Skip to content

Advertisement

  • Research article
  • Open Access
  • Open Peer Review

Lack of evidence of viral reactivation in HBsAg-negative HBcAb-positive and HCV patients undergoing immunosuppressive therapy for psoriasis

  • 1Email author,
  • 1,
  • 2,
  • 2,
  • 1,
  • 2 and
  • 2
BMC Gastroenterology201414:214

https://doi.org/10.1186/s12876-014-0214-x

©  Morisco et al.; licensee BioMed Central. 2014

  • Received: 9 September 2014
  • Accepted: 9 December 2014
  • Published:
Open Peer Review reports

Abstract

Background

HBV and HCV reactivation have been widely reported in patients undergoing immunosuppressive therapy (IT); however, few data are available on the risk of reactivation in patients with psoriasis receiving IT. The aim of our study was to assess the prevalence of HBV and HCV infection in patients with psoriasis and to evaluate the effects of IT during the course of the infection.

Methods

The study included psoriatic patients who attended an Italian tertiary referral hospital from 2009 to 2012. A total of 224 patients were enrolled. We evaluated: HBV and HCV markers, type of IT and the occurrence of viral reactivation. The observational period ranged from the beginning of IT to the last visit, with a mean follow-up period of 54 months.

Results

Two hundred and twenty patients (135 males and 89 females; mean age 59 years; range 18–86 years) with psoriasis, with or without psoriatic arthritis, receiving conventional IT and/or biological drugs were tested for markers of infection. We identified 23/224 patients (10.2%) with isolated positivity for HBcAb positivity, 36/224 (16%) with positivity for HBsAb/HBcAb, and 15/224 (6.6%) with positivity for HCV-Ab. No patient was HBsAg positive, none of them underwent pre-emptive therapy with lamivudine or other antiviral drugs and no one showed episodes of viral reactivation.

Conclusions

The prevalence of HBsAg in patients with psoriasis is lower than that observed in the general population. The prevalence of isolated positivity for HBcAb and of combined positivity for HBcAb and HBsAb is 10.2% and 16%, respectively. The prevalence of HCV infection (HCV-RNA+) is 4%. In patients with psoriasis and HCV-Ab or HBcAb positivity, the IT seems to be safe, regardless of the type of drugs.

Keywords

  • Biological drugs
  • HBV reactivation
  • HCV infection
  • Immunosuppressive therapy
  • Lamivudine
  • Psoriasis

Background

Psoriasis is a chronic, immune-mediated relapsing and remitting inflammatory skin and joint disease. The prevalence of psoriasis estimates as high as 2.8% in western populations [1],[2]. Currently, different immunosuppressive therapeutic regimens are indicated for patients with psoriasis. The best treatment is determined on an individual basis and depends on the type of disease, the Psoriasis Area Severity Index (PASI) and comorbidities. For mild disease (PASI <10), involving only small areas of the body, topical treatments such as corticosteroids or calcineurin inhibitors or vitamin D derivates may be very effective and safe to use [3]. Up to 30% of 70% of psoriatic patients (PASI >/=10 that involves much larger areas of the body or for psoriatic artrhritis), require traditional systemic treatments such as retinoids, methotrexate and cyclosporine. Many of them imply long-term toxicity, treatment resistance and potential drug interactions; therefore, only 25% of psoriatic patients are completely satisfied with their treatment [4]. Advances in psoriasis therapies have introduced biologic agents, whose immune targeting is successful in treating many immunemediated inflammatory diseases [4]. Psoriatic patients who are refractory or intolerant to traditional therapy are the main candidates for biological anti-tumor necrosis factor alpha (TNF-a) drugs, for instance, infliximab, adalimumab, etanercept, golimumab or the anti-IL-12/23p40 monoclonal antibody, such as ustekinumab [5]. Several reports and studies have highlighted the risk of adverse events related to immunosuppressive therapy (IT) [4]. Under immunosuppression conditions, all patients with a history of exposure to HBV or HCV are at risk of reactivation [6]-[18]. The widespread use of biological drugs have raised these issues concerning the safety and the potential risks related to its administration, including patients with psoriasis [19]-[28]. Although a large amount of information on the relationship between IT for psoriasis and the behavior of HBV/HCV infections have become more available, the impact of different immunosuppressive drugs on the risk of reactivation remains poorly investigated.

The aim of our study was to assess the prevalence of HBV and HCV infection in a consecutive series of patients with psoriasis and to evaluate the effects of different schedules of immunosuppressive therapy during the course of the infection.

