in the anti-HBs negative group when compared to that in the anti-HBs positive group (15.2%, 95% confidence interval [CI]: 3.6%–26.7% vs. 1.3%, 95% CI: 0.0–3.0; p < 0.001). Table 2 presents the details of patients experiencing HBV reactivation: six in the anti-HBs negative group and two in the anti-HBs positive group. HBV reactivation happened during the period of 2–6 years after kidney transplant, and often appeared within 1 year after tapering steroid administration from its peak dose. Reappearance of HBsAg also combined with HBV DNA level >2,000 IU/mL and ALT elevation > 2x ULN in all of these patients. Moreover, five anti-HBs negative patients and one anti-HBs positive patient experienced hepatitis flare, which is defined as ALT increase >3 times baseline and >100 U/L (10). Eight patients who developed HBV reactivation were all hepatitis B e antigen (HBeAg) negative at baseline, and three with antibody to HBeAg. Four (4/8; 50%) patients became HBeAg positive during HBV reactivation.
FIGURE 2
FIGURE 2. The cumulative incidence of (A) HBV reactivation and (B) hepatitis flare was higher in patients without anti-HBs than in patients with anti-HBs in competing risks regression. Anti-HBs, antibody to hepatitis B surface antigen; HBV, hepatitis B virus.
TABLE 2
TABLE 2. Characteristics of the patients with HBV reactivation.
Regarding HBV vaccination, among 47 patients were initially anti-HBs negative prior to kidney transplantation, 14 patients (14/47; 29.8%) received HBV vaccination: Two patients (2/14; 14.3%) produced durable anti-HBs, and they were thus sorted into the anti-HBs positive group. Only one vaccinated patient (1/14; 7.1%), who failed to produce durable anti-HBs, experienced HBV reactivation after kidney transplantation. In univariable regression analysis for all the initially anti-HBs negative patients, HBV vaccination prior to transplantation was not significantly associated with a lower risk of HBV reactivation (SHR 0.61, 95% CI: 0.07–5.28; p = 0.656). The efficacy of HBV vaccination in preventing HBV reactivation might not be sufficiently evaluated due to the limited case numbers in this study.
The 10-year cumulative incidence of hepatitis flare was significantly higher in the anti-HBs negative group when compared to that in the anti-HBs positive group (12.6%, 95% CI: 1.9%–23.3% vs. 0.7%, 95% CI: 0.0–2.0; p < 0.001) (Figure 2B). Severe hepatitis flare, i.e., jaundice and ALT > 5x ULN (1), was noted in one anti-HBs negative patient. All patients diagnosed with HBV reactivation received NA therapy within 1 month after HBsAg seroreversion. Fortunately, no patient died of hepatic failure. After NA therapy, three patients (37.5%) experienced HBsAg loss again thereafter (1.2, 4 and 8.7 years after their HBV reactivation episodes).
The Risk Factors of HBV Reactivation
As shown in Table 3, in univariable regression analysis, a negative anti-HBs status (SHR 14.3, 95% CI: 2.97–68.8; p < 0.001), increased average steroid daily dose (SHR 1.13 per mg of prednisolone equivalent, 95% CI: 1.04–1.23; p = 0.003), and a peak steroid dose ≥20 mg/day of prednisolone equivalent (SHR 8.96, 95% CI: 1.05–76.2; p = 0.045) were associated with the occurrence of HBV reactivation. The peak dose was defined as the maximal steroid dosage which persisted ≥4 weeks in maintenance. Furthermore, in multivariable regression analysis (Model 1), both a negative anti-HBs status (SHR 13.3, 95% CI: 2.75–64.4; p = 0.001) and increased average steroid daily dose (SHR 1.12 per mg of prednisolone equivalent, 95% CI: 1.02–1.23; p = 0.023) were significantly associated with the development of HBV reactivation. In addition, as shown in Model 2, a negative anti-HBs status (SHR 14.2, 95% CI: 3.09–65.2; p < 0.001) and a peak steroid dose ≥20 mg/day of prednisolone equivalent (SHR 9.20, 95% CI: 1.06–79.8; p = 0.044) remained the independent risk factors for HBV reactivation.
