4.4 Article

Bioinformatics identification of hub genes and signaling pathways regulated by intravenous immunoglobulin treatment in acute Kawasaki disease

Journal

EXPERIMENTAL AND THERAPEUTIC MEDICINE
Volume 22, Issue 1, Pages -

Publisher

SPANDIDOS PUBL LTD
DOI: 10.3892/etm.2021.10216

Keywords

Kawasaki disease; mechanism of action; intravenous immunoglobulin; bioinformatics analysis

Funding

  1. National Natural Science Foundation of China [81971477, 81870365, 82070512, 81970436]
  2. Jiangsu Provincial Medical Young Talents [QNRC2016756]
  3. Applied Foundational Research of Medical and Health Care of Suzhou City [SYS2019086]
  4. Suzhou Medical Key Discipline Pediatric Cardiology [Szxk201507]
  5. Key Medical Talents in Jiangsu Province [ZDRCA2016049]
  6. Second cycle key subjects of maternal and child health in Jiangsu Province [FXK201740]
  7. Introduction Project of Clinical Medical Expert Team in Suzhou City [SZYJTD201805]

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The study revealed that IVIG treatment affects myeloid cells and neutrophils in patients with Kawasaki disease, and pathway analysis indicated that hematopoietic cell lineages and osteoclast differentiation may play important roles in the mechanism of action of IVIG treatment. Furthermore, immune cell analysis showed significant changes in levels of monocytes, M1 macrophages, neutrophils, and platelets in patients with Kawasaki disease following IVIG treatment, suggesting the involvement of these cells in the treatment mechanism.
Kawasaki disease (KD) is an acute, self-limiting form of vasculitis commonly encountered in infants and young children. Intravenous immunoglobulin (IVIG) is the primary drug used for the treatment of KD, which may significantly reduce the occurrence of coronary artery lesions. However, the specific molecular profile changes of KD caused by IVIG treatment have remained elusive and require further research. The present study was designed to identify key genes, pathways and immune cells affected by IVIG treatment using multiple bioinformatics analysis methods. The results suggested that myeloid cells and neutrophils were affected by IVIG treatment. Kyoto Encyclopedia of Genes and Genomes pathway analysis identified that hematopoietic cell lineages and osteoclast differentiation may have an important role in the mechanism of action of IVIG treatment. Immune cell analysis indicated that the levels of monocytes, M1 macrophages, neutrophils and platelets were markedly changed in patients with KD after vs. prior to IVIG treatment. The key upregulated genes, including ZW10 interacting kinetochore protein, GINS complex subunit 1 and microRNA-30b-3p in whole blood cells of patients with KD following treatment with IVIG indicated that these IVIG-targeted molecules may have important roles in KD. In addition, these genes were further examined by literature review and indicated to be involved in cell proliferation, apoptosis and virus-related immune response in patients with KD. Therefore, the present results may provide novel insight into the mechanisms of action of IVIG treatment for KD.

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