- Research Article
- Open Access
Hepatitis B virus infection in undocumented immigrants and refugees in Southern Italy: demographic, virological, and clinical features
Infectious Diseases of Poverty volume 6, Article number: 33 (2017)
The data on hepatitis b virus (HBV) infection in immigrants population are scanty. The porpoise of this study was to define the demographic, virological, and clinical characteristics of subjects infected with HBV chronic infection in a cohort of immigrants living in Naples, Italy.
A screening for HBV infection was offered to 1,331 immigrants, of whom 1,212 (91%) (831 undocumented immigrants and 381 refugees) accepted and were screened for hepatitis B surface antigen (HBsAg) and anti-hepatitis B core antibody (HBc). Those found to be HBsAg positive were further investigated at third-level infectious disease units.
Of the 1,212 immigrants screened, 116 (9.6%) were HBsAg positive, 490 (40.4%) were HBsAg negative/anti-HBc positive, and 606 (50%) were seronegative for both. Moreover, 21 (1.7%) were anti-human immunodeficiency virus positive and 45 (3.7%) were anti-hepatitis C virus positive. The logistic regression analysis showed that male sex (OR: 1.79; 95%CI: 1.28–2.51), Sub-Saharan African origin (OR: 6.18; 95%CI: 3.37–11.36), low level of schooling (OR: 0.96; 95%CI: 0.94–0.99), and minor parenteral risks for acquiring HBV infection (acupuncture, tattoo, piercing, or tribal practices, OR: 1.54; 95%CI: 1.1–2.16) were independently associated with ongoing or past HBV infection. Of the 116 HBsAg-positive immigrants, 90 (77.6%) completed their diagnostic itinerary at a third-level infectious disease unit: 29 (32.2%) were asymptomatic non-viremic HBsAg carriers, 43 (47.8%) were asymptomatic viremic carriers, 14 (15.6%) had chronic hepatitis, and four (4.4%) had liver cirrhosis, with superimposed hepatocellular carcinoma in two.
The data illustrate the demographic, clinical and virological characteristics of HBV infection in immigrants in Italy and indicate the need for Italian healthcare authorities to enhance their support for providing screening, HBV vaccination, treatment, and educational programs for this populations.
Please see Additional file 1 for translation of the abstract into the five official working languages of the United Nations.
The hepatitis B virus (HBV) is the most common agent of hepatitis worldwide, with around 350–400 million people chronically infected  and 600,000 deaths reported each year due to a fulminant course of acute hepatitis B (AHB) or, more frequently, to liver decompensation in hepatitis B surface antigen (HBsAg)-positive patients with cirrhosis or hepatocellular carcinoma (HCC) [2–4]. The HBV is transmitted from infected mothers to their new-born babies at birth and in childhood, and in adulthood by parenteral (unsafe blood transfusion, intravenous drug use, surgery, dialysis, tattooing, piercing) or sexual (heterosexual or homosexual) routes. The level of HBV endemicity differs from one country to another: it is low in Western Europe, USA, Canada, and some South American and Northern African countries (with an HBsAg chronic carrier rate below 2%); intermediate in Eastern Europe, Central Asia, and some Eastern Asian countries (from 2 to 8%); and high in some Asian and Sub-Saharan African countries and in Alaska (above 8%) . In Italy, HBsAg seroprevalence is estimated to be around 1% and the yearly incidence rate of AHB is nearly 1/100,000 inhabitants [3, 4].
Due to the socioeconomic and political crises in Northern Africa, Sub-Saharan Africa (SSA), Eastern Europe, and Central and Eastern Asia in recent decades, Western countries have become lands of immigration from these subcontinents with intermediate or high HBV, hepatitis C virus (HCV), and human immunodeficiency virus (HIV) endemicities. At present, approximately 5.4 million legal immigrants live in Italy, making up 8.2% of the resident population (http://www.dossierimmigrazione.it/docnews/file/Scheda%20Dossier%202015(4).pdf). In addition, Italian immigration authorities estimate that around 500,000 undocumented immigrants live in Italy at present, prevalently coming from Northern Africa and SSA, Eastern Europe, and Central and Eastern Asia [5, 6]. The immigrant population is prevalently young, sexually active [7, 8], and has broken family ties. They often have no fixed abode or live in crowded homes; are not socially integrated due to language, cultural, and socioeconomic barriers ; and consequently, have limited access to healthcare services.
