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©The Author(s) 2024.
World J Gastroenterol. Mar 14, 2024; 30(10): 1295-1312
Published online Mar 14, 2024. doi: 10.3748/wjg.v30.i10.1295
Published online Mar 14, 2024. doi: 10.3748/wjg.v30.i10.1295
Table 1 Mechanisms of immune cell response in hepatitis B virus reactivation
| Immune cells | Mechanism of impairment | Outcomes | Ref. |
| Innate immune cell responses | |||
| Natural killer cells | Downregulation of activating receptors (NKp30, NKp46, and CD56dim), inhibitory cytokine production (IFN- and TNF-) | Reduced viral clearance, increased reactivation risk | [62,64] |
| Dendritic cells | Reduced antigen presentation (CD8+ CTLs), impaired cytokine (IL-12 and IL-18) production | Impaired antiviral response, increased viral persistence | [40,65] |
| Macrophages | Dysregulated cytokine secretion (IL-1β, IL-6, and TNF-α) | Altered immune balance, increased inflammation | [49] |
| Neutrophils | Impaired chemotaxis, reduced phagocytosis | Ineffective pathogen clearance, prolonged viremia | [55] |
| Adaptive immune cell responses | |||
| CD8+ T cells | Exhaustion (CD8+ T cells), reduced cytotoxic activity | Inadequate viral control, viral persistence | [66] |
| CD4+ T cells | Decreased help for B and CD8+ T cells | Impaired adaptive immune response | [67] |
| B cells | Altered antibody production | Reduced neutralizing antibodies, prolonged viremia | [68] |
| Regulatory T cells | Dysfunction, reduced suppression | Dysregulated immune response, increased inflammation | [69] |
Table 2 Strategies for the management of hepatitis B virus reactivation
| Therapy | Model | Mechanism | Efficacy | Success rate, % | Resistance | Ref. |
| Anti-viral therapy | ||||||
| Nucleos(t)ide | Lamivudine | Inhibits viral DNA synthesis | High | 80% | Low | [30] |
| Entecavir | Potent viral DNA polymerase | High | 90% | Rare | [120] | |
| Adefovir | Inhibits viral DNA polymerase | Moderate | 70%-80% | Occasional | [128] | |
| Tenofovir | Inhibits viral DNA synthesis | High | 90% | Rare | [124] | |
| Monoclonal antibodies | Anti-HBV antibodies | Viral neutralization | Moderate | 70% | Occasional | [137] |
| Combination therapy | Tenofovir + emtricitabine | Inhibits viral DNA synthesis | High | 95% | Low | [138] |
| Immune-modulating therapy | ||||||
| Toll-like receptor agonists | Immune activation | Moderate | 70% | Variable | [139] | |
| Interferon | Antiviral and immune activation | High | 80% | Occasional | [140] | |
| Personalized treatment approaches | ||||||
| Tailored | Targeted antiviral therapy based on genomic profile | Variable | 75%-90% | Variable | [141] | |
| Treatment | ||||||
| Combination therapy | Nucleos(t)ide + immune-modulating therapy | Antiviral + immunomodulation | High | 90%-95% | Low | [142] |
| Monoclonal antibodies | Individualized treatment | Targeted viral neutralization based on antibody profiling | Varies | 60%-80% | Occasional | [143] |
- Citation: Ma H, Yan QZ, Ma JR, Li DF, Yang JL. Overview of the immunological mechanisms in hepatitis B virus reactivation: Implications for disease progression and management strategies. World J Gastroenterol 2024; 30(10): 1295-1312
- URL: https://www.wjgnet.com/1007-9327/full/v30/i10/1295.htm
- DOI: https://dx.doi.org/10.3748/wjg.v30.i10.1295
