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Inverse correlation between serum complement component C1q levels and whole blood type-1 interferon signature in active tuberculosis and QuantiFERON-positive uveitis: implications for diagnosis

Authors :
Schrijver, B. (Benjamin)
Dijkstra, D.J.
Borggreven, N.V.
Nora, R.L.
Huijser, E.
Versnel, M.A. (Marjan)
Hagen, P.M. (Martin) van
Joosten, S.A.
Trouw, L.A. (L.)
Dik, W.A. (Willem)
Schrijver, B. (Benjamin)
Dijkstra, D.J.
Borggreven, N.V.
Nora, R.L.
Huijser, E.
Versnel, M.A. (Marjan)
Hagen, P.M. (Martin) van
Joosten, S.A.
Trouw, L.A. (L.)
Dik, W.A. (Willem)
Publication Year :
2020

Abstract

Objectives To examine the relation between serum C1q levels and blood type‐1 interferon signature (type‐1 IFN signature) in active pulmonary tuberculosis (APTB) and to determine whether combined measurement of serum C1q and type‐1 IFN signature may add to the diagnosis of QuantiFERON‐positive (QFT+) patients with uveitis of unknown cause. Methods C1q was determined (ELISA) in serum from two distinct Indonesian cohorts, and in total, APTB (n = 72), QFT+ uveitis of unknown aetiology (n = 58), QFT− uveitis (n = 51) patients and healthy controls (HC; n = 73) were included. The type‐1 IFN signature scores were previously determined. Results Serum C1q was higher in APTB than HC (P < 0.001). APTB patients with uveitis had higher serum C1q than APTB patients without uveitis (P = 0.0207). Serum C1q correlated inversely with type‐1 IFN signature scores in APTB (P = 0.0036, r2 = 0.3526), revealing that these biomarkers for active TB disease can be mutually exclusive. Stratification of QFT+ patients with uveitis of unknown cause, by serum C1q and type‐1 IFN signature, yielded four groups with different likelihood of suffering from active TB uveitis. Conclusion Serum C1q is elevated in APTB, es

Details

Database :
OAIster
Notes :
application/pdf, Clinical & Translational Immunology vol. 9 no. 10, English
Publication Type :
Electronic Resource
Accession number :
edsoai.on1236257010
Document Type :
Electronic Resource
Full Text :
https://doi.org/10.1002.cti2.1196