Methods

This is a retrospective, observational study carried out at the Dermatology Unit of the University of Naples “Federico II,” a tertiary referral centre in Southern Italy. The target population consisted of adult patients with plaque-type psoriasis (Pso) with or without psoriatic arthritis (PsA) candidate to immunosuppressive therapy, observed from 1 January 2009 to 31 December 2012.

This study was independently designed by the authors, conducted in compliance with the 1975 Declaration of Helsinki and approved by the Ethic Committee of the University of Naples Federico II (protocol n° 175/2012).

Records for 224 outpatients were reviewed in relation to the markers of previous disease or active HBV and HCV infection. Among them, patients with almost 1 positive marker of HBV or HCV infection were identified for the inclusion in the study. All of the selected patients underwent immunosuppressive therapy, such as conventional immunosuppressive treatment (cyclosporine A, methotrexate (MTX)) or biological treatment (adalimumab, etanercept, infliximab, golimumab, ustekinumab) or combined biological plus methotrexate. The medical records of these selected patients were retrospectively reviewed.

Before starting the immunosuppressive therapy, all psoriatic patients had been routinely tested for serology of HBV and HCV infection. For patients with HBV or HCV infection, a scheduled monitoring had been applied: transaminases every 1 month, complete liver function test (bilirubin, INR, γ-Glutamyltransferase, alkaline phosphatase, albumin) every 3 months and HBV/HCV serological status (HBsAg and HBV-DNA for HBV infection, HCV-RNA for HCV infection) every 3 months from the start of therapy, until the last follow-up visit.

Definition of HBV and HCV infection

HBV chronic infection was defined according to the EASL guidelines [29] as patients positive for HBsAg, independently from the HBeAg/HBeAb positivity and the levels of HBV-DNA. “Occult” HBV infection (OBI) represents a particular clinical entity that is characterized by the persistence of HBV DNA in the liver tissue, without the evidence of overt HBV infection in individuals who are HBsAg negative and HBcAb positive either with or without serum HBV-DNA positivity [29]. The difficulty in identifying HBV-DNA in liver biopsy (frequently not justified in patients without clinical signs of hepatitis) and the rarity of detectable serum viremia, even with sensitive techniques, lead to consider all HBcAb positive patients (HBsAg and HBV-DNA negative, with or without HBsAb positivity) as potential OBI. Patients with HBsAg negativity but positivity for HBcAb with HBsAb positivity, were considered as a resolved HBV infection [29].

Potential OBI and resolved HBV infection were analyzed for the same parameters as the HBsAg-positive patients. HCV infection was defined as patients positive for anti-HCV, with or without positivity for HCV-RNA [30].

Definition of HBV and HCV reactivation

In HBV- positive patients, the following biochemical events were considered significant for a viral reactivation:

in HBsAg-positive patients (active or inactive carriers), the increase of at least one logarithm of HBV-DNA with or without the concomitant increase of transaminases;

in potential OBI and resolved HBV infection (HBsAb positive and/or HBcAb positive patients), the re-emergence of HBsAg or the appearance or increase of at least one logarithm of HBV-DNA.

Reactivation of HCV was defined as a significant increase of HCV-RNA (at least one logarithm), with or without a concomitant increase of transaminases. In HCV-Ab positive but HCV-RNA negative patients, the re-appearance of HCV-RNA was considered as a relevant event.

Serological profile

HBsAg, HBcAb and HBsAb were determined by conventional commercial assay kits (Abbott AxSYM AUSAB, Germany; HBsAg EIA, Abbott, North Chicago, IL). HCV-Ab and HDV-Ab were determined by commercial enzyme linked immunosorbent assay III, Abbot Laboratories Chicago. All HBcAb-positive samples were assayed for serum HBV-DNA by a commercial qualitative target amplification method (Cobas Ampliscreen, Roche Molecular Systems, Branchburg, New Jersey, USA). In order to achieve the highest sensitivity allowed by this method (20 IU/mL), testing was performed on each individual sample without pooling and increasing the volume for extraction (500 μL). The specimens that resulted positive were further tested by a quantitative method (Cobas Amplicor HBV Monitor, Roche Molecular Systems, Branchburg, NJ, USA) to determine the viral load.

All HCV-Ab positive samples were assayed for serum HCV-RNA by a qualitative method (Cobas Ampliscreen, Roche Molecular Systems, Branchburg, New Jersey, USA). In order to achieve the highest sensitivity allowed by this method (15 IU/mL), testing was performed on each individual sample - without pooling- and increasing the volume for extraction (500 μL). The specimens that resulted positive were further tested by quantitative method (Light Cycler Instrument, Roche Molecular Biochemicals, Mannheim, Germany) to determine the viral load.