TABLE 3
TABLE 3. Subdistribution hazard ratio of risk factors for HBV reactivation in univariate and multivariate competing-risks regression.
Figure 3 shows the cumulative incidence of HBV reactivation in the patient groups receiving different peak steroid doses (<10, 10–19 and ≥20 mg/day of prednisolone equivalent for 4 weeks). The 10-year cumulative incidence of HBV reactivation was highest in patients who received high-dose steroids (≥20 vs. 10–19 vs. < 10 mg/day: 13.1%, 95% CI: 2.1%–24.0% vs. 1.9%, 95% CI: 0.0%–4.4% vs. 1.3%, 95% CI: 0.0–4.0, p = 0.007). Moreover, as demonstrated in Figure 4, we performed a risk stratification based on the independent risk factors of HBV reactivation, i.e., absence of baseline serum anti-HBs and high-dose steroids, and the 10-year cumulative incidence of HBV reactivation occurring in patients with two, one and zero risk factors was 42.7% (95% CI: 0.0–87.1), 7.9% (95% CI: 1.2–14.7) and 0%, respectively (p < 0.001).
FIGURE 3
FIGURE 3. The cumulative incidence of HBV reactivation after kidney transplant according to different peak daily doses of prednisolone, or equivalent. HBV, hepatitis B virus.
FIGURE 4
FIGURE 4. The cumulative incidence of HBV reactivation after kidney transplant in the patient groups stratified by the risk factors of HBV reactivation. The two risk factors are defined as follows (1): absence of baseline serum anti-HBs and (2) high-dose steroids, i.e., a peak steroid dose ≥20 mg/day of prednisolone equivalent which persisted ≥4 weeks in maintenance. HBV, hepatitis B virus.
Discussion
Although HBV reactivation in 1%–10% of cases can be classified as moderate risk (24), the prophylaxis strategy for HBV reactivation in KTRs with resolved HBV infection remains unclear in the current practice guidelines. In the present study, we comprehensively collected the data on immunosuppressants and analyzed the dosages and durations of corticosteroid use. This cohort study is able to provide evidence that the absence of anti-HBs and high-dose steroid use (≥20 mg/day of prednisolone equivalent ≥4 weeks in maintenance) were both independent risk factors associated with HBV reactivation. The cumulative incidence of HBV reactivation will be the highest (>40%) among anti-HBs negative patients who received high-dose steroids, in which case antiviral therapy prophylaxis should be mandatory. In contrast to the high-risk patients, the risk of HBV reactivation in anti-HBs positive patients who did not receive high-dose steroids is very low (0%), therefore a long-term antiviral therapy prophylaxis may be waived. In these low-risk patients, a strategy involving periodic surveillance for HBV reactivation, such as HBsAg testing, may be more cost-effective than NA therapy prophylaxis. The findings of this study may provide an effective and cost-saving strategy in the use of antiviral prophylaxis, which should be valuable to both clinicians and patients.
Similar to the findings in previous studies for KTRs with resolved HBV infection, our study also demonstrates that the absence of baseline serum anti-HBs is a strong risk factor of HBsAg seroreversion after kidney transplantation (12–14). However, other risk factors may be also involved in HBV reactivation (13–15). Although the presence of anti-HBs lowered HBV reactivation risk, the risk is not totally eliminated. For patients with only one risk factor of HBV reactivation, i.e., positive anti-HBs patients who will receive high-dose steroids or negative anti-HBs patients who do not need to use high-dose steroids in this study, NA therapy prophylaxis or close monitoring for HBV reactivation should be considered. However, which strategy is more cost-effective needs further investigated. In addition, the other risk factors found in other similar studies (13–15), including age, ABO-incompatibility, rituximab use, and acute rejection, were not significantly related to HBV reactivation in this study, and their effects should be further clarified in the future studies.
