Clinical significance of airway inflammation in bronchcial asthma. Comparison with chronic obstructive bronchiolitis.

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24 Airway inflammation in asthma Clinical significance of airway inflammation in bronchcial asthma. Comparison with chronic obstructive bronchiolitis. Yoshiro Tanizaki, Hikaru Kitani, Takashi Mifune, Fumihiro Mitsunobu, Kazuhiro Kajimoto, Keisuke Sugimoto, Satoshi Yokota, Junichi Hiramatsu, Masashi Kawaraya, Koji Ochi 1), Hideo Harada 1), Shinya Tada 2), and Ikuro Kimura 2) Division of Medicine, Misasa Medical Branch, lldepartment of Laboratory Medicine, 2)Second Department of Medicine, Okayama University Medical School Abstract: Clinical significanoce of airway inflammation was assessed in 28 patients with bronchial asthma, and the results were compared with those in 9 patients with chronic obstructive bronchiolitis (COB). 1. Total cell number in bronchoalveolar lavage (BAL) fluid was markedly increased in patients with COB (51. X 1 6 ), which was significantly greater than that in those with bronchial asthma (9.6 X 1 6 ). 2. The proportion of BAL macrophages was significantly higher in patients with bronchial asthma than in those with COB. However, the, absolute number of BAL macrophages was not significantly different between them. 3. The proportion of BAL lymphocytes was higher in patients with bronchial asthma than in those with COB, but this difference was not signifcant. In contrast, the absolute number of BAL lymphocytes was significantly greater in patients with COB than in those with bronchial asthma. 4. The proportion and the number of BAL neutrophils were markedly increased in patients with COB compared to those with bronchial asthma. 5. The proportion and the number of BAL eosinophils were higher in patients with bronchial asthma than in those with COB, although these defferences were not significant. The results suggest that airway inflammation in bronchial asthma is not so intensive as that in COB. Key words: airway inflammation, bronchial asthma, chronic obstructive bronchiolitis, lymphocytes, neutrophils. Introduction 19E-mediated allergy, in which chemical mediators are released from tissue mast cells by bridging of 19E receptors on the cell membranes, has been evaluated as a major

Airway inflammation in asthma 25 reaction participating in the mechanism of onset of bronchial asthma (1-5).However, recently, attention has been focused on airway inflammation in the pathogenesis of bronchial asthma (6-8). Inflammatory cell infiltration in the airways of asthma has been found by analyzing humoral and cellular components in bronchoalveolar lavage (BAL) fluid (9-12) : lymphocytes, neutrophils, eosinophils and basophils are assessed as inflammatory cells in the airways of asthma. These findings suggest that airway inflammation is assessed sa a major mechanism related to asthma attack. There are many kinds of respiratory diseases with airway inflammation. Of these respiratory diseases, chronic obstructive bronchiolitis (or diffuse panbronchiolitis : DPB) is one the chronic obstructive pulmonary diseases (COPD), which IS clearly caused by airway inflammation. In the present study, airway inflammation is evaluated in patients with bronchial asthma and chronic obstructive bronchiolitis (COB) by analyzing the proportions and the numbers of bronchoalveolar lavage (BAL) cells such as macrophages, lymphocytes, neutrophils and eosinophils. Subjects and Methods The subjects of this study were 28 patients with bronchial asthma (18 females and 1 males, age 52. 6 years, range 24-72 years). Nine patients with chronic obstructive bronchiolitis (COB) (5 females and 4 males, mean age 48. 9 years, range 21-73) were selected as controls. To compare the numbers of bronchoalveolar lavage (BAL) cells between patients with asthma and those with COB, asthma patients whose recovery rate at BAL examination was more than 3% were selected in this study, SInce recovery rate at BAL examination was sometimes very low in patients with asthma (this may be due to bronchoconstriction induced by BAL examination). All patients were admitted to our hospital, and all of them were non-smokers. Bronchial asthma was diagnosed according to the criteria of American Thoracic Society (13). Chronic obstructive bronchiolitis (COB) was diagnosed by clinical symptom, finding on auscultation and micronodular shadow on chest X-ray films. Bronchoalveolar lavage (BAL) was performed by a previously reported method (14, 15) in all the patients when their symptoms were stable. Informed consent for the BAL examination was obtained from all study subjects. The aspirates obtained by a bronchofiberscope were filtered through a sterile steel mesh and centrifuged at 12 rpm for 1 min at 4ce. The cell pellet was resuspended in Tris ACM which comprises 1m of.1 M Ca,