In our previous study, conducted from January 2012 to June 2013, we screened 882 immigrants; the resulting HBsAg seroprevalence was 8% . In the present study, we report on the demographic, virological, and clinical characteristics of 116 HBsAg-positive subjects, after screening 1,212 undocumented immigrants and low-income refugees from January 2012 to December 2014 using the same methodology as in the previous study .
The design of this study was extensively described in a previous paper . Briefly, this is a multicentre prospective study with the participation of six centres: three in Naples (two first-level clinical centres and one tertiary unit of infectious diseases) and three in Caserta (two first-level clinical centres and one tertiary unit of infectious diseases). All immigrants—undocumented immigrants and low-income refugees—consecutively seen for a clinical consultation at one of the four first-level centres from January 2012 to December 2014 were enrolled in the study. Undocumented immigrant and low-income refugee populations living in Italy have similar characteristics: they are all prevalently young; not integrated due to language, cultural, and social barriers; and have low incomes, most frequently from casual work.
The first-level clinical centres are hospital centres of the national healthcare system or clinical centres of international charity organizations supported by the national healthcare system, with proven experience in clinical, psychological, and legal management of vulnerable groups, such as undocumented immigrants, low-income refugees, the homeless, and alcoholics. Each first-level clinical centre is an outpatients clinic providing general medical services. The most frequent pathological conditions inducing undocumented immigrants and refugees to refer to one of these centres are lumbago, headaches, pruritus, coughs, high blood pressure, and allergy symptoms.
Screening of patients
During a clinical consultation, a physician from the clinical centre and a cultural mediator explained to the immigrants the importance of testing for HBV, HCV, and HIV serum markers, and offered them to be screened free of charge, in anonymity (centre number, patient number), and in full accordance with the privacy law. Acceptance of screening and a signed informed consent, written in the immigrant’s native language, was obtained on a voluntary basis from more than 91% (1,212) of the 1,331 undocumented immigrants and low-income refugees at one of the four first-level clinical units during the study period. These were the subjects who participated in the study.
An anonymous questionnaire collecting information on the demographics (age, sex, race/ethnicity, place of birth, language); socioeconomic status (education, annual household income); environmental factors (alcohol, diet, etc); and clinical data and risk factors for acquiring HBV, HCV (sexual contact, drug, use, surgery, etc), and HIV infections was completed by the 1212 subjects who agreed to participate in this study.
Serum sampling and clinical definitions
For all subjects enrolled, a serum sample was obtained to test for HBsAg, total anti- hepatitis B core antibody (HBc), anti-HCV, anti-HIV, and serum aminotransferases. HBsAg positivity was considered a marker of ongoing HBV infection, and HBsAg negativity/anti-HBc positivity as markers of a past HBV infection; HBsAg/anti-HBc-negative subjects were considered as having no HBV infection.
The HBsAg-positive subjects were referred for further investigation, monitoring, and possible treatment to one of the two tertiary units of infectious diseases, both of which are affiliated with the Second University of Naples and have cooperated for nearly 15 years in several clinical investigations on HBV infection using the same clinical approach and laboratory methods [11, 12]. Each HBsAg-positive subject was assigned to the care of a cultural mediator, who, acting as a support, assisted him/her at the third-level clinical centre throughout the monitoring and/or treatment period.
HBsAg-positive patients were classified as asymptomatic carriers when, in the absence of clinical, biochemical, and ultrasound signs of chronic liver disease, alanine aminotransferase (ALT) values were persistently normal. Chronic hepatitis was diagnosed based on liver histology or, if not performed, based on abnormal ALT values. Liver cirrhosis was diagnosed with a liver biopsy or, if not performed, from the presence of unequivocal clinical, biochemical, and ultrasound signs . The diagnosis of HCC was based on histology, imaging techniques, or biochemical parameters (α1-feto protein greater than 400 ng/mL) .
Serum samples were tested for HBsAg, anti-HCV, anti-HIV, total anti-HBc, and anti-hepatitis B surface antibody (HBs) using commercial immunoenzymatic assays (Abbott Laboratories, North Chicago, IL, USA: AxSYM® HBsAg (v2) M/S for HBsAg, AxSYM® HCV (v3) for anti-HCV, AxSYM® HIV 1/2 Combo for HIV, AxSYM® CORE™ (v2) for total anti-HBc, and AxSYM® AUSAB® for anti-HBs). Anti-HIV reactivity was always confirmed by a western blot assay (Genelabs Diagnostics, Science Park Drive, Singapore), which identifies both HIV-1 and HIV-2 strains.
