HBeAg Levels Vary across the Different Stages of HBV Infection According to the Extent of Immunological Pressure and Are Associated with Therapeutic Outcome in the Setting of Immunosuppression-Driven HBV Reactivation

Autor: Carla Fontana, Patrick T F Kennedy, Elisa Basile, Carlotta Cerva, Valentina Svicher, Maria De Cristofaro, A. Iuvara, L. Piermatteo, Stefano D’Anna, Francesca Ceccherini-Silberstein, Mariantonietta Pisaturo, Loredana Sarmati, Carmine Minichini, Mohammad Alkhatib, Mario Starace, Romina Salpini, Eleonora Andreassi, Sandro Grelli, Massimo Andreoni, Upkar S. Gill, Ada Bertoli, Vincenzo Malagnino, Nicola Coppola, Giuseppina Cappiello
Přispěvatelé: Piermatteo, Lorenzo, Alkhatib, Mohammad, D'Anna, Stefano, Malagnino, Vincenzo, Bertoli, Ada, Andreassi, Eleonora, Basile, Elisa, Iuvara, Alessandra, De Cristofaro, Maria, Cappiello, Giuseppina, Cerva, Carlotta, Minichini, Carmine, Pisaturo, Mariantonietta, Starace, Mario, Coppola, Nicola, Fontana, Carla, Grelli, Sandro, Ceccherini-Silberstein, Francesca, Andreoni, Massimo, Gill, Upkar S, Kennedy, Patrick T F, Sarmati, Loredana, Salpini, Romina, Svicher, Valentina, Piermatteo, L., Alkhatib, M., D'Anna, S., Malagnino, V., Bertoli, A., Andreassi, E., Basile, E., Iuvara, A., De Cristofaro, M., Cappiello, G., Cerva, C., Minichini, C., Pisaturo, M., Starace, M., Coppola, N., Fontana, C., Grelli, S., Ceccherini-Silberstein, F., Andreoni, M., Gill, U. S., Kennedy, P. T. F., Sarmati, L., Salpini, R., Svicher, V.
Rok vydání: 2021
Předmět:
Zdroj: Biomedicines
Volume 9
Issue 10
Biomedicines, Vol 9, Iss 1352, p 1352 (2021)
ISSN: 2227-9059
Popis: HBeAg is a marker of HBV-activity, and HBeAg-loss predicts a favorable clinical outcome. Here, we characterize HBeAg-levels across different phases of HBV infection, their correlation with virological/biochemical markers and the virological response to anti-HBV therapy. Quantitative HBeAg (qHBeAg, DiaSorin) is assessed in 101 HBeAg+ patients: 20 with acute-infection, 20 with chronic infection, 32 with chronic hepatitis and 29 with immunosuppression-driven HBV-reactivation (HBV-R). A total of 15/29 patients with HBV-R are monitored for >
12 months after starting TDF/ETV. qHBeAg is higher in immunosuppression-driven HBV-R (median[IQR]:930[206–1945]PEIU/mL) and declines in chronic hepatitis (481[28–1393]PEIU/mL, p = 0.03), suggesting HBeAg production, modulated by the extent of immunological pressure. This is reinforced by the negative correlation between qHBeAg and ALT in acute infection (Rho = −0.66, p = 0.006) and chronic hepatitis (Rho = −0.35
p = 0.05). Interestingly, qHBeAg strongly and positively correlates with qHBsAg across the study groups, suggesting cccDNA as a major source of both proteins in the setting of HBeAg positivity (with limited contribution of integrated HBV-DNA to HBsAg production). Focusing on 15 patients with HBV-R starting TDF/ETV, virological suppression and HBeAg-loss are achieved in 60% and 53.3%. Notably, the combination of qHBeAg >
2000 PEIU/mL + qHBsAg >
52,000 IU/mL at HBV-R is the only factor predicting no HBeAg loss (HBeAg loss: 0% with vs. 72.7% without qHBeAg >
52,000 IU/mL, p = 0.03). In conclusion, qHBeAg varies over the natural course of HBV infection, according to the extent of immunological pressure. In the setting of HBV-R, qHBeAg could be useful in predicting the treatment response under immunosuppression.
Databáze: OpenAIRE