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Open Access Highly Accessed Research article

Occult Hepatitis B Virus infection in ART-Naive HIV-Infected Patients seen at a Tertiary Care Centre in North India

Swati Gupta and Sarman Singh*

Author Affiliations

Division of Clinical Microbiology, Department of Laboratory Medicine, All India Institute of Medical Sciences, New Delhi-110029, India

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BMC Infectious Diseases 2010, 10:53  doi:10.1186/1471-2334-10-53

The electronic version of this article is the complete one and can be found online at: http://www.biomedcentral.com/1471-2334/10/53


Received:25 March 2009
Accepted:7 March 2010
Published:7 March 2010

© 2010 Gupta and Singh; licensee BioMed Central Ltd.

This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

Abstract

Background

Co-infections of hepatitis B and C viruses are frequent with HIV due to shared routes of transmission. In most of the tertiary care health settings, HIV reactive patients are routinely tested for HBsAg and anti-HCV antibodies to rule out these co-infections. However, using the routine serological markers one can only detect active HBV infection while the occult HBV infection may be missed. There is insufficient data from India on HIV-HBV co-infection and even scarce on occult HBV infection in this group.

Methods

We estimated the burden of HBV infection in patients who were tested positive for HIV at a tertiary care centre in north India. We also attempted to determine the prevalence and clinical characteristics of occult HBV infection among these treatment-naïve patients and compare their demographic features with other HIV patients. During a period of 6 years between January 2002 to December 2007, 837 HIV positive patients (631 males and 206 females (M: F :: 3.06:1) were tested for serological markers of HBV (HBsAg) and HCV (anti-HCV antibodies) infections in our laboratory. For comparison 1000 apparently healthy, HIV-negative organ donors were also included in the study. Data on demographics, sexual behaviour, medical history, laboratory tests including the serum ALT and CD4 count of these patients were recorded. A sub-group of 53 HBsAg negative samples from HIV positive patients were assessed for anti-HBs, anti-HBc total (IgG+IgM) and HBV-DNA using a highly sensitive qualitative PCR and analysed retrospectively.

Results

Overall, 7.28% of HIV positive patients showed presence of HBsAg as compared to 1.4% in the HIV negative control group. The prevalence of HBsAg was higher (8.55%) in males than females (3.39%). The study revealed that occult HBV infection with detectable HBV-DNA was prevalent in 24.5% of patients positive for anti-HBc antibodies; being 45.5% in HBsAg negative patients. Most importantly the occult infection was seen in 20.7% patients who were positive for anti-HBs antibodies. However, in none of the seronegative patient HBV-DNA was detected. Five of the nine HBV-DNA positive (55.6%) patients showed raised alanine aminotransferase levels and 66.7% had CD4+ T cell counts below 200 cells/cumm.

Conclusions

High prevalence of HIV-HBV co-infection was found in our patients. A sizeable number of co-infected patients remain undiagnosed, if only conventional serological markers are used. Presence of anti-HBs antibodies was not a reliable surrogate marker to rule out occult HBV infection. The most reliable method to diagnose occult HBV co-infection in HIV seropositive patients is the detection of HBV-DNA.

Background

Human immunodeficiency virus (HIV) establishes a chronic and latent infection in the body that induces extensive damage to the immune system through virus-related as well as indirect pathogenic mechanisms [1]. HIV infected individuals show not only a quantitative depletion of CD4+ T cells but also an overall immune dysregulation. Hepatitis B virus (HBV) is a frequent co-contaminant with HIV, mainly because both share common modes of transmission. Whether the presence of one facilitates the sexual transmission of the other is a matter under investigation, but both are easily transmitted through infected blood, unsafe injections and equipments. Over the years, much evidence has accumulated that co-infection with HIV significantly modifies the natural history of HBV infection [2,3]. Highly active antiretroviral therapy (HAART) is well known to prolong the survival of HIV-infected individuals which allows a longer time for cirrhosis to develop in HBV co-infected patients. Therefore, HAART increases the relative proportion of deaths attributable to liver disease in these patients. HAART may also have a major impact on HBV co-infection because of restoration of specific and non-specific immune responses and decrease of aberrant activation and dysregulation of the immune system [4]. Withdrawal or development of resistance to drugs that are dually active against both HIV and HBV has been associated with reactivation of HBV infection and with flares of liver enzyme elevations and hepatic decompensation in patients with advanced liver disease [5,6].