Serum HBV-DNA levels were determined by real-time polymerase chain reaction (PCR) with a detection limit of 20 copies/mL, as previously described . The HBV genotype was determined in HBV DNA positive samples, as previously described .
Continuous variables were summarized as mean and standard deviations (SD), and categorical variables as absolute and relative frequencies. Differences in mean values were evaluated using the Student’s t-test, while the chi-square test was used for categorical variables. The odds ratio (OR), with a 95% confidence interval (CI), was estimated using a logistic regression model to identify possible independent associations between the presence of HBV infection (ongoing or past) with sex, age, country of origin, years of schooling, and possible risk factors for its acquisition. A P < 0.05 was considered to be statistically significant.
The Ethics Committee of the Azienda Ospedaliera Universitaria of the Second University of Naples (214/2012) approved this study. Signed informed consent, written in the immigrant’s native language, was obtained on a voluntary basis from more than 91% (1,212) of the 1,331 undocumented immigrants and low-income refugees at one of the four first-level clinical units during the study period. All patients signed an informed consent for the collection and storage of biological samples and for the anonymous use of their data for research purposes these subjects participated in the study.
The initial demographic and serological data pertaining to the 1,212 immigrants investigated in this study are shown in Table 1. The subjects were mostly young (median age 32 years, range 12–74 years), prevalently males (75.2%), and had been living in Italy for a mean period of 50.3 months (SD ± 53.0). Of the 1,212 immigrants, 668 (55.1%) came from SSA, 237 (19.5%) from Eastern Europe, 88 (7.3%) from Northern Africa, 207 (17.1%) from Asia, 10 (0.8%) from South America, and 2 (0. 2%) did not state their country of origin (see Table 1).
Of the 1 212 immigrants, 116 (9.6%) were HBsAg positive (113 with HBsAg alone, two had HBsAg and were anti-HIV positive, and one was HBsAg, anti-HCV, and anti-HIV positive); 490 (40.4%) were HBsAg negative/anti-HBc positive, and 606 (50%) were HBsAg/anti-HBc negative (see Table 1). Of the 1 096 HBsAg-negative subjects, 40 (3.6%) were anti-HCV positive, 14 (1.3%) were anti-HIV positive, and 4 (0.4%) were anti-HCV/anti-HIV positive. Thus, 21 (1.7%) subjects were anti-HIV positive and 45 (3.7%) were anti-HCV positive. All subjects were unaware of their serological status.
The demographic and initial characteristics of the 1 212 subjects were also analysed according to their HBV serological condition. Compared with the HBsAg/anti-HBc-negative subjects, HBsAg-positive or HBsAg-negative/anti-HBc-positive patients were more frequently males (81.5 and 80.8% vs. 70%, P = 0.001) and more frequently came from SSA (76.5 and 70.4% vs. 37.4%, P = 0.001). The HBsAg-positive subjects had fewer years of schooling than the HBsAg/anti-HBc-negative (4.5 ± 3.9 vs. 8.1 ± 5.3, P = 0.000) and the HBsAg-negative/anti-HBc-positive (12.9 ± 2.9 years, P = 0.000) patients (see Table 2).
To identify the factors independently associated with the acquisition of an ongoing or previous HBV infection, a logistic regression analysis was performed with sex, age, country of origin, years of schooling, and sexual and parenteral risk factors as covariates. The analysis identified the male sex (OR: 1.79; 95%CI: 1.28–2.51, P = 0.001), fewer years of schooling (OR: 0.96; 95%CI: 0.94–0.99, P = 0.007), and a history of acupuncture, tattooing, piercing, or other tribal practices (OR: 1.54; 95%CI: 1.1–2.16, P = 0.011) as being independently associated with acquiring a HBV infection. In addition, compared with immigrants from Northern Africa, those from SSA (OR: 6.18; 95%CI: 3.37–11.36, P = 0.000), Asia (OR: 2.65; 95%CI: 1.35–5.21, P = 0.005), and Eastern Europe (OR: 2.00; 95%CI: 1.02–3.91, P = 0.043) more frequently had HBV infection (see Table 3).
