HIV-HBV Coinfection
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Good Response to Hepatitis B Treatment is Associated Sustained Response to Antiretroviral Therapy in HIV-HBV Coinfected Patients

Due to overlapping transmission routes, many people with HIV also have evidence of past or present hepatitis B virus (HBV) infection. However, little is known about the natural history of chronic hepatitis B and its treatment in HIV-HBV coinfected individuals, nor about the effects of antiretroviral therapy in this population.

As reported in the September 1, 2007 issue of Clinical Infectious Diseases, French researchers retrospectively analyzed data from 92 HIV-HBV coinfected patients collected before and after HAART and lamivudine (3TC, Epivir) treatment. The investigators aimed to determine the impact of treatment on chronic hepatitis B and factors associated with hepatitis B "e" antigen (HBeAg) or hepatitis B surface antigen (HBsAg) seroconversion.

Lamivudine is active against both HIV and HBV, and is approved for the treatment of both diseases. Two other approved anti-HIV drugs, emtricitabine (Emtriva) and tenofovir (Viread), are also active against hepatitis B, but not yet approved for this indication. Two additional approved anti-HBV drugs, adefovir (Hepsera) and entecavir (Baraclude), have low-level activity against HIV at standard doses.

Results

During the follow-up period, 82 patients received antiretroviral therapy, 79 of whom received combination HAART.

76 patients received lamivudine, 28 of whom (36.8%) developed lamivudine resistance mutations.

While receiving antiretroviral therapy, 10 of 59 HBeAg positive patients (17%) developed antibodies to HBeAg, 3 of 10 (30%) cleared HBsAg, and 2 of 3 (66%) developed antibodies to HBsAg.

2 of 23 initially HBeAg negative patients (9%) cleared HBsAg and developed antibodies to HBsAg.

Patients who responded to anti-HBV therapy with HBeAg and/or HBsAg seroconversion combined with an undetectable HBV DNA level were more likely to achieve sustained response to anti-HIV treatment (P = 0.001).

This occurred despite the fact that these patients had a shorter average duration of antiretroviral therapy and more severe HIV disease (higher CDC stage).

For patients with elevated baseline alanine aminotransferase (ALT) levels, response to anti-HBV therapy correlated with a larger CD4 cell increase while receiving HAART.

Conclusion

In conclusion, the authors wrote, "In HIV-HBV coinfected patients, HBV response correlated with a sustained HIV response to antiretroviral therapy, usually HAART including lamivudine."

In an editorial accompanying the report, Hans Tillmann, MD, from the University of Leipzig in Germany noted that the study yielded some unexpected results, among them that a shorter course of antiretroviral therapy and lower CD4 cell count were associated with a higher likelihood of HBeAg and/or HBsAg seroconversion

Given that HBV infection B is preventable with a vaccine -- which has been shown to be effective in people with HIV -- Tillman emphasized the need for better prevention and screening efforts rather than waiting to treat HIV positive people until after they develop chronic hepatitis B.

09/28/07

References

P Miailhes, MA Trabaud, P Pradat, and others. Impact of highly active antiretroviral therapy (HAART) on the natural history of hepatitis B virus (HBV) and HIV coinfection: relationship between prolonged efficacy of HAART and HBV surface and early antigen seroconversion. Clinical Infectious Diseases 45(5): 624-632. September 1, 2007.

HL Tillman. Screening for and treating hepatitis B virus in patients with HIV infection. Clinical Infectious Diseases 45(5): 633-636. September 1, 2007.