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Immunome perturbation is present in patients with juvenile idiopathic arthritis who are in remission and will relapse upon anti-TNFα withdrawal.

Authors :
Jing Yao Leong
Chen, Phyllis
Joo Guan Yeo
Ally, Fauziah
Chua, Camillus
Hazirah, Sharifah Nur
Su Li Poh
Lu Pan
Liyun Lai
Choon Lee, Elene Seck
Loshinidevi
Arkachaisri, Thaschawee
Lovell, Daniel
Albani, Salvatore
Leong, Jing Yao
Yeo, Joo Guan
Nur Hazirah, Sharifah
Poh, Su Li
Pan, Lu
Lai, Liyun
Source :
Annals of the Rheumatic Diseases; Dec2019, Vol. 78 Issue 12, p1712-1721, 10p, 1 Diagram, 5 Graphs
Publication Year :
2019

Abstract

<bold>Objectives: </bold>Biologics treatment with antitumour necrosis factor alpha (TNFα) is efficacious in patients with juvenile idiopathic arthritis (JIA). Despite displaying clinical inactivity during treatment, many patients will flare on cessation of therapy. The inability to definitively discriminate patients who will relapse or continue to remain in remission after therapy withdrawal is currently a major unmet medical need. CD4 T cells have been implicated in active disease, yet how they contribute to disease persistence despite treatment is unknown.<bold>Methods: </bold>We interrogated the circulatory reservoir of CD4+ immune subsets at the single-cell resolution with mass cytometry (cytometry by time of flight) of patients with JIA (n=20) who displayed continuous clinical inactivity for at least 6 months with anti-TNFα and were subsequently withdrawn from therapy for 8 months, and scored as relapse or remission. These patients were examined prior to therapy withdrawal for putative subsets that could discriminate relapse from remission. We verified on a separate JIA cohort (n=16) the dysregulation of these circulatory subsets 8 months into therapy withdrawal. The immunological transcriptomic signature of CD4 memory in relapse/remission patients was examined with NanoString.<bold>Results: </bold>An inflammatory memory subset of CD3+CD4+CD45RA-TNFα+ T cells deficient in immune checkpoints (PD1-CD152-) was present in relapse patients prior to therapy withdrawal. Transcriptomic profiling reveals divergence between relapse and remission patients in disease-centric pathways involving (1) T-cell receptor activation, (2) apoptosis, (3) TNFα, (4) nuclear factor-kappa B and (5) mitogen-activated protein kinase signalling.<bold>Conclusions: </bold>A unique discriminatory immunomic and transcriptomic signature is associated with relapse patients and may explain how relapse occurs. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
00034967
Volume :
78
Issue :
12
Database :
Complementary Index
Journal :
Annals of the Rheumatic Diseases
Publication Type :
Academic Journal
Accession number :
139712926
Full Text :
https://doi.org/10.1136/annrheumdis-2019-216059