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Differences in the distribution of CD20, CD3, CD34 and CD45RO in nasal mucosa and polyps from patients with chronic rhinosinusitis

  • Authors:
    • Mihaela Mitroi
    • Dana Albulescu
    • Alina Capitanescu
    • Anca Oana Docea
    • Gabriela Musat
    • George Mitroi
    • Ovidiu Zlatian
    • Aristidis Tsatsakis
    • George Tzanakakis
    • Demetrios A. Spandidos
    • Daniela Calina
  • View Affiliations / Copyright

    Affiliations: Department of Otorhinolaryngology, University of Medicine and Pharmacy of Craiova, 200349 Craiova, Romania, Department of Radiology, University of Medicine and Pharmacy of Craiova, 200349 Craiova, Romania, Department of Toxicology, University of Medicine and Pharmacy of Craiova, 200349 Craiova, Romania, Department of Otorhinolaryngology, University of Medicine and Pharmacy ‘Carol Davila’, 050474 Bucharest, Romania, Department of Urology, University of Medicine and Pharmacy of Craiova, 200349 Craiova, Romania, Department of Microbiology, University of Medicine and Pharmacy of Craiova, 200349 Craiova, Romania, Laboratory of Toxicology, Medical School, University of Crete, 71003 Heraklion, Greece, Laboratory of Anatomy-Histology-Embryology, Medical School, University of Crete, 71003 Heraklion, Greece, Laboratory of Clinical Virology, Medical School, University of Crete, 71003 Heraklion, Greece, Department of Clinical Pharmacy, University of Medicine and Pharmacy of Craiova, 200349 Craiova, Romania
    Copyright: © Mitroi et al. This is an open access article distributed under the terms of Creative Commons Attribution License.
  • Pages: 2792-2800
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    Published online on: February 5, 2019
       https://doi.org/10.3892/mmr.2019.9932
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Abstract

