December 29, 2013

Immunological alterations in hepatitis C virus infection

World J Gastroenterol 2013 December 21; 19(47): 8916-8923

Copyright ©2013 Baishideng Publishing Group Co., Limited. All rights reserved.

Vincenza Calvaruso, Antonio Craxì, Gastroenterologia and Epatologia, DIBIMIS, Università di Palermo, 90127 Palermo, Italy

Author contributions: Both authors contributed equally to this paper.

Correspondence to: Vincenza Calvaruso, MD, PhD, Gastroenterologia and Epatologia, DIBIMIS, Università di Palermo, Piazza delle Cliniche n.2, 90127 Palermo, Italy. vincenza.calvaruso@unipa.it

Telephone: +39-91-6552280 Fax: +39-91-6552156

Received July 31, 2013; Revised October 23, 2013; Accepted November 12, 2013;

Abstract

A higher prevalence of immunological processes has recently been reported in patients with hepatitis C virus (HCV) infection, focusing the attention of physicians and researchers on the close association between HCV and immune disorders. HCV lymphotropism represents the most important step in the pathogenesis of virus-related immunological diseases and experimental, virologic, and clinical evidence has demonstrated a trigger role for HCV both in systemic autoimmune diseases, such as rheumatoid arthritis, Sjögren syndrome, hemolytic anemia and severe thrombocytopenia, and in organ-specific autoimmune diseases, such as autoimmune hepatitis, thyroid disorders and diabetes. This review will outline the principal aspects of such HCV-induced immunological alterations, focusing on the prevalence of these less characterized HCV extrahepatic manifestations.

Keywords: Hepatitis C virus, Immune disorders, Cytopenia, Extrahepatic manifestation, Autoantibody

Core tip: Hepatitis C virus (HCV)-infected lymphoid tissue of the host represents a site for the persistence of HCV infection which exerts a chronic stimulus to the immune system, facilitating clonal B-lymphocyte expansion and consequent wide autoantibody production, including cryo- and non-cryo-precipitable immune complexes which may lead to organ- and non-organ-specific immunological alterations. This review outlines the principal aspects of such HCV-induced immunological alterations, focusing on the prevalence of these less characterized HCV extrahepatic manifestations.

INTRODUCTION

Autoimmunity and viral infections are closely related, and the hepatitis C virus (HCV), is recognized as one of the viruses most often associated with autoimmune features. For this reason HCV is not only associated with chronic hepatic inflammation but also an array of extrahepatic complications. In the majority of these associated extrahepatic manifestations, the pathogenic mechanism appears to be immunologically driven, with many having features of autoimmunity. HCV infection has been associated with both organ-specific [thyroiditis, diabetes, autoimmune hepatitis (AIH)] and systemic autoimmune diseases and this association has generated growing interest in recent years since it is often observed in patients with chronic HCV infection.

PATHOGENESIS OF HCV RELATED IMMUNE DISORDERS

HCV lymphotropism represents the most relevant step in the pathogenesis of virus-related immunological disorders[1]. Indeed, infected lymphoid tissue of the host represents a site for the persistence of the HCV infection[2-6]. HCV exerts a chronic stimulus to the immune system, facilitating the clonal B-lymphocyte expansion and consequent wide autoantibody production, including cryo- and non-cryoprecipitable immune complexes[3,7-9] which may lead to organ- and non-organ-specific immunological alterations[3,7,8,10]. The first step is translocation, demonstrated in a high percentage of HCV-infected patients, with consequent Bcl-2 proto-oncogene activation, antiapoptotic activity and prolonged survival of lymphocytes[3,7,9,10]. Besides, the identification of HCV envelope protein E2 able to bind the CD81 molecule expressed on both hepatocytes and B-lymphocytes seems to be crucial for HCV-driven autoimmunity[3,7,9,10].

Dysregulation of cytokine networks skewing regulatory T-cells to a Th2 phenotype, which may be associated with enhanced humoral immune responses and autoantibody production has also been related to the expansion of autoantibody-producing B-cells and chronic lymphoproliferation in HCV infection[11]. HCV infections induce a massive chemokine and cytokine burst and therefore recruit leukocytes to the site of infection with the goal to stop viral spread. This excitation of the human defense system could stimulate a potentially self-reactive lymphocytes inducing autoimmunity in susceptible individuals[11].

Many studies have linked Th1 immune response with HCV infection[12], mixed cryoglobulinemia (MC)[13] and organ specific autoimmune disorders[14]. These findings suggest that a possible common immunological Th1 pattern could be the pathophysiological base of the association of autoimmunity related HCV infections.

Several studies have shown an increased expression of interferon-gamma (IFN-γ), and IFN-γ inducible chemokines (C-X-C motif chemokine 10 - CXCL10), in hepatocytes and in lymphocytes of HCV-infected patients[12,15,16], which are directly related to the degree of inflammation and an increase in circulating levels of IFN-γ and CXCL10[17,18].

Furthermore, it has been shown that NS5A and core proteins, alone or by a synergistic effect with Th1 cytokines [IFN-γ and tumor necrosis factor-α (TNF-α)], are capable of upregulating CXCL10 and monokine induced by gamma interferon (MIG) gene expression and secretion in cultured human hepatocyte derived cells. These data suggest that CXCL10 produced by HCV-infected hepatocytes could play a key role regulating T-cell trafficking into a Th1-type inflammatory site by recruiting Th1 lymphocytes, that secrete IFN-γ and TNF-α, with a synergistic effect on CXCL10 secretion by hepatocytes, thus perpetuating the immune cascade[19].

