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Organ-specificity and Diagnostic Value of Cell-mediated Immunity Against a Liver-specific Membrane Protein: Studies in Hepatic and Non-hepatic Diseases

Overview
Journal Klin Wochenschr
Specialty General Medicine
Date 1975 Nov 15
PMID 1083922
Citations 12
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Abstract

In chronic active hepatitis (CAH, n=58) 70% of the HBsAg negative and 48% of the HBsAg positive cases showed a CMI against human liver specific proteins (HLPI). Using HBsAg as antigen only 12% of the HBsAg negative and 24% of the HBsAg positive cases gave a CMI response. On the basis of HBsAg and autoantibodies in the serum CAH patients could be divided into 4 subgroups. A close correlation between CMI against HLPI, sex, ANA and HL-A-8 could be detected. In a follow-up study of patients with acute virus B hepatitis (n=62) CMI against HBsAg was detected in 60% of the cases in the acute phase of the disease but in 15% only 3-6 months after the onset of the illness (n=40). In patients who developed a chronic HBsAg carrier status 3 of 5 cases remained persistently positive with HLPI as antigen in the migration inhibition test. - In non-hepatic diseases in which immunological abnormalities may be present (malignant diseases n=46, diabetes mellitus n=27, active tuberculosis, n=18 and untreated systemic lupus erythematodes, n=5) only 26% of patients with malignant diseases showed a migration inhibition with HLPI. - Using different antigens such as human liver specific proteins (HLP), rabbit liver specific proteins (RLP), brucella suis antigen and tuberculin it was possible to demonstrate the validity of the two-step migration inhibition test to detect CMI. The results with different antigens in hepatic and non-hepatic diseases demonstrated that cell-mediated immunity of HLPI is an organ specific immune reaction which is associated with acute and chronic active liver diseases as a time limited or long-lasting phenomenon. Positive reactions in some tumor patients suggest that different mechanisms may elicit an autoimmune reaction against liver antigens.

Citing Articles

Immune response to rabbit liver-specific lipoprotein in acute viral hepatitis.

ORTONA L, Laghi V, Cauda R, Nervo P Clin Exp Immunol. 1980; 42(3):436-40.

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The immunopathology of acute type B hepatitis.

Bianchi L Springer Semin Immunopathol. 1981; 3(4):421-38.

PMID: 7022717 DOI: 10.1007/BF01951491.


The role of liver membrane antigens as targets in autoimmune type liver disease.

Meyer zum Buschenfelde K, Hutteroth T, Manns M, Moller B Springer Semin Immunopathol. 1980; 3(3):297-315.

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The immunopathogenesis of chronic HBV induced liver disease.

Levy G, Chisari F Springer Semin Immunopathol. 1981; 3(4):439-59.

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The diagnostic significance of intrahepatocellular hepatitis-B-surface-antigen (HBsAg), hepatitis-B-core-antigen (HBcAg) and IgG for the classification of inflammatory liver diseases. (Studies on HBsAg-positive and -negative patients).

Arnold W, Meyer zum Buschenfelde K, Hess G, Knolle J Klin Wochenschr. 1975; 53(22):1069-74.

PMID: 1226039 DOI: 10.1007/BF01614383.


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