Interleukin-18 in hemophagocytic lymphohistiocytosis

H. Takada, A. Nomura, S. Ohga, T. Hara

Research output: Contribution to journalReview article

38 Citations (Scopus)

Abstract

Hemophagocytic lymphohistiocytosis (HLH) is characterized by dysregulated hyperactivation of macrophages and T helper 1 (Th1) cells accompanied by excessive secretion of inflammatory cytokines. Although TNF-α and IFN-γ are known to be important factors for the development of the disease, the mechanism of their overproduction has not been clarified, yet. We measured serum IL-18 levels of patients with HLH to investigate the possible significance of IL-18 in its pathophysiology, especially in IFN-γ production. IL-18 levels were significantly increased in all patients with HLH compared with healthy controls. A significant correlation was observed between IL-18 and IFN-γ levels. In addition to IFN-γ and soluble Fas ligand (sFasL), IL-18 levels significantly correlated with disease activity. IL-18 may play important roles in the pathogenesis of HLH, particularly through induction of Th1 cells. In addition, IL-18 measurement may not only be useful for the diagnosis, but also for the evaluation of disease activity.

Original languageEnglish
Pages (from-to)21-28
Number of pages8
JournalLeukemia and Lymphoma
Volume42
Issue number1-2
DOIs
Publication statusPublished - Jan 1 2001

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Hemophagocytic Lymphohistiocytosis
Interleukin-18
Th1 Cells
Fas Ligand Protein
Macrophages
Cytokines
Serum

All Science Journal Classification (ASJC) codes

  • Hematology
  • Oncology
  • Cancer Research

Cite this

Interleukin-18 in hemophagocytic lymphohistiocytosis. / Takada, H.; Nomura, A.; Ohga, S.; Hara, T.

In: Leukemia and Lymphoma, Vol. 42, No. 1-2, 01.01.2001, p. 21-28.

Research output: Contribution to journalReview article

Takada, H. ; Nomura, A. ; Ohga, S. ; Hara, T. / Interleukin-18 in hemophagocytic lymphohistiocytosis. In: Leukemia and Lymphoma. 2001 ; Vol. 42, No. 1-2. pp. 21-28.
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