At our institute all HIV reactive patients are also screened for hepatitis B surface antigen (HBsAg), if treating physician has any suspicion of co-infection. However, not all hepatitis B virus co-infections are symptomatic and even routine serological markers can miss the diagnosis of HBV disease. Those patients who turn out to be positive for HBV-DNA in the absence of serum HBsAg are known as occult hepatitis B virus (HBV) infections [7]. Occult HBV infection is characterised by long lasting persistence of HBV-DNA in serum, and/or hepatic tissues of individuals negative for serum HBsAg. The presence of antibodies to HBV core antigen (anti-HBc-IgM) is now recognized as a better indicator of progressing occult HBV infection. But, recent estimates suggest that up to 20% of individuals with occult HBV could be negative even for anti-HBc antibodies or any other serological indicator of exposure to HBV [7]. Some studies also show that the detection of naturally acquired antibodies to HBsAg (anti-HBs) does not exclude the existence of occult infection [8], indicating that diagnosis of occult HBV co-infection is a challenging task for laboratory physicians.

True prevalence and clinical significance of occult HBV infections is scarcely reported in the literature. Occult HBV has been implicated in the transmission of the HBV via transfusion of blood and blood products [9,10] and transplanted solid organs [11] leading to hepatitis in recipients. Reactivation of occult infection has also been reported in hematologic malignancies [12], and immunosuppressed states [13] with reconstitution of immune surveillance associated with activation of virus and cytotoxic T-cell mediated hepatitis. However, the prevalence of occult HBV infection in HIV-infected persons is more so controversial because of the lack of standardization of diagnostic methods and fewer prospective studies. Studies have reported rates of occult HBV markedly varying from as low as nil to as high as 89.5% [14-17] in these patients. However, there are only a few reports of occult HBV infection, as such from India and even scarce in HIV seropositive patients. In this study, we estimated the burden of HBV in patients who tested positive for HIV at a tertiary care centre in north India. We also attempted to determine the prevalence and clinical characteristics of occult HBV among HIV-infected, treatment- naïve patients.

Methods

Study population

The study was carried out in the Clinical Microbiology Division, Department of Laboratory Medicine at the All India Institute of Medical Sciences (AIIMS). At this referral institute patients suspected with HIV associated illnesses are seen in the medicine out-patient clinics. Here they are counselled by a social worker and informed consent is taken for testing. As a routine, our laboratory follows the World Health Organization (WHO) testing strategies for HIV test followed by post-test counselling of the patients and this is documented. As an investigative protocol at the institute, all confirmed HIV positive patients are screened for Hepatitis B (HBsAg) and C viruses (anti-HCV antibodies) as a part of their pre-ART work-up beside other tests. A retrospective analysis was performed on data collected from January 2002 to December 2007 in the laboratory.

Laboratory analysis

Serum samples from 837 proven HIV seropositive patients (WHO testing strategy III, as mentioned above) were collected, labelled with a laboratory identification serial number and stored at -20°C in separate aliquots for further testing upto 10 years or till the storage space is available. From these samples one aliquot was tested for HBsAg and for anti-HCV antibodies using enzyme linked immunosorbent assay kits (bio Merieux, France). All serum samples were tested in duplicate.

