Cellular comparison of sinus mucosa vs polyp tissue from a single sinus cavity in chronic rhinosinusitis

被引:32
作者
Ho, Jacqueline [1 ,2 ]
Bailey, Michelle [3 ,4 ]
Zaunders, John [3 ,4 ]
Mrad, Nadine [2 ]
Sacks, Raymond [2 ,5 ]
Sewell, William [1 ,6 ]
Harvey, Richard J. [1 ,2 ,5 ]
机构
[1] Univ New S Wales, St Vincents Clin Sch, Fac Med, Sydney, NSW, Australia
[2] Univ New S Wales, Rhinol & Skull Base Res Grp, St Vincents Ctr Appl Med Res, Sydney, NSW, Australia
[3] Univ New S Wales, St Vincents Ctr Appl Med Res, Sydney, NSW, Australia
[4] Univ New S Wales, Kirby Inst Infect & Immun, Sydney, NSW, Australia
[5] Macquarie Univ, Australian Sch Adv Med, Sydney, NSW 2109, Australia
[6] Garvan Inst Med Res, Dept Immunol, Sydney, NSW, Australia
关键词
chronic rhinosinusitis; sinus; mucosa; nasal polyp; sinonasal; tissue; flow cytometry; type 2 innate lymphoid cells; lymphocytes; human; INNATE LYMPHOID-CELLS; PLASMACYTOID DENDRITIC CELLS; HUMAN NASAL POLYPS; INCREASED EXPRESSION; PATHOGENESIS; CYTOKINE; PROLIFERATION; INFLAMMATION; HOMEOSTASIS; SECRETION;
D O I
10.1002/alr.21417
中图分类号
R76 [耳鼻咽喉科学];
学科分类号
100213 ;
摘要
BackgroundNasal polyposis is a common development in chronic rhinosinusitis (CRS), and sinus mucosa and polyp tissue have been used interchangeably in studies investigating CRS. However, potential differences may exist between these 2 tissue types, which have not been entirely characterized. MethodsA cross-sectional study of CRS with nasal polyposis (CRSwNP) patients undergoing endoscopic sinus surgery was conducted. Sinus mucosal biopsies and corresponding polyp tissue were obtained from the same sinus cavity via flow cytometry, single-cell suspensions identified type 2 innate lymphoid cells (ILC2s), CD4 and CD8 T cells, activated CD4 and CD8 T cells, plasma cells, plasmacytoid dendritic cells (pDCs), regulatory T cells, T follicular helper cells, B cells, and immunoglobulin A (IgA)(+) and IgG(+) B cells. Cells were measured as a percentage of CD45(+) cells. Paired nonparametric comparisons between sinus and polyp tissue were performed. ResultsTen patients (50% female; age 48 16 years) were recruited. Significantly elevated ILC2 levels were found in polyp tissue compared to sinus mucosa (0.12 [0.07 to 0.23] vs 0.07 [0.04 to 0.16], p=0.02), as well as plasma cells (2.25 [0.84 to 3.68] vs 1.18 [0.74 to 2.41], p=0.01); pDCs (0.15 [0.12 to 0.50[ vs 0.04 [0.02 to 0.17], p=0.03); activated CD8 T cells (29.22 [17.60 to 41.43] vs 16.32 [10.07 to 36.16], p=0.04) and IgG(+) B cells (6.96 [0.06 to 11.82] vs 1.51 [0.38 to 5.13], p=0.04). Other cell populations showed no significant differences. ConclusionPolyps have a similar cellular composition to that of mucosa. Higher levels of ILC2s, plasma cells, pDCs, activated CD8 T cells, and IgG(+) B cells in polyp tissue may be reflective of cell populations driving nasal polyp development. The cellular machinery of CRS is present in polyps and representative of the disease process. This pilot study strongly suggests that a larger study would provide significant insights into the relationship of sinus mucosa to pathogenesis of nasal polyps. (C) 2014 ARS-AAOA, LLC.
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页码:14 / 27
页数:14
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    Wang, Jong Hwan
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    Jang, Yong Ju
    [J]. AMERICAN JOURNAL OF RHINOLOGY & ALLERGY, 2010, 24 (06) : 422 - 427
  • [52] Innate lymphoid cells wield a double-edged sword
    Wills-Karp, Marsha
    Finkelman, Fred D.
    [J]. NATURE IMMUNOLOGY, 2011, 12 (11) : 1025 - 1027
  • [53] Similar cellular proliferation activities m nasal polyps and adjacent inferior turbinate
    Wu, Chia-Chen
    Lee, Ta-Jen
    Chang, Po-Hung
    Tsai, Chi-Neu
    Lee, Yun-Shien
    Fu, Chia-Hsiang
    Huang, Chi-Che
    [J]. AMERICAN JOURNAL OF OTOLARYNGOLOGY, 2012, 33 (01) : 14 - 19
  • [54] RKIP and BRAF aberrations in human nasal polyps and the adjacent turbinate mucosae
    Zaravinos, Apostolos
    Bizakis, John
    Spandidos, Demetrios A.
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