Department of Microbiology and Immunology, Tulane University School of Medicine, New Orleans, LA, USA.
Department of Epidemiology, Tulane University School of Public Health and Tropical Medicine, New Orleans, LA, USA.
Sci Rep. 2021 May 6;11(1):9686. doi: 10.1038/s41598-021-88956-4.
Mast cells are potent mediators of allergy and asthma, yet their role in regulating adaptive immunity remains ambiguous. On the surface of mast cells, the crosslinking of IgE bound to FcεRI by a specific antigen recognized by that IgE triggers the release of immune mediators such as histamine and cytokines capable of activating other immune cells; however, little is known about the mast cell contribution to the induction of endogenous, antigen-specific CD4 T cells. Here we examined the effects of specific mast cell activation in vivo on the initiation of an antigen-specific CD4 T cell response. While CD4 T cells were not enhanced by FcεRI stimulation alone, their activation was synergistically enhanced when FcεRI activation was combined with TLR4 stimulation. This enhanced activation was dependent on global TLR4 stimulation but appeared to be less dependent on mast cell expressed TLR4. This study provides important new evidence to support the role of mast cells as mediators of the antigen-specific adaptive immune response.
肥大细胞是过敏和哮喘的强效介质,但它们在调节适应性免疫中的作用仍不明确。在肥大细胞表面,与特定 IgE 结合的 IgE 通过该 IgE 识别的特定抗原与 FcεRI 的交联触发免疫介质的释放,如组胺和细胞因子,能够激活其他免疫细胞;然而,关于肥大细胞对诱导内源性、抗原特异性 CD4 T 细胞的贡献知之甚少。在这里,我们研究了体内特定肥大细胞激活对诱导抗原特异性 CD4 T 细胞反应的影响。虽然单独的 FcεRI 刺激不会增强 CD4 T 细胞,但当 FcεRI 激活与 TLR4 刺激结合时,其激活会协同增强。这种增强的激活依赖于全局 TLR4 刺激,但似乎对肥大细胞表达的 TLR4 的依赖性较小。这项研究提供了重要的新证据,支持肥大细胞作为抗原特异性适应性免疫反应的介质的作用。