HCV AND SYSTEMIC AUTOIMMUNE DISEASES

Mixed cryoglobulinemia

MC is the most well documented extrahepatic manifestation of HCV infection[2,20]. MC, which is defined by documenting cryoprecipitates in serum (Ig precipitates from serum at temperatures under 37 °C and dissolves upon re-warming), is characterized by the presence of circulating immunocomplexes produced by a benign proliferation of B-cells. MC represents the link between HCV and various autoimmune and lymphoproliferative disorders. Although serum cryoglobulins (CGs) are frequently present in patients with chronic HCV[3-5,21,22], in many of them CGs are present at low levels and symptoms are often absent or very mild. Only about 5% of HCV-infected subjects have clinically overt MC syndrome.

HCV-related arthritis

Chronic oligo-polyarthritis during chronic HCV infection is often associated with MC but can also represent an independent entity. Indeed, it is not rare to observe a simple association between HCV infection and classical rheumatoid arthritis (RA) that can co-exist by chance or can be related to the ability of HCV to act as a trigger of the immune disease in individuals genetically predisposed to RA.

A polyarthritis, which is often non-erosive and rarely progressive, and involves small joints is the most common kind of arthritis associated with HCV chronic infection without the coexistence of cryoglobulinemia. Instead, 40%-80% of HCV-infected patients with MC[23] are reported to have a bilateral and symmetric arthralgia, which is non-deforming and includes mainly the knees and hands, and, more seldom, the elbows and ankles. Rheumatoid factor (RF) activity is found in 70%-80% of MC patients but is not correlated with the presence of articular disease, as patients chronically infected with HCV in the absence of HCV-MC or RF may have prominent articular symptoms. Usually there is no evidence of joint destruction, and antibodies to cyclic citrullinated peptide, which are highly specific to rheumatoid arthritis, are absent[24]. These evidences suggest that HCV infection should be considered in the differential diagnosis of patients with atypical arthritis.

Sjögren syndrome

Another autoimmune condition associated with HCV is a chronic lymphocytic sialoadenitis similar to sialoadenitis associated with idiopathic Sjögren syndrome (SS), which has been reported in approximately 50% of patients with HCV infection[25].

Some authors have distinguished the HCV-related sicca syndrome from Sjogren’s syndrome based on several differences, including absence of anti-SSA and anti-SSB antibodies, pericapillary and non pericanalary lymphocytic infiltration, lack of glandular canal damage, high prevalence of mixed cryoglobulinemia (50%), hypocomplementemia (51%), and systemic vasculitic manifestations (58%)[25-28]. Moreover, the lymphocytic type of the infiltrate in the minor salivary gland shows a predominance of CD8 lymphocytes which is not observed in primary SS[29]. Although the possible etiopathogenetic role of HCV in SS remains a controversial issue[27], the explanation for this extrahepatic manifestation could be a cross reactivity between the HCV envelope and host salivary tissue which lead to an immune reaction directed against salivary glands[26]. The correct classification of patients with sialoadenitis related to HCV chronic infection have important clinical, prognostic and therapeutic implications since it may evolve into a B cell malignant lymphoma, especially in the presence of MC[10,30].

HCV related cardiac disorders

Several observations suggest that HCV infection is an important cause of a variety of otherwise unexplained heart diseases. Indeed, it was reported that (+) or (-) chain HCV-RNAs can be detected in the biopsied myocardial tissue or in the autopsied heart suggesting that HCV might proliferate in the myocardium[31], resulting in induction of cardiomyopathy. Frustaci et al[32] have shown that HCV replicates in myocardial tissue of patients with myocarditis, and that HCV infection may contribute to the development of an autoimmune myocarditis, frequently associated with myocardial antibodies and responsive to immunosuppressive therapy. In 2000, Matsumori suggested that some specific HCV clones with high affinity for the heart can develop and cause cardiomyopathy[33] and in 2006, in a large study involving more than 1000 patients, the same group identified anti-HCV antibodies, HCV RNA, NT-proBNP, and cardiac troponin I and T in sera stored for up to 17 years, and found the anti-HCV antibodies were more prevalent in patients with myocarditis than in the general US population[34]. These results suggest that in regions where its prevalence is high, HCV infection may be an important cause of myocarditis and heart failure. Moreover, the same authors concluded that NT-proBNP is a more sensitive marker of myocardial injury than cardiac troponins in patients with heart failure from HCV myocarditis. More recently, other studies confirmed that NT-proBNP is a sensitive biomarker for identifying patients with heart failure caused by HCV-related myocarditis[35,36]. Antonelli et al[36] assessed serum NTproBNP in 50 HCV-positive patients and in 50 sex- and age-matched controls. HCV patients showed significantly higher mean NT-proBNP level than controls[35]. This result was confirmed by the same group in another study where TNF-α was also found to be higher in HCV+ patients with respect to controls, suggesting the presence of subclinical cardiac dysfunction[36].

AUTOIMMUNE CYTOPENIAS IN PATIENT WITH HCV INFECTION

Hemolytic anemia and severe thrombocytopenia were the most frequent cytopenias observed in patients with HCV infection. The different types of immune-mediated cytopenias may be severe and clinically significant.

