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Autoantibodies and human immunodeficiency viruses infection: a case-control study
P Chretien1, J C Monier, F Oksman
1Laboratory of Hematology and Immunology, CHI de Créteil, Créteil, France.
Clinical and Experimental Rheumatology
|May 16, 2003
Summary
HIV patients show increased prevalence of certain autoantibodies like anticardiolipin and antiplatelet, but not specific markers like anti-ds DNA. The autoantibody profile in HIV is similar to other chronic viral infections, suggesting HIV is not uniquely autoimmunogenic.
Area of Science:
- Immunology
- Virology
- Infectious Diseases
Background:
- Autoantibodies are implicated in various autoimmune and chronic conditions.
- Understanding autoantibody profiles in Human Immunodeficiency Virus (HIV) infection is crucial for comprehending disease pathogenesis and potential autoimmune comorbidities.
Purpose of the Study:
- To investigate the prevalence of organ-specific and non-specific autoantibodies in individuals with HIV infection.
- To compare the autoantibody profile of HIV patients with that of HIV-negative controls.
Main Methods:
- A multicentric case-control study involving 105 HIV patients and 100 HIV-negative healthy volunteers.
- Screening for a wide range of autoantibodies including antinuclear, anti-ds DNA, anticardiolipin, antiplatelet, anti-smooth muscle, and anti-thyroid antibodies across six European laboratories.
Main Results:
- HIV patients exhibited a statistically significant higher frequency of IgG and IgM anticardiolipin, IgG antiplatelet, anti-smooth muscle, and anti-thyroglobulin antibodies compared to controls.
- Specific autoantibodies such as anti-ds DNA, anti-Sm, and anti-beta 2 glycoprotein 1 were not detected more frequently in HIV patients.
- A correlation between CD4+ cell counts and autoantibodies was observed only for anti-smooth muscle antibodies.
Conclusions:
- The autoantibody profile observed in HIV infection is comparable to that seen in other chronic viral infections.
- HIV does not appear to be more autoimmunogenic than other viruses, suggesting a common immunopathological response in chronic viral infections.
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