Torque Teno Virus quantification for monitoring of immunomodulation with biologic compounds in the treatment of rheumatoid arthritis

Author:

Studenic Paul12ORCID,Bond Gregor3ORCID,Kerschbaumer Andreas1,Bécède Manuel1,Pavelka Karel45,Karateev Dmitry6,Stieger Jutta7,Puchner Rudolf8,Mueller Ruediger B9,Puchhammer-Stöckl Elisabeth10,Durechova Martina1,Loiskandl Michaela1,Perkmann Thomas11,Olejarova Martina45,Luchikhina Elena6,Steiner Carl-Walter1,Bonelli Michael1,Smolen Josef S1,Aletaha Daniel1ORCID

Affiliation:

1. Department of Internal Medicine 3, Division of Rheumatology, Medical University of Vienna, Vienna, Austria

2. Division of Rheumatology, Department of Medicine (Solna), Karolinska Institutet, Solna, Sweden

3. Division of Nephrology and Dialysis, Medical University of Vienna, Vienna, Austria

4. Institute of Rheumatology

5. Department of Rheumatology, First Faculty of Medicine, Charles University, Prague, Czech Republic

6. Department of Rheumatology, Moscow Regional Research and Clinical Institute (MONIKI), Moscow, Russia

7. 2nd Department of Medicine, Hietzing Hospital, Vienna

8. Rheumatologist in Private Practice, Wels, Austria

9. Cantonal Hospital Lucerne, Division of Rheumatology, Medical University Department, Rheumazentrum Ostschweiz, St. Gallen, Switzerland

10. Center of Virology

11. Department of Laboratory Medicine, Medical University of Vienna, Vienna, Austria

Abstract

Abstract Objectives RA patients who fail to respond to MTX can receive biologic dMARDs (bDMARDs). The Torque Teno Virus (TTV) is a potential novel candidate for monitoring of immunosuppression. We explore TTV in these patients and its association with clinical response to bDMARDs. Methods The BioBio Study is a multicentre randomized open-label trial, including RA patients with insufficient response to MTX. Patients were randomized to either TNFi (infliximab, INF), anti-IL-6 (tocilizumab, TCZ), CTLA4-Ig (abatacept, ABA) or anti-CD20 (rituximab, RTX) in addition to MTX. PCR was used to quantify TTV in the peripheral blood. Results TTV was measured in 95 patients (INF, n = 23; TCZ, n = 22; ABA, n = 27; RTX; n = 23). TTV increased by a median of 4.5 × 104 copies/ml [c/ml; interquartile range (IQR) 0–7.5 × 105] after 3 months. TTV levels at month 3 were associated with the Simplified Disease Activity Index (SDAI) (P = 0.03) and the Clinical Disease Activity Index (CDAI) response (P = 0.026) at month 6. A TTV cut-off level of 1.2 × 106 c/ml at month 3 had a positive likelihood ratio of 2.7 for prediction of an 85% reduction in SDAI at month 6. Conclusion Our data suggest that TTV levels increase upon TNF, CD20 and costimulation blockade and are associated with the clinical response to bDMARDs in RA patients. Trial registration ClinicalTrials.gov; https://clinicaltrials.gov; NCT01638715

Funder

Austrian Science Fund

Research Project of the Ministry of Health of the Czech Republic

Publisher

Oxford University Press (OUP)

Subject

Pharmacology (medical),Rheumatology

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