The Role of Mast Cells in IgE-Independent Lung Diseases

Publication date

2020

Authors

Komi, Daniel Elieh Ali
Mortaz, EsmaeilISNI 0000000396269831
Amani, Saeede
Tiotiu, Angelica
Folkerts, GertISNI 000000038703888X
Adcock, Ian M.

Editors

Advisors

Supervisors

Document Type

Article
Open Access logo

License

cc_by

Abstract

Mast cells (MCs) are granular cells of the innate immune system which develop from CD34+/CD117+ progenitors and play a role in orchestrating adaptive immune responses. They have a well-known role in allergic reactions following immunoglobulin (Ig)E-mediated activation of the cell-surface expressed IgE high-affinity receptor (FcεRI). MCs can also respond to various other stimuli due to the expression of a variety of receptors including toll-like receptors (TLRs), immunoglobulin (IgG) receptors (FcγR), complement receptors such as C5a (CD88) expressed by skin MCs, neuropeptides receptors including nerve growth factor receptor, (NGFR), cytokines receptors such as (IL)-1R and IL-3R, and chemokines receptors including CCR-1 and CCR-3. MCs release three groups of mediators upon degranulation differentiated according to their chemical composition, storage, and time to release. These include preformed mediators (mainly histamine, tryptase, and chymase), de novo synthesized mediators such as prostaglandin (PG)D2, leukotriene (LT)B4 and LTD4, and cytokines including IL-1β, IL-3, tumor necrosis factor (TNF)α, and transforming growth factor(TGF)-β. Emerging evidence indicates a role for IgE-independent MC activation in the late-stage asthmatic response as well as in non-allergic airway diseases including chronic obstructive pulmonary disease (COPD), idiopathic pulmonary fibrosis (IPF), and lung cancer. MC infiltration/activation has been reported in some, but not all, studies of lung cancer. MC-derived TNF-α possesses tumor-suppressive activity while IL-1β supports tumor progression and metastasis. In IPF lungs, an increase in density of tryptase- and chymase-positive MCs (MCTC) and overexpression of TGF-β support the fibrosis progression. MC-derived chymase activates latent TGF-β that induces the differentiation of fibroblasts to matrix-producing myofibroblasts. In summary, increasing evidence highlights a critical role of MCs in non-allergic diseases that may indicate new approaches for therapy.

Keywords

Antigen-independent, COPD, IPF, Lung cancer, Mast cells, Non-IgE mast cell activation, Immunology and Allergy, SDG 3 - Good Health and Well-being

Citation

Komi, D E A, Mortaz, E, Amani, S, Tiotiu, A, Folkerts, G & Adcock, I M 2020, 'The Role of Mast Cells in IgE-Independent Lung Diseases', Clinical Reviews in Allergy and Immunology, vol. 58, pp. 377–387. https://doi.org/10.1007/s12016-020-08779-5