Ickrath Pascal, Sprügel Lisa, Beyersdorf Niklas, Scherzad Agmal, Hagen Rudolf, Hackenberg Stephan
Department of Oto-Rhino-Laryngology, Plastic, Aesthetic and Reconstructive Head and Neck Surgery, University of Wuerzburg, 97080 Wuerzburg, Germany.
Institute for Virology and Immunobiology, University of Wuerzburg, 97078 Wuerzburg, Germany.
J Fungi (Basel). 2021 May 21;7(6):403. doi: 10.3390/jof7060403.
is ubiquitously present, and colonization in the nose and oral cavity is common. In healthy patients, it usually does not act as a pathogen, but in some cases can cause diseases. The influence of as a trigger of T cell activation on the pathogenesis of chronic rhinosinusitis (CRS) is controversial, and its exact role is not clear to date. The aim of the present study was to detect and characterize -specific CD4+ and CD8+ T cells in patients with CRS, with and without nasal polyps. Tissue and blood samples were collected from patients suffering from chronic rhinosinusitis with (CRSwNP) and without nasal polyps (CRSsNP), and from healthy controls. A peptide pool derived from antigen was added to tissue and blood samples. After 6 days, lymphocytes were analyzed by multicolor flow cytometry. Activation was assessed by the intracellular marker Ki-67, and the cytokine secretion was measured. Tissue CD8+ T cells of CRSsNP patients showed a significantly higher proportion of Ki-67+ cells after activation with antigen compared to peripheral blood CD8+ T cells. Cytokine secretion in response to antigen was similar for all study groups. In this study, -specific CD4+ and CD8+ T cells were detected in peripheral blood and mucosal tissue in all study groups. In patients suffering from CRSsNP, -specific CD8+ T cells were relatively enriched in the nasal mucosa, suggesting that they might play a role in the pathogenesis of CRSsNP.
普遍存在,在鼻腔和口腔定植很常见。在健康患者中,它通常不充当病原体,但在某些情况下可导致疾病。作为T细胞活化触发因素对慢性鼻窦炎(CRS)发病机制的影响存在争议,其确切作用至今尚不清楚。本研究的目的是检测和表征有鼻息肉和无鼻息肉的CRS患者中特异性CD4+和CD8+T细胞。从患有慢性鼻窦炎伴鼻息肉(CRSwNP)和无鼻息肉(CRSsNP)的患者以及健康对照中采集组织和血液样本。将源自抗原的肽库添加到组织和血液样本中。6天后,通过多色流式细胞术分析淋巴细胞。通过细胞内标志物Ki-67评估活化情况,并测量细胞因子分泌。与外周血CD8+T细胞相比,用抗原激活后,CRSsNP患者的组织CD8+T细胞显示出显著更高比例的Ki-67+细胞。所有研究组对抗原的细胞因子分泌相似。在本研究中,在所有研究组的外周血和黏膜组织中均检测到特异性CD4+和CD8+T细胞。在患有CRSsNP的患者中,特异性CD8+T细胞在鼻黏膜中相对富集,表明它们可能在CRSsNP的发病机制中起作用。