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Cofactor dependence and isotype distribution of anticardiolipin antibodies in viral infections
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  1. H Guglielmonea,b,
  2. S Vitozzia,
  3. O Elbarchaa,
  4. E Fernandeza
  1. aLaboratorio de Análisis Clínicos Especializados (LACE), Córdoba, Argentina, bDepartamento de Bioquímica Clínica, Facultad de Ciencias Químicas, Universidad Nacional de Córdoba, Argentina
  1. Dr Guglielmone, Laboratorio de Análisis Clínicos Especializados (LACE), Av Velez Sarsfield 562-4to Piso, (5000) Córdoba, Argentinahgugli{at}bioclin.fcq.unc.edu.ar

Abstract

BACKGROUND Antibodies to cardiolipin (aCLs) are often detected in patients with autoimmune disorders or infectious diseases.

OBJECTIVE To investigate the distribution of aCL isotypes and requirement of protein cofactor in viral infections in order to establish the importance, if any, of these antibodies in these infectious diseases.

PATIENTS AND METHODS The isotype distribution of aCLs in the sera from 160 patients with infection caused by HIV-1 (n=40), hepatitis A virus (n=40), hepatitis B virus (n=40), or hepatitis C virus (n=40) was studied by standardised enzyme linked immunosorbent assay (ELISA) in the presence and absence of protein cofactor (mainly β2-glycoprotein I). Serum samples from healthy volunteers and patients with syphilis and antiphospholipid syndrome were also included and served as negative and positive control groups respectively.

RESULTS The prevalence of one or more aCL isotypes in serum of patients with HIV-1, hepatitis A virus, hepatitis B virus, or hepatitis C virus infection was 47%, 92%, 42%, and 17% respectively (principally IgM and/or IgA). Most of these antibodies were mainly cofactor independent.

CONCLUSIONS The presence of aCLs in viral infections is principally cofactor independent, suggesting that cofactor dependence of the aCLs should be assessed to distinguish subjects most likely to suffer from clinical symptoms observed in the presence of these antibodies.

  • antibodies
  • phospholipid antibodies
  • anticardiolipin antibodies
  • β2-glycoprotein I
  • viral diseases

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