All HBsAg-positive subjects were referred to one of the two tertiary units of infectious diseases for further investigation, monitoring, and possible treatment. Of the 116 HBsAg-positive subjects, 29 (25%) were serum HBV DNA negative with normal aminotransferase serum values in two determinations at a 3–6 month interval and were considered asymptomatic non-viremic HBsAg carriers. Hepatitis B virus DNA was detected in 87 (75%) HBsAg-positive subjects, with a HBV DNA load ≤ 2 000 IU/ml in 58 (50%) and >2 000 IU/ml in the remaining 29 (25%). However, three (10.3%) of the 29 subjects with a serum HBV load >2 000 IU/ml and 23 (39.7%) of the 58 with a HBV DNA load ≤ 2 000 IU/ml did not complete the diagnostic itinerary (see Fig. 1).
Of the 26 HBsAg-positive subjects with a HBV DNA load >2 000 IU/ml who completed the diagnostic procedures, 10 (38.5%) were considered asymptomatic viremic HBsAg carriers because they showed persistently normal aminotransferase serum values and a normal liver at ultrasound examination; all were anti-hepatitis Be antibody (HBe) positive and had a HBV load between 2 001 and 10 000 IU/ml. Another 13 (50%) showed clinical, laboratory, and US patterns characteristic of chronic hepatitis, and the remaining three (11.5%) had liver cirrhosis, with superimposed HCC in two patients (see Fig. 1).
Of the 35 subjects with serum HBV DNA ≤2 000 IU/ml who completed the diagnostic procedures, 33 (94.3%) were conclusively diagnosed as asymptomatic HBsAg carriers with low viremia, one (2.9%) with chronic hepatitis, and one (2.9%) with liver cirrhosis (see Fig. 1).
Overall, a conclusive diagnosis was obtained for 90 (77.6%) of the 116 HBsAg-positive subjects. Of these, 29 (32.2%) were asymptomatic non-viremic HBsAg carriers, 43 (47.8%) were asymptomatic viremic HBsAg carriers, 14 (15.6%) had chronic hepatitis, and four (4.4%) had liver cirrhosis, with superimposed HCC in two patients. Of these 90 HBsAg-positive subjects, two (2.2%) were anti-Delta positive, six (6.7%) were hepatitis B e antigen (HBeAg) positive, and 84 (93.3%) were anti-HBe positive. The HBV genotype was identified in 47 of the 61 HBV-DNA-positive subjects with a conclusive diagnosis; a low HBV DNA serum concentration did not allow sequencing in 14 cases. Of the 47 genotyped patients, 11 (23.4%) had HBV genotype A, seven (14.9%) had genotype D, 28 (59.6%) had genotype E, and only one (2.1%) had genotype C.
The demographic, serological, and virological characteristics of the 90 HBsAg-positive subjects with a conclusive diagnosis are shown in Table 4, according to the disease stage. Compared with patients with a less active liver disease, those with chronic hepatitis or liver cirrhosis showed a higher viral load and higher aminotransferase serum levels and were more frequently HBeAg positive (see Table 4).
The HBsAg-positive subjects admitted to the present study received treatment or remained untreated in accordance with the current international guidelines . In particular, five of the 14 patients with chronic hepatitis were treated with peginterferon α-2a (180ug once a week) for 12–24 months; a favourable response was observed only in one, a HBV-genotype-A Romanian patient. Another six patients with chronic hepatitis and three of the four cirrhotic patients were treated with nucleos(t)ide analogues: entecavir was given to five cases and tenofovir to four. All nine nucleos(t)ide-analogue-treated patients became serum HBV DNA negative within the 48th week of treatment and remained so after. For the remaining three patients with chronic hepatitis, antiviral treatment was not indicated and they were left untreated. Also untreated was a patient from SSA with advanced liver cirrhosis and multifocal HCC who died after a few weeks of observation.
Despite their long-term stay in Italy, the undocumented immigrants and low-income refugees investigated in this study were poorly integrated due to language, cultural, and socioeconomic barriers. This immigrant population came to Italy from various countries with intermediate or high HBV endemicities and with different socioeconomic, religious, and cultural backgrounds, all of which makes their access to Italian healthcare services difficult. Nevertheless, the presence of skilled physicians and cultural mediators operating in the four first-level centres overcame any language and cultural barriers and allowed successful screening with an over-90% acceptance rate. The rate of the interviewed immigrants who agreed to be screened seems a useful parameter for evaluating the efficacy of screening and representative of the immigrant population. However, a possible bias on the enrolment may not be excluded.
The HBsAg-positive subjects were referred to a tertiary clinical centre to complete their diagnostic itinerary and receive treatment, if indicated. Overall, the strategies used in this study could be recommended for screening undocumented immigrants and low-income refugees in several clinical settings.
