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Predictive value of ex-vivo drug-inhibited cytokine production for clinical response to biologic DMARD therapy in rheumatoid arthritis
L. Tweehuysen1, A.A. Den Broeder2, K. Schraa3, M.G. Netea4, F.H. Van Den Hoogen5, L.A. Joosten6
- Department of Rheumatology, Sint Maartenskliniek, Nijmegen, the Netherlands. l.tweehuysen@maartenskliniek.nl
- Department of Rheumatology, Sint Maartenskliniek, Nijmegen, and Department of Rheumatology, Radboud University Medical Center, Nijmegen, the Netherlands.
- Department of Internal Medicine and Radboud Center for Infectious Diseases (RCI), Radboud University Medical Center, Nijmegen, the Netherlands.
- Department of Internal Medicine and Radboud Center for Infectious Diseases (RCI), Radboud University Medical Center, Nijmegen, and Department for Genomics & Immunoregulation, Life and Medical Sciences Institute (LIMES), University of Bonn, Germany.
- Department of Rheumatology, Sint Maartenskliniek, Nijmegen, and Department of Rheumatology, Radboud University Medical Center, Nijmegen, the Netherlands.
- Department of Internal Medicine and Radboud Center for Infectious Diseases (RCI), Radboud University Medical Center, Nijmegen, the Netherlands.
CER11120
2019 Vol.37, N°3
PI 0367, PF 0372
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PMID: 30767874 [PubMed]
Received: 20/01/2018
Accepted : 23/05/2018
In Press: 07/02/2019
Published: 10/05/2019
Abstract
OBJECTIVES:
To investigate ex-vivo drug-inhibited cytokine production before the start of a biological DMARD (bDMARD) as predictor of treatment response in rheumatoid arthritis (RA).
METHODS:
In a prospective RA cohort study [BIO-TOP], blood samples were obtained from patients before the start of a bDMARD (abatacept, adalimumab, etanercept, rituximab or tocilizumab). Peripheral blood mononuclear cells were pre-incubated for 1 hour with the therapeutic in-vivo concentration of the bDMARD and stimulated for 24 hours with heat-killed Candida albicans or Pam3Cys. Concentrations of IL-1β, IL-6, TNFα, IL-17 and IFNγ were determined by ELISA. EULAR response (good vs. moderate/no) was assessed at month 6. Area under the receiver operating characteristic curves (AUCs) were generated to evaluate the predictive value of baseline characteristics and ex-vivo cytokine production (including stimulated cytokine concentrations and absolute changes after inhibition by a bDMARD). Logistic prediction models were created to assess the added value of potential cytokine predictors.
RESULTS:
277 RA patients were included with 330 blood samples. Good response was reached in 39% of the cases. DAS28-CRP was predictive for response to adalimumab (AUC 0.70, 95%CI 0.57–0.83), etanercept (AUC 0.68, 95%CI 0.58–0.78) and rituximab (AUC 0.76, 95%CI 0.65–0.86). ACPA was modestly predictive for response to abatacept (AUC 0.63, 95%CI 0.52–0.75). In the ex-vivo analysis, 4 of 64 (6%) tests showed some predictive value but these had no added value to clinical factors routinely measured in RA, such as DAS28-CRP.
CONCLUSIONS:
Ex-vivo inhibition of cytokine production by bDMARDs is unable to help prediction of treatment response to bDMARDs in RA.