From the stored serum samples of 776 HIV positive but HBsAg negative patients, we selected 53 serum samples randomly, for reasons of feasibility and availability of reagents and quantity of samples. These were tested for occult HBV infection viz. for anti-HBs antibodies (bio Merieux, France), anti HBc total (IgG+ IgM; biokit, Spain) and a qualitative PCR for HBV DNA (SORPOline™ HBV end-point PCR kit) was also done. This PCR kit has a reported sensitivity of 10-30 copies of HBV. Risk factors and transaminase levels weer ascertained at the time of sample collection. Data on demographics, sexual behaviour, medical history, other laboratory tests including., serum ALT and CD4+ count were also analysed from the records. All tests were performed in accordance with the institutional ethical guidelines at that time. Data of 1000 age and sex matched HIV-negative healthy organ donors was also analysed to compare the prevalence of hepatitis markers. These organ donors are screened with due consent for viral markers as a routine work-up for their family members requiring organ transplantation, as described earlier [18].

Statistical analysis

Comparison of proportions among different groups and characteristics was done using Fisher's exact test. p < 0.05 was taken as significant.

Results

A retrospective analysis was performed on laboratory data from 837 HIV sero-reactive patients who were tested in our laboratory from January 2002 to December 2007. Among the study subjects, there were 631 males and 206 females (M: F - 3.06:1). These patients aged between 1-73 years (median 32 years). Overall, HBsAg positivity (HBV co-infection) was seen in 61 (7.28%) HIV positive patients. This rate was highly significant (p < 0.0001) when compared to 1.4% in the control group which comprised of age and sex matched HIV-negative healthy persons. Further, out of the 61 serologically (HBsAg positive) reactive subjects for HIV and HBV co-infection; 54 were males and 7 female. Our patients were in the age range of 14-69 years (median 36 years), but the HBsAg positivity rate was significantly higher in males (8.55%) as compared to 3.39% in female patients (p = 0.0129). Majority (635 of 837) of the HIV positive patients were aged between 21-40 years. This trend was similar in HIV-HBV co-infected patients also (table 1).

Table 1. Comparative distribution of HIV positive patients by age and gender divided into two groups on the basis of presence or absence of HBsAg.

Among the 53 HBsAg negative samples tested for occult HBV infection, 41 (77.4%) were males and 12 (22.6%) females. The age group of these patients ranged from 21-59 years (median 32 years). The patients belonged to different risk groups, but the heterosexual risk group was the most predominant. None of these patients gave history of vaccination against HBV. Serological markers of HBV exposure (other than HBsAg, i.e. either anti-HBs or anti-HBc antibody positivity) were seen in 45.3% (24 out of 53) patients. While in 29 patients no marker was detected (table 2). Among these 53 patients, 20.7% (11) showed anti-HBs antibodies and 35.8% (19) anti-HBc (total) antibodies. There was no statistical difference in the prevalence of these markers in two genders; being 46.3% in males and 41.7% in females (table 2). Of the various risk factors for occult HBV infection, male gender combined with low CD4+ counts below 200 cells/cumm and raised alanine aminotransferase levels (>40 IU/L) were most significant (table 3).

Table 2. Characteristics and positivity rate of other HBV serological markers in HBsAg-negative HIV-seropositive patients in whom the occult HBV infection rate was investigated.

Table 3. Characteristics and HBV-DNA positivity in HBsAg negative HIV positive patients with or without the presence of other marker of HBV infection.

HCV co-infection was seen in only 5 (9.4%) of the 53 HBsAg negative patients. This rate was only marginally lower (6.2%) in 61 HBsAg positive pool. Among the HIV-HCV co-infected patients, positivity for anti-HBs/anti-HBc was seen in 80% samples as compared to 41.7% in HCV negative samples (p = 0.163). Tuberculosis (TB) is a common infection in Indian HIV positive patients; hence we compared the presence of these serological markers of occult HBV infection in HIV-TB co-infected and uninfected patients. We found that presence of either of the HBV markers was seen in 35.2% of TB positive patients and in 50% of TB uninfected patients. This difference was statistically insignificant. Anti-HBc alone (in absence of anti-HBs) as a marker of occult infection was seen in 11.3% of samples tested and was associated with lower CD4+ levels below 200 cells/cumm in 84.6% patients (p = 0.032) as compared to higher CD4+ levels (table 3). None of the other characteristics showed a significant association with anti-HBc positivity.