To the best of our knowledge, our cohort is the first study designed to evaluate the effects of steroid therapy on the risk of HBV reactivation in KTRs with resolved HBV infection. Corticosteroids are the most widely used immunosuppressive agents, and a daily dose above 20 mg for longer than 2 weeks of prednisolone, or its equivalent, is generally considered to induce significant immunosuppression (27). HBV reactivation with active viral replication maybe occur when the host is immune suppressed (5). A systemic review suggested that steroid therapy longer than 4 weeks at a moderate (10–20 mg/day of prednisolone equivalent) or high-dose (>20 mg/day of prednisolone equivalent) may lead to HBV reactivation in 1%–10% of patients resolved HBV infection (24). In a cohort study involving rheumatic patients with resolved HBV infection, individuals experiencing HBsAg seroreversion had been exposed to a daily dose of prednisolone over 20 mg (7). Our analysis demonstrates that receiving a peak steroid dose ≥20 mg/day of prednisolone equivalent ≥4 weeks in maintenance had a major impact on risk of HBV reactivation. In addition, most HBsAg seroreversion and hepatitis flare occurred within 1 year after the tapering off of steroid administration from its peak dose. Host immune may rebound and hepatitis may develop after the withdrawal of immunosuppressants. Therefore, close surveillance of liver biochemistries, HBsAg status and HBV DNA remains essential while steroids are given in a decremental fashion. On the other hand, episodes of methylprednisolone (MTP) pulse therapy for acute rejection did not associate with HBV reactivation. Similar to our previous study for rheumatic patients with resolved HBV infection, maintained high dose oral steroid therapy, rather than short-term ultra-high dose MTP pulse therapy, increased the risk of HBV reactivation (28).
Several commonly used immunosuppressants, such as rituximab, have been evaluated for their HBV reactivation risk in previous studies, but the results remain conflicting (13–16). In studies mainly for hematologic malignancy patients receiving multi-course high-dose rituximab during chemotherapy, rituximab could lead to HBV reactivation in more than 10% of patients with resolved HBV infection (24). However, only a single-dose rituximab may be used for KTRs during induction or acute rejection. In two Japanese studies for KTRs with resolved HBV infection, rituximab was not related to an increased HBV reactivation risk (15, 16). In contrast to two Korean studies, rituximab was identified as a risk factor related to HBV reactivation, and patients might die of hepatic failure (13, 14). In the present study, the case number of rituximab users was limited (12 cases during induction and 15 cases for acute rejection), and HBV reactivation was not found during the follow-up period. However, due to the potentially fatal outcome and long-term effect reported in previous studies, careful surveillance for rituximab users remains required.
While there is insufficient evidence to recommend long-term antiviral prophylaxis for KTRs with resolved HBV infection, a limited duration of NA prophylaxis during the period of induction therapy with intensified immunosuppression may be an alternative option (10). However, the consensus regarding short-term NA prophylaxis has not been made in our hospital. Moreover, NA prophylaxis for KTRs with resolved HBV infection was not reimbursed by the National Health Insurance in Taiwan during the study period, therefore only a minority of KTRs received short-term NA prophylaxis during induction out of pocket. However, NA prophylaxis during induction was not significantly associated with HBV reactivation in our analysis.
Several limitations should be acknowledged with regards to this study. First, this is a retrospective study conducted in a transplant referral center, and some data were not completely collected, such as serum HBV DNA prior to transplantation, serum anti-HBc in donors, and the duration between resolving HBV infection and transplantation. However, the prevalence rate of occult HBV infection in patients with resolved HBV infection was low (29), and no HBV DNA was detected in our limited data. In addition, a Korean study reported that a positive anti-HBc in kidney donors was not related to HBV reactivation (14). With a high prevalence of anti-HBs positivity in Taiwanese donors, we believe that the effect of anti-HBc in donors should be insignificant in our study. A well-designed prospective study should be helpful to address the effects of these factors. Second, the incidence of HBsAg seroreversion may have been underestimated in this retrospective study. In patients without positive HBsAg, HBsAg and HBV DNA are usually performed when hepatitis has been suspected. However, our study demonstrates an increased risk not only for HBV reactivation but also for hepatitis flare; therefore, the conclusion of this study should be convincing. Third, the efficacy of long-term NA prophylaxis for kidney transplant patients with resolved HBV infection remains unclear. Although this study may stratify HBV-resolved patients in high risk of HBV reactivation, i.e., absence of anti-HBs and high-dose steroid maintenance, antiviral therapy prophylaxis cannot be directly recommended. A prospective study involving long-term NA prophylaxis versus periodic surveillance as controls would be valuable towards investigating both the risk of HBV reactivation and whether long-term NA prophylaxis could benefit liver and renal outcome.
