4.7 Article

IgM anti-phosphorylcholine antibodies associate with senescent and IL-17+ T cells in SLE patients with a pro-inflammatory lipid profile

Journal

RHEUMATOLOGY
Volume 59, Issue 2, Pages 407-417

Publisher

OXFORD UNIV PRESS
DOI: 10.1093/rheumatology/kez264

Keywords

atherosclerosis; IgM anti-phosphorylcholine antibodies; lipid profile; Th17; Treg; CD4(+)CD28(null) cells; systemic lupus erythematosus

Categories

Funding

  1. European Union FEDER funds
  2. Fondo de Investigacion Sanitaria [FIS PI16/00113]
  3. Plan de Ciencia, Tecnologia e Innovacion del Principado de Asturias [IDI-2018-000152]

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Objective The aim was to evaluate whether T cell subsets and the lipid profile could be linked to the cardioprotective effect of IgM anti-phosphorylcholine (PC) antibodies in SLE. Methods Anti-PC antibodies were quantified by ELISA in 197 patients and 99 controls and analysed in relationship to clinical features, treatments and serum lipids. Carotid atheromatosis was evaluated by ultrasonography; Th1, Th17, Treg and CD4(+)CD28(null) cells by flow cytometry; and cytokine serum levels by immunoassays, in a subgroup of 120 SLE patients and 33 controls. Results IgM anti-PC serum levels were reduced in SLE patients compared with controls (P < 0.001) and were associated with age (beta= -0.252; P = 0.002), high-density lipoprotein (HDL; beta = 0.271; P = 0.001), low-density lipoprotein (LDL; beta= -0.192; P = 0.017) and glucocorticoid treatment (beta= -0.201; P = 0.012), whereas the IgG-to-IgM anti-PC ratio was increased (P = 0.007) and associated with age (beta = 0.194; P = 0.028) and SLEDAI (beta = 0.250; P = 0.005). Also, patients with clinical or subclinical cardiovascular disease exhibited reduced IgM anti-PC levels compared with their cardiovascular disease-free counterparts, regardless of glucocorticoid usage (P = 0.001). CD4(+)CD28(null) and Th17 cells were increased in SLE patients compared with controls (P < 0.01) and correlated inversely with IgM anti-PC levels. These associations were observed in patients displaying high triglyceride or low HDL levels, even after adjusting for clinical parameters and treatments (CD4(+)CD28(null): beta = -0.455, P = 0.001; Th17: beta= -0.280, P = 0.035), but not in those with a normal lipid profile. High triglyceride and low HDL profiles were related to low IgM anti-PC and Treg levels, respectively, whereas both lipid profiles were associated with inflammatory markers and cytokines. Conclusion The present study provides evidence for an association of IgM anti-PC antibodies with pro-atherogenic T cell subsets in SLE, with a high triglyceride/low HDL lipid profile playing a facilitating major role.

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