Abstract:Liver-related mortality is an increasing problem in human immunodeficiency virus (HIV)/hepatitis B virus (HBV)-coinfected patients receiving highly active antiretroviral therapy (HAART). In HIV-negative patients, HBV chronicity is associated with a reduction in specific T cell responses that can be partially restored by treatment with lamivudine. We studied 5 HIV/HBV-coinfected patients treated with HAART, either with or without addition of a drug with specific anti-HBV activity. Our data show that reconstitut… Show more
“…A previous immunologic study involving 5 patients coinfected with HIV and HBV found evidence of the reconstitution of a functionally active HBV-specific CD8 cell response when HAART was combined with an anti-HBV drug [14]. More recently [15], the same group demonstrated that an HBV-specific CD8 cell response had been reconstituted in 50% of the HIV-infected patients receiving HAART.…”
“…A previous immunologic study involving 5 patients coinfected with HIV and HBV found evidence of the reconstitution of a functionally active HBV-specific CD8 cell response when HAART was combined with an anti-HBV drug [14]. More recently [15], the same group demonstrated that an HBV-specific CD8 cell response had been reconstituted in 50% of the HIV-infected patients receiving HAART.…”
“…HBV-specific CD8 T-cell responses recover in patients on ART, but this has not been related to LEE (75,76). A lack of HBV-specific CD4 T-cell help in HIV-HBV-coinfected individuals may lead to an inefficient or dysregulated HBV-specific CD8 T-cell response and/or a greater role for innate immunity (24).…”
Section: Ird May Present As Lee Following Initiation Of Art In Hiv-hbmentioning
SUMMARY
Up to one in four patients infected with human immunodeficiency virus type 1 and given antiretroviral therapy (ART) experiences inflammatory or cellular proliferative disease associated with a preexisting opportunistic infection, which may be subclinical. These immune restoration diseases (IRD) appear to result from the restoration of immunocompetence. IRD associated with intracellular pathogens are characterized by cellular immune responses and/or granulomatous inflammation. Mycobacterial and cryptococcal IRD are attributed to a pathological overproduction of Th1 cytokines. Clinicopathological characteristics of IRD associated with viral infections suggest different pathogenic mechanisms. For example, IRD associated with varicella-zoster virus or JC polyomavirus infection correlate with a CD8 T-cell response in the central nervous system. Exacerbations or de novo presentations of hepatitis associated with hepatitis C virus (HCV) infection following ART may also reflect restoration of pathogen-specific immune responses as titers of HCV-reactive antibodies rise in parallel with liver enzymes and plasma markers of T-cell activation. Correlations between immunological parameters assessed in longitudinal sample sets and clinical presentations are required to illuminate the diverse immunological scenarios described collectively as IRD. Here we present salient clinical features and review progress toward understanding their pathogeneses.
“…Independent of the use of lamivudine, HAART may induce reconstitution of the adaptive immune response and this is a 'double-edged sword' in patients infected with HBV: on one side, anecdotal reports suggest the induction of HBV seroconversion and therefore a better control of HBV replication with or without flares of necro-inflammatory activity [41][42][43][44]; on the other side, flares of necroinflammatory activity have been reported without modification of HBV markers and of HBV replication levels [45][46][47][48]. However, the incidence of HAART-induced HBsAg seroconversion has not been accurately determined, but occurred in one out of 24 HBsAg-positive patients prospectively followed during HAART in one of the largest published studies [49].…”
Section: Natural History Of Hbv-related Disease In Hiv-infected Patiementioning
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