Statistical analysis

Demographical, clinical, biochemical, histological, virological and therapeutic data were collected from medical records by case report forms. Baseline characteristics were expressed as median and range for continuous and not normally distributed data, as a mean and standard deviation (SD) for normally distributed data and as a percentage for categorical data.

Results

Seventy-four patients with plaque-type psoriasis (Pso) with or without psoriatic arthritis (Psa) and with active or previous HBV or HCV infection were identified in a population of 224 patients, receiving conventional or biological treatment. All of these patients are still being treated for psoriasis. The characteristics of our population are illustrated in Table 1.
Table 1

Characteristics of patients with psoriasis at baseline

 

Overall

Isolated HBcAb positive

HBcAb/HBsAb positive

HCV-Ab positive

N° of patients

224

23

36

15

Age, yrs (mean ± SD)

49 [±13.3]

66 [±10.6]

52 [±12.4]

62 [±11.8]

Gender (M/F) N°%

135/89 [60.2/39.7%]

10/13 [43.4/56.5%]

27/9 [75/25%]

11/4 [73.3/26.6%]

Pso

113 [50.5%]

10 [43.5%]

22 [61.1%]

9 [60%]

PsA

111 [49.5%]

13 [56.5%]

14 [38.9%]

6 [40%]

ALT, U/L (mean ± SD)

23 [±5.3]

27 [±2.3]

24 [±3.2]

25 [±2.1]

HBV-DNA positivity

0/224

0/23

0/36

0/15

HCV-RNA positivity

9/224

0/23

0/36

9/15

HBsAg positivity

0/224

0/23

0/36

0/15

HBV infection

No patient was HBsAg positive. Globally, 59 patients showed almost 1 marker of HBV infection; 23/224 (10.2%) patients were isolated HBcAb positive (OBI) and 36/224 (16%) patients were HBsAb and HBcAb positive (resolved HBV infection). The main features of the 59 patients are reported in Table 1. Thirty-two patients were affected by plaque-type psoriasis and 27 by psoriatic arthritis. None of them showed signs of cirrhosis. At baseline all patients had normal aminotransferase levels and negative HBV-DNA. All HBV patients underwent immunosuppressive therapy. The treatment schedules are reported in Table 2. Nineteen patients (32%) were treated with conventional drugs only (Metotrexate, Cyclosporine or a combination of the two drugs) for a mean time of 24 months, 34 patients (58%) were treated with conventional and biological drugs, sequentially, for a mean time of 42 months, and 6 patients (10%) were treated with conventional drugs followed by a combination of biological drug plus methotrexate) for a mean time of 72 months. No patients were treated with prophylactic Lamivudine. In all of the cases serum liver functional tests showed no significant changes in AST or ALT levels and HBV-DNA positivity, from baseline to the last follow-up visit.
Table 2

Schedules of treatment in patients with HBV or HCV infection

Schedules of treatment [#]

Isolated HBcAb positive (23 patients)

HBcAb/HBsAb positive (36 patients)

HCV-Ab positive (15 patients)

Conventional therapy

   

  MTX, n.

3

5

0

  Duration, months (mean ± SD)

11 ± 7,54

24 ± 23,62

-

  Cyclosporine, n.

0

4

4

  Duration, months (mean ± SD)

-

5,75 ± 4,5

20,25 ± 10,34

  MTX + Cyclosporine, n.

2

5

5

  Duration, months (mean ± SD)

12

26,4 ± 21,46

30,4 ± 22,19

Conventional > Biological * therapy, n.

16

18

6

  Duration, months (mean ± SD)

33,8 ± 16,9

48,1 ± 26,55

46 ± 34,77

Conventional > Biological * therapy + MTX, n.

2

4

0

  Duration, months (mean ± SD)

35,5 ± 4,94

90,75 ± 65,06

-

* Adalimumab, etanercept, infliximab, golimumab, ustekinumab.

[#] The treatment schedule was standardized, the doses were used as follows.

● MTX (7.5 vs15 mg/ week -per os or intramuscular injections).

● Cyclosporine (2.5 vs 5 mg/prokilo/die- per os).

● Adalimumab (40 mg every other week-subcutaneous injections).

● Etanercept (50 mg weekly- subcutaneous injections).

● Infliximab (5 mg/kg at 0, 2 and 6 weeks, then every 8 weeks-endovenous infusion).