Hemolytic anemia

Although autoimmune hemolytic anemia (AHA) has frequently been reported in association with HCV in the setting of interferon (IFN) treatment[37,38], it has also been observed as an isolated extrahepatic manifestation. The existence of AHA in patients with chronic hepatitis was first described in 1951, when Hyman et al[39] described AHA in 3 patients with chronic liver involvement. In 1973, Panush et al[40] described a patient with chronic active hepatitis who presented with AHA with a positive Coombs test, who responded to treatment with steroids. In 1982, Portell et al[41] reported 5 patients with chronic hepatopathy (3 with active chronic hepatitis and 2 with cirrhosis) and a positive Coombs AHA, with positive ANA in 4 and sicca syndrome in 1. In 2001, 2 cases of HCV infection associated with Coombs-positive AHA, in the absence of treatment with IFN, were reported by Srinivasan[42] and Chao et al[43], respectively. In 2003, Ramos-Casals et al[44] presented the largest series of cases of HCV-related AHA not treated with antiviral therapy. Seventeen HCV patients, mostly women with a mean age of 56 years, presented a high level of association with autoimmune diseases, with cryoglobulinemia as the most frequent immunologic marker. Most patients had a history of liver cirrhosis and even if they had a good response to corticosteroids, the prognosis was poor (56% mortality).

HCV-associated immune thrombocytopenic purpura

Although thrombocytopenia during the course of chronic liver disease is usually attributed to hypersplenism, an autoimmune mechanism has been suggested as playing a role in some patients with HCV infection. This hypothesis is based on the observation of a greater prevalence of thrombocytopenia and antiplatelet antibodies in HCV patients compared with HBV patients[45], and of the frequency of HCV infection seen among patients initially diagnosed with idiopathic thrombocytopenic purpura (ITP)[46-48]. The pathophysiology of infection-related ITP involves diverse immunologic pathways as well as nonimmune mechanisms that accelerate platelet destruction and/or decrease platelet production.

High affinity binding of HCV to the platelet membrane with subsequent binding of anti-HCV antibody might lead to phagocytosis of platelets[49]. Dysregulation of the host immune system triggering the production of autoantibodies against platelet glycoproteins has also been postulated[45,50]. However there have been conflicting data on the presence of specific antibodies in platelets in patients with HCV-related ITP[45,50-52].

Thrombocytopenia in HCV patients may be present even in the absence of clinically evident liver disease or splenomegaly and may be mistakenly diagnosed as primary chronic immune thrombocytopenic purpura (CITP)[48,53]. Six cross-sectional studies have reported serologic evidence of HCV infection in 20% of patients with a clinical diagnosis of CITP[48,53-57], and in the largest series published to date, HCV antibodies were identified in 30% of 250 patients fulfilling the American Society of Hematology criteria for CITP[54]. There were significant differences in the demographic characteristics of patients with HCV-positive compared with patients with HCV-negative CITP. Patients positive for HCV were older and the incidence was distributed equally between the sexes compared with the female predominance in HCV-negative CITP.

ORGAN-SPECIFIC AUTOIMMUNE DISEASES

Thyroid disorders and HCV

Autoimmune thyroid involvement and hypothyroidism were significantly more frequent in patients with chronic hepatitis C (CHC) than in comparison groups such as patients with viral hepatitis B or D[58-60] or normal subjects[61,62]. The most frequent thyroid disorder in this setting is the presence of circulating anti-thyroid antibodies which is more commonly reported in female subjects[58]. The prevalence of abnormally high levels of anti-thyroid antibodies observed in these patients ranges from 2% to 48%[58,61,63,64], with heterogeneous geographic distribution[65]. These discrepancies are related to variable genetic predisposition and environmental co-factors, such as iodine intake or other infectious agents[66]. The evidence of a subclinical hypothyroidism was observed in 2%-9% of patients with chronic HCV infection, particularly in those patients with MC[59,60,62,63,67], and these patients seem to be susceptible to Hashimoto’s autoimmune thyroiditis and Grave’s disease when treated with interferon.

Antonelli et al[21] in 2004 analyzed 630 consecutive patients affected by CHC compared with a large control group of subjects from iodine-deficient and sufficient areas and with 86 patients with chronic hepatitis B. They demonstrated that patients with CHC were more likely to have hypothyroidism, anti-thyroglobulin and anti-thyroid peroxidase antibodies than any of the other groups. The same group evaluated thyroid function, the presence of thyroid autoantibodies, thyroid nodules and thyroid cancer, in 93 HCV + MC consecutive patients matched by sex and age to 93 patients with CHC without MC and 93 healthy (HCV-negative) controls. Subclinical hypothyroidism and thyroid autoimmunity were significantly more frequent in HCV + MC patients than in HCV-negative controls. Moreover, serum thyroid peroxidase antibodies were also significantly more frequent in HCV + MC patients than in CHC patients. Finally, the prevalence of thyroid nodules was not significantly different in the three groups[68]. In conclusion, pooling all data about HCV-positive patients (with CHC or HCVAb positivity) and using as control healthy subjects and HBV-infected patients, there was a significant increase in the prevalence of both thyroid autoimmune disorders (OR = 1.6; 95%CI: 1.4-1.9) and hypothyroidism (OR = 2.9; 95%CI: 2.0-4.1)[69].

Some authors have reported that patients with chronic HCV have a higher prevalence of papillary thyroid carcinoma[70,71]. In 2002, the prevalence of thyroid cancer in a series of 94 HCV-related mixed cryoglobulinemic patients was investigated[70]. A control group was obtained from a sample of the general population (2401 subjects) who had undergone thyroid ultrasonography. The prevalence of thyroid nodules was higher, although not significantly so, in control subjects than in MC patients but 2 patients with papillary thyroid cancer were found in the MC series, while no case was observed among controls.