In agreement with the recommendations of the Centers for Disease Control and Prevention in Atlanta, USA, the data from our study underscore the need for universal screening for HBV infection for people from countries with an HBsAg prevalence higher than 2% . In fact, the individuals from SSA, who accounted for over half of the subjects in this study, showed an ongoing HBV infection in 11.3% and a past HBV infection in more than half of the cases. The rate of HBsAg positivity observed in this subcontinent is very high, thus suggesting that in most cases HBV infection was acquired early in life, at birth from HBsAg-positive mothers, or in early youth from infected parents or siblings [3, 18, 19]. In addition, the immigrants from Eastern Europe, the India-Pakistan subcontinent, and Northern Africa investigated in this study showed intermediate HBsAg-positivity rates. The prevalences observed in undocumented immigrants and low-income refugees in this study indicate the widespread HBV infection in their countries of origin, since the rate of HBsAg positivity in Italy is estimated to be below 1% [20–23].
Subjects participating in the present study were relatively young, prevalently males, and had been living in Italy for a mean period of four and a half years. All immigrants with an ongoing or previous HBV infection were unaware of their serological status and, compared with the HBsAg/anti-HBc-negative patients, were more frequently males and more frequently from SSA. Accordingly, a logistic regression analysis identified the male sex and Sub-Saharan African origin as independent predictors of a persisting or past HBV infection. The other independent predictors identified in this study were a low level of schooling and the presence of ‘minor’ parenteral risk factors (acupuncture, tattooing, piercing, or tribal practices). Worthy of note is the observation that in our immigrant population, in which the ‘main’ routes of parenteral transmission played a minor role in transmitting HBV infection, the so-called ‘minor’ risk factors were instead identified as being independently associated with transmission. Furthermore, that education plays a major role in the prevention of infectious diseases is once again demonstrated in the present study, as a low level of schooling was independently associated with HBV transmission [4, 24–28].
Referred to one of the two tertiary units of infectious diseases for further investigation, monitoring, and possible treatment, approximately 10% of the subjects with a serum HBV load >2 000 IU/ml and nearly 40% of those with a lower HBV replication did not complete the diagnostic course. This partial success suggests that an improvement in the skills of some cultural mediators is necessary.
A conclusive diagnosis was obtained for 90 of the 116 HBsAg-positive immigrants: 29 were asymptomatic non-viremic HBsAg carriers, 43 were asymptomatic viremic carriers, and 18 had viremic chronic hepatitis or cirrhosis. Moreover, those with a HBV load above 2,000 IU/ml had chronic hepatitis or liver cirrhosis more frequently than those with lower viremia and, conversely, were less frequently asymptomatic viremic HBsAg carriers. These data indicate that, when applying only the HBV DNA serum value of 2,000 IU/ml to distinguish low from high viremic subjects for clinical and therapeutic decisions, as suggested by the current international guidelines , over 5% of the low viremic and nearly 40% of the high viremic immigrants in the present study could have been misclassified. It is very likely that the current international guidelines do not consider patients with HBV-genotype E chronic hepatitis, a genotype detected in recent years mostly in populations from SSA and which predominated in this study. We believe that more attention should be given to this genotype, the epidemiological impact of which is steadily increasing [29–33].
Literature on the treatment of HBV-related chronic hepatitis in immigrants is scanty [34–36] and does not allow for any conclusive evaluation. All chronic hepatitis and cirrhosis patients in the present study were considered for anti-HBV treatment and, in accordance with the current national guidelines [13, 37, 38], some were left untreated and some were treated with either peginterferon α-2a or nucleos(t)ide analogues, with results similar to those observed for the local Italian population [39–42].
The present investigation provides interesting information on the presence of HBV infection in undocumented immigrants and refugee populations from different geographical areas [43–47], and could be useful for devising healthcare strategies in Italy. Virtually all Italian citizens aged 0–35 years have HBV vaccination coverage , whereas none of the 1,212 undocumented immigrants or refugees in our study received active immune-prophylaxis against HBV nor had they been tested for HBV markers after an average stay in Italy of 4.5 years. Taking care of this vulnerable group of individuals should be a moral duty for every government or national healthcare system in developed countries [22, 47]. Extending monitoring and treatment of HBV chronic infection and HBV universal vaccination to undocumented immigrants and low-income refugees is a mandatory epidemiological approach towards eradicating HBV infection in this vulnerable group and in their host countries.
