Hullegie Sebastiaan J, Arends Joop E A, Groothuismink Zwier M A, Pas Suzan D, Rijnders Bart J A, Boonstra Andre, Claassen Mark A A
Department of Infectious Diseases, Erasmus MC, Rotterdam, The Netherlands.
Department of Infectious Diseases, University Medical Center Utrecht, Utrecht, The Netherlands.
J Gen Virol. 2017 Jun;98(6):1294-1298. doi: 10.1099/jgv.0.000768. Epub 2017 Jun 8.
Patients in high-risk groups continue to transmit the hepatitis C virus (HCV) and frequently experience reinfections. Since little is known regarding the immune response to HCV during reinfection, we compared primary and consecutive acute HCV infections in patients with an HIV infection, and focused on the cytokine bridging innate to adaptive immunity. We observed that the serum levels of IL-12p40, MIP-1β, MIG and IP-10 increased during primary acute HCV infection, but not during subsequent secondary acute reinfections. The weaker pro-inflammatory cytokine responses observed during HCV reinfections suggest more limited secondary acute immune responses, which may prevent damage to the infected liver.
高危人群中的患者持续传播丙型肝炎病毒(HCV),并经常发生再次感染。由于对再次感染期间HCV的免疫反应了解甚少,我们比较了HIV感染患者的初次和连续急性HCV感染,并重点关注连接固有免疫和适应性免疫的细胞因子。我们观察到,在初次急性HCV感染期间,血清IL-12p40、MIP-1β、MIG和IP-10水平升高,但在随后的二次急性再感染期间则没有升高。在HCV再感染期间观察到的较弱的促炎细胞因子反应表明二次急性免疫反应更有限,这可能会防止对受感染肝脏的损伤。