A more recent study[71] prospectively investigated the prevalence and features of thyroid cancer in 308 patients with CHC in comparison with 2 large sex- and age-matched control groups from the general population with different iodine intake. Thyroid status was assessed by measurement of circulating thyroid hormones and autoantibodies, thyroid ultrasonography, and, when indicated, fine-needle aspiration cytology. The authors have found that circulating thyrotropin, anti-thyroglobulin, and anti-thyroperoxidase antibodies levels, and the prevalence of hypothyroidism were significantly higher in HCV patients and 6 cases of papillary thyroid cancer were detected among HCV patients, whereas only 1 case was observed in controls, suggesting a high prevalence of thyroid papillary cancer in HCV patients. Because of this high prevalence of thyroid disorders, the guidelines on management of CHC recommend investigation of thyroid function, including free T4 and TSH in all patients, and since interferon-based therapy could exacerbate thyroid dysfunction, thyroid function tests should be fully evaluated prior to initiating HCV treatment.

Diabetes mellitus and HCV

Data from the literature have shown a higher incidence of type 2 diabetes mellitus with chronic HCV when compared with patients with other liver disorders[72-74]. In a large study[75] involving 229 consecutively recruited MC-HCV patients compared with 217 sex- and age-matched controls without HCV infection, the prevalence of type 2 diabetes was significantly higher in MC-HCV patients than in controls. Moreover, MC-HCV diabetic patients more often had non-organ-specific autoantibodies than non-diabetic MC-HCV patients.

Another study conducted in 2005 by the same group[22], established the prevalence and clinical phenotype of type 2 diabetes in a large series of non-cirrhotic HCV patients. The prevalence of type 2 diabetes was significantly higher in HCV patients compared with control subjects or non-cirrhotic HBV patients. Moreover, type 2 diabetic HCV patients had a significantly lower BMI than type 2 diabetic control subjects and significantly higher BMI than non-diabetic HCV patients. In contrast, no association with diabetes mellitus type 1 has been identified[22,72,73,76-78]. The association between chronic HCV and diabetes mellitus seems to be independent of the severity of the liver disease and is associated with insulin-resistance, but not with the presence of pancreatic anti-insulin antibodies[79]. In contrast, interferon treatment of HCV has been associated with the appearance of diabetes mellitus type 1 and development of anti-pancreas autoimmunity[80-82].

AIH and HCV infection

Finally, an intriguing, still controversial aspect is the possible etiopathogenetic role of HCV in AIH[3,6,8,9,65]. Patients with AIH may present with mixed cryoglobulins, HCV infection, and extrahepatic manifestations such as thyroiditis, sicca syndrome, and arthritis[6], while patients with HCV infection show one or more non-organ-specific auto-antibodies. The antigenic target specificity of HCV-related autoantibodies shows only quantitative differences compared with those associated with “primary” AIH[8].

In clinical practice, the search for serum autoantibodies should be limited to cases for whom treatment with IFN is planned. An exception may be cases where clinical data (female gender, young age), high biochemical activity (transaminase-globulins) and histological aspects (interfaces hepatitis) of liver disease may suggest the presence of AIH with superimposed HCV infection.

The heterogeneous geographical distribution of HCV-associated AIH[65] suggests a possible involvement of various pathogenetic co-factors; among these, HCV might trigger a particular AIH clinico-serological subset, which is prevalent in specific geographical areas.

CONCLUSION

In the case of patients with chronic HCV infection, the possible existence of extrahepatic manifestations should be taken into account and an accurate analysis of clinical and anamnestic data is recommended. Some patients may display the entire complex spectrum of HCV-related disorders which could be mild for many years and progress, generally during a long follow-up, to more severe systemic manifestations. In the last few years, very consistent data have been accumulated through different in vivo and in vitro models, suggesting that a more accurate characterization of the modalities and consequences at the molecular level of HCV infection of lymphatic cells may be of great importance in the future for the clarification of the pathogenesis of several pathological manifestations of HCV.

Footnotes

P- Reviewers: Kato T, Seya T, Tetsuya T S- Editor: Zhai HH L- Editor: Cant MR E- Editor: Liu XM

References

1. Zignego AL, Macchia D, Monti M, Thiers V, Mazzetti M, Foschi M, Maggi E, Romagnani S, Gentilini P, Bréchot C. Infection of peripheral mononuclear blood cells by hepatitis C virus. J Hepatol. 1992;15:382-386.[PubMed] [DOI]

2. Ferri C, Monti M, La Civita L, Longombardo G, Greco F, Pasero G, Gentilini P, Bombardieri S, Zignego AL. Infection of peripheral blood mononuclear cells by hepatitis C virus in mixed cryoglobulinemia. Blood. 1993;82:3701-3704. [PubMed]

3. Ferri C, Mascia MT. Cryoglobulinemic vasculitis. Curr Opin Rheumatol. 2006;18:54-63. [PubMed]

4. Ferri C, Antonelli A, Mascia MT, Sebastiani M, Fallahi P, Ferrari D, Giunti M, Pileri SA, Zignego AL. B-cells and mixed cryoglobulinemia. Autoimmun Rev. 2007;7:114-120. [PubMed] [DOI]

5. Sansonno D, Carbone A, De Re V, Dammacco F. Hepatitis C virus infection, cryoglobulinaemia, and beyond. Rheumatology (Oxford). 2007;46:572-578. [PubMed] [DOI]

