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Serum levels of tumour necrosis factor family members a proliferation-inducing ligand (APRIL) and B lymphocyte stimulator (BLyS) are inversely correlated in systemic lupus erythematosus
  1. J Morel1,2,
  2. C Roubille1,
  3. L Planelles3,
  4. C Rocha4,
  5. L Fernandez3,
  6. C Lukas1,
  7. M Hahne,
  8. B Combe2
  1. 1
    Service d’Immuno-Rhumatologie Université Montpellier 1 et CHU Montpellier, Montpellier, France
  2. 2
    Institut de Génétique Moléculaire de Montpellier, CNRS UMR5535, Montpellier, France
  3. 3
    Department of Immunology and Oncology, Centro Nacional de Biotecnología/CSIC, Madrid, Spain
  4. 4
    Laboratory on Thymus Research, Oswaldo Cruz Institute, Oswaldo Cruz Foundation, Rio de Janeiro, Brazil
  1. Dr J Morel, Department of Immuno-Rheumatology, Montpellier I University and Lapeyronie Teaching Hospital, 34295 Montpellier, Cedex 5, France; j-morel{at}chu-montpellier.fr

Abstract

Objective: To determine whether serum levels of a proliferation-inducing ligand (APRIL) are altered in patients with systemic lupus erythematosus (SLE), and correlate with disease parameters.

Methods: Clinical and biological parameters were analysed for 43 patients that fulfilled American College of Rheumatology (ACR) criteria for SLE classification and were positive for anti-double-stranded DNA (dsDNA) antibodies at least once in their medical records. Tests included measurement of serum levels of the tumour necrosis factor (TNF) family members APRIL and B lymphocyte stimulator (BLyS; a cytokine shown to promote SLE disease).

Results: Median APRIL levels were elevated in patients with SLE compared to patients with osteoarthritis and healthy controls, but did not correlate with the SLE Disease Activity Index (SLEDAI). APRIL serum levels showed an inverse correlation with BLyS serum levels (r = −0.339; p = 0.03). For patients with SLE with positive anti-dsDNA titres (>40 arbitrary units (AU)/ml) at inclusion (n = 25), circulating APRIL was inversely correlated with BLyS levels (r = −0.465; p = 0.022) and anti-dsDNA antibody titres (r = −0.411; p = 0.046). In a follow-up study at their second visit, 27 patients showed an inverse correlation of APRIL serum levels with BLyS (r = −0.398; p = 0.03) as well as with anti-dsDNA (r = −0.408; p = 0.03) titres and SLEDAI (r = −0.408; p = 0.01).

Conclusion: The inverse correlation observed between APRIL and BLyS suggests that APRIL acts as a protective factor. APRIL and BLyS may thus have opposite roles in SLE, which must be considered when defining therapeutic applications of these cytokines.

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Footnotes

  • Competing interests: None declared.

  • Funding: This study was supported by a grant (AOI, UF 7821) from the CHU Montpellier and the contract interface no. 05.524-DRV/MC/SS. LP holds a contract from the Spanish Ramón y Cajal Programme. MH and LF are supported by the Fondation de France, Fondation pour la Recherche Médicale and Association pour la Recherche sur le Cancer; CR by the CNRS PICS programme. The Department of Immunology and Oncology at the CNB was founded and is supported by the Spanish National Research Council (CSIC) and by Pfizer.

  • Ethics approval: The Ethics Committee of the CHU Montpellier approved the study protocol, and informed consent was obtained from each participant.

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