Determination of ANA specificity using multiplexed fluorescent microsphere immunoassay in patients with ANA positivity at high titres after infliximab treatment: preliminary results

To evaluate ANA specificity using the fully automated multiplexed fluorescent microsphere immunoassay in patients affected either by rheumatoid arthritis or ankylosing spondylitis who developed strong positivity for ANA as assessed by indirect immunofluorescent method on HEp-2 cells during infliximab treatment. Three men affected by ankylosing spondylitis and 12 women affected by rheumatoid arthritis who developed ANA positivity at high titres during infliximab treatment underwent the identification of ANA specificity by multiplexed fluorescent microsphere immunoassay; moreover anti-DNA and anti-ENA antibodies were tested by indirect immunofluorescence and ELISA method, respectively. In 4 out of 15 cases, the determination of ANA reactivity by multiplexed fluorescent microsphere immunoassay was also performed on the serum collected before infliximab administration. One patient affected by rheumatoid arthritis showed multiple ANA reactivities against SS-A, SS-B, RNP, Sm, Jo-1 and histones; one patient affected by ankylosing spondylitis resulted positive for the same autoantibodies, except for anti-Sm antibody. Moreover, two patients, one with rheumatoid arthritis and one with ankylosing spondylitis, showed single antibody specificity to SS-B and RNP, respectively. The remaining 11 cases did not show any positivity. Instead, all the patients resulted negative for anti-ENA antibodies by the ELISA method. In the four cases tested for ANA specificity by multiplexed fluorescent microsphere immunoassay before and after infliximab administration no difference was found. The search for anti-DNA antibody always resulted negative by both the traditional immunofluorescent assay and the novel technique. The use of multiplexed fluorescent microsphere immunoassay in patients treated with infliximab with ANA positivity at high titres allowed to find some ANA specificities which were not revealed by ELISA method. Nevertheless, the majority of patients resulted negative in spite of ANA positivity at high titres; the molecular target of ANA which develop after infliximab administration still remains to be identified.

[1]  R. Croft A prospective cohort study comes of age. , 2000, Leprosy review.

[2]  F. Finkelman,et al.  In vivo neutralization of TNF-alpha promotes humoral autoimmunity by preventing the induction of CTL. , 2001, Journal of immunology.

[3]  Y. Shoenfeld,et al.  Multiplexed AtheNA multi-lyte immunoassay for ANA screening in autoimmune diseases , 2005, Autoimmunity.

[4]  D. Baeten,et al.  Infliximab, but not etanercept, induces IgM anti-double-stranded DNA autoantibodies as main antinuclear reactivity: biologic and clinical implications in autoimmune arthritis. , 2005, Arthritis and rheumatism.

[5]  S. Hanauer,et al.  A lupus-like syndrome associated with infliximab therapy. , 2003, Inflammatory bowel diseases.

[6]  K. Van Steen,et al.  Autoimmunity associated with anti-tumor necrosis factor alpha treatment in Crohn's disease: a prospective cohort study. , 2003, Gastroenterology.

[7]  J. Bienvenu,et al.  Infliximab therapy in rheumatoid arthritis and ankylosing spondylitis-induced specific antinuclear and antiphospholipid autoantibodies without autoimmune clinical manifestations: a two-year prospective study , 2004, Arthritis research & therapy.

[8]  O. Meyer,et al.  Anti-TNF-α-induced systemic lupus syndrome , 2003, Clinical Rheumatology.

[9]  P. Sarzi-Puttini,et al.  Adalimumab clinical efficacy is associated with rheumatoid factor and anti-cyclic citrullinated peptide antibody titer reduction: a one-year prospective study , 2005, Arthritis research & therapy.

[10]  G. Ferraccioli,et al.  Drug-induced systemic lupus erythematosus and TNF-alpha blockers. , 2002, Lancet.

[11]  F. Breedveld,et al.  Therapeutic efficacy of multiple intravenous infusions of anti-tumor necrosis factor alpha monoclonal antibody combined with low-dose weekly methotrexate in rheumatoid arthritis. , 1998, Arthritis and rheumatism.

[12]  P. Sarzi-Puttini,et al.  Infliximab-induced lupus in Crohn's disease: a case report. , 2003, Digestive and liver disease : official journal of the Italian Society of Gastroenterology and the Italian Association for the Study of the Liver.

[13]  M. Oppermann,et al.  Clinical significance of anti-dsDNA antibody isotypes: IgG/IgM ratio of anti-dsDNA antibodies as a prognostic marker for lupus nephritis , 2004, Lupus.

[14]  F. Finkelman,et al.  In Vivo Neutralization of TNF-α Promotes Humoral Autoimmunity by Preventing the Induction of CTL1 , 2001, The Journal of Immunology.

[15]  Harry R. Hill,et al.  Evaluation of Multiplexed Fluorescent Microsphere Immunoassay for Detection of Autoantibodies to Nuclear Antigens , 2004, Clinical Diagnostic Laboratory Immunology.

[16]  N. Shakoor,et al.  Drug-induced systemic lupus erythematosus and TNF-α blockers , 2002, The Lancet.

[17]  A D GUNN,et al.  Case of Anaphylaxis after Anaesthesia , 1943, British medical journal.

[18]  E. Tan,et al.  Autoantibodies in the diagnosis of systemicrheumatic diseases , 1995 .

[19]  E. Favalli,et al.  Drug-induced lupus following treatment with infliximab in rheumatoid arthritis , 2002, Lupus.

[20]  M. Feldmann,et al.  Assessment of antibodies to double-stranded DNA induced in rheumatoid arthritis patients following treatment with infliximab, a monoclonal antibody to tumor necrosis factor alpha: findings in open-label and randomized placebo-controlled trials. , 2000, Arthritis and rheumatism.

[21]  R Hal Scofield,et al.  Development of autoantibodies before the clinical onset of systemic lupus erythematosus. , 2003, The New England journal of medicine.

[22]  P. Lipsky,et al.  Infliximab (chimeric anti-tumour necrosis factor α monoclonal antibody) versus placebo in rheumatoid arthritis patients receiving concomitant methotrexate: a randomised phase III trial , 1999, The Lancet.

[23]  M. Braun,et al.  Drug-induced systemic lupus erythematosus and TNF-α blockers , 2002, The Lancet.

[24]  H. McQuay,et al.  Dipyrone and agranulocytosis: what is the risk? , 2002, The Lancet.

[25]  P. Butler,et al.  Serum amyloid P component controls chromatin degradation and prevents antinuclear autoimmunity , 1999, Nature Medicine.

[26]  S. Hanauer Review article: safety of infliximab in clinical trials , 1999, Alimentary pharmacology & therapeutics.

[27]  X. Mariette,et al.  Systemic lupus erythematosus induced by anti-tumour necrosis factor alpha therapy: a French national survey , 2005, Arthritis research & therapy.

[28]  N. Martinelli,et al.  Anti-TNFα therapy in rheumatoid arthritis and autoimmunity , 2004, Rheumatology International.

[29]  N. Brot,et al.  C-Reactive Protein Binds to Apoptotic Cells, Protects the Cells from Assembly of the Terminal Complement Components, and Sustains an Antiinflammatory Innate Immune Response , 2000, The Journal of experimental medicine.

[30]  Carole Foy,et al.  A comparability study of the emerging protein array platforms with established ELISA procedures. , 2005, Journal of immunological methods.