Haemolysis in hepatitis A virus infections coinciding with the occurrence of autoantibodies against triosephosphate isomerase and the reactivation of latent persistent Epstein-Barr virus infection
Haemolysis has been observed frequently as a complication of acute hepatitis A virus (HAV) infection. However, the pathogenic mechanism has not been elucidated completely. In individual cases the detection of anti‐erythrocyte antibodies of unknown specificity was described. The raised serum IgM frac...
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Veröffentlicht in: | Journal of medical virology 1996-11, Vol.50 (3), p.272-275 |
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Zusammenfassung: | Haemolysis has been observed frequently as a complication of acute hepatitis A virus (HAV) infection. However, the pathogenic mechanism has not been elucidated completely. In individual cases the detection of anti‐erythrocyte antibodies of unknown specificity was described. The raised serum IgM fraction was shown to consist partially of autoantibodies. Previously, we detected autoantibodies of immunoglobulin class M directed against triosephosphate isomerase (IgM anti‐TPI) in patients with infectious mononucleosis. These autoantibodies are able to induce haemolysis.
In this study the occurrence of IgM anti‐TPI in acute HAV infections and other viral diseases has been investigated. In 33 of 134 patients suffering from HAV infection (IgM anti‐TPI was detected. Haematological and chemical data were available from seven of these 33 patients. Mild‐to‐moderate signs of haemolysis correlating with the IgM anti‐TPI titre in the follow‐up examinations were demonstrated. The presence of IgM anti‐TPI in HAV infections is connected with a reactivation of a latent persistent EBV infection. In other viral infections both the detection of IgM anti‐TPI and evidence of a reactivated EBV infection is rare. Thus, we anticipate that IgM anti‐TPI antibodies occurring with the reactivation of a latent persistent EBV infection take part in provoking haemolysis in acute HAV infections. © 1996 Wiley‐Liss, Inc. |
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ISSN: | 0146-6615 1096-9071 |
DOI: | 10.1002/(SICI)1096-9071(199611)50:3<272::AID-JMV10>3.0.CO;2-M |