Frontiers in Immunology (Apr 2016)

Tertiary lymphoid organs in Takayasu Arteritis

  • Marc eClement,
  • Marc eClement,
  • Adrien eGaly,
  • Patrick eBruneval,
  • Marion eMorvan,
  • Fabien eHyafil,
  • Fabien eHyafil,
  • Khadija eBenali,
  • Nicoletta ePasi,
  • Lydia eDeschamps,
  • Quentin ePellenc,
  • Quentin ePellenc,
  • Thomas ePapo,
  • Antonino eNicoletti,
  • Antonino eNicoletti,
  • Karim eSacre

DOI
https://doi.org/10.3389/fimmu.2016.00158
Journal volume & issue
Vol. 7

Abstract

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Objective: The role of B cells in the pathogenesis of Takayasu arteritis (TA) is controversial. We aimed to study the presence of tertiary lymphoid organs (TLOs) in the aortic wall of TA patients.Methods: Hematoxylin and eosin–stained sections from aorta specimens from patients with TA were screened for TLOs. The presence of B cell aggregates (CD20), follicular dendritic cells (FDCs, CD21), and high endothelial venules (HEVs, PNAd) was investigated by immunohistochemistry. Immune cells from the adventitial layer of one patient were characterized by flow cytometry. Demographic, medical history, laboratory, imaging, treatment and follow up data were extracted from medical records.Results: Aorta specimens from Bentall procedures were available from 7 patients (five female, aged 22 to 57 years) with TA. Surgical treatment was performed at TA diagnosis (n=4) or at a median of 108 months [84-156] after TA diagnosis. Disease was active at surgery in four patients according to NIH score. B cell aggregates-TLOs containing HEVs were observed in the adventitia of all but one patient.. Of note, ectopic follicles containing CD21+ FDCs were found in all patients (4/4) with increased aortic FDG uptake before surgery but were absent in all but one patients (2/3) with no FDG uptake. In addition, flow cytometry analysis confirmed the accumulation of memory/germinal center–like B cells in the adventitial layer and showed the presence of antigen-experienced T follicular helper cells.Conclusion: Ectopic lymphoid neogenesis displaying functional features can be found in the aortic wall of a subset of patients with active TA. The function of these local B cell clusters on the pathogenesis of TA remains to be elucidated.

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