In conclusion, the absence of baseline serum anti-HBs and the use of high-dose steroids may result in a higher risk of HBV reactivation in KTRs with resolved HBV infection, and the strategy of antiviral therapy prophylaxis may be defined according to the risk stratification for HBV reactivation.
Data Availability Statement
The original contributions presented in the study are included in the article/Supplementary Material, further inquiries can be directed to the corresponding authors.
Ethics Statement
The studies involving human participants were reviewed and approved by the Institutional Review Board of Taichung Veterans General Hospital (CE21059B). Written informed consent for participation was not required for this study in accordance with the national legislation and the institutional requirements.
Author Contributions
H-JT, C-HC, M-JW, S-SY, Y-HH, Y-ZC, H-RC, and T-YL participated in study design and the performance of the research. H-JT, C-HC, S-SY, Y-HH, Y-ZC, H-RC, and T-YL collected and analyzed data. H-JT, H-RC, and T-YL participated in writing the manuscript. C-HC, M-JW, S-SY, Y-HH, Y-ZC, H-RC, and T-YL participated in results interpretation and critical review of the manuscript.
Funding
This work was supported in part by Taichung Veterans General Hospital (TCVGH-1103301B, TCVGH-1113301B, TCVGH-1113301C, VTA111-V1-2-3, VTA112-V1-3-3) and Chung Shan Medical University Hospital (CSH-2015-C-024), Taiwan.
Conflict of Interest
The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.
Acknowledgments
The authors thank the Clinical Informatics Research & Development Center of Taichung Veterans General Hospital. This study is based in part on data taken from the Taichung Veterans General Hospital Research Database, which is managed by the Clinical Informatics Research & Development Center of Taichung Veterans General. We also thank the Biostatistics Task Force of Taichung Veterans General Hospital, Taichung, Taiwan, for the statistical assistance.
Supplementary Material
The Supplementary Material for this article can be found online at: https://www.frontierspartnerships.org/articles/10.3389/ti.2023.11122/full#supplementary-material
Abbreviations
ALT, alanine aminotransferase; anti-HBc, antibody to hepatitis B core antigen; anti-HBs, antibody to hepatitis B surface antigen; CI, confidence interval; DNA, deoxyribonucleic acid; HBeAg, hepatitis B e antigen; HBsAg, hepatitis B surface antigen; HBV, hepatitis B virus; HCV, hepatitis C virus; HLA, human leukocyte antigens; IQR, interquartile range; KTRs, kidney transplant recipients; MTP, methylprednisolone; NA, nucleos(t)ide analogue; SHR, subdistribution hazard ratio; ULN, upper limit of normal.
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Keywords: immunosuppression, renal transplantation, hepatitis B, reversion, antiviral therapy
Citation: Tsai H-J, Wu M-J, Chen C-H, Yang S-S, Huang Y-H, Chang Y-Z, Chang H-R and Lee T-Y (2023) Risk Stratification for Hepatitis B Virus Reactivation in Kidney Transplant Recipients With Resolved HBV Infection. Transpl Int 36:11122. doi: 10.3389/ti.2023.11122
Received: 11 December 2022; Accepted: 31 March 2023;
Published: 13 April 2023.
Copyright © 2023 Tsai, Wu, Chen, Yang, Huang, Chang, Chang and Lee. This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
*Correspondence: Horng-Rong Chang, chrcsmu@gmail.com; Teng-Yu Lee, tylee@vghtc.gov.tw
