Effect of experimental rhinovirus 16 colds on airway hyperresponsiveness to histamine and interleukin-8 in nasal lavage in asthmatic subjects in vivo

K Grünberg, M C Timmers, H H Smits, E P de Klerk, E C Dick, W J Spaan, P S Hiemstra, P J Sterk, K Grünberg, M C Timmers, H H Smits, E P de Klerk, E C Dick, W J Spaan, P S Hiemstra, P J Sterk

Abstract

Background: Asthma exacerbations are closely associated with respiratory virus infections. However, the pathophysiological consequences of such infections in asthma are largely unclear.

Objective: To examine the effect of rhinovirus 16 (RV16) infection on airway hypersensitivity to histamine, and on interleukin-8 (IL-8) in nasal lavage.

Methods: Twenty-seven non-smoking atopic, mildly asthmatic subjects participated in a placebo-controlled, parallel study. A dose of 0.5-2.9 x 10(4) TCID50 RV16 or placebo was nasally administered. Cold symptoms were recorded by questionnaire throughout the study. Histamine challenges were performed at entry, and on days 4 and 11 after inoculation. Nasal lavages were obtained at entry, and on days 2 and 9. The response to histamine was measured by PC20 (changes expressed as doubling doses: DD) IL-8 levels were obtained by ELISA, and were expressed in ng/ml.

Results: RV infection was confirmed by culture of nasal lavage and/or by antibody titre rise in each of the RV16-treated subjects. Among the 19 RV 16-treated subjects, eight developed severe cold symptoms. Baseline FEV1, did not change significantly during the study in either treatment group (P = 0.99). However, in the RV16-treated subjects there was a decrease in PC20 at day 4, which was most pronounced in those with a severe cold (mean change +/- SEM: -1.14 +/- 0.28 DD, P = 0.01). In addition, IL-8 levels increased in the RV16 group at days 2 and 9 (P < 0.001). The increase in nasal IL-8 at day 2 correlated significantly with the change in PC20 at day 4 (r = -0.48, P = 0.04).

Conclusion: We conclude that the severity of cold, as induced by experimental RV16 infection, is a determinant of the increase in airway hypersensitivity to histamine in patients with asthma. Our results suggest that this may be mediated by an inflammatory mechanism, involving the release of chemokines such as IL-8.

