» Articles » PMID: 25938736

Early Decreased Plasma Levels of Factor B and C5a Are Important Biomarkers in Children with Kawasaki Disease

Overview
Journal Pediatr Res
Specialties Biology
Pediatrics
Date 2015 May 5
PMID 25938736
Citations 2
Authors
Affiliations
Soon will be listed here.
Abstract

Background: The mechanisms underpinning Kawasaki disease (KD) are incompletely understood. There is an unmet need for specific biomarkers for the early diagnosis of KD.

Methods: Eighty-five KD patients suffering from acute-phase and subacute-phase KD, 40 healthy children, and 40 febrile children comprised the study cohort. An enzyme-linked immunosorbent assay was used to measure plasma levels of C1q, C1q-circulating immune complex (C1q-CIC), mannan-binding lectin-associated serine protease (MASP)-1, factor B, C4d, C3d, C5a, C5b-9 and CD59.

Results: Plasma concentrations of factor B and C5a in the acute phase were lower than those in healthy and febrile control groups (all P < 0.05). Compared with acute-phase KD patients, plasma concentrations of C1q, factor B, and C3d in KD patients were increased significantly (P < 0.05), but those of C4d, MASP-1 and CD59 decreased significantly (P < 0.05), in patients with sub-acute KD.

Conclusion: These data suggest that more than one pathway in the complement system is activated in KD. Importantly, decreased plasma concentrations of factor B and C5a in the acute phase (6-10 d) could be employed as biomarkers for the early diagnosis of KD.

Citing Articles

Identification of 10 Hub Genes and an miRNA-mRNA Regulatory Network in Acute Kawasaki Disease.

Ma J, Gui H, Tang Y, Ding Y, Qian G, Yang M Front Genet. 2021; 12:585058.

PMID: 33868359 PMC: 8044791. DOI: 10.3389/fgene.2021.585058.


Does the Lectin Complement Pathway Link Kawasaki Disease and SARS-CoV-2?.

Polycarpou A, Grigoriadou S, Klavinskis L, Sacks S Front Immunol. 2021; 11:604512.

PMID: 33584675 PMC: 7874141. DOI: 10.3389/fimmu.2020.604512.

References
1.
Matsushita M, Fujita T . Activation of the classical complement pathway by mannose-binding protein in association with a novel C1s-like serine protease. J Exp Med. 1992; 176(6):1497-502. PMC: 2119445. DOI: 10.1084/jem.176.6.1497. View

2.
Murata K, Baldwin 3rd W . Mechanisms of complement activation, C4d deposition, and their contribution to the pathogenesis of antibody-mediated rejection. Transplant Rev (Orlando). 2009; 23(3):139-50. PMC: 2797368. DOI: 10.1016/j.trre.2009.02.005. View

3.
Gorter A, Blok V, Haasnoot W, Ensink N, Daha M, Fleuren G . Expression of CD46, CD55, and CD59 on renal tumor cell lines and their role in preventing complement-mediated tumor cell lysis. Lab Invest. 1996; 74(6):1039-49. View

4.
Salo E, Kekomaki R, Pelkonen P, Ruuskanen O, Viander M, Wagner O . Kawasaki disease: monitoring of circulating immune complexes. Eur J Pediatr. 1988; 147(4):377-80. DOI: 10.1007/BF00496414. View

5.
Newburger J, Takahashi M, Gerber M, Gewitz M, Tani L, Burns J . Diagnosis, treatment, and long-term management of Kawasaki disease: a statement for health professionals from the Committee on Rheumatic Fever, Endocarditis, and Kawasaki Disease, Council on Cardiovascular Disease in the Young, American Heart.... Pediatrics. 2004; 114(6):1708-33. DOI: 10.1542/peds.2004-2182. View