The Role of TGFβ and Other Cytokines in Regulating Mast Cell Functions in Allergic Inflammation

• Published in: International journal of molecular sciences Vol. 23; no. 18; p. 10864
• Main Authors: Haque, Tamara T., Frischmeyer-Guerrerio, Pamela A.
• Format: Journal Article
• Language: English
• Published: Basel MDPI AG 17.09.2022; MDPI
• Subjects: Allergic diseases; allergy; Apoptosis; Atopy; Bone marrow; Cytokines; Degranulation; Gallbladder diseases; Gene expression; Hypersensitivity; Immune response; Immunoglobulin E; Inflammation; Interleukin 10; Literature reviews; Liver; Mast cells; Phosphorylation; Public health; Review; TGFβ
• ISSN: 1422-0067; 1661-6596; 1422-0067
• DOI: 10.3390/ijms231810864

Mast cells (MC) are a key effector cell in multiple types of immune responses, including atopic conditions. Allergic diseases have been steadily rising across the globe, creating a growing public health problem. IgE-mediated activation of MCs leads to the release of potent mediators that can have dire clinical consequences. Current therapeutic options to inhibit MC activation and degranulation are limited; thus, a better understanding of the mechanisms that regulate MC effector functions in allergic inflammation are necessary in order to develop effective treatment options with minimal side effects. Several cytokines have been identified that play multifaceted roles in regulating MC activation, including TGFβ, IL-10, and IL-33, and others that appear to serve primarily anti-inflammatory functions, including IL-35 and IL-37. Here, we review the literature examining cytokines that regulate MC-mediated allergic immune responses.