Acute hepatitis B
Hepatitis B core antibody
Hepatitis Be antibody
Hepatitis B envelope antigen
Hepatitis B surface antibody
Hepatitis B surface antigen
Hepatitis B virus
Hepatitis C virus
Human immunodeficiency virus
Hepatitis B. World Health Organization Fact Sheet No. 2004. Available from: http://who.int/mediacentre/factsheets/fs204/en accessed 5 June 2005.
Sagnelli E, Stroffolini T, Mele A, Imparato M, Sagnelli C, Coppola N, et al. Impact of comorbidities on the severity of chronic hepatitis B at presentation. World J Gastroenterol. 2012;18:1616–21.
Sagnelli E, Sagnelli C, Pisaturo M, Macera M, Coppola N. Epidemiology of acute and chronic hepatitis B and delta over the last 5 decades in Italy. World J Gastroenterol. 2014;20:7635–43.
Sagnelli E, Stroffolini T, Mele A, Imparato M, Almasio PL. Chronic hepatitis B in Italy: new features of an old disease-approaching the universal prevalence of hepatitis B e antigen-negative cases and the eradication of hepatitis D infection. Clin Infect Dis. 2008;46:110–3.
Rapporto ISTAT - Popolazione residente straniera per età e sesso al 1° Gennaio 2014. http://www.istat.it/it/archivio/132657.
Rapporto ISTAT - Popolazione residente per età, sesso e stato civile al 1° Gennaio 2014. http://dati.istat.it/Index.aspx?DataSetCode=DCIS_POPRES1 .
Walker PF, Jaranson J. Refugee and immigrant health care. Med Clin North Am. 1999;83:1103–20.
Mabey D, Mayaud P. Sexually transmitted disease in mobile populations. Genitourin Med. 1997;73:18–22.
Tiedje K, Wieland ML, Meiers SJ. A focus group study of healthy eating knowledge, practices, and barriers among adult and adolescent immigrants and refugees in the United States. Int J Behav Nutr Phys Act. 2014;11:63.
Coppola N, Alessio L, Gualdieri L, Pisaturo M, Sagnelli C, Caprio N et al. Hepatitis B Virus, Hepatitis C Virus and Human Immunodeficiency Virus infection in undocumented migrants and refugees in southern Italy, January 2012 to June 2013. EuroSurv. 2015; 20. doi: 10.2807/1560-7917
Coppola N, Sagnelli C, Pisaturo M, Minichini C, Messina V, Alessio L, et al. Clinical and virological characteristics associated with severe acute hepatitis B. Clinic Microb Inf Dis. 2014;20:991–7.
Coppola N, Zampino R, Cirillo G, Stanzione M, Macera M, Boemio A, et al. TM6SF2 E167K variant is associated with severe steatosis in chronic hepatitis C, regardless of PNPLA3 polymorphism. Liv Intern. 2015;35:1959–63.
European Association For The Study Of The Liver. EASL Clinical Practice Guidelines: Management of chronichepatitis B virus infection. J Hepatol. 2012;55:167–85.
Mancuso A. Management of hepatocellular carcinoma: Enlightening the gray zones. World J Hepatol. 2013;5:302–10.
Coppola N, Potenza N, Pisaturo M, Mosca N, Tonziello G, Signoriello G, et al. Liver microRNA hsa-miR-125a-5p in HBV Chronic Infection: Correlation with HBV Replication and Disease Progression. PLoS One. 2013;8:e65336.
Coppola N, Masiello A, Tonziello G, Pisapia R, Pisaturo M, Sagnelli C, et al. Factors affecting the changes in molecular epidemiology of acute hepatitis B in a Southern Italian area. J Viral Hep. 2010;17:493–500.
Weinbaum CM, Williams I, Mast EE, Wang SA, Finelli L, Wasley A, et al. Recommendations for identification and public health management of persons with chronic hepatitis B virus infection. MMWR Recomm Rep. 2008;57(RR-8):1–20.
Ott JJ, Stevens GA, Groeger J, Wiersma ST. Global epidemiology of hepatitis B virus infection: new estimates of age-specific HBsAg seroprevalence and endemicity. Vaccine. 2012;30:2212–9.
Lavanchy D. Hepatitis B, virus epidemiology, disease burden, treatment, and current and emerging prevention and control measures. J Viral Hepat. 2004;11:97–107.
Bonanni P, Pesavento G, Bechini A, et al. Impact of universal vaccination programmes on the epidemiology of hepatitis B: 10 years of experience in Italy. Vaccine. 2003;21:685–91.
