Immunohistochemical detection of IL-17 and IL-23 improves the identification of patients with a possible diagnosis of Sjogren's syndrome

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Fusconi M, Musy I, Valente D, Maggi E, Priori R, Pecorella I, Mastromanno L, Di Cristofano C, Greco A, Armeli F, Candelori F, de Vincentiis M, Gallo A, Businaro R.
ISSN: 0344-0338

Objectives: The diagnosis of primary Sjogren’s syndrome (pSS) continues to be difficult and several patients keep
symptomatic for years with different diagnoses before confirmation of pSS. Since the IL-23-IL-17 axis is involved
in the etiopathogenesis of pSS we evaluated by immunohistochemistry and morphometric methods the presence
of IL-17 as well as IL-23 within minor salivary glands (MSG) obtained from patients with uncertain diagnosis of
pSS.
Materials and Methods: 42 patients, with symptoms attributable to pSS, and 8 patients used as a control, were
enrolled for the study. Autoantibody detection, histological analysis for the presence of Germinal Centers
(GC+), immunohistochemistry to detect IL-23 and IL-17 were performed.
Results: The detection of GC + anti-SSA and anti-SSB antibody in parallel with the detection of IL-17 and IL-23,
displays only a diagnostic reinforcement value. Instead, the detection of a positive reaction for both IL-17 and IL23 without GC + or autoantibody within minor salivary glands, as detected in 36 % of patients with uncertain
diagnosis, may be hold as a sensitive and specific marker to identify those patients who are likely to evolve into
pSS.
Conclusion: we suggest to use the IL-17/ IL-23 immunohistochemical detection to improve the identification of
patients with a possible diagnosis in all cases which do not fully meet the American-European criteria for pSS, in
particular when the GC + are not present at histopathological analysis and anti-SSA and anti-SSB antibody are
undetectable in the serum.

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