Author/Authors :
Xibing, Gu Wuxi Hospital for Infectious Diseases - Wuxi, China , Xiaojuan, Yang Wuxi Hospital for Infectious Diseases - Wuxi, China , Zhonghua, Lu Wuxi Hospital for Infectious Diseases - Wuxi, China , Juanhua, Wang Wuxi Hospital for Infectious Diseases - Wuxi, China
Abstract :
Background: It is difficult to predict what type of chronic hepatitis B (CHB) progresses to
chronic severe hepatitis B.
Objectives: This study aimed to observe changes in the HBV-specific and -nonspecific cellmediated
immune responses after CHB deteriorates into severe hepatic disease and explore
the significance of such changes.
Patients and Methods: This study aimed to observe changes in the HBV-specific and -nonspecific
cell-mediated immune responses after CHB deteriorates into severe hepatic disease
and explore the significance of such changes.
Results: In 49 of 255 CHB patients (19.22%), the disease developed into chronic severe
hepatitis (early stage) an average of 10.06 ± 1.73 days after admission. CD4+ and NK cells
levels in Group A were lower after progression into severe hepatitis than on the second
day of admission (baseline) (P < 0.01). CD8+ cells and nonspecific CTL levels in Group A
were higher after progression than at baseline (P < 0.01), and latter was higher than in
Group B at baseline (P < 0.01); the levels of CD8+ cells and nonspecific CTLs in Group A
after progression were significantly higher than those of Group B 10 days after admission
(P < 0.01). There were no significant differences in HBV-specific CTL levels in Group A
before and after progression to severe hepatitis (P > 0.05).
Conclusions: Our results suggest that the immunological pathogenesis of chronic severe
hepatitis B is related to significant rises in CD8+ and nonspecific CTL levels and that such
increases predict that the disease will deteriorate into severe hepatitis.
Keywords :
Hepatitis B, Chronic , T-Lymphocytes , Killer Cells, Natural