Improved Immune Status Corresponds with Long-Term Decline of Quantitative Serum Hepatitis B Surface Antigen in HBV/HIV Co-infected Patients

被引:13
作者
Arendt, Eduard [1 ]
Jaroszewicz, Jerzy [1 ,2 ]
Rockstroh, Juergen [3 ]
Meyer-Olson, Dirk [4 ]
Zacher, Behrend J. [1 ]
Mederacke, Ingmar [1 ]
Manns, Michael P. [1 ]
Wedemeyer, Heiner [1 ]
Cornberg, Markus [1 ]
Wursthorn, Karsten [1 ]
机构
[1] Hannover Med Sch, Dept Gastroenterol Hepatol & Endocrinol, D-30625 Hannover, Germany
[2] Med Univ Bialystok, Dept Infect Dis & Hepatol, Bialystok, Poland
[3] Univ Bonn, Dept Internal Med 3, Bonn, Germany
[4] Hannover Med Sch, Dept Immunol & Rheumatol, D-30625 Hannover, Germany
关键词
HUMAN-IMMUNODEFICIENCY-VIRUS; PEGINTERFERON ALPHA-2A; SUSTAINED RESPONSE; NATURAL-HISTORY; HBV; PREDICTION; HBSAG; COINFECTION; KINETICS;
D O I
10.1089/vim.2012.0036
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
In HBV/HIV-co-infected individuals, the course of hepatitis B is aggravated, leading to higher morbidity and mortality rates. Increasing evidence suggests an important role for hepatitis B surface antigen (HBsAg) quantification in monitoring treatment efficacy in HBV monoinfection. However, data concerning any HBsAg decline during treatment of HBV/HIV coinfection are limited. Fifty-one HBV/HIV-co-infected patients were retrospectively followed for a mean of 43 months (median 2 years, interquartile range 2 years). Baseline and on-treatment parameters were associated with longitudinal HBsAg levels. At baseline, serum HBsAg levels were comparable between patients on antiretroviral therapy (ART; n = 43) and patients without (n = 8). Longitudinally, HBsAg decreased in ART patients (-0.20 +/- 0.09 log(10) IU/mL/y), but slightly increased in subjects without therapy (0.22 +/- 0.26 log(10) IU/mL/y; p < 0.001). In 58% of the ART subjects an HBsAg decline > 10% was seen during the initial 24 mo. They showed higher baseline CD4 counts (401 +/- 42 versus 265 +/- 50 cells/mu L, p = 0.03), and had significantly higher CD4 counts at the last follow-up compared to patients without a decline (506 +/- 39 versus 310 +/- 51 cells/mu L, p = 0.01). A significant correlation was found between HBsAg decline from baseline to the last follow-up and the absolute increase of CD4 cells (r = 0.44, p = 0.003), as well the last CD4 count (r = 0.41, p = 0.006). This association was strongest in patients with complete suppression of HBV-DNA and HIV-RNA at the last follow-up visit. The highest HBsAg decline (-1.63 +/- 0.32 versus -0.43 +/- 0.24 log(10) IU/mL, p = 0.001), and yearly HBsAg decline (-0.47 +/- 0.13 versus -0.19 +/- 0.12 log(10) IU/mL, p = 0.03), were found in patients with CD4 increases > 100 cells/mu L at the last follow-up (n = 21, 49%). Four cases of HBsAg loss were observed (8%). HBsAg declines steadily in > 50% of HBV/HIV patients on ART. Long-term follow-up of HBV/HIV-co-infected patients is needed to identify distinct HBsAg patterns. Increasing CD4 counts indicating the restoration of immune competence in HBV/HIV-co-infected patients is associated with a stronger HBsAg decline.
引用
收藏
页码:442 / 447
页数:6
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