● Golimumab (50 mg monthly-subcutaneus injections).

● Ustekinumab ( For patients weighing ≤100 kg (220 lbs), the recommended dose is 45 mg initially and 4 weeks later, followed by 45 mg every 12 weeks. For patients weighing >100 kg (220 lbs), the recommended dose is 90 mg initially and 4 weeks later, followed by 90 mg every 12 weeks. – subcutaneous injections).

The data in bold represent "macro-categories", while the data not in bold represent their "sub-categories".

HCV infection

Overall, 15/224 (6.6%) patients had a positive serology for anti-HCV (11 males and 4 females, mean age 62 yrs). The main features of the 15 patients with HCV infection are reported in Table 1. Nine patients were affected by plaque-type psoriasis and 6 by psoriatic arthritis. None of them showed signs of cirrhosis. All HCV patients had baseline normal aminotransferase levels, 6/15 were HCV-RNA negative and 9/15 were positive (mean levels of HCV-RNA: 16.207.071 UI/ml, range 43600 – 515.000.000), and underwent immunosuppressive therapy. The schedules of treatment are reported in Table 2. Nine patients (60%) were treated with conventional drugs only (Metotrexate, Cyclosporine or a combination of the two drugs) for a mean time of 26 months and 6 patients (40%) were treated with conventional and biological drug, sequentially, for a mean time of 46 months. Serum liver functional tests in all cases showed no significant changes in AST or ALT levels and in viral load, from baseline to the last follow-up visit.

Discussion

The reactivation of viral hepatitis, in particular HBV disease, has been widely reported in patients undergoing IT in different clinical conditions with particular frequency and severity in onco-haematological and transplant settings._Conversely, very few data are available in literature on the course of liver disease and the risk of HBV or HCV reactivation in patients with psoriasis receiving IT [19]-[25], the major part of them are case reports and series of patients.

Our study is the first observational analysis conducted in a larger cohort of psoriatic patients with a serological pattern of active or previous HBV or HCV infection, assessing the safety of different schedules of immunosuppressive therapy for a mean follow-up period of 48 months.

The main results of our investigation is represented by the absence of episodes of viral reactivation in HBsAg negative-HBcAb positive patients independently of the type of immunosuppressive (conventional or biological) drugs.

The risk of reactivation for the category of potential occult HBV infection is controversial and might be related to the clinical setting and type of IT. There are several reported cases of HBV reactivation in HBcAb positive patients with and without concomitant HBsAb positivity in patients who have undergone bone marrow transplantation or cytotoxic chemotherapy for lymphoma [31]. In these patients, the use of intense immunosuppression, monoclonal antibodies anti-lymphocyte B and T (anti-CD20) are particularly considered as risk factors. Conversely, in other clinical settings (gastroenterology, rheumatology and dermatology) the risk of reactivation in isolated HBcAb positive patients seems to be negligible or absent [20],[22],[32],[33].

Our result seems to be in agreement with other previous reports limited by the observation of a small number of patients using biological agents for a short follow-up period. For example, the study of Prignano et al. [23] conducted in a cohort of 17 patients with psoriasis, using etanercept and/or adalimumab showed no significant changes in aminotransferase and in viral load levels during a follow-up period of only 6–8 months. Moreover, in the latest study by Navarro et al. [28], the safety of anti-TNF agents in 13 psoriatic HBsAg negative – HbcAb positive patients during a mean follow-up time of 28.6 months has been pointed out, suggesting a low risk of HBV reactivation in potential occult HBV infection.

Concerning patients with resolved HBV infection (HBsAg negative, HBcAb positive, HBsAb positive), there is only one reported case of viral reactivation in a dermatological setting during immunosuppressive therapy with ustekinumab, as described by Koskinas et al. [19]. In our study, no viral reactivation was observed in this category, confirming a low risk of viral reactivation in resolved HBV infection.

On the other hand, more data are available in literature for patients with chronic HBV infection (HBsAg positive). In total, 103 patients HBsAg positive with concomitant psoriasis and IT have been described in literature [20],[24],[25],[34],[35]; 56/103 of these patients were treated with concomitant antiviral therapy and only 5/56 (8.9%) showed HBV reactivation [35]. Differently, among the remaining patients without antiviral prophylaxis, 32/47 (68%) patients showed HBV reactivation during biological therapy [25],[35]. We did not observe HBsAg positive patients in our series of patients; therefore, we can add nothing to what is already known in this category, which seems to be the only one at high risk of reactivation during biological therapies. In this perspective, the European guidelines for the use of anti-TNF therapy in psoriasis published in 2009 [36], the British Association of dermatologist guidelines for the use of biological interventions in psoriasis published in 2005 [37] and the Japanese guidance for use of biologics for psoriasis published in 2013 [38] consider active chronic hepatitis B as relative or absolute contraindication to the use of anti-TNF agents. Considering the success of biological IT in HBsAg patients using concomitant antiviral therapy, these guidelines seem far from clinical reality and current evidence. Only 5 cases of HBV reactivation in psoriatic patients treated with biological drugs (3 etanercept and 2 infliximab), using concomitant antiviral therapy (lamivudine) are reported in literature until now [35].