HBV-DNA was positive in 45.3% (24/53) samples which were negative for HBsAg but positive for other HBV serological marker. As mentioned above, none of 29 patients who were negative for all HBV seromarkers was positive for HBV-DNA. In patients who were positive only for anti-HBc antibodies, we found a 24.5% (13/53) prevalence rate of occult HBV infection (HBV-DNA positive). However, the most significant finding of this study was that HBV-DNA was detected in 20.7% (11/53) patients in whom circulating anti-HBs antibodies were detectable. Of the HBV-DNA positives 55.6% (5 of 9) patients showed raised alanine aminotransferase levels while 66.7% (6 of 9) had a CD4+ T cell counts below 200 cells/cu mm. The prevalence rates of HBV-DNA were comparable in both males (36.8%) and females (40%). The demographic and laboratory characteristics of HBV-DNA positive and negative patients were significantly indifferent (table 3).

Discussion

Co-infection of HIV significantly modifies the natural history of HBV infection. Before availability of HAART it was associated with a higher chronicity rate of acute hepatitis B, higher levels of HBV replication, a lower rate of spontaneous loss of HBV antigens and a high rate of reactivation [2-4]. However, even after widespread institution of HAART, studies have shown increased number of deaths attributed to liver disease possibly due to prolonged survival and time for development of cirrhosis. Reports of flares of necro-inflammatory activity in liver are also documented due to restoration of adaptive HBV specific immune response and innate non-specific immune responses [4]. The treatment of HBV in HIV co-infected patients is complex because the drug(s) used are associated with drug-resistance, cross-resistance, hepatotoxicity and unresponsiveness. Another major concern is reactivation of HBV replication after withdrawal of dually active antiviral drugs leading to emergence of resistant strains.

Our study findings indicate that HIV-infected patients are at a higher risk of HBV co-infection in our set-up, as illustrated by the high prevalence of HBsAg (7.28%) in HIV positive patients in comparison to HIV negative patients (1.4%). Male patients were found more likely to be co-infected with HBV as compared to females (table. 1). This trend can be explained on the basis of higher rate of sexual promiscuity and other exposure risks in males. The majority of HIV-HBV co-infections were seen in the sexually active population indicating a common mode of transmission to these viruses, as has been previously documented [19]. Our study also shows a very high persistence of HBV genome (overall 37.5%) even in those patients who are HBsAg negative. The study further shows that like HBsAg other serological markers were also of lesser value to rule out the occult infection of HBV which is supported by the data that occult HBV infection was frequent in those who were positive for anti-HBc antibodies and also those who had significant levels of anti-HBs antibodies in their serum. Presence of Anti-HBc antibodies alone was also found associated with low CD4+ cell counts (less than 200), even though these patients were treatment naive. Interestingly presence of naturally acquired antibodies to HBsAg (anti-HBs) did not exclude the existence of occult infection.

The clinical relevance of occult HBV infection in humans is not limited to blood banks but it is a still ongoing process. HBV particles may persist for decades after self-limited acute hepatitis and clinical recovery [20]. Thus, though occult infection alone may not have clinical consequences but may become injurious only when the virus is reactivated after immunosuppression [12,13]. A number of explanations for the persistence of HBV-DNA in HBsAg negative samples have been proposed, including the presence of HBV-DNA at a low copy number [21], genetic variations in the S gene [22] and the presence of immune complexes in which HBsAg may be hidden [23]. Many epidemiologic and molecular studies indicate that persistent HBV infection may have a critical role in the development of hepatocellular carcinoma in HBsAg-negative patients. Occult HBV infection and its potential oncogenicity are traditionally considered a consequence of the capacity of the virus to be integrated into the host genome, although many observations now show that free episomal HBV genomes may persist in the liver cells during occult infection. It may induce mild long lasting necroinflammation [20] and may progress to cirrhosis and hepatocellular carcinoma [24]. Studies have also shown that mutations in the hepatitis B X gene (HBx) protein modify the functioning of p53, a tumor suppressor gene [25]. It is still unclear if there is an altered prevalence of such mutations in occult HBV infections or if coinfection with HIV could play a catalytic role.