6. Ferri C, Antonelli A, Mascia MT, Sebastiani M, Fallahi P, Ferrari D, Pileri SA, Zignego AL. HCV-related autoimmune and neoplastic disorders: the HCV syndrome. Dig Liver Dis. 2007;39 Suppl 1:S13-S21.[PubMed] [DOI]

7. Zignego AL, Ferri C, Pileri SA, Caini P, Bianchi FB. Extrahepatic manifestations of Hepatitis C Virus infection: a general overview and guidelines for a clinical approach. Dig Liver Dis. 2007;39:2-17. [PubMed] [DOI]

8. Ferri C, Sebastiani M, Giuggioli D, Cazzato M, Longombardo G, Antonelli A, Puccini R, Michelassi C, Zignego AL. Mixed cryoglobulinemia: demographic, clinical, and serologic features and survival in 231 patients. Semin Arthritis Rheum. 2004;33:355-374. [PubMed] [DOI]

9. Ferri C, Zignego AL, Pileri SA. Cryoglobulins. J Clin Pathol. 2002;55:4-13. [PubMed] [DOI]

10. Rosa D, Saletti G, De Gregorio E, Zorat F, Comar C, D’Oro U, Nuti S, Houghton M, Barnaba V, Pozzato G. Activation of naïve B lymphocytes via CD81, a pathogenetic mechanism for hepatitis C virus-associated B lymphocyte disorders. Proc Natl Acad Sci USA. 2005;102:18544-18549. [PubMed] [DOI]

11. Antonelli A, Ferri C, Ferrari SM, Colaci M, Fallahi P. Immunopathogenesis of HCV-related endocrine manifestations in chronic hepatitis and mixed cryoglobulinemia. Autoimmun Rev. 2008;8:18-23. [PubMed] [DOI]

12. Patzwahl R, Meier V, Ramadori G, Mihm S. Enhanced expression of interferon-regulated genes in the liver of patients with chronic hepatitis C virus infection: detection by suppression-subtractive hybridization. J Virol. 2001;75:1332-1338. [PubMed] [DOI]

13. Zignego AL. Enhanced TH1 cytokine production in hepatitis C virus-infected patients with mixed cryoglobulinemia: understanding the pathological issues. J Hepatol. 2004;41:1045-1049. [PubMed] [DOI]

14. Antonelli A, Rotondi M, Fallahi P, Romagnani P, Ferrari SM, Buonamano A, Ferrannini E, Serio M. High levels of circulating CXC chemokine ligand 10 are associated with chronic autoimmune thyroiditis and hypothyroidism. J Clin Endocrinol Metab. 2004;89:5496-5499. [PubMed] [DOI]

15. Matskevich AA, Strayer DS. Exploiting hepatitis C virus activation of NFkappaB to deliver HCV-responsive expression of interferons alpha and gamma. Gene Ther. 2003;10:1861-1873. [PubMed] [DOI]

16. Murata M, Nabeshima S, Maeda N, Nakashima H, Kashiwagi S, Hayashi J. Increased frequency of IFN-gamma-producing peripheral CD8+ T cells with memory-phenotype in patients with chronic hepatitis C. J Med Virol. 2002;67:162-170. [PubMed] [DOI]

17. Itoh Y, Morita A, Nishioji K, Narumi S, Toyama T, Daimon Y, Nakamura H, Kirishima T, Okanoue T. Clinical significance of elevated serum interferon- inducible protein-10 levels in hepatitis C virus carriers with persistently normal serum transaminase levels. J Viral Hepat. 2001;8:341-348. [PubMed] [DOI]

18. Shields PL, Morland CM, Salmon M, Qin S, Hubscher SG, Adams DH. Chemokine and chemokine receptor interactions provide a mechanism for selective T cell recruitment to specific liver compartments within hepatitis C-infected liver. J Immunol. 1999;163:6236-6243. [PubMed]

19. Apolinario A, Majano PL, Lorente R, Núñez O, Clemente G, García-Monzón C. Gene expression profile of T-cell-specific chemokines in human hepatocyte-derived cells: evidence for a synergistic inducer effect of cytokines and hepatitis C virus proteins. J Viral Hepat. 2005;12:27-37. [PubMed] [DOI]

20. Ferri C, Greco F, Longombardo G, Palla P, Moretti A, Marzo E, Mazzoni A, Pasero G, Bombardieri S, Highfield P. Association between hepatitis C virus and mixed cryoglobulinemia [see comment]. Clin Exp Rheumatol. 1991;9:621-624. [PubMed]

21. Antonelli A, Ferri C, Pampana A, Fallahi P, Nesti C, Pasquini M, Marchi S, Ferrannini E. Thyroid disorders in chronic hepatitis C. Am J Med. 2004;117:10-13. [PubMed] [DOI]

22. Antonelli A, Ferri C, Fallahi P, Pampana A, Ferrari SM, Goglia F, Ferrannini E. Hepatitis C virus infection: evidence for an association with type 2 diabetes. Diabetes Care. 2005;28:2548-2550. [PubMed] [DOI]

23. Leone N, Pellicano R, Ariata Maiocco I, Modena V, Marietti G, Rizzetto M, Ponzetto A. Mixed cryoglobulinaemia and chronic hepatitis C virus infection: the rheumatic manifestations. J Med Virol. 2002;66:200-203. [PubMed] [DOI]

24. Wener MH, Hutchinson K, Morishima C, Gretch DR. Absence of antibodies to cyclic citrullinated peptide in sera of patients with hepatitis C virus infection and cryoglobulinemia. Arthritis Rheum. 2004;50:2305-2308.[PubMed] [DOI]

