Asthma and lower airway disease
Activin A and TGF-β promote TH9 cell–mediated pulmonary allergic pathology

https://doi.org/10.1016/j.jaci.2011.12.965Get rights and content

Background

IL-9–secreting (TH9) T cells are thought to represent a distinct T-cell subset. However, evidence for their functionality in disease is uncertain.

Objective

To define a functional phenotype for TH9-driven pathology in vivo.

Methods

We used fluorescence-activated cell sorting to identify circulating TH9 cells in atopic and nonatopic subjects. In mice we utilized a model of allergic airways disease induced by house dust mite to determine TH9 cell function in vivo and the role of activin A in TH9 generation.

Results

Allergic patients have elevated TH9 cell numbers in comparison to nonatopic donors, which correlates with elevated IgE levels. In a murine model, allergen challenge with house dust mite leads to rapid TH9 differentiation and proliferation, with much faster kinetics than for TH2 cell differentiation, resulting in the specific recruitment and activation of mast cells. The TGF-β superfamily member activin A replicates the function of TGF-β1 in driving the in vitro generation of TH9 cells. Importantly, the in vivo inhibition of TH9 differentiation induced by allergen was achieved only when activin A and TGF-β were blocked in conjunction but not alone, resulting in reduced airway hyperreactivity and collagen deposition. Conversely, adoptive transfer of TH9 cells results in enhanced pathology.

Conclusion

Our data identify a distinct functional role for TH9 cells and outline a novel pathway for their generation in vitro and in vivo. Functionally, TH9 cells promote allergic responses resulting in enhanced pathology mediated by the specific recruitment and activation of mast cells in the lungs.

Section snippets

Mice

BALB/c and severe combined immunodeficiency mice (6-8 weeks) were purchased from Charles River (Morgate, United Kingdom [UK]). All experiments were performed in accordance with UK Home Office guidelines.

Induction and analysis of allergic airway inflammation

Mice received 15 μg of house dust mite (HDM) extract (Dermatophagoides pteronyssinus in saline; Greer Laboratories, Lenoir, NC) or saline intranasally 3 days a week for 1 or 3 weeks. In adoptive transfer experiments, 1 × 106 in vitro generated TH9 cells (more than 90% CD4+IL-9+IL-13IFN-γ) were

TH9 cells are generated in the lungs following exposure to allergen and are associated with atopy in patients

PBMCs isolated from asthmatic children generate greater numbers of TH9 cells in vitro when compared with nonasthmatic controls.9 However, direct evidence for the existence of TH9 cells during an allergic response in vivo is lacking. In order to directly evaluate the TH9 subset in human subjects, we isolated PBMCs from allergic or nonallergic donors, and quantified them by flow. We found significantly higher numbers of circulating TH9 cells, defined as CD4+IL-9+IL-13IFN-γ, in allergic donors

Discussion

Asthma is a complex heterogeneous disease thought to occur as a consequence of aberrant TH2 immunity to innocuous environmental particles such as dust and animal dander. However, it is clear that a range of other T cells contribute to disease pathology, which might account for this heterogeneity.22 We demonstrate here that TH9 cells are present in human peripheral blood, since previous studies have shown IL-9 levels only in plasma or TH9 cells generated in vitro from PBMCs. Importantly,

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    This work was supported by the Wellcome Trust (grant nos. 057704 and 085851/Z/08/Z). Part of this data was presented as a poster and the abstract published in the journal Immunology (2011;135:71).

    Disclosure of potential conflict of interest: The authors declare that they have no relevant conflicts of interest.

    These authors contributed equally to this work.

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