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Updated: May 31, 2026

Methodology for Sputum Induction and Laboratory Processing
Published on: December 17, 2017
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.
Background:
TPI ASM8 contains two modified phosphorothioate antisense oligonucleotides (AON), one targeting the common beta chain (βc) of the IL-3/IL-5/GM-CSF receptors and the other targeting the chemokine receptor CCR3. Inhalation of TPI ASM8 significantly improves lung function and sputum eosinophilia after allergen inhalation challenge in asthmatics.
Objective:
This study assessed whether TPI ASM8 reduces airway levels of haemopoietic progenitor cells.
Methods:
This open-label study was conducted in 14 stable, allergic mild asthmatic subjects with early- and late-phase allergen-induced bronchoconstriction. Subjects underwent allergen challenges after 4-day treatment with placebo, 4 mg b.i.d. and 8 mg o.d. of TPI ASM8. Sputum was induced before, 7 and 24 h after allergen challenges for progenitor measurements. Treatments were separated by 2-3 weeks.
Results:
TPI ASM8 reduced allergen-induced sputum eosinophils, and the early and late asthmatic responses (P<0.05). TPI ASM8 also reduced the number of CD34(+) CCR3(+) cells (P=0.004) and CD34(+) IL-5Rα(+) cells (P=0.016), and the proportion of CD34(+) cells expressing IL-5Rα (P=0.036).
Conclusions And Clinical Relevance:
TPI ASM8 was safe and well tolerated. The results of this study demonstrate blocking of CCR3 and βc expression by TPI ASM8 significantly inhibits the accumulation of eosinophils and eosinophil progenitors in the airways after allergen challenge. Inhibition of airway progenitor cell accumulation presents a novel therapeutic target.
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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