25. Haddad J, Deny P, Munz-Gotheil C, Ambrosini JC, Trinchet JC, Pateron D, Mal F, Callard P, Beaugrand M. Lymphocytic sialadenitis of Sjögren’s syndrome associated with chronic hepatitis C virus liver disease. Lancet. 1992;339:321-323. [PubMed] [DOI]

26. Koike K, Moriya K, Ishibashi K, Yotsuyanagi H, Shintani Y, Fujie H, Kurokawa K, Matsuura Y, Miyamura T. Sialadenitis histologically resembling Sjogren syndrome in mice transgenic for hepatitis C virus envelope genes. Proc Natl Acad Sci USA. 1997;94:233-236. [PubMed] [DOI]

27. Ramos-Casals M, Loustaud-Ratti V, De Vita S, Zeher M, Bosch JA, Toussirot E, Medina F, Rosas J, Anaya JM, Font J. Sjögren syndrome associated with hepatitis C virus: a multicenter analysis of 137 cases. Medicine (Baltimore). 2005;84:81-89. [PubMed] [DOI]

28. Ramos-Casals M, García-Carrasco M, Cervera R, Rosas J, Trejo O, de la Red G, Sánchez-Tapias JM, Font J, Ingelmo M. Hepatitis C virus infection mimicking primary Sjögren syndrome. A clinical and immunologic description of 35 cases. Medicine (Baltimore). 2001;80:1-8. [PubMed] [DOI]

29. Scott CA, Avellini C, Desinan L, Pirisi M, Ferraccioli GF, Bardus P, Fabris C, Casatta L, Bartoli E, Beltrami CA. Chronic lymphocytic sialoadenitis in HCV-related chronic liver disease: comparison of Sjögren’s syndrome. Histopathology. 1997;30:41-48. [PubMed] [DOI]

30. De Vita S, Sacco C, Sansonno D, Gloghini A, Dammacco F, Crovatto M, Santini G, Dolcetti R, Boiocchi M, Carbone A. Characterization of overt B-cell lymphomas in patients with hepatitis C virus infection. Blood. 1997;90:776-782. [PubMed]

31. Okabe M, Fukuda K, Arakawa K, Kikuchi M. Chronic variant of myocarditis associated with hepatitis C virus infection. Circulation. 1997;96:22-24. [PubMed] [DOI]

32. Frustaci A, Calabrese F, Chimenti C, Pieroni M, Thiene G, Maseri A. Lone hepatitis C virus myocarditis responsive to immunosuppressive therapy. Chest. 2002;122:1348-1356. [PubMed] [DOI]

33. Matsumori A, Yutani C, Ikeda Y, Kawai S, Sasayama S. Hepatitis C virus from the hearts of patients with myocarditis and cardiomyopathy. Lab Invest. 2000;80:1137-1142. [PubMed] [DOI]

34. Matsumori A, Shimada T, Chapman NM, Tracy SM, Mason JW. Myocarditis and heart failure associated with hepatitis C virus infection. J Card Fail. 2006;12:293-298. [PubMed] [DOI]

35. Antonelli A, Ferri C, Ferrari SM, Colaci M, Sebastiani M, Zignego AL, Ghiri E, Goglia F, Fallahi P. High levels of circulating N-terminal pro-brain natriuretic peptide in patients with hepatitis C. J Viral Hepat. 2010;17:851-853.[PubMed] [DOI]

36. Antonelli A, Ferri C, Ferrari SM, Marchi S, De Bortoli N, Sansonno D, Chiavacci C, Ferrannini E, Fallahi P. N-terminal pro-brain natriuretic peptide and tumor necrosis factor-alpha both are increased in patients with Hepatitis C. J Interferon Cytokine Res. 2010;30:359-363. [PubMed] [DOI]

37. de-la-Serna-Higuera C, Bárcena-Marugán R, Sanz-de-Villalobos E. Hemolytic anemia secondary to alpha-interferon treatment in a patient with chronic C hepatitis. J Clin Gastroenterol. 1999;28:358-359. [PubMed] [DOI]

38. European Association for the Study of the Liver.EASL Clinical Practice Guidelines: management of hepatitis C virus infection. J Hepatol. 2011;55:245-264. [PubMed] [DOI]

39. Hyman GA, Southworth H. Hemolytic anemia associated with liver disease. Am J Med Sci. 1951;221:448-456.[PubMed] [DOI]

40. Panush RS, Wilkinson LS, Fagin RR. Chronic active hepatitis associated with eosinophilia and Coombs’-positive hemolytic anemia. Gastroenterology. 1973;64:1015-1019. [PubMed]

41. Portell A, Pedreira JD, Richart C, Vargas V, Martín C, Guardia J. [Autoimmune hemolytic anemia associated with chronic liver disease]. Rev Clin Esp. 1982;164:101-103. [PubMed]

42. Srinivasan R. Autoimmune hemolytic anemia in treatment-naïve chronic hepatitis C infection. J Clin Gastroenterol. 2001;32:245-247. [PubMed] [DOI]

43. Chao TC, Chen CY, Yang YH, Chen PM, Chang FY, Lee SD. Chronic hepatitis C virus infection associated with primary warm-type autoimmune hemolytic anemia. J Clin Gastroenterol. 2001;33:232-233. [PubMed] [DOI]

