By Dr. A. Vallbracht, B. Fleischer (auth.), Prof. Dr. C. De Bac, Dr. G. Taliani, Prof. Dr. W. H. Gerlich (eds.)
Chronic viral hepatitis is mentioned right here in a multidisciplinary process. The editors' aim used to be to collect contributions from clinicians, laboratory physicians, epidemiologists, pathologists, and molecular biologists to supply a synopsis of the entire vital elements of this disorder. A key point within the persistent evolution of viral hepatitis is the continual coexistence of a cytotoxic immune reaction and viral gene expression that is mentioned in 11 articles on immune pathogenesis. The oncogenicity of hepatitis B virus on the molecular point and of hepatitis C virus on the epidemiological point is mentioned in chapters. the applying of PCR for the detection of hepatitis viruses and their editions is a huge subject of either functional and theoretical curiosity. The medical value of newly built serological assays for prognosis and prevention is mentioned intensive by way of experts from clinics, transfusion facilities and virological laboratories. The treatment of persistent viral hepatitis remains to be unsatisfactory, yet a few sluggish growth is defined in numerous articles. in addition, the quantity has a distinct bankruptcy at the frequently ignored subject of power hepatitis in childhood.
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U. B. , Roslagstull Hospital, Box 5651, S-11489 Stockholm, Sweden. Arch Virol (1992) [Suppl] 4: 39-41 © Springer-Verlag 1992 Absence of free core antigen in anti-HBc negative viremic hepatitis B carriers Ch. , R. -H. , E. Korec\ A. Uyl, and W. H. Gerlich! 2 ! Department of Medical Microbiology, University of Gottingen Pediatric Clinic, University of Giessen, Federal Republic of Germany, 3 Institute of Molecular Biology, Prague, CSFR Summary. Using enzyme immune assay and immune electron microscopy, we have examined the sera of immune-suppressed anti-HBc negative HBVinfected patients for the presence of HBcAg.
Autologous irradiated PBMC were incubated overnight with anti-HLA class I (W6/ 32) or anti-HLA class II (D 1- 12 specific for DR molecules; BT3/4 recognizing DQ molecules; B7/21 specific for DP antigens) monoclonal antibodies and the relevant synthetic peptide. The cells were washed and added to T cells from the peptide-primed T cell lines. , Geneva, Switzerland, for providing rHBeAg; Sorin Biomedica Spa, Saluggia, Italy, for supplying rHBcAg; Marie Anne Petit, Inserm U 131, Clamart, France, for hHBcAg; Roberto Accolla, University of Verona, Italy, for the generous gift of anti-HLA monoclonal antibodies.
N Engl J Med 303: 178-182 Stahl SJ, Murray K (1989) Immunogenicity of peptide fusions to hepatitis B virus core antigen. Proc Nat! Acad Sci USA 86: 6283-6287 Wen YM, Duan SC, Howard CR, Frew AF, Steward MW (1990) The affinity of antiHBc antibodies in acute and chronic hepatitis B infection. Clin Exp Immunol 79: 83-86 Authors' address: Dr. S. P. E. Sylvan, Department of Infectious Diseases, Karolinska In'stitute, Roslagstull Hospital, Box 5651, S-11489 Stockholm, Sweden. Arch Virol (1992) [Suppl] 4: 36-38 © Springer-Verlag 1992 Divergent anti-HBc reactivities in HB-immune and chronic HBsAg carriers U.
Chronically Evolving Viral Hepatitis by Dr. A. Vallbracht, B. Fleischer (auth.), Prof. Dr. C. De Bac, Dr. G. Taliani, Prof. Dr. W. H. Gerlich (eds.)
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