Characterization of inflammatory reaction in upper airways of cystic fibrosis patients

被引:0
|
作者
Lesprit, E
Escudier, E
Roger, G
Prulière, V
Lenoir, G
Reinert, P
Coste, A
机构
[1] Hop Intercommunal Creteil & Necker Enfants Malad, Serv Pediat, Paris, France
[2] Hop Henri Mondor & Intercommunal Creteil & Trouss, Serv ORL, Paris, France
[3] Hop Henri Mondor & Intercommunal Creteil & Trouss, Serv Chirurg Cervicofaciale, Paris, France
[4] Grp Hosp Pitie Salpetriere, Serv Histol & Embryol, F-75634 Paris, France
[5] Fac Med Pitie Salpetriere, Serv Histol& Embryol, Paris, France
关键词
cystic fibrosis; inflammation; nasal polyps; sinusitis; airways;
D O I
暂无
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Inflammatory cell populations have not been yet precisely evaluated in cystic fibrosis (CF) airways. We intended to characterize morphological modifications, inflammatory cell infiltration and cell proliferation in nasal tissues obtained from 15 CF patients and from 6 non-CF patients with nasal polyposis. Morphological analysis showed an intense inflammatory infiltration in CF and non-CF tissues with only few modifications in the epithelium from CF tissues. Inflammatory cell populations characterized by specific immunolabeling were quantified, showing a predominance of macrophages and T- and B-lymphocytes and only moderate numbers of neutrophils in CF tissues; in non-CF polyps, lymphocytes and eosinophils were abundant. Proliferating cell percentages quantified after proliferating cell nuclear antigen immunolabeling were 5.3+/-4.1% (mean +/- SD) in CF polyps and 3.1+/-1.2% in non-CF polyps in epithelium but were very low in lamina propria. Intense inflammation in nasal tissues from CF patients is therefore dominated by macrophages and lymphocytes rather than by neutrophils. While morphology is preserved, proliferation is high in epithelium from CF polyps. These findings should be regarded in the future for a better understanding of inflammation in CF airway disease.
引用
收藏
页码:395 / 402
页数:8
相关论文
共 50 条
  • [41] Upper Airway Findings and Markers of Lung Disease Progression in Patients with Cystic Fibrosis
    Steffen, Luciane Mazzini
    Pezzin, Luise Sgarabotto
    Sulis, Natassia
    Steffen, Nedio
    Pinto, Leonardo Araujo
    INTERNATIONAL ARCHIVES OF OTORHINOLARYNGOLOGY, 2020, 24 (04) : E434 - E437
  • [42] Evaluation of Inflammatory Biomarkers in Iranian Patients with Cystic Fibrosis
    Ghaffaripour, Hosseinali
    Mirkarimi, Mohammadreza
    Hassanzad, Maryam
    Boloursaz, Mohammadreza
    Mohammadi, Shooka
    CURRENT RESPIRATORY MEDICINE REVIEWS, 2020, 16 (03) : 184 - 192
  • [43] The Cystic Fibrosis Upper and Lower Airway Metagenome
    Pienkowska, Katarzyna
    Pust, Marie-Madlen
    Gessner, Margaux
    Gaedcke, Svenja
    Thavarasa, Ajith
    Rosenboom, Ilona
    Moran Losada, Patricia
    Minso, Rebecca
    Arnold, Christin
    Hedtfeld, Silke
    Dorda, Marie
    Wiehlmann, Lutz
    Mainz, Jochen G.
    Klockgether, Jens
    Tuemmler, Burkhard
    MICROBIOLOGY SPECTRUM, 2023, 11 (02):
  • [44] CT characterization of inflammatory paranasal sinus disease in cystic fibrosis
    Eggesbo, HB
    Sovik, S
    Dolvik, S
    Kolmannskog, F
    ACTA RADIOLOGICA, 2002, 43 (01) : 21 - 28
  • [45] Detection of bile acids in bronchoalveolar lavage fluid defines the inflammatory and microbial landscape of the lower airways in infants with cystic fibrosis
    Jose A. Caparrós-Martín
    Montserrat Saladie
    S. Patricia Agudelo-Romero
    F. Jerry Reen
    Robert S. Ware
    Peter D. Sly
    Stephen M. Stick
    Fergal O’Gara
    Microbiome, 11
  • [46] Detection of bile acids in bronchoalveolar lavage fluid defines the inflammatory and microbial landscape of the lower airways in infants with cystic fibrosis
    Caparros-Martin, Jose
    Saladie, Montserrat
    Agudelo-Romero, S. Patricia
    Reen, F. Jerry
    Ware, Robert S.
    Sly, Peter D.
    Stick, Stephen M.
    O'Gara, Fergal
    MICROBIOME, 2023, 11 (01)
  • [47] Genetic characterization of cystic fibrosis patients in Portugal
    Pereira, Luisa
    Azevedo, Pilar
    Cavaco, Jose
    Felix, Miguel
    Gamboa, Fernanda
    Amorim, Adelina
    Vaz, Luisa
    Rocha, Herculano
    Goncalves, Juan
    Freitas, Cristina
    Barreto, Celeste
    EUROPEAN RESPIRATORY JOURNAL, 2013, 42
  • [48] Characterization of Patients with Cystic Fibrosis in Multidisciplinary Consultation
    Llull Tombo, Caridad
    Fonseca Hernandez, Mercedes
    Garcia Rodriguez, Ileana
    Yanes Macias, Juan Carlos
    Tio Gonzalez, Daymi
    Leon Rayas, Yoandra
    FINLAY, 2020, 10 (01): : 33 - 40
  • [49] Targeting Antibiotics to Pseudomonas aeruginosa in Small airways (TAPAS) in patients with Cystic Fibrosis
    Guidetti, Beatrice
    Bos, Aukje C.
    Van der Wiel, Els
    Meneghelli, Ilaria
    Van der Eerden, Menno
    Tiddens, Harm A. W. M.
    Volpi, Sonia
    Janssens, Hettie M.
    EUROPEAN RESPIRATORY JOURNAL, 2021, 58
  • [50] Bacteria in the airways of patients with cystic fibrosis are genetically capable of producing VOCs in breath
    Bos, Lieuwe D. J.
    Meinardi, Simone
    Blake, Donald
    Whiteson, Katrine
    JOURNAL OF BREATH RESEARCH, 2016, 10 (04)