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Cigarette smoke aggravates asthma by inducing memory-like type 3 innate lymphoid cells

Author

Listed:
  • Jongho Ham

    (Seoul National University College of Medicine
    Seoul National University College of Medicine)

  • Jihyun Kim

    (Seoul National University College of Medicine
    Seoul National University Medical Research Center)

  • Kyoung-Hee Sohn

    (Kyung Hee University Medical Center)

  • In-Won Park

    (Chung-Ang University College of Medicine)

  • Byoung-Whui Choi

    (Chung-Ang University College of Medicine
    Chung-Ang University H.C.S. Hyundae l Hospital)

  • Doo Hyun Chung

    (Seoul National University College of Medicine
    Seoul National University College of Medicine
    Seoul National University College of Medicine)

  • Sang-Heon Cho

    (Seoul National University Medical Research Center
    Seoul National University Hospital)

  • Hye Ryun Kang

    (Seoul National University Medical Research Center
    Seoul National University Hospital)

  • Jae-Woo Jung

    (Chung-Ang University College of Medicine)

  • Hye Young Kim

    (Seoul National University College of Medicine
    Seoul National University College of Medicine
    Seoul National University Medical Research Center)

Abstract

Although cigarette smoking is known to exacerbate asthma, only a few clinical asthma studies have been conducted involving smokers. Here we show, by comparing paired sputum and blood samples from smoking and non-smoking patients with asthma, that smoking associates with significantly higher frequencies of pro-inflammatory, natural-cytotoxicity-receptor-non-expressing type 3 innate lymphoid cells (ILC3) in the sputum and memory-like, CD45RO-expressing ILC3s in the blood. These ILC3 frequencies positively correlate with circulating neutrophil counts and M1 alveolar macrophage frequencies, which are known to increase in uncontrolled severe asthma, yet do not correlate with circulating eosinophil frequencies that characterize allergic asthma. In vitro exposure of ILCs to cigarette smoke extract induces expression of the memory marker CD45RO in ILC3s. Cigarette smoke extract also impairs the barrier function of airway epithelial cells and increases their production of IL-1β, which is a known activating factor for ILC3s. Thus, our study suggests that cigarette smoking increases local and circulating frequencies of activated ILC3 cells, plays a role in their activation, thereby aggravating non-allergic inflammation and the severity of asthma.

Suggested Citation

  • Jongho Ham & Jihyun Kim & Kyoung-Hee Sohn & In-Won Park & Byoung-Whui Choi & Doo Hyun Chung & Sang-Heon Cho & Hye Ryun Kang & Jae-Woo Jung & Hye Young Kim, 2022. "Cigarette smoke aggravates asthma by inducing memory-like type 3 innate lymphoid cells," Nature Communications, Nature, vol. 13(1), pages 1-12, December.
  • Handle: RePEc:nat:natcom:v:13:y:2022:i:1:d:10.1038_s41467-022-31491-1
    DOI: 10.1038/s41467-022-31491-1
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    References listed on IDEAS

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    1. Junko Irie-Sasaki & Takehiko Sasaki & Wataru Matsumoto & Anne Opavsky & Mary Cheng & Grant Welstead & Emily Griffiths & Connie Krawczyk & Christopher D. Richardson & Karen Aitken & Norman Iscove & Gar, 2001. "CD45 is a JAK phosphatase and negatively regulates cytokine receptor signalling," Nature, Nature, vol. 409(6818), pages 349-354, January.
    2. Lauriane Galle-Treger & Yuzo Suzuki & Nisheel Patel & Ishwarya Sankaranarayanan & Jennifer L. Aron & Hadi Maazi & Lin Chen & Omid Akbari, 2016. "Nicotinic acetylcholine receptor agonist attenuates ILC2-dependent airway hyperreactivity," Nature Communications, Nature, vol. 7(1), pages 1-13, December.
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