TPI ASM8 reduces eosinophil progenitors in sputum after allergen challenge

H Imaoka1, H Campbell, I Babirad

  • 1Department of Medicine, Division of Respirology, Neurology and Rheumatology, Kurume University School of Medicine, Kurume, Japan.

Abstract

Insights

TPI ASM8, a novel asthma therapy, effectively reduces airway eosinophils and progenitor cells by blocking CCR3 and beta common receptor (βc) pathways. This demonstrates a new therapeutic target for asthma management.

Area of Science:

  • Respiratory Medicine
  • Immunology
  • Pharmacology

Background:

  • TPI ASM8 comprises two antisense oligonucleotides (AONs) targeting IL-3/IL-5/GM-CSF receptor beta chain (βc) and CCR3.
  • Inhaled TPI ASM8 improves lung function and reduces sputum eosinophilia in asthmatics post-allergen challenge.

Purpose of the Study:

  • To evaluate the efficacy of TPI ASM8 in reducing airway levels of haemopoietic progenitor cells in asthmatic subjects.
  • To assess the impact of TPI ASM8 on airway inflammation markers following allergen exposure.

Main Methods:

  • An open-label study involving 14 stable allergic mild asthmatics with early and late asthmatic responses.
  • Subjects received placebo or TPI ASM8 (4 mg b.i.d. or 8 mg o.d.) for 4 days before allergen challenge.
  • Sputum induction was performed pre-challenge and 7, 24 hours post-challenge for progenitor cell analysis.

Main Results:

  • TPI ASM8 significantly reduced allergen-induced sputum eosinophils and early/late asthmatic responses (P<0.05).
  • A significant reduction was observed in CD34(+) CCR3(+) cells (P=0.004) and CD34(+) IL-5Rα(+) cells (P=0.016).
  • The proportion of CD34(+) cells expressing IL-5Rα also decreased significantly (P=0.036).

Conclusions:

  • TPI ASM8 is safe and well-tolerated in mild asthmatics.
  • Blocking CCR3 and βc receptors with TPI ASM8 inhibits airway eosinophil and progenitor cell accumulation post-allergen challenge.
  • Inhibition of airway progenitor cell accumulation represents a novel therapeutic strategy for asthma.

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