Literature DB >> 2962795

An immunogenetic study of suppressor cell activity in autoimmune chronic active hepatitis.

E L Krawitt1, A E Kilby, R J Albertini, M S Schanfield, B F Chastenay, P C Harper, R M Mickey, T L McAuliffe.   

Abstract

Some patients with autoimmune chronic active hepatitis as well as their disease-free first degree relatives show decreased suppressor cell activity of peripheral blood T lymphocytes. Studies were therefore undertaken in families ascertained by the presence of a single chronic active hepatitis patient to determine if this abnormality of immune regulation represents a genetic phenotype simply controlled by a gene or genes at a putative disease susceptibility locus and, further, if this locus showed linkage to either the HLA or the immunoglobulin constant region loci. In addition to determining circulating autoantibody status and genotyping for HLA and immunoglobulin allotypes, suppressor T cells were evaluated by surface markers and by determining their ability to suppress IgG secretion in vitro. The results suggest that immunoregulatory dysfunction in autoimmune chronic active hepatitis is a familial abnormality, but that this abnormality occurs independent of circulating autoantibody status and of the segregation of genes for HLA or immunoglobulin allotypes.

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Year:  1988        PMID: 2962795     DOI: 10.1016/0090-1229(88)90187-0

Source DB:  PubMed          Journal:  Clin Immunol Immunopathol        ISSN: 0090-1229


  5 in total

1.  Suppressor T-cell deficiency in primary sclerosing cholangitis. Case and family study.

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Review 2.  Primary biliary cirrhosis: considerations on pathogenesis based on identification of the M2 autoantigens.

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Review 3.  Autoimmune hepatitis. Evolving concepts and treatment strategies.

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5.  Emperipolesis mediated by CD8 T cells is a characteristic histopathologic feature of autoimmune hepatitis.

Authors:  Qi Miao; Zhaolian Bian; Ruqi Tang; Haiyan Zhang; Qixia Wang; Shanshan Huang; Xiao Xiao; Li Shen; Dekai Qiu; Edward L Krawitt; M Eric Gershwin; Xiong Ma
Journal:  Clin Rev Allergy Immunol       Date:  2015-06       Impact factor: 8.667

  5 in total

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