Skip to main content
Anais Brasileiros de Dermatologia logoLink to Anais Brasileiros de Dermatologia
. 2014 May-Jun;89(3):423–426. doi: 10.1590/abd1806-4841.20142566

Hepatitis C and hepatitis B virus infections in the etiopathogenesis of pemphigus*

Gulsen Tukenmez Demirci 1,, Ikbal Esen Aydingoz 2, Ayse Tulin Mansur 3, Guldehan Atis 4, Ilknur Kivanc Altunay 5
PMCID: PMC4056699  PMID: 24937815

Abstract

BACKGROUND

Previous studies have shown that some viral infections may be triggers for autoimmune diseases. The role of viral infections in the etiopathogenesis of pemphigus has also been investigated.

OBJECTIVES

To investigate the relationship between pemphigus and the hepatitis B and C virus infections.

METHODS

This retrospective study included 62 patients with pemphigus and 50 healthy controls of matching ages and genders. The control group included relatives who accompanied the orthopedic patients to the hospital but had no history of systemic and/or autoimmune diseases.

RESULTS

The group of patients with pemphigus was composed of 43 (69.3%) females and 19 (29.7%) males, and the mean age was 48.08 ± 15.38. The hepatitis C virus antibody was negative in all of the patients. Hepatitis B surface antigen (HBsAg), hepatitis B surface antibody (HBsAb), or both, were studied in 44 of the 62 patients. Two (4.3%) of these patients were positive for HBsAg and found to have HBV infection. Fourteen of them were HBsAb positive. Two (4%) of the 50 control subjects showed hepatitis C virus antibody positivity, while only 1 (2%) patient with pemphigus displayed HBsAg positivity. There was no statistically significant difference between the two groups for hepatitis B and C virus infections.

CONCLUSIONS

This study does not support an association between pemphigus and hepatitis B and/or C virus infections.

Keywords: Hepatitis B vírus, Hepatitis antibodies, Pemphigus

INTRODUCTION

Pemphigus is a rare autoimmune disease of the skin and mucous membranes. Previous studies have shown that some viral infections may be triggers for autoimmune diseases in patients with genetic susceptibility to them.1 The role of viral infections in the etiopathogenesis of pemphigus has also been investigated.2 The role of HCV in the etiopathogenesis of secondary anti-phospholipid syndrome, Sjögren syndrome, autoimmune trombocytic purpura and cryoglobulinemia, have been reported.3,4 Similarly, the mechanisms involved in HBV infection have been proposed as a trigger in some autoimmune diseases such as diabetes mellitus type 1, polyarteritis nodosa and vitiligo.5,6,7 However, there are few studies that evaluate the relationship between pemphigus and HCV and HBV infections.8-11 The purpose of this study is to investigate the frequency of HCV and HBV infections in our patients who had recently been diagnosed with pemphigus.

MATERIALS AND METHODS

Sixty-two patients with a new diagnosis of pemphigus were included in this retrospective study. In addition to clinical and histopathological findings, diagnosis of pemphigus had been confirmed through direct immunofluorescent microscopy. The control group was composed of 50 subjects of matching ages and genders, gathered from among the relatives of the orthopedic patients. The controls all had a negative history for systemic and/or autoimmune diseases and had provided verbal informed consent for the study. In our departments, all patients with pemphigus are screened for HBsAg, HBsAb and anti-HCV, using ELISA, before starting appropriate immunosuppressive therapy, since this treatment can exacerbate viral infections such as HBV and HCV infections. The control group was set up after the decision had been taken to conduct a retrospective study. This group was informed about viral hepatitis and the vaccination for HBV, and those who were found to be eligible for the study were included. The study used their patient records or face-to face interviews to obtain their ages, genders, serologic test results, family history of HBV and HCV occurrences and the risk factors for HBV and HCV infections, such as blood transfusion, hemodialysis, past operations, transplantation, ear piercing, dental surgery and similar trauma histories. The serological test results of pemphigus patients were acquired from the database of our patients' records.

