Interleukin-7 is decreased and maybe plays a pro-inflammatory function in primary immune thrombocytopenia

Platelets. 2015;26(3):243-9. doi: 10.3109/09537104.2014.903392. Epub 2014 Apr 21.

Abstract

Primary immune thrombocytopenia (ITP) is an autoimmune disease with many immune dysfunctions, including over-proliferation and apoptosis resistance of auto-reactive lymphocytes. This study aimed to determine the effects of interleukin (IL)-7 on the cytokine production and survival of peripheral blood mononuclear cells and bone marrow mononuclear cells from ITP patients. We found that the plasma IL-7 levels in peripheral blood from ITP patients were lower than that of the normal controls, and it had positive correlation with platelet counts. However, the levels of IL-7 did not change in bone marrow serum of ITP patients compared with that of normal controls. The result of further stimulation experiments in vitro showed that IL-7 up-regulated the apoptosis of autologous platelets, promoted the proliferation and secretion of interferon-γ, tumor necrosis factor-α as well as IL-10 of lymphocyte both from peripheral blood and bone marrow. As the role of IL-7 in apoptosis-resistance and stimulation of pro-inflammatory cytokines, we speculated that decreased IL-7 in peripheral blood, maybe, is a consequence of the negative feedback of the pro-inflammatory function in ITP patients.

Keywords: Apoptosis; cell activation; interleukin 7; primary immune thrombocytopenia.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adolescent
  • Adult
  • Aged
  • Apoptosis / drug effects
  • Blood Platelets / drug effects
  • Case-Control Studies
  • Child
  • Child, Preschool
  • Cytokines / blood
  • Female
  • Humans
  • Inflammation Mediators / blood*
  • Inflammation Mediators / pharmacology
  • Interleukin-7 / blood*
  • Interleukin-7 / pharmacology
  • Lymphocytes / drug effects
  • Male
  • Middle Aged
  • Platelet Count
  • Purpura, Thrombocytopenic, Idiopathic / blood*
  • Purpura, Thrombocytopenic, Idiopathic / drug therapy
  • Young Adult

Substances

  • Cytokines
  • Inflammation Mediators
  • Interleukin-7