Zanetti AR, Tanzi E, Romanò L, Grappasonni I. Vaccination against hepatitis B: the Italian strategy. Vaccine. 1993;11:521–4.
Da Villa G, Sepe A. Immunization programme against hepatitis B virus infection in Italy: cost-effectiveness. Vaccine. 1999;17:1734–8.
Coppola N, Corvino AR, De Pascalis S, Signoriello G, Di Fiore E, Nienhaus A, Sagnelli E, Lamberti M. The long-term immunogenicity of recombinant hepatitis B virus (HBV) vaccine: contribution of universal HBV vaccination in Italy. BMC Infect Dis. 2015;15:149.
de Paula Machado DF, Martins T, Trevisol DJ, Silva RA VE, Narciso-Schiavon JL, Schuelter Trevisol F, Schiavon Lde L. Prevalence and factors associated with hepatitis B virus infection among senior citizens in a southern brazilian city. Hepat Mon. 2013;135:e7874.
Al-Thaqafy MS, Balkhy HH, Memish Z, Makhdom YM, Ibrahim A, Al-Amri A, Al-Thaqafi A. Hepatitis B virus among Saudi National Guard personnel: seroprevalence and risk of exposure. J Infect Public Health. 2013;6:237–45.
Tozun N, Ozdogan O, Cakaloglu Y, Idilman R, Karasu Z, Akarca U, Kaymakoglu S, Ergonul O. Seroprevalence of hepatitis B and C virus infections and risk factors in Turkey: a fieldwork TURHEP study. Clin Microbiol Infect. 2015;21:1020–6.
Ma GX, Zhang GY, Zhai S, Ma X, Tan Y, Shive SE, Wang MQ. Hepatitis B screening among Chinese Americans: a structural equation modeling analysis. BMC Infect Dis. 2015;15:120.
Sagnelli E, Stroffolini T, Sagnelli C, Smedile A, Morisco F, Furlan C, et al. Epidemiological and clinical scenario of chronic liver diseases in Italy: Data from a multicenter nationwide survey. Dig Liver Dis. 2016 In press. doi: 10.1016/j.dld.2016.05.014
Hübschen JM, Andernach IE, Muller CP. Hepatitis B virus genotype E variability in Africa. J Clin Virol. 2008;43:376–80.
Araujo NM. Hepatitis B, virus intergenotypic recombinants worldwide: An overview. Infect Genet Evol. 2015;36:500–10.
Liu CJ, Kao JH, Chen DS. Therapeutic implications of hepatitis B virus genotypes. Liver Int. 2005;25:1097–107.
Liu CJ, Kao JH. Genetic variability of hepatitis B virus and response to antiviral therapy. Antivir Ther. 2008;13:613–24.
Croagh CM, Desmond PV, Bell SJ. Genotypes and viral variants in chronic hepatitis B: A review of epidemiology and clinical relevance. World J Hepatol. 2015;27(7):289–303.
Zhang S, Ristau JT, Trinh HN, Garcia RT, Nguyen HA, Nguyen MH. Undertreatment of asian chronic hepatitis B patients on the basis of standard guidelines: a community-based study. Dig Dis Sci. 2012;57:1373–83.
Giannini EG, Torre F, Basso M, Feasi M, Boni S, Grasso A, et al. A significant proportion of patients with chronic hepatitis B who are candidates for antiviral treatment are untreated: a region-wide survey in Italy. J Clin Gastroenterol. 2009;43:1001–7.
Veldhuijzen IK, Wolter R, Rijckborst V, Mostert M, Voeten HA, Cheung Y, et al. Identification and treatment of chronic hepatitis B in Chinese migrants: Results of a project offering on-site testing in Rotterdam. Neth J Hepat. 2012;57:1171–6.
AASLD, Terrault NA, Bzowej NH, Chang KM, Hwang JP, Jonas MM, Murad MH. Guidelines for Treatment of Chronic Hepatitis B. Hepatol. 2016;63:261–83.
Carosi G, Rizzetto M, et al. Treatment of chronic hepatitis B: update of recommendations from the 2007 Italian Workshop. Dig Liv Dis. 2011;43:259.
Bonino F, Marcellin P, Lau GK, Hadziyannis S, Jin R, Piratvisuth T, et al. Predicting response to peginterferon alpha-2a, lamivudine and the two combined for HBeAg-negative chronic hepatitis B. Gut. 2007;56:699–705.
