The SLE-key test serological signature: New insights into the course of lupus

Chaim Putterman, David S. Pisetsky, Michelle Petri, Roberto Caricchio, Alan H.B. Wu, Ignacio Sanz, Jim C. Oates, Steve Wallace, Rachel Sorek, Robert Gerwien, Pennina Safer, Keren Jakobi-Brook, Irun R. Cohen

Research output: Contribution to journalArticlepeer-review

10 Scopus citations

Abstract

Objective. We previously described the multiplex autoantibody SLE-key Rule-Out test, which detects a signature of autoantibody reactivity that distinguishes healthy subjects from SLE patients with 94% sensitivity, 75% specificity and 93% negative predictive value; thus, an individual manifesting a positive Rule-Out test score is unlikely to have SLE (e.g. lupus is excluded). The objective of this current study was to evaluate the stability of the lupus-associated signature over time. Methods. We used banked serum samples from healthy subjects (n = 51) and lupus patients (n = 50 individual samples and n = 181 paired samples, for a total of n = 412 serum samples). The samples were drawn at different times after diagnosis to analyse the impact on the SLE-key Rule-Out test of time elapsed since diagnosis and any changes in disease activity (as reflected by the SLEDAI score). Results. The SLE signature remains stable for the first 10 years after diagnosis; in this time frame, <10% of patients manifested a positive Rule-Out score and the SLE-key Rule-Out score was independent of the underlying disease activity as reflected by the SLEDAI score. After 510 years, 30% of lupus subjects scored as SLE Ruled-Out; the proportion of patients manifesting this status was even greater in the subset of individuals with a SLEDAI score of 0. Conclusion. These findings raise the possibility that a significant number of SLE patients manifest a change in their serological signature over time, and that such a signature change may signify an evolution in the immunological features of their disease relevant to patient management.

Original languageEnglish
Pages (from-to)1632-1640
Number of pages9
JournalRheumatology
Volume57
Issue number9
DOIs
StatePublished - 1 Sep 2018
Externally publishedYes

Bibliographical note

Publisher Copyright:
© 2018 The Author(s).

Funding

The authors wish to acknowledge the invaluable contributions of Yakov Blumenstein, Ilana Gilkaite, Miriam Lerner, Ornit Cohen-Gindi, Olga Tarnapolski, Adrian Javaherian, Annmarie Goldstein, Vanessa Cabra-Hodge, Justin Pitts, Maggie Barton and Emileigh Wong The Hopkins Lupus Cohort is supported by the National Institute of Arthritis and Musculoskeletal Diseases at the National Institutes of Health [grant numbers R01 AR 43727 and 69572]. The MUSC cohort and authors were funded by the National Center for Research Resources at the National Institutes of Health [grant number UL1 RR029882], MUSC General and Clinical Research Center [grant number M01 RR001070], South Carolina Clinical & Translational Research Institute [grant number UL1 RR029882], the Multidisciplinary Clinical Research Center at MUSC [grant number P60 AR062755] and the Core Center for Clinical Research [grant number P30 AR072582]. Funding: This study was funded by ImmunArray.

FundersFunder number
Core Center for Clinical ResearchP30 AR072582
ImmunArray
MUSC General and Clinical Research CenterM01 RR001070
Multidisciplinary Clinical Research CenterP60 AR062755
South Carolina Clinical & Translational Research Institute
National Institutes of HealthR01 AR 43727, 69572
National Institute of Arthritis and Musculoskeletal and Skin DiseasesP30AR072582
National Center for Research ResourcesUL1 RR029882

    Keywords

    • Autoantibodies
    • Diagnosis
    • Microarray
    • Multivariate classifier
    • Natural history
    • SLE-key
    • Systemic lupus erythematosus
    • iCHIP

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