Experimental rhinovirus 16 infection. Effects on cell differentials and soluble markers in sputum in asthmatic subjects - PubMed (original) (raw)
Clinical Trial
. 1997 Aug;156(2 Pt 1):609-16.
doi: 10.1164/ajrccm.156.2.9610079.
Affiliations
- PMID: 9279247
- DOI: 10.1164/ajrccm.156.2.9610079
Clinical Trial
Experimental rhinovirus 16 infection. Effects on cell differentials and soluble markers in sputum in asthmatic subjects
K Grünberg et al. Am J Respir Crit Care Med. 1997 Aug.
Abstract
Asthma exacerbations are often associated with respiratory virus infections, particularly with rhinovirus. In the present study we investigated the effect of experimental rhinovirus 16 (RV16) infection on airway inflammation as assessed by analysis of hypertonic saline-induced sputum. Twenty-seven nonsmoking atopic, mildly asthmatic subjects participated in a placebo-controlled parallel study. RV16 (n = 19) or its diluent (n = 8) was nasally administered. Sputum inductions were performed at entry and on Days 2 and 9 after inoculation, and airway responsiveness to histamine (PC20) was measured on Days 4 and 11. Cell differentials and levels of albumin, eosinophil cationic protein (ECP), IL-8, and IL-6 were determined. The cellular origin of IL-8 was investigated by intracellular staining. RV infection was confirmed by culture and/or by antibody titer rise in each of the RV16-treated subjects. There were no significant changes in the sputum differentials of nonsquamous cells (MANOVA, p > or = 0.40). In the RV16 group, there was a significant increase in the levels of ECP, IL-8, and IL-6 at Day 2 after infection (p < 0.05), whereas the albumin levels did not change (p = 0.82). The levels of IL-8 and IL-6 remained elevated for as long as 9 d after infection (p < 0.05). The increase in the percentage of IL-8 positive cells at Day 2 after infection could be attributed to the increase in IL-8 positive neutrophils (p < 0.02). There was a significant decrease in PC20 at Day 4 (p = 0.02), which was no longer significant at Day 11 (p = 0.19). The decrease in PC20 correlated significantly with the increase in ECP in the first week (r = -0.60) and with the change in the percentage eosinophils in the second week after inoculation (r = -0.58). We conclude that experimental RV16 infection in atopic asthmatic subjects increases airway hyperresponsiveness in conjunction with augmented airway inflammation, as reflected by an increase in ECP, IL-8, and IL-6 in sputum. Our results suggest that the RV16-enhanced airway hyperresponsiveness is associated with eosinophilic inflammation.
Similar articles
- Experimental rhinovirus 16 infection causes variable airway obstruction in subjects with atopic asthma.
Grünberg K, Timmers MC, de Klerk EP, Dick EC, Sterk PJ. Grünberg K, et al. Am J Respir Crit Care Med. 1999 Oct;160(4):1375-80. doi: 10.1164/ajrccm.160.4.9810083. Am J Respir Crit Care Med. 1999. PMID: 10508832 - Effects of experimental rhinovirus 16 infection on airway hyperresponsiveness to bradykinin in asthmatic subjects in vivo.
Grünberg K, Kuijpers EA, de Klerk EP, de Gouw HW, Kroes AC, Dick EC, Sterk PJ. Grünberg K, et al. Am J Respir Crit Care Med. 1997 Mar;155(3):833-8. doi: 10.1164/ajrccm.155.3.9117013. Am J Respir Crit Care Med. 1997. PMID: 9117013 Clinical Trial. - Effect of experimental rhinovirus 16 colds on airway hyperresponsiveness to histamine and interleukin-8 in nasal lavage in asthmatic subjects in vivo.
Grünberg K, Timmers MC, Smits HH, de Klerk EP, Dick EC, Spaan WJ, Hiemstra PS, Sterk PJ. Grünberg K, et al. Clin Exp Allergy. 1997 Jan;27(1):36-45. doi: 10.1111/j.1365-2222.1997.tb00670.x. Clin Exp Allergy. 1997. PMID: 9117878 Free PMC article. Clinical Trial. - The immunology of virus infection in asthma.
Message SD, Johnston SL. Message SD, et al. Eur Respir J. 2001 Dec;18(6):1013-25. doi: 10.1183/09031936.01.00228701. Eur Respir J. 2001. PMID: 11829084 Review. - Update on sputum methodology.
Holz O, Kips J, Magnussen H. Holz O, et al. Eur Respir J. 2000 Aug;16(2):355-9. doi: 10.1034/j.1399-3003.2000.16b26.x. Eur Respir J. 2000. PMID: 10968514 Review.
Cited by
- Role of Virus-Induced EGFR Trafficking in Proviral Functions.
Noh SS, Shin HJ. Noh SS, et al. Biomolecules. 2023 Dec 9;13(12):1766. doi: 10.3390/biom13121766. Biomolecules. 2023. PMID: 38136637 Free PMC article. Review. - Anionic Pulmonary Surfactant Lipid Treatment Inhibits Rhinovirus A Infection of the Human Airway Epithelium.
Numata M, Sajuthi S, Bochkov YA, Loeffler J, Everman J, Vladar EK, Cooney RA, Reinhardt RL, Liu AH, Seibold MA, Voelker DR. Numata M, et al. Viruses. 2023 Mar 14;15(3):747. doi: 10.3390/v15030747. Viruses. 2023. PMID: 36992456 Free PMC article. - Analysis of Exosomal MicroRNA Dynamics in Response to Rhinovirus Challenge in a Longitudinal Case-Control Study of Asthma.
Wang W, Sinha A, Lutter R, Yang J, Ascoli C, Sterk PJ, Nemsick NK, Perkins DL, Finn PW. Wang W, et al. Viruses. 2022 Nov 3;14(11):2444. doi: 10.3390/v14112444. Viruses. 2022. PMID: 36366542 Free PMC article. - Strong and consistent associations of precedent chronic rhinosinusitis with risk of non-cystic fibrosis bronchiectasis.
Schwartz BS, Al-Sayouri SA, Pollak JS, Hirsch AG, Kern R, Tan B, Kato A, Schleimer RP, Peters AT. Schwartz BS, et al. J Allergy Clin Immunol. 2022 Sep;150(3):701-708.e4. doi: 10.1016/j.jaci.2022.03.006. Epub 2022 Mar 18. J Allergy Clin Immunol. 2022. PMID: 35314187 Free PMC article. - Peripheral blood T cells response in human parainfluenza virus-associated lower respiratory tract infection in children.
Gul A, Khan S, Arshad M, Anjum SI, Attaullah S, Ali I, Rauf A, Arshad A, Alghanem SM, Khan SN. Gul A, et al. Saudi J Biol Sci. 2020 Oct;27(10):2847-2852. doi: 10.1016/j.sjbs.2020.07.005. Epub 2020 Jul 10. Saudi J Biol Sci. 2020. PMID: 32994745 Free PMC article.
Publication types
MeSH terms
Substances
LinkOut - more resources
Full Text Sources
Other Literature Sources
Medical