The prophylactic use of antiviral drugs is an important issue. Lamivudine prophylaxis has been suggested on the basis of its well demonstrated efficacy; however, other nucleotides/nucleosides should be preferred for their lower propensity to provoke drug resistance, especially if immunosuppressive therapy is scheduled for more than 12 months. The role of alternative anti-viral drugs, including entecavir and tenofovir, is still unknown and further studies are needed.

With regard to patients with HCV infection, the use of IT appears to induce lower frequency and severity of viral reactivation than in HBV. This finding is confirmed in our series of 15 HCV patients undergoing IT in which no viral reactivation was observed. Only one case of HCV reactivation during treatment with ustekinumab for psoriasis is reported in the literature [25].

Conclusions

In conclusion, screening for HBV and HCV is now recommended for all patients with psoriasis, before starting all types of IT therapy. All patients with psoriasis should be tested for HBV (including HBsAg, HBcAb, HBsAb and HBV-DNA if needed) and HCV (including HCV-Ab and HCV-RNA if HCV-Ab positive) to assess the infection or vaccination status. HBV vaccination is mandatory in all seronegative patients. The current data that are available suggest that anti-TNFα and IL-12 and IL-23 blockers may also represent a therapeutic option in patients with concomitant HBV and/or HCV infection. The risk of HBV or HCV reactivation related to TNFα inhibitors seems to be low. The best strategy to adopt in HBsAg negative/HBcAb positive patients with or without HBsAb positivity and HCV positive patients would appear to be represented by periodic clinical and laboratoristic monitoring.

Abbreviations

HBV: 

Hepatitis B virus

HCV: 

Hepatitis C virus

HBsAg: 

HB surface antigen

HBcAb: 

Hepatitis B core antibody

HBsAb: 

Hepatitis B surface antibody

IT: 

Immunosuppressive Therapy

TNF-a: 

Tumour Necrosis Factor-alpha

MTX: 

Methotrexate

OBI: 

Occult HBV Infection

ALT: 

Alanine Aminotransferase

AST: 

Aspartate Aminotransferase

GGT: 

Gamma-Glutamiltransferase

SD: 

Standard Deviation

Pso: 

Plaque-type Psoriasis

PsA: 

Psoriatic Arthritis

Declarations

Acknowledgements

The authors wish to thank Dr Alfonso Gruosso for the English revision of the manuscript.

Fundings

This study was supported by Gilead Fellowship Program 2012.

Authors’ Affiliations

(1)
Department of Clinical Medicine and Surgery, Gastroenterology Unit, University of Naples “Federico II”, Via S. Pansini, 5, Naples, 80131, Italy
(2)
Dermatology Units, University of Naples “Federico II”, Via S. Pansini, 5, Naples, 80131, Italy