References

    1. National Heart Lung and Blood Institute. International consensus report on diagnosis and treatment of asthma. Eur Respir J 1992; 5:601–41.
    1. Djukanovic R, Roche WR, Wilson JW et al. Mucosal inflammation in asthma. Am Rev Respir Dis 1990; 142: 434–57.
    1. Pattemore PK, Johnston SL, Bardin PG. Viruses as precipitants of asthma syniptoms I. Epidemiology. Clin Exp Allergy 1992; 22:325–36.
    1. Beasley R, Coleman ED, Hermon Y et al. Viral respiratory tract infection and exacerbations of asthma in adult patients. Thorax 1988; 43:679–83.
    1. Nicholson KG, Kent J, Ireland DC. Respiratory viruses and exacerbations of asthma in adults. Br Med J 1993; 307:982–6.
    1. McIntosh K, Ellis EE, Hoffman LS et al. The association of viral and bacterial respiratory inlections with exacerbations of wheezing in young asthmatic children. J Pediatr 1973; 82: 578–90.
    1. Minor TE, Dick EC, DeMeo AN et al. Viruses as precipitants of asthmatic attacks in children. JAMA 1974; 227:292–8.
    1. Horn MEC, Brain EA, Gregg I et al. Respiratory viral infection and wheezy bronchitis in childhood. Thorax 1979; 34:23–8.
    1. Johnston SL, Pattemore PK, Sanderson G et al. A community study of the role of virus infections in exacerhations of asthma in 9–11 ye:ir old children. Br Med J 1995; 310:1225–8.
    1. Lemanske RF Jr, Dick EC, Swenson CA, Vrtls RF, Busse WW. Rhinovirus upper respiratory infection increases airway hyperreactivity and late asthmatic reactions. J Clin Invest 1989; 83:1–10.
    1. Summers QA, Higgins PG, Barrow IG, Tyrrell DA, Holgate ST. Bronchial reactivity to histamine and bradykinin is unchanged after rhinovirus infection in normal subjects. Eur Respir J 1992; 5:313–7.
    1. Skoner DP, Doyle WJ, Seroky J, Van Deusen MA, Fireman P. Lower airway responses to rhinovirus 39 in healthy allergic and nonallergic subjects. Eur Respir J 1996; 9:1402–6.
    1. Halperin SA, Eggleston PA, Beasley P et al. Exacerbations of asthma in adults during experimental rhinovirus infection. Am Rev Respir Dis 1985; 132:976–80.
    1. Fraenkel DJ, Bardin PG, Sanderson G et al. Lower airways intlammalion during rhinovirus colds in nomial and in asthmatic subjects. Am J Respir Crit Care Med 1995; 151:879–86.
    1. Cheung D, Dick EC, Timmers MC et al. Rhinovirus inhalation causes long‐lasling excessive airway narrowing in response to methacholine in asthmatic subjects in vivo . Am J Respir Crit Care Med 1995; 152:1490–6.
    1. Naclerio RM, Proud D, Lichtenstein LM et al. Kinins are generated during experimental rhinovirus colds. J Infect Dis 1988; 157:133–42.
    1. Levandowski RA, Weaver CW, Jackson GG. Nasal‐secretion leukocyte populations determined by flow cytometry during acute rhinovirus infection. J Med Virol 1988; 25:423–32.
    1. Winlher B, Earr B, Turner RB et al. Histopathologic examination and enumeration of polymorphonuclear leukocytes in the nasal mucosa during experimental rhinovirus colds. Acta Otolaryngol SuppI 1984; 413:19–24.
    1. Gern JE, Dick EC, Ming Lee W et al. Rhinovirus enters but does not replicate inside monocytes and airway macrophages. J Immunol 1996; 156:621–7.
    1. Subauste MC, Jacoby DB, Richards SM, Proud D. Infection of a human respiratory epithelial cell line with rhinovirus. Induction of cytokine release and modulation of susceptibility to infection by cytokine exposure. J Clin Invest 1995; 96:549–57.
    1. Johnston SL, Mastronarde JG, Monick MM, Hunninghake GW. Rhinoviruses induce prolonged interleukin‐8 release, increases in mRNA and promotor activation in pulmonary epithelial and peripheral blood mononuclear cells. Am J Respir Crit Care Med 1995; 151:A773.
    1. Teran LM, Johnston SL, Shute JK, Church MK, Holgale ST. Increased levels of interIeukin‐8 in the nasal aspirates of children with virus‐associatetl asthma. J Allergy Clin Immunol 1994; 93:272.
    1. Teran LM, Johnston SL, Holgate ST. Immunoreactive RANTES and MIP‐1α are increased in the nasal aspirates of children with virus‐associated asthma. Am J Respir Crit Care Med 1995; 151:A385.
    1. Baggiolini M, Dewald B, Moser B. Interleukin‐8 and related chemotactic cytokines ‐ CXC and CC chemokines. Adv in Immunol 1994; 55:97–179.
    1. Gwaliney JM Jr, Hendley O, Hayden FG et al. Updated recommendations for safety‐testing of viral inocula used in volunteer experiments on rhinovirus colds. Prog Med Virol 1992; 39:256–63.
    1. Sierk PJ, Fabbri LM, Quanjer FH et al. Airway responsiveness. Standardized challenge testing with pharmacological, physical and sensitizing stimuli in adults. Eur Respir J Suppl 1993; 6:53–83.
    1. Greiff L, Pipktim U, Alkner V, Persson CG. The ‘nasal pool’ device applies controlled concentralions of solutes on human nasal airway mucosa and samples its surface exudations/secretions. Clin Exp Allergy 1990; 20:253–9.
    1. O'Byrne PM. Allergen‐induced airway hyperresponsiveness. J Allergy Clin Immunol 1988; 81:119–27.
    1. Bardin PG, Eraenkel DJ, Sanderson G et al. Amplified rhinovirus colds in atopic subjects. Clin Exp Allergy 1994; 24:457–64.
    1. Las Hcras J, Swanson VL. Sudden death of an infant with rhinovirus infection complicating bronchial asthma: case report. Pediatr Pathol 1983; 1:319–23.
    1. Dick EC, Inhorn SL. Rhinoviruses In: Feigin RD, Cherry JD, eds. Textbook of pediatric infectious diseases. Philadelphia . WB Saunders; 1992:1507–32.
    1. Everard ML, Hardy JG, Milner AD. Comparison of nebulised aerosol deposition in the kings of healthy adults following oral and nasal inhalation. Thorax 1993; 48:1045–6.
    1. Hegele RG, Hayashi S, Hogg JC. Pare PD. Mechanisms of airway narrowing and hypernesponsiveness in viral respiratory tract infections. Am J Respir Crit Care Med 1995; 151: 1659–65.
    1. Proud D, Naclerio RM, Gwaltney JM, Hendley JO. Kinins are generated in nasal secretions during natural rhinovirus colds. J Infect Dis 1990; 161:120–3.
    1. Proud D, Gwaltney JM Jr, Hendley JO et al. Increased levels of interleukin‐1 are detected in nasal secretions of volunteers during experimental rhinovirus colds. J Infect Dis 1994; 169:1007–13.
    1. Calhoun WJ, Dick EC, Schwartz LB, Busse WW. A common cold virus, rhinovirus 16, potentiates airway inflammation after segmental antigen bronchoprovocation in allergic subjects. J Clin Invest 1994; 94:2200–8.
    1. Yousefi S, Hemniann S, Weber M et al. IL‐8 is expressed by human peripheral blood eosinophils. Evidence for increased secretion in asthma. J Immunol 1995; 154:5481–90.
    1. Baggiolini M, Dahinden CA. CC chemokines in allergic inflammation. Immunol Today 1994; 15:127–33.
    1. Warringa RAJ, Mengelers HJJ, Raaijmakers JAM, Bruijnzeel PLB, Koendcmian L. Upregulation of formyl‐peptide and interleukin‐8‐induced eosinophil chemotaxis in patients with allergic asthma. J Allergy Clin Immunol 1993; 91:1198–1205.
    1. Zhu Z, Tang W, Ray A et al. Rhinovirus stimulation of intereukin‐6 in vivo and in vino. Evidence for nuclear factor kB‐dependent transcriptional activation. J Clin Invest 1996; 97:421–30.

Source: PubMed

3
Abonnere