Statistical Analysis:

SPSS Statistics 17.0 for Windows was used for statistical analysis. The distribution of the data was tested using Kolmogrov-Smirnov and Anova tests. The independent test was used for the analysis of the data; p<0.05 was considered to be significant.

RESULTS

The study group involved 62 pemphigus patients, including 43 women and 19 men (age range: 10-78 years, mean 48.08 ± 15.38) and 50 controls with 35 women and 15 men (age range 18-82 years, mean 48.56 ± 15.50). Of the 62 pemphigus patients, 57 (92%) had pemphigus vulgaris, 2 (3.2%) had pemphigus foliaceus, 2 (3.2%) had pemphigus vegetans and 1 (1.6%) had pemphigus erythematosus.

Anti-HCV Ab was negative in all of the pemphigus patients. Among this group, only one had a family member with HCV infection. In the control group, anti-HCV test results were found to be positive in 2 (4%) individuals who were also positive for HCV-RNA, confirming HCV infection. We did not find a statistically significant difference between the two groups for HCV infection (p=0.114) (Table 1). In the assessment of risk factors, only one of the HCV-positive controls declared a past surgery, but that had been more than three months before and was not interpreted as a risk factor.

TABLE 1.

The comparison of HBsAg, Anti HBsAg and Anti-HCV test results and the existence of risk factors for hepatitis virus infections between the pemphigus group and the control group

    Pemphigus patients n % Control group n % P
Anti-HCV   Positive: 0 0 Positive: 2 4 0.114
    Negative: 62 100 Negative: 48 96  
HBsAg   Positive: 2 4.56 Positive: 1 2 0.526
    Negative: 42 95.44 Negative: 49 98  
AntiHBsAg   Positive: 14 31.8 Positive: 14 28 0.848
    Negative: 30 68.2 Negative: 36 72  
Risk Factors Abnormality in hepatic function tests Yes: 2 3.2 Yes: 3 6 0.932
    No: 60 96.8 No: 47 94  
  Hepatitis B and/ or C virus infection in family members Yes: 1 1.6 Yes: 0 0 0.159
    No: 61 98.4 No: 50 100  
  Past operation (operations done under local or general anesthesia) Yes: 14 22.6 Yes: 10 20 0.960
    No: 48 77.4 No: 40 80  
  Ear piercing Yes: 11 17,75 Yes: 13 26 0.294
    No: 51 82,25 No: 37 76  
  Blood transfusion Yes: 2 3.2 Yes: 1 2 0,381
    No: 60 96.8 No: 49 98  
  Hemodialysis Yes: 0 0 Yes: 0 0 1
    No: 62 100 No: 50 100  
  Transplantation Yes: 0 0 Yes: 0 0 1
    No: 62 100 No: 50 100  
  Blood transfusion or past operation in the last 3 months Yes: 0 0 Yes: 0 0 1
    No: 62 100 No: 50 100  

We could only evaluate HBV screening in 44 of the 62 pemphigus patients because of temporary technical problems. Fourteen (31.8%) of the patients were HBsAb positive and 2 (4.3%) were HBsAg positive, denoting HBV infection. We did not find any of the risk factors in the two pemphigus patients with Hepatitis B infection (Table 2). In the control group, 14 (28%) individuals were HBsAb positive and 1 (2%) was HBsAg positive. There were no statistically significant differences between the two groups for HBsAb and HBsAg positivity (p=0.848, p=0.526, respectively) (See Table 1). We did not encounter any of the risk factors in the patients and controls with positive serology for HBV.

TABLE 2.

