| Literature DB >> 1808224 |
M C Jung1, U Spengler, W Schraut, R Hoffmann, R Zachoval, J Eisenburg, D Eichenlaub, G Riethmüller, G Paumgartner, H W Ziegler-Heitbrock.
Abstract
Since the hepatitis B virus is noncytopathic, it is generally believed that the individual specific immune response determines the course of infection. The lack of data about hepatitis B virus-specific T-cell reactions in acute infection led us to investigate the specific cellular immune response of infected individuals in terms of proliferation, and gamma-interferon and lymphotoxin production. Our results demonstrate that peripheral blood mononuclear cells (PBMNC) from patients with acute and chronic hepatitis B respond weakly to HBsAg. In contrast, patients with acute hepatitis show a vigorous response to the nucleocapsid antigen (HBcAg) in terms of proliferation and lymphokine production, while only few chronic virus carriers gave a proliferative response. Either of the antigens could activate lymphocytes to produce gamma-interferon and lymphotoxin, cytokines which may modulate antiviral immune response.Entities:
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Year: 1991 PMID: 1808224 DOI: 10.1016/0168-8278(91)90074-l
Source DB: PubMed Journal: J Hepatol ISSN: 0168-8278 Impact factor: 25.083