The present study focused on the assessment of the inflammatory infiltrate that characterizes nasal polyps in patients with chronic rhinosinusitis and nasal polyposis. Inflammatory cell type was determined using specific markers. This evaluation was made possible by determining the expression of the following markers: CD20, a marker of B lymphocytes [using activated T cells (ATC) armed with CD20 antibody]; CD3, a marker of T lymphocytes (using ATC armed with anti‑CD3 antibody); CD45, the leukocyte common antigen (using ATC armed with anti‑CD45 antibody; and CD34, for the microvasculature of the nasal polyp (using anti‑CD34 antibody). The diagnosis of chronic rhinosinusitis with nasal polyps (CRSwNP) was made according to current EPOS guidelines based on patient history, clinical examination and nasal endoscopy. We examined surgically resected nasal polyps from 127 patients diagnosed with CRSwNP, who benefited from surgical procedures at the Department of Otorhinolaryngology of our institution. The polyps were analyzed at the Department of Pathology of our institution utilizing histopathological and immunohistochemical methods as follows: Firstly, the tissues were paraffin‑impregnated, sectioned and stained with hematoxylin and eosin. We then examined the expression of CD3, CD20, CD34 and CD45RO by immunohistochemistry with soluble labeled streptavidin biotin (LSAB)/horseradish peroxidase (HRP) complexes. We observed the following histopathological changes: The structure of the epithelium was evidenced by collagenous subjacent stroma with mixed areas, sometimes associated with hyaline zones. In all types of polyps, we also observed a diffuse underlayer or periglandular lymphoplasmacytic in filtrate composed predominantly from T lymphocytes and eosinophils. The histopathological changes suggest the chronic inflammation of the sinus mucosa, which was diffusely distributed in allergic polyps and with nodular distribution in fibro‑inflammatory polyps. The number of B lymphocytes was greater in the fibro‑inflammatory polyps. On the whole, the findings of this study indicate that the inflammatory infiltrate in nasal polyps from patients with CRSwNP is mainly composed of T cells and eosinophils in all types of polyposis. In addition, a diffuse distribution of allergic polyps and the nodular distribution of fibro‑inflammatory polyps, and the hyperplasia of the seromucous glands was observed. The determination of CD20, CD3, CD34 and CD45RO could be used to assess the inflammatory infiltrate of the nasal poplyps in these patients.
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Mitroi M, Albulescu D, Capitanescu A, Docea AO, Musat G, Mitroi G, Zlatian O, Tsatsakis A, Tzanakakis G, Spandidos DA, Spandidos DA, et al: Differences in the distribution of CD20, CD3, CD34 and CD45RO in nasal mucosa and polyps from patients with chronic rhinosinusitis. Mol Med Rep 19: 2792-2800, 2019.
APA
Mitroi, M., Albulescu, D., Capitanescu, A., Docea, A.O., Musat, G., Mitroi, G. ... Calina, D. (2019). Differences in the distribution of CD20, CD3, CD34 and CD45RO in nasal mucosa and polyps from patients with chronic rhinosinusitis. Molecular Medicine Reports, 19, 2792-2800. https://doi.org/10.3892/mmr.2019.9932
MLA
Mitroi, M., Albulescu, D., Capitanescu, A., Docea, A. O., Musat, G., Mitroi, G., Zlatian, O., Tsatsakis, A., Tzanakakis, G., Spandidos, D. A., Calina, D."Differences in the distribution of CD20, CD3, CD34 and CD45RO in nasal mucosa and polyps from patients with chronic rhinosinusitis". Molecular Medicine Reports 19.4 (2019): 2792-2800.
Chicago
Mitroi, M., Albulescu, D., Capitanescu, A., Docea, A. O., Musat, G., Mitroi, G., Zlatian, O., Tsatsakis, A., Tzanakakis, G., Spandidos, D. A., Calina, D."Differences in the distribution of CD20, CD3, CD34 and CD45RO in nasal mucosa and polyps from patients with chronic rhinosinusitis". Molecular Medicine Reports 19, no. 4 (2019): 2792-2800. https://doi.org/10.3892/mmr.2019.9932
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Spandidos Publications style
Mitroi M, Albulescu D, Capitanescu A, Docea AO, Musat G, Mitroi G, Zlatian O, Tsatsakis A, Tzanakakis G, Spandidos DA, Spandidos DA, et al: Differences in the distribution of CD20, CD3, CD34 and CD45RO in nasal mucosa and polyps from patients with chronic rhinosinusitis. Mol Med Rep 19: 2792-2800, 2019.
APA
Mitroi, M., Albulescu, D., Capitanescu, A., Docea, A.O., Musat, G., Mitroi, G. ... Calina, D. (2019). Differences in the distribution of CD20, CD3, CD34 and CD45RO in nasal mucosa and polyps from patients with chronic rhinosinusitis. Molecular Medicine Reports, 19, 2792-2800. https://doi.org/10.3892/mmr.2019.9932
MLA
Mitroi, M., Albulescu, D., Capitanescu, A., Docea, A. O., Musat, G., Mitroi, G., Zlatian, O., Tsatsakis, A., Tzanakakis, G., Spandidos, D. A., Calina, D."Differences in the distribution of CD20, CD3, CD34 and CD45RO in nasal mucosa and polyps from patients with chronic rhinosinusitis". Molecular Medicine Reports 19.4 (2019): 2792-2800.
Chicago
Mitroi, M., Albulescu, D., Capitanescu, A., Docea, A. O., Musat, G., Mitroi, G., Zlatian, O., Tsatsakis, A., Tzanakakis, G., Spandidos, D. A., Calina, D."Differences in the distribution of CD20, CD3, CD34 and CD45RO in nasal mucosa and polyps from patients with chronic rhinosinusitis". Molecular Medicine Reports 19, no. 4 (2019): 2792-2800. https://doi.org/10.3892/mmr.2019.9932
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