References

  1. Schon MP, Boehncke WH: Psoriasis. N Engl J Med. 2005, 352 (18): 1899-1912. 10.1056/NEJMra041320.View ArticlePubMedGoogle Scholar
  2. Naldi L: Epidemiology of psoriasis. Curr Drug Targets Inflamm Allergy. 2004, 3 (2): 121-128. 10.2174/1568010043343958.View ArticlePubMedGoogle Scholar
  3. Kivelevitch DN, Hebeler KR, Patel M, Menter A: Emerging topical treatments for psoriasis. Expert Opin Emerg Drugs. 2013, 18 (4): 523-532. 10.1517/14728214.2013.861418.View ArticlePubMedGoogle Scholar
  4. Balato N, Di Costanzo L, Ayala F, Balato A, Sanduzzi A, Bocchino M: Psoriatic disease and tuberculosis nowadays. Clin Dev Immunol. 2012, 2012: 747204-10.1155/2012/747204.View ArticlePubMedPubMed CentralGoogle Scholar
  5. Daudén E, Castañeda S, Suárez C, García-Campayo J, Blasco AJ, Aguilar MD, Ferrándiz C, Puig L, Sánchez-Carazo JL, Working Group on Comorbidity in Psoriasis: Clinical practice guideline for an integrated approach to comorbidity in patients with psoriasis. J Eur Acad Dermatol Venereol. 2013, 27 (11): 1387-1404. 10.1111/jdv.12024. doi:10.1111/jdv.12024View ArticlePubMedGoogle Scholar
  6. Picardi M, De Rosa G, Selleri C, Pane F, Rotoli B, Muretto P: Clinical relevance of intrahepatic hepatitis B virus DNA in HBsAg-negative HBcAb-positive patients undergoing hematopoietic stem cell transplantation for haematological malignancies. Transplantation. 2006, 82 (1): 141-142. 10.1097/01.tp.0000225828.27850.fc.View ArticlePubMedGoogle Scholar
  7. Sansone S, Guarino M, Castiglione F, Rispo A, Auriemma F, Loperto I, Rea M, Caporaso N, Morisco F: Hepatitis B and C virus reactivation in immunosuppressed patients with inflammatory bowel disease. World J Gastroenterol. 2014, 20 (13): 3516-3524. 10.3748/wjg.v20.i13.3516.View ArticlePubMedPubMed CentralGoogle Scholar
  8. Liang R, Lau G, Kwong Y: Chemotherapy and bone marrow transplantation for cancer patients who are also chronic hepatitis B carriers: a review of the problem. J Clin Oncol. 1999, 17 (1): 394-398.PubMedGoogle Scholar
  9. Persico M, De Marino F, Di Giacomo Russo G, Morante A, Rotoli B, Torella R, De Renzo A: Efficacy of lamivudine to prevent hepatitis reactivation in hepatitis B virus-infected patients treated for non-Hodgkin lymphoma. Blood. 2002, 99 (2): 724-725. 10.1182/blood.V99.2.724.View ArticlePubMedGoogle Scholar
  10. Dervite I, Hober D, Morel P: Acute hepatitis B in a patient with antibodies to hepatitis B surface antigen who was receiving rituximab. N Engl J Med. 2001, 344 (1): 68-69. 10.1056/NEJM200101043440120.View ArticlePubMedGoogle Scholar
  11. Francisci D, Falcinelli F, Schiaroli E, Capponi M, Belfiori B, Flenghi L, Baldelli F: Management of hepatitis B virus reactivation in patients with hematological malignancies treated with chemotherapy. Infection. 2010, 38 (1): 58-61. 10.1007/s15010-009-9019-1.View ArticlePubMedGoogle Scholar
  12. Yağci M, Ozkurt Z, Yeğin Z, Aki Z, Sucak GT, Haznedar R: Hepatitus B virus reactivation in HBV-DNA negative and positive patients with hematological malignancies. Hematology. 2010, 15 (4): 240-244. 10.1179/102453309X12583347114059.View ArticlePubMedGoogle Scholar
  13. Sugauchi F, Tanaka Y, Kusumoto S, Matsuura K, Sugiyama M, Kurbanov F, Ueda R, Mizokami M: Virological and clinical characteristics on reactivation of occult hepatitis B in patients with hematological malignancy. J Med Virol. 2011, 83 (3): 412-418. 10.1002/jmv.21995.View ArticlePubMedGoogle Scholar
  14. Picardi M, Pane F, Quintarelli C, De Renzo A, Del Giudice A, De Divitiis B, Persico M, Ciancia R, Salvatore F, Rotoli B: Hepatitis B virus reactivation after fludarabine-based regimens for indolent non-Hodgkin’s lymphomas: high prevalence of acquired viral genomic mutations. J Haematol. 2003, 88 (11): 1296-1303.Google Scholar
  15. Huang Y, Lin H, Lee S: Management of chemotherapy-induced hepatitis B virus reactivation. J Chin Med Assoc. 2012, 75 (8): 359-362. 10.1016/j.jcma.2012.06.006.View ArticlePubMedGoogle Scholar