Though reactivation of HBV infection (in the absence of HBsAg) has been described anecdotally in HIV-infected patients following severe immune depletion and/or lamivudine withdrawal, yet the true prevalence and clinical impact of occult HBV infection in HIV- infected subjects is controversial due to lack of methodological standardisation and fewer prospective studies. The available data on prevalence of occult HBV are wildly divergent and inadequate. In fact, the published prevalence rates range from 0% to 89%, with a considerable number of other studies reporting results between these two extremes [26]. One basis for difference could be the difference in methodologies adopted by various workers and the number of samples tested. One recent study which tested a prospective cohort of 909 HIV positive patients for occult HBV showed a prevalence of 1.3% [17], but the sera were pooled in this study which makes it incomparable to ours. However, there is no study from Indian sub-continent to compare our results.

HBV-DNA detection has made significant impact on the management of these patients. According to treatment guidelines for HIV co-infected individuals, it is advocated that HBsAg positive patients should be treated in presence of elevated HBV-DNA, raised aminotransferases or significant hepatic fibrosis [27]. But, as yet no clear guidelines have been established for occult HBV co-infection in HIV positive patients. Moreover, the issue needs to be addressed whether to offer HBV vaccine to HBsAg negative HIV positive patients harbouring occult HBV infection. This study even though had some limitations, clearly indicates that routinely used serological markers of HBV infection do not rule out occult and ongoing Hepatitis B virus infection and emphasizes application of molecular methods for the detection of occult HBV infection in these patients. Some blood banks around the world have now routinely started nucleic acid testing (NAT) to ensure safe blood transfusion practices. However, this practice needs to be extended at every blood bank and specially when managing the HIV positive patients.

Limitation of The study

A major limitation in our study was the small sample size and that it was a single time point testing without any follow-up. The sample size of the studied patients was small even though we have a large pool of patients due to cost constraints. The HBV-DNA estimation along with all serological marker costs us approximately US 100 per patients. We are in process of getting funds to test all our patients to assess the prevalence of occult HBV infection in all HIV positive patients. We also had limitation of not doing multivariate analysis of the data. Since it was a cross-sectional study we could not comment on the clinical significance of occult HBV in HIV patients included in our study. Lastly, since ours is a tertiary care referral centre, hence a patient selection bias cannot be completely ruled out.

Conclusion

A sizeable number of HIV-HBV co-infected patients remain undiagnosed, if only conventional serological markers for HBV are used. The presence of anti-HBs antibodies is also an unreliable surrogate marker to rule out occult HBV infection. Though the most reliable method to diagnose occult HBV co-infection in HIV seropositive patients remains the detection of HBV DNA, it would not be practical yet to recommend this highly sensitive molecular assay for each and every patient in resource limited countries.

Competing interests

The authors declare that they have no competing interests.

Authors' contributions

SS was responsible for conceptualizing the study, arranging diagnostic services and facilities and critically reviewing the manuscript. SG analysed the data and prepared the draft of manuscript with data analysis and manuscript preparation. Both authors read and approved the manuscript.

Acknowledgements

The authors wish to thank Mrs. Veena Balooni for technical assistance. Partial funding for the study was provided by the Department of Science and Technology, Government of India.

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Pre-publication history

The pre-publication history for this paper can be accessed here:

http://www.biomedcentral.com/1471-2334/10/53/prepub