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      Human foamy virus bel1 sequence in patients with autoimmune rheumatic diseases.

      Clinical Rheumatology
      Adolescent, Adult, Aged, Arthritis, Rheumatoid, blood, diagnosis, virology, Autoimmune Diseases, Child, DNA, Viral, DNA-Binding Proteins, genetics, Humans, Leukocytes, Mononuclear, Lupus Erythematosus, Systemic, Middle Aged, RNA, Viral, Retroviridae Infections, complications, Retroviridae Proteins, Scleroderma, Systemic, Simian foamy virus, isolation & purification, pathogenicity, Trans-Activators

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          Abstract

          Since the association between human foamy virus (HFV) with rheumatic autoimmune diseases remains controversial, this study was designed to determine the relationship between HFV and systemic lupus erythematosus (SLE), rheumatoid arthritis (RA), or progressive systemic sclerosis (PSS). The bel1 and Pol sequences of HFV were measured by reverse transcriptase-polymerase chain reaction (RT-PCR) in plasma and by PCR in peripheral blood mononuclear cells (PBMC) from patients with SLE, RA, and PSS. Antibodies against Bel1 and Pol were assessed by enzyme-linked immunosorbent assay. Active HFV infections were detected by a Bel1-responsive indicator cell line. The bel1 sequence was detected in the plasma (SLE 59, RA 32, and PSS 63%) and PBMC (SLE 54, RA 71, and PSS 57%). However, active HFV infection existed only in patients with the bel1 sequence in both plasma and PBMC. In SLE patients, antibodies against Bel1 (7.1%) and Pol (4.5%) were also detected. The results suggest a possible association between HFV infection and these autoimmune rheumatic diseases.

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