  16. Lee I, Huang Y, Chu C, Lee PC, Lin HC, Lee SD: Hepatitis B virus reactivation after 23 months of rituximab-based chemotherapy in an HBsAg-negative, anti-HBs-positive patient with follicular lymphoma. J Chin Med Assoc. 2010, 73 (3): 156-160. 10.1016/S1726-4901(10)70031-9.View ArticlePubMedGoogle Scholar
  17. Hui C, Cheung W, Zhang H, Au WY, Yueng YH, Leung AY, Leung N, Luk JM, Lie AK, Kwong YL, Liang R, Lau GK: Kinetics and risk of de novo hepatitis B infection in HBsAg-negative patients undergoing cytotoxic chemotherapy. Gastroenterology. 2006, 131 (1): 59-68. 10.1053/j.gastro.2006.04.015.View ArticlePubMedGoogle Scholar
  18. Wu J, Huang Y, Lee P, Lin HC, Lee SD: Fatal reactivation of hepatitis B virus in a patient who was hepatitis B surface antigen negative and core antibody positive before receiving chemotherapy for non-Hodgkin lymphoma. J Clin Gastroenterol. 2009, 43 (5): 496-498. 10.1097/MCG.0b013e3181945942.View ArticlePubMedGoogle Scholar
  19. Koskinas J, Tampaki M, Doumba PP, Rallis E: Hepatitis B virus reactivation during therapy with ustekinumab for psoriasis in a hepatitis B surface-antigen-negative anti-HBs-positive patient. Br J Dermatol. 2013, 168 (3): 679-680. 10.1111/bjd.12120.View ArticlePubMedGoogle Scholar
  20. Fotiadou C, Lazaridou E, Ioannides D: Safety of anti-tumour necrosis factor- agents in psoriasis patients who were chronic hepatitis B carriers: a retrospective report of seven patients and brief review of the literature. JEADV. 2011, 25 (4): 471-474.PubMedGoogle Scholar
  21. Marinos G, Naoumov NV, Rossol S, Torre F, Wong PY, Gallati H, Portmann B, Williams R: Tumor necrosis factor receptors in patients with chronic hepatitis B virus infection. Gastroenterology. 1995, 108 (5): 1453-1463. 10.1016/0016-5085(95)90694-0.View ArticlePubMedGoogle Scholar
  22. Cassano N, Mastrandrea V, Principi M, Loconsole F, De Tullio N, Di Leo A, Vena GA: Anti-tumor necrosis factor treatment in occult hepatitis B virus infection: a retrospective analysis of 62 patients with psoriatic disease. J Biol Regul Homeost Agents. 2011, 25 (2): 285-289.PubMedGoogle Scholar
  23. Prignano F, Ricceri F, Pescitelli L, Zanieri F, Lotti T: Tumour necrosis factor-a antagonists in patients with concurrent psoriasis and hepatitis B or hepatitis C: a retrospective analysis of 17 patients. Br J Dermatol. 2011, 164 (3): 645-647.PubMedGoogle Scholar
  24. Navarro R, Vilarrasa E, Herranz P, Puig L, Bordas X, Carrascosa JM, Taberner R, Ferrán M, García-Bustinduy M, Romero-Maté A, Pedragosa R, García-Diez A, Daudén E: Safety and effectiveness of ustekinumab and antitumour necrosis factor therapy in patients with psoriasis and chronic viral hepatitis B or C: a retrospective, multicentre study in a clinical setting. Br J Dermatol. 2013, 168 (3): 609-616. 10.1111/bjd.12045.View ArticlePubMedGoogle Scholar
  25. Chiu HY, Chen CH, Wu MS, Cheng YP, Tsai TF: The safety profile of ustekinumab in the treatment of psoriasis patients with concurrent hepatitis B or hepatitis C. Br J Dermatol. 2013, 169 (6): 1295-1303. 10.1111/bjd.12461.View ArticlePubMedGoogle Scholar
  26. Navarro R, Concha-Garzon MJ, Castano C, Casal C, Guiu A, Daudén E: Outcome of patients with serology suggestive of past hepatitis B virus infection during antitumor necrosis factor therapy for psoriasis. Intern J Dermatol. 2014, 65: 1241-1245.Google Scholar
  27. Costa L, Caso F, Atteno M, Giannitti C, Spadaro A, Ramonda R, Vezzù M, Del Puente A, Morisco F, Fiocco U, Galeazzi M, Punzi L, Scarpa R: Long-term safety of anti-TNF-α in PsA patients with concomitant HCV infection: a retrospective observational multicenter study on 15 patients. Clin Rheumatol. 2014, 33 (2): 273-276. 10.1007/s10067-013-2378-0.View ArticlePubMedGoogle Scholar