44. Ramos-Casals M, García-Carrasco M, López-Medrano F, Trejo O, Forns X, López-Guillermo A, Muñoz C, Ingelmo M, Font J. Severe autoimmune cytopenias in treatment-naive hepatitis C virus infection: clinical description of 35 cases. Medicine (Baltimore). 2003;82:87-96. [PubMed] [DOI]

45. Nagamine T, Ohtuka T, Takehara K, Arai T, Takagi H, Mori M. Thrombocytopenia associated with hepatitis C viral infection. J Hepatol. 1996;24:135-140. [PubMed] [DOI]

46. Hernández F, Blanquer A, Linares M, López A, Tarín F, Cerveró A. Autoimmune thrombocytopenia associated with hepatitis C virus infection. Acta Haematol. 1998;99:217-220. [PubMed] [DOI]

47. Linares M, Pastor E, Hernández F, Montagud M, Blanquer A. Autoimmune thrombocytopenia and hepatitis C virus infection. Am J Hematol. 1996;53:284. [PubMed]

48. Pivetti S, Novarino A, Merico F, Bertero MT, Brunetto MR, Bonino F, Caligaris-Cappio F. High prevalence of autoimmune phenomena in hepatitis C virus antibody positive patients with lymphoproliferative and connective tissue disorders. Br J Haematol. 1996;95:204-211. [PubMed] [DOI]

49. Hamaia S, Li C, Allain JP. The dynamics of hepatitis C virus binding to platelets and 2 mononuclear cell lines. Blood. 2001;98:2293-2300. [PubMed] [DOI]

50. Pockros PJ, Duchini A, McMillan R, Nyberg LM, McHutchison J, Viernes E. Immune thrombocytopenic purpura in patients with chronic hepatitis C virus infection. Am J Gastroenterol. 2002;97:2040-2045. [PubMed] [DOI]

51. Rajan S, Liebman HA. Treatment of hepatitis C related thrombocytopenia with interferon alpha. Am J Hematol. 2001;68:202-209. [PubMed] [DOI]

52. Panzer S, Seel E, Brunner M, Körmöczi GF, Schmid M, Ferenci P, Peck-Radosavljevic M. Platelet autoantibodies are common in hepatitis C infection, irrespective of the presence of thrombocytopenia. Eur J Haematol. 2006;77:513-517. [PubMed] [DOI]

53. García-Suárez J, Burgaleta C, Hernanz N, Albarran F, Tobaruela P, Alvarez-Mon M. HCV-associated thrombocytopenia: clinical characteristics and platelet response after recombinant alpha2b-interferon therapy. Br J Haematol. 2000;110:98-103. [PubMed] [DOI]

54. Rajan SK, Espina BM, Liebman HA. Hepatitis C virus-related thrombocytopenia: clinical and laboratory characteristics compared with chronic immune thrombocytopenic purpura. Br J Haematol. 2005;129:818-824.[PubMed] [DOI]

55. Zhang L, Li H, Zhao H, Ji L, Yang R. Hepatitis C virus-related adult chronic idiopathic thrombocytopenic purpura: experience from a single Chinese center. Eur J Haematol. 2003;70:196-197. [PubMed] [DOI]

56. Pawlotsky JM, Bouvier M, Fromont P, Deforges L, Duval J, Dhumeaux D, Bierling P. Hepatitis C virus infection and autoimmune thrombocytopenic purpura. J Hepatol. 1995;23:635-639. [PubMed] [DOI]

57. Sakuraya M, Murakami H, Uchiumi H, Hatsumi N, Akiba T, Yokohama A, Matsushima T, Tsukamoto N, Morita K, Karasawa M. Steroid-refractory chronic idiopathic thrombocytopenic purpura associated with hepatitis C virus infection. Eur J Haematol. 2002;68:49-53. [PubMed] [DOI]

58. Fernandez-Soto L, Gonzalez A, Escobar-Jimenez F, Vazquez R, Ocete E, Olea N, Salmeron J. Increased risk of autoimmune thyroid disease in hepatitis C vs hepatitis B before, during, and after discontinuing interferon therapy. Arch Intern Med. 1998;158:1445-1448. [PubMed] [DOI]

59. Marazuela M, García-Buey L, González-Fernández B, García-Monzón C, Arranz A, Borque MJ, Moreno-Otero R. Thyroid autoimmune disorders in patients with chronic hepatitis C before and during interferon-alpha therapy. Clin Endocrinol (Oxf). 1996;44:635-642. [PubMed] [DOI]

60. Deutsch M, Dourakis S, Manesis EK, Gioustozi A, Hess G, Horsch A, Hadziyannis S. Thyroid abnormalities in chronic viral hepatitis and their relationship to interferon alfa therapy. Hepatology. 1997;26:206-210.[PubMed] [DOI]

61. Huang MJ, Wu SS, Liaw YF. Thyroid abnormalities in patients with chronic viral hepatitis. Hepatology. 1994;20:1651-1652. [PubMed] [DOI]

62. Ganne-Carrie N, Medini A, Coderc E, Seror O, Christidis C, Grimbert S, Trinchet JC, Beaugrand M. Latent autoimmune thyroiditis in untreated patients with HCV chronic hepatitis: a case-control study. J Autoimmun. 2000;14:189-193. [PubMed] [DOI]

63. Preziati D, La Rosa L, Covini G, Marcelli R, Rescalli S, Persani L, Del Ninno E, Meroni PL, Colombo M, Beck-Peccoz P. Autoimmunity and thyroid function in patients with chronic active hepatitis treated with recombinant interferon alpha-2a. Eur J Endocrinol. 1995;132:587-593. [PubMed] [DOI]