There were no risk factors in the two pemphigus patients with Hepatitis B infection

    Patient 1 Patient 2
Risk factors Hepatitis B infection in family members Absent Absent
  Past operation (operations done under local or general anesthesia) Absent Absent
  Ear piercing Absent Absent
  Blood transfusion Absent Absent
  Hemodialysis Absent Absent
  Transplantation Absent Absent
  Blood transfusion or past operation in the last 3 months Absent Absent

DISCUSSION

Pemphigus is an autoimmune disease characterized by painful oral mucosa erosions and fragile bullous skin lesions. The IgG-type antibodies targeting the keratinocytic antigens, desmoglein 1 and desmoglein 3, play a major role in the etiopathogenesis of the disease, by inducing acantholysis.12

Although there is some conflicting evidence, the hypothesis that some infections trigger autoimmune disease in genetically predisposed individuals is still up to date. The association of cryoblobulinemia and Sjögren syndrome with chronic HCV infections is well-known. Furthermore, the antinuclear, anti-smooth muscle, anticardiolipin and antithyroid antibody positivity accompanying these infections, support this view.4

The exact pathogenetic mechanism involved in HCV and autoimmunity is not known. However, this microorganism has been incriminated in the elimination of tolerance that is protected from autoimmunity.13 In addition, the activation of B lymphocytes resulting from HCV residence on these cells has been seen as responsible for autoimmunity.14

Some studies have investigated the association of HCV with autoimmune diseases. Agmon-Levin et al. found that the frequency of HCV infection in 1,322 patients with various autoimmune diseases was significantly higher (8.7%), compared with the control group (%0.4). In this study, the prevalence of HCV was found to be 14% among the pemphigus vulgaris patients, and the authors emphasized a new association between HCV and pemphigus.8 The prevalence of HBV infection in anti-HCV-positive pemphigus foliaceus patients was also found to be considerable.10 Sagi et al. found that the frequency of HBV, HCV, H. pylori, T. gondii, T. pallidum and CMV was significantly higher than in the control group in pemphigus and bullous pemphigoid patients.9 In accordance with these results, a pemphigus case has been reported after a hepatitis B vaccination.11 However, there are also opposing results: Rosa et al. did not find any association between HCV infection and pemphigus in 126 patients with fogo selvage, in their study group.10 In terms of our findings, although the prevalence of HCV infection was 4% in the control group, none of our 62 pemphigus patients had HCV infection. Nevertheless, the prevalence of HBV infection in our pemphigus patients was 4.3%, while it was 2 % in the control group. There was no statistically significant difference between the two groups for HBV and HCV infections. According to the surveys, 1% of the Turkish population has been found to be infected by HCV, and 2.7% by HBV. 15 The results are also slightly different from the general population. We believe that the results obtained may have been caused by the small numbers in our study groups. If the number of patients and controls were higher, the prevalence of these viral infections would probably be closer to the prevalence within the general population.

CONCLUSION

The controversy surrounding the role of viral infections in the etiopathogenesis of autoimmune diseases still exists today. However, the findings of our study do not support any association between pemphigus and HBV and/or HCV infections.

Footnotes

Conflict of interest: None

Financial funding: None

How to cite this article: Demirci GT, Aydingoz IE, Mansur AT, Atis G, Altunay IK. Hepatitis C and hepatitis B virus infections in the etiopathogenesis of pemphigus. An Bras Dermatol. 2014;89(3):423-6.

*

Work performed at the Sisli Etfal Egitim ve Arastırma Hastanesi, Haydarpasa Numune Egitim ve Arastırma Hastanesi - İstanbul, Turkey.

