Allergic diseases have emerged as a major health care burden, especially in the western hemisphere. They are defined by overshooting reactions of an aberrant immune system to harmless exogenous stimuli. The T1/T2 paradigm assumes that a dominance of T2 cell activation and an inadequate T1 cell response are responsible for the development of allergies. However, the characterization of additional T helper cell subpopulations such as T9, T17, T22, TGM-CSF and their interplay with regulatory T cells suggest further layers of complexity. This review summarizes state-of-the-art knowledge on T cell diversity and their induction, while revisiting the T1/T2 paradigm. With respect to these numerous contributors, it offers a new perspective on the pathogenesis of asthma, allergic rhinitis (AR) and atopic dermatitis (AD) incorporating recent discoveries in the field of T cell plasticity.
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http://dx.doi.org/10.1016/j.clim.2016.11.001 | DOI Listing |
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