Fibroproliferative activity in patients with immune thrombocytopenia (ITP) treated with thrombopoietic agents

Br J Haematol. 2011 Oct;155(2):248-55. doi: 10.1111/j.1365-2141.2011.08845.x. Epub 2011 Sep 9.

Abstract

This study assessed the grade of bone marrow (BM) fibrosis and its association with a seromarker for collagen-III formation and fibrosis-related cytokines in 25 immune thrombocytopenia (ITP) patients treated with thrombopoietin receptor agonists (Tpo-RA) who had at least one BM biopsy. Assessment of 8 pre- and on-treatment BM biopsies revealed statistically significant increases in reticulin. Reticulin in biopsies performed after a median of 1·4 years of treatment was graded: MF-0 in 3 (12%), MF-1 in 19 (76%), MF-2 in 2 (8%) and MF-3 in 1 (4%). No cytogenetic or flow-cytometric abnormalities were detected. Median pretreatment Procollagen III N-propeptide (PIIINP) (6·6 μg/l) was significantly higher than on-treatment levels (5·6 μg/l); both were higher than controls (3·4 μg/l; P < 0·001). PIIINP was negatively correlated with treatment duration (r = -0·49) suggesting a decelerated reticulin production over time. There was a trend towards an association between grade of reticulin and PIIINP. Transforming growth factor (GF)-beta and basic-Fibroblast GF were not different between patients and controls but Hepatocyte GF (HGF), an anti-fibrotic cytokine, was significantly elevated in patients. In conclusion, low-grade BM reticulin fibrosis is seen in most ITP patients on Tpo-RA. The novel findings of decreasing PIIINP and elevated HGF need further investigation to explore their significance in BM fibrogenesis.

MeSH terms

  • Adult
  • Benzoates / administration & dosage
  • Benzoates / adverse effects*
  • Benzoates / therapeutic use
  • Bone Marrow / metabolism
  • Bone Marrow / pathology*
  • Combined Modality Therapy
  • Cytokines / blood
  • Female
  • Hepatocyte Growth Factor / blood*
  • Humans
  • Hydrazines / administration & dosage
  • Hydrazines / adverse effects*
  • Hydrazines / therapeutic use
  • Intercellular Signaling Peptides and Proteins / blood
  • Male
  • Middle Aged
  • Peptide Fragments / blood*
  • Primary Myelofibrosis / blood
  • Primary Myelofibrosis / chemically induced*
  • Procollagen / blood*
  • Purpura, Thrombocytopenic, Idiopathic / blood
  • Purpura, Thrombocytopenic, Idiopathic / drug therapy*
  • Purpura, Thrombocytopenic, Idiopathic / pathology
  • Purpura, Thrombocytopenic, Idiopathic / surgery
  • Pyrazoles / administration & dosage
  • Pyrazoles / adverse effects*
  • Pyrazoles / therapeutic use
  • Receptors, Fc / administration & dosage
  • Receptors, Fc / therapeutic use
  • Receptors, Thrombopoietin / agonists*
  • Recombinant Fusion Proteins / administration & dosage
  • Recombinant Fusion Proteins / adverse effects*
  • Recombinant Fusion Proteins / therapeutic use
  • Reticulin / analysis*
  • Splenectomy
  • Thrombopoietin / administration & dosage
  • Thrombopoietin / adverse effects*
  • Thrombopoietin / therapeutic use

Substances

  • Benzoates
  • Cytokines
  • HGF protein, human
  • Hydrazines
  • Intercellular Signaling Peptides and Proteins
  • Peptide Fragments
  • Procollagen
  • Pyrazoles
  • Receptors, Fc
  • Receptors, Thrombopoietin
  • Recombinant Fusion Proteins
  • Reticulin
  • procollagen Type III-N-terminal peptide
  • MPL protein, human
  • Hepatocyte Growth Factor
  • Thrombopoietin
  • romiplostim
  • eltrombopag