REFERENCES

  • 1.Miller SD, Katz-Levy Y, Neville KL, Vanderlugt CL. Virus-induced autoimmunity: epitope spreading to myelin autoepitopes in Theiler's virus infection of the central nervous system. Adv Virus Res. 2001;56:199–217. doi: 10.1016/s0065-3527(01)56008-x. [DOI] [PubMed] [Google Scholar]
  • 2.Sagi L, Sherer Y, Trau H, Shoenfeld Y. Pemphigus and infectious agentes. Autoimmun Rev. 2008;8:33–35. doi: 10.1016/j.autrev.2008.07.021. [DOI] [PubMed] [Google Scholar]
  • 3.Harada M, Fujisawa Y, Sakisaka S, Kawaguchi T, Taniguchi E, Sakamoto M, et al. High prevalence of anticardiolipin antibodies in hepatitis C virus infection: lack of effects on thrombocytopenia and thrombotic complications. J Gastroenterol. 2000;35:272–277. doi: 10.1007/s005350050345. [DOI] [PubMed] [Google Scholar]
  • 4.Jadali Z, Alavian SM. Autoimmune Diseases Co-Existing with Hepatitis C Virus Infection. Iran J Allergy Asthma Immunol. 2010;9:191–206. [PubMed] [Google Scholar]
  • 5.Halota W, Muszynska M, Pawlowska M. Hepatitis B virus serologic markers and anti-hepatitis B vaccination in patients with diabetes. Med Sci Monit. 2002;8:CR516–CR519. [PubMed] [Google Scholar]
  • 6.Guillevin L, Mahr A, Callard P, Godmer P, Pagnoux C, Leray E, et al. Hepatitis B virus-associated polyarteritis nodosa: clinical characteristics, outcome, and impact of treatment in 115 patients. Medicine (Baltimore) 2005;84:313–322. doi: 10.1097/01.md.0000180792.80212.5e. [DOI] [PubMed] [Google Scholar]
  • 7.Soylu S, Gül U, Gönül M, Kiliç A, Cakmak SK, Demiriz M. An uncommon presentation of the co-existence of morphea and vitiligo in a patient with chronic hepatitis B virus infection: is there a possible association with autoimmunity? Am J Clin Dermatol. 2009;10:336–338. doi: 10.2165/11310800-000000000-00000. [DOI] [PubMed] [Google Scholar]
  • 8.Agmon-Levin N, Ram M, Barzilai O, Porat-Katz BS, Parikman R, Selmi C, et al. Prevalence of hepatitis C serum antibody in autoimmune diseases. J Autoimmun. 2009;32:261–266. doi: 10.1016/j.jaut.2009.02.017. [DOI] [PubMed] [Google Scholar]
  • 9.Sagi L, Baum S, Agmon-Levin N, Sherer Y, Katz BS, Barzilai O, et al. Autoimmune bullous diseases the spectrum of infectious agent antibodies and review of the literature. Autoimmun Rev. 2011;10:527–535. doi: 10.1016/j.autrev.2011.04.003. [DOI] [PubMed] [Google Scholar]
  • 10.Rosa H, Martins R, Vanderborght B. Hepatitis C virus investigation in pemfigus foliaceus (fogo selvagem) patients. Arq Gastroenterol. 2000;37:42–43. doi: 10.1590/s0004-28032000000100009. [DOI] [PubMed] [Google Scholar]
  • 11.Berkun Y, Mimouni D, Shoenfeld Y. Pemphigus following hepatitis B vaccination-coincidence or causality? Autoimmunity. 2005;38:117–119. doi: 10.1080/08916930400027078. [DOI] [PubMed] [Google Scholar]
  • 12.Karıncaoğlu Y. Pemfigus: epidemiyoloji ve patogenez. Türkderm. 2008;42:1–4. [Google Scholar]
  • 13.Bach JF. Infections and autoimmune diseases. J Autoimmun. 2005;25:74–80. doi: 10.1016/j.jaut.2005.09.024. [DOI] [PubMed] [Google Scholar]
  • 14.Soylu S, Gül Ü, Kiliç A. Cutaneous manifestations in patients positive for anti-hepatitis C virus antibodies. Acta Derm Venereol. 2007;87:49–53. doi: 10.2340/00015555-0186. [DOI] [PubMed] [Google Scholar]
  • 15.Tozun N, Ozdogan OC, Cakaloglu Y, Idilman R, Karasu Z, Akarca US, et al. A nationwide prevalence study and risk factors for hepatitis A, B, C and D infections in Turkey. Hepatology. 2010;52:697A. [Google Scholar]

Articles from Anais Brasileiros de Dermatologia are provided here courtesy of Sociedade Brasileira de Dermatologia

RESOURCES