Lampertico P, Viganò M, Di Costanzo GG, Sagnelli E, Fasano M, Di Marco V, Fargion S, Giuberti T, Iannacone C, Regep L, Massetto B, Facchetti F, Colombo M, PegBeLiverStudy Group, et al. Randomised study comparing 48 and 96 weeks peginterferonα-2a therapy in genotype D HBeAg-negative chronic hepatitis B. Gut. 2013;62:290–8.
Fasano M, Lampertico P, Marzano A, Di Marco V, Niro GA, Brancaccio G, Marengo A, Scotto G, Brunetto MR, Gaeta GB, Rizzetto M, Angarano G, Santantonio T. HBV DNA suppression and HBsAg clearance in HBeAg negative chronic hepatitis B patients on lamivudine therapy for over 5 years. J Hepatol. 2012;56:1254–8.
Lampertico P, Invernizzi F, Viganò M, Loglio A, Mangia G, Facchetti F, Primignani M, Jovani M, Iavarone M, Fraquelli M, Casazza G, de Franchis R, Colombo M. The long-term benefits of nucleos(t)ide analogs in compensated HBV cirrhotic patients with no or small esophageal varices: A 12-year prospective cohort study. J Hepatol. 2015;63:1118–25.
Williams R. Global challenges in liver disease. Hepatology. 2006;44:521–6.
World Health Organization statistics, available at: http://www.who.int/countries/rus/en/. Accessed 28 Dec 2016.
Van Sighem A, Nakagawa F, De Angelis D, Quinten C, Bezemer D, de Coul EO, et al. Estimating HIV Incidence, Time to Diagnosis, and the Undiagnosed HIV Epidemic Using Routine Surveillance Data. Epidemiology. 2015;26:653–60.
Maartens G, Celum C, Lewin SR. HIV infection: epidemiology, pathogenesis, treatment, and prevention. Lancet. 2014;384:258–71.
Papadakis G, Okoba NA, Nicolaou C, Boufidou F, Ioannidis A, Bersimis S, et al. Serologic markers for HBV, HCV and HIV in immigrants visiting the Athens’ polyclinic of ‘Doctors of the World - Greece’. Public Health. 2013;127:1045–7.
We thank Doctors Laura Paradiso, Nicolina Capoluongo, Valerio Rosato, Gaetano Pergola, Paolo Francesco Marino, Ciro Esposito, and Stefania De Pascalis, and the registered nurses Salvatore Auricchio, Vincenza Cangiano, Giacomo Sabatino, and Mrs. Asli Ahmed Abdulle for their invaluable technical assistance.
This study was supported in part by a grant from Gilead Sciences S.r.l. ‘L’infezione da HBV nelle popolazioni speciali (donne in gravidanza, popolazioni immigrate, popolazioni in età pediatrica): progetti di awareness ed accesso alla diagnosi’ Fellowship Program 2011 and 2013; and by a grant from 2014 goSHAPE program.
Availability of data and materials
The clinical data pertaining to the subjects enrolled in the study are anonymously collected in a dataset. The readers may contact the authors to access these data. At the time of the first observation, all subjects signed their informed consent according to the rules of the Ethics Committee of the Azienda Ospedaliera Universitaria-Seconda Università di Napoli for the collection and storage of plasma samples, and for the collection and use of their data in clinical research.
NC, LA, and ES were responsible for the conception and design of the study, interpreted the data, and wrote the paper. MS and CM performed the analysis of HBV serological and molecular assays. LG, CS, MP, LO, GDC, MM, and GP enrolled and followed up the patients. GS and IFA interpreted and analyzed the data and performed the statistical analysis. All authors read and approved the final paper.
The authors declare that they have no competing interests.
Ethics approval and consent to participate
The Ethics Committee of the Azienda Ospedaliera Universitaria of the Second University of Naples (214/2012) approved this study. Signed informed consent, written in the immigrant’s native language, was obtained on a voluntary basis from almost 91% of the 1 331 undocumented immigrants and low-income refugees at one of the four first-level clinical units during the study period. These were the subjects who participated in the study.
214/2012 at the Ethics Committee of the Azienda Ospedaliera Universitaria-Seconda Università di Napoli. Registered 3 November 2011
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Cite this article
Coppola, N., Alessio, L., Gualdieri, L. et al. Hepatitis B virus infection in undocumented immigrants and refugees in Southern Italy: demographic, virological, and clinical features. Infect Dis Poverty 6, 33 (2017). https://doi.org/10.1186/s40249-016-0228-4
- Hepatitis B
- Chronic hepatitis B virus infection
- Illegal immigrants