  28. Navarro R, Concha-Garzón MJ, Castaño C, Casal C, Guiu A, Daudén E. Outcome of patients with serology suggestive of past hepatitis B virus infection during antitumor necrosis factor therapy for psoriasis. Int J Dermatol. 2014 Feb 14. doi:10.1111/ijd.12313. [Epub ahead of print]Google Scholar
  29. European Association for the Study of the Liver: EASL clinical practice guidelines: management of chronic hepatitis B virus infection. J Hepatol. 2012, 57: 167-185.View ArticleGoogle Scholar
  30. European Association for the Study of the Liver: EASL clinical practice guidelines: management of hepatitis C virus infection. J Hepatol. 2014, 60 (2): 392-420. 10.1016/j.jhep.2013.11.003.View ArticleGoogle Scholar
  31. Masarone M, De Renzo A, La Mura V, Sasso FC, Romano M, Signoriello G, Rosato V, Perna F, Pane F, Persico M: Management of the HBV reactivation in isolated HBcAb positive patients affected with Non Hodgkin Lymphoma. BMC Gastroenterol. 2014, 14: 31-10.1186/1471-230X-14-31.View ArticlePubMedPubMed CentralGoogle Scholar
  32. Morisco F, Castiglione F, Rispo A, Stroffolini T, Sansone S, Vitale R, Guarino M, Biancone L, Caruso A, D'Inca R, Marmo R, Orlando A, Riegler G, Donnarumma L, Camera S, Zorzi F, Renna S, Bove V, Tontini G, Vecchi M, Caporaso N: Effect of immunosuppressive therapy on patients with inflammatory bowel diseases and hepatitis B or C virus infection. J Viral Hepat. 2013, 20 (3): 200-208. 10.1111/j.1365-2893.2012.01643.x.View ArticlePubMedGoogle Scholar
  33. Modesti V, Ramonda R, Ortolan A, Lorenzin M, Lo Nigro A, Frallonardo P, Oliviero F, Campana C, Punzi L: Infection relapse in spondyloarthritis treated with biological drugs: a single-centre study. Scand J Rheumatol. 2012, 41 (6): 490-491. 10.3109/03009742.2012.698393.View ArticlePubMedGoogle Scholar
  34. Núñez-Rodríguez MH, Santamaría-Martínez A, Mata-Román L, Caro-Patón A: Reactivation of hepatitis B treated with adefovir after infliximab administration. Med Clin (Barc). 2006, 126 (14): 558-559. 10.1157/13087150.View ArticleGoogle Scholar
  35. Pérez-Alvarez R, Díaz-Lagares C, García-Hernández F, Lopez-Roses L, Brito-Zerón P, Pérez-de-Lis M, Retamozo S, Bové A, Bosch X, Sanchez-Tapias JM, Forns X, Ramos-Casals M, BIOGEAS Study Group: Hepatitis B virus (HBV) reactivation in patients receiving tumor necrosis factor (TNF)-targeted therapy: analysis of 257 cases. Medicine (Baltimore). 2011, 90 (6): 359-371. 10.1097/MD.0b013e3182380a76.View ArticleGoogle Scholar
  36. Dernis E, Lavie F, Salliot C, Flipo RM, Saraux A, Maillefert JF, Paul C, Goupille P, Cantagrel A, Claudepierre P, Gaudin P, Tebib J, Wendling D, Schaeverbeke T, Le Loët X, Combe B: Pharmacological treatment (biotherapy excluded) of peripheral psoriatic arthritis: development of recommendations for clinical practice based on data from the literature and experts opinion. Joint Bone Spine. 2009, 76 (5): 524-531. 10.1016/j.jbspin.2009.03.002.View ArticlePubMedGoogle Scholar
  37. Smith CH, Anstey AV, Barker JN, Burden AD, Chalmers RJ, Chandler D, Finlay AY, Griffiths CE, Jackson K, McHugh NJ, McKenna KE, Reynolds NJ, Ormerod AD, British Association of Dermatologists: British association of dermatologists guidelines for use of biological interventions in psoriasis 2005. Br J Dermatol. 2005, 153 (3): 486-497. 10.1111/j.1365-2133.2005.06893.x.View ArticlePubMedGoogle Scholar
  38. Ohtsuki M, Terui T, Ozawa A, Morita A, Sano S, Takahashi H, Komine M, Etoh T, Igarashi A, Torii H, Asahina A, Nemoto O, Nakagawa H, Biologics Review Committee of the Japanese Dermatological Association: Japanese guidance for use of biologics for psoriasis (the 2013 version). J Dermatol. 2013, 40 (9): 683-695. 10.1111/1346-8138.12239.View ArticlePubMedGoogle Scholar

Copyright

© Morisco et al.; licensee BioMed Central. 2014

This article is published under license to BioMed Central Ltd. This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly credited. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.

Advertisement

BMC Gastroenterology

ISSN: 1471-230X

Contact us