64. Quaranta JF, Tran A, Régnier D, Letestu R, Beusnel C, Fuzibet JG, Thiers V, Rampal P. High prevalence of antibodies to hepatitis C virus (HCV) in patients with anti-thyroid autoantibodies. J Hepatol. 1993;18:136-138.[PubMed]

65. Lenzi M, Johnson PJ, McFarlane IG, Ballardini G, Smith HM, McFarlane BM, Bridger C, Vergani D, Bianchi FB, Williams R. Antibodies to hepatitis C virus in autoimmune liver disease: evidence for geographical heterogeneity. Lancet. 1991;338:277-280. [PubMed] [DOI]

66. Minelli R, Braverman LE, Giuberti T, Schianchi C, Gardini E, Salvi M, Fiaccadori F, Ugolotti G, Roti E. Effects of excess iodine administration on thyroid function in euthyroid patients with a previous episode of thyroid dysfunction induced by interferon-alpha treatment. Clin Endocrinol (Oxf). 1997;47:357-361. [PubMed] [DOI]

67. Cacoub P, Poynard T, Ghillani P, Charlotte F, Olivi M, Piette JC, Opolon P. Extrahepatic manifestations of chronic hepatitis C. MULTIVIRC Group. Multidepartment Virus C. Arthritis Rheum. 1999;42:2204-2212.[PubMed]

68. Antonelli A, Ferri C, Fallahi P, Giuggioli D, Nesti C, Longombardo G, Fadda P, Pampana A, Maccheroni M, Ferrannini E. Thyroid involvement in patients with overt HCV-related mixed cryoglobulinaemia. QJM. 2004;97:499-506. [PubMed] [DOI]

69. Antonelli A, Ferri C, Fallahi P, Ferrari SM, Ghinoi A, Rotondi M, Ferrannini E. Thyroid disorders in chronic hepatitis C virus infection. Thyroid. 2006;16:563-572. [PubMed] [DOI]

70. Antonelli A, Ferri C, Fallahi P, Nesti C, Zignego AL, Maccheroni M. Thyroid cancer in HCV-related mixed cryoglobulinemia patients. Clin Exp Rheumatol. 2002;20:693-696. [PubMed]

71. Antonelli A, Ferri C, Fallahi P, Pampana A, Ferrari SM, Barani L, Marchi S, Ferrannini E. Thyroid cancer in HCV-related chronic hepatitis patients: a case-control study. Thyroid. 2007;17:447-451. [PubMed] [DOI]

72. Caronia S, Taylor K, Pagliaro L, Carr C, Palazzo U, Petrik J, O’Rahilly S, Shore S, Tom BD, Alexander GJ. Further evidence for an association between non-insulin-dependent diabetes mellitus and chronic hepatitis C virus infection. Hepatology. 1999;30:1059-1063. [PubMed] [DOI]

73. Mason A. Viral induction of type 2 diabetes and autoimmune liver disease. J Nutr. 2001;131:2805S-2808S.[PubMed]

74. Petta S. Insulin resistance and diabetes mellitus in patients with chronic hepatitis C: spectators or actors?. Dig Liver Dis. 2012;44:359-360. [PubMed] [DOI]

75. Antonelli A, Ferri C, Fallahi P, Sebastiani M, Nesti C, Barani L, Barale R, Ferrannini E. Type 2 diabetes in hepatitis C-related mixed cryoglobulinaemia patients. Rheumatology (Oxford). 2004;43:238-240. [PubMed] [DOI]

76. Mehta SH, Brancati FL, Sulkowski MS, Strathdee SA, Szklo M, Thomas DL. Prevalence of type 2 diabetes mellitus among persons with hepatitis C virus infection in the United States. Ann Intern Med. 2000;133:592-599.[PubMed] [DOI]

77. Noto H, Raskin P. Hepatitis C infection and diabetes. J Diabetes Complications. 2006;20:113-120.[PubMed] [DOI]

78. Mason AL, Lau JY, Hoang N, Qian K, Alexander GJ, Xu L, Guo L, Jacob S, Regenstein FG, Zimmerman R. Association of diabetes mellitus and chronic hepatitis C virus infection. Hepatology. 1999;29:328-333.[PubMed] [DOI]

79. Petit JM, Bour JB, Galland-Jos C, Minello A, Verges B, Guiguet M, Brun JM, Hillon P. Risk factors for diabetes mellitus and early insulin resistance in chronic hepatitis C. J Hepatol. 2001;35:279-283. [PubMed] [DOI]

80. Betterle C, Fabris P, Zanchetta R, Pedini B, Tositti G, Bosi E, de Lalla F. Autoimmunity against pancreatic islets and other tissues before and after interferon-alpha therapy in patients with hepatitis C virus chronic infection. Diabetes Care. 2000;23:1177-1181. [PubMed] [DOI]

81. Piquer S, Hernández C, Enriquez J, Ross A, Esteban JI, Genescà J, Bonifacio E, Puig-Domingo M, Simó R. Islet cell and thyroid antibody prevalence in patients with hepatitis C virus infection: effect of treatment with interferon. J Lab Clin Med. 2001;137:38-42. [PubMed] [DOI]

82. Bosi E, Minelli R, Bazzigaluppi E, Salvi M. Fulminant autoimmune Type 1 diabetes during interferon-alpha therapy: a case of Th1-mediated disease?. Diabet Med. 2001;18:329-332. [PubMed] [DOI]

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