Expression of cytokine mRNA in bronchoalveolar lavage cells from atopic asthmatics before late antigen-induced reaction

A. Miadonna, S. Gibelli, M. Lorini, A. Tedeschi, S. Oddera, G. A. Rossi, E. Crimi

Research output: Contribution to journalArticle

Abstract

Recently, much attention has been given to the possible role of lymphocytes and their soluble products in causing and maintaining allergic inflammation. The aim of this study was to assess the production of mRNAs for interleukins (IL) in bronchoalveolar lavage (BAL) cells obtained from allergic asthmatics after challenge with the relevant allergen in the period between early and late reactions. We evaluated BAL fluid cells obtained from six asthmatic subjects and four nonatopic controls. Challenge was performed with the relevant allergen. BAL fluid cells were obtained by fiberoptic bronchoscopy and bronchoalveolar lavage. To detect mRNA encoding each cytokine in BAL cells we used a reverse transcriptase polymerase chain reaction method. We evaluated IL-1α, -2, -4, -5, -6, -13, and granulocyte- macrophage colony-stimulating factor (GM-CSF), and interferon-γ (IFN-γ). mRNAs for IL-1α, -2, -4, -5, and IFN-γ were detected in all of the atopic subjects; mRNAs for IL-6 and GM-CSF were found in five asthmatics; and mRNA for IL-1 3 was found in one patient only. In contrast, no mRNAs for IL-2, - 4, -5, -6, -13, and GM-CSF were detected in the nonatopic healthy controls; mRNA for IL-1α was found in one out of four normal subjects; and mRNA for IFN-γ was evidenced in two of four subjects. The cellular environment in BAL fluids from allergic asthmatics before the clinical appearance of the late airway reaction shows an unrestricted expression of mRNA for cytokines. The local cytokine milieu could have an important role in the modulation of bronchial inflammation and in the appearance of allergic symptoms.

Original languageEnglish
Pages (from-to)195-209
Number of pages15
JournalLung
Volume175
Issue number3
DOIs
Publication statusPublished - 1997

Fingerprint

Bronchoalveolar Lavage
Cytokines
Antigens
Messenger RNA
Interleukin-1
Bronchoalveolar Lavage Fluid
Granulocyte-Macrophage Colony-Stimulating Factor
Interferons
Interleukin-2
Allergens
Inflammation
Interleukin-3
Interleukins
Bronchoscopy
Reverse Transcriptase Polymerase Chain Reaction
Interleukin-4
Interleukin-6
Lymphocytes

Keywords

  • Asthma
  • Bronchoalveolar lavage cells
  • Cytokines
  • mRNA

ASJC Scopus subject areas

  • Physiology
  • Pulmonary and Respiratory Medicine

Cite this

Miadonna, A., Gibelli, S., Lorini, M., Tedeschi, A., Oddera, S., Rossi, G. A., & Crimi, E. (1997). Expression of cytokine mRNA in bronchoalveolar lavage cells from atopic asthmatics before late antigen-induced reaction. Lung, 175(3), 195-209. https://doi.org/10.1007/PL00007567

Expression of cytokine mRNA in bronchoalveolar lavage cells from atopic asthmatics before late antigen-induced reaction. / Miadonna, A.; Gibelli, S.; Lorini, M.; Tedeschi, A.; Oddera, S.; Rossi, G. A.; Crimi, E.

In: Lung, Vol. 175, No. 3, 1997, p. 195-209.

Research output: Contribution to journalArticle

Miadonna, A, Gibelli, S, Lorini, M, Tedeschi, A, Oddera, S, Rossi, GA & Crimi, E 1997, 'Expression of cytokine mRNA in bronchoalveolar lavage cells from atopic asthmatics before late antigen-induced reaction', Lung, vol. 175, no. 3, pp. 195-209. https://doi.org/10.1007/PL00007567
Miadonna, A. ; Gibelli, S. ; Lorini, M. ; Tedeschi, A. ; Oddera, S. ; Rossi, G. A. ; Crimi, E. / Expression of cytokine mRNA in bronchoalveolar lavage cells from atopic asthmatics before late antigen-induced reaction. In: Lung. 1997 ; Vol. 175, No. 3. pp. 195-209.
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AB - Recently, much attention has been given to the possible role of lymphocytes and their soluble products in causing and maintaining allergic inflammation. The aim of this study was to assess the production of mRNAs for interleukins (IL) in bronchoalveolar lavage (BAL) cells obtained from allergic asthmatics after challenge with the relevant allergen in the period between early and late reactions. We evaluated BAL fluid cells obtained from six asthmatic subjects and four nonatopic controls. Challenge was performed with the relevant allergen. BAL fluid cells were obtained by fiberoptic bronchoscopy and bronchoalveolar lavage. To detect mRNA encoding each cytokine in BAL cells we used a reverse transcriptase polymerase chain reaction method. We evaluated IL-1α, -2, -4, -5, -6, -13, and granulocyte- macrophage colony-stimulating factor (GM-CSF), and interferon-γ (IFN-γ). mRNAs for IL-1α, -2, -4, -5, and IFN-γ were detected in all of the atopic subjects; mRNAs for IL-6 and GM-CSF were found in five asthmatics; and mRNA for IL-1 3 was found in one patient only. In contrast, no mRNAs for IL-2, - 4, -5, -6, -13, and GM-CSF were detected in the nonatopic healthy controls; mRNA for IL-1α was found in one out of four normal subjects; and mRNA for IFN-γ was evidenced in two of four subjects. The cellular environment in BAL fluids from allergic asthmatics before the clinical appearance of the late airway reaction shows an unrestricted expression of mRNA for cytokines. The local cytokine milieu could have an important role in the modulation of bronchial inflammation and in the appearance of allergic symptoms.

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