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AI-09 T follicular helper (Tfh) cells are increased in asymptomatic anti-nuclear antibody (ANA)+ individuals and appear to play a role in epitope spreading
  1. Joan Wither1,2,3,4,
  2. Nan-Hua Chang1,
  3. Sindhu R Johnson3,4,5,6,
  4. Waleed Hafiz3,
  5. Kieran Manion1,2,
  6. Dario Ferri1,2,
  7. Ariana Karanxha1,
  8. Babak Noamani1,
  9. Dennisse Bonilla1,
  10. Sina Rusta-Sellehy1,
  11. Larissa Lisnevskaia7,
  12. Zahi Touma3,4,
  13. Earl Silverman8,9,
  14. Arthur Bookman3,4,
  15. Carolina Landolt-Marticorena1 and
  16. Yuriy Baglaenko1,2
  1. 1Krembil Research Institute, University Health Network, Toronto, Canada
  2. 2Department of Immunology, University of Toronto, Toronto, Canada
  3. 3Division of Rheumatology, University Health Network, Toronto, Canada
  4. 4Department of Medicine, University of Toronto, Toronto, Canada
  5. 5Division of Rheumatology, Mount Sinai Hospital, Toronto, Canada
  6. 6Institute of Health Policy, Management and Evaluation, University of Toronto, Toronto, Canada
  7. 7Lakeridge Heath Services, Oshawa, Canada
  8. 8Division of Rheumatology, Sick Children’s Hospital, Toronto, Canada
  9. 9Department of Pediatrics, University of Toronto, Toronto, Canada


Background The diagnosis of Systemic Autoimmune Rheumatic Diseases (SARD), including Systemic Lupus Erythematosus (SLE), relies on the presence of ANAs, many of which can be detected years before clinical manifestations. However, ANAs are also seen in healthy individuals most of whom will not develop SARD. A number of cellular immune changes are seen in SARD, and thus could constitute potential biomarkers/treatment targets for SARD, however it is not known at what point in disease progression these develop.

Methods Healthy ANA- controls (n=32) and ANA+ (≥1:160 by immunofluorescence) participants with no (asymptomatic ANA+, n=61), at least one (UCTD, n=35), or meeting SARD classification criteria (n=59) were recruited. Peripheral blood cellular immunological changes were assessed by flow cytometry.

Results Consistent with previous reports, SARD patients had increased proportions of activated B cells (CD86+ or CD95+) and in the SLE patient subset there were increased proportions of plasma cells/plasmablasts, as compared to ANA- controls. SARD patients also had reduced proportions of iNKT and IFN-γ producing cells, as well as, increased proportions of memory Tfh (CD4+CXCR5hiPD1hi) and T regulatory (Treg, CD4+FOXP3+HELIOS+) cells, especially in the SLE and Sjogren’s Disease patient subsets. In asymptomatic ANA+ individuals and UCTD patients, similar increases in the proportion of activated B cells, Tfh, and Treg cells, and decreases in the proportion of iNKT and IFN-γ producing cells were seen to those in SARD. In asymptomatic ANA+ individuals and SARD patients, the extent of serologic changes (number of specific ANAs detected by Bioplex® 2200 ANA screening system) positively correlated with activation in the switched memory B cell compartment and the proportion of Tfh cells, with the later being an independent predictor of serologic status in a multivariate analysis. However, significantly elevated levels of Tfh cells could still be seen in asymptomatic ANA+ individuals who lacked specific ANAs. Consistent with a role for Tfh cell in ANA production there was a strong correlation between the proportion of Tfh and plasma cells in asymptomatic ANA+ individuals. In preliminary studies, the majority of Tfh cells in asymptomatic ANA+ and UCTD patients were Tfh2 cells, with a trend to increased proportions of Tfh2 cells and decreased proportions Tfh17 cells as compared to active SLE patients.

Conclusions Tfh cells appear to play an important role in the development of a positive ANA and in the epitope spreading that may accompany disease progression, and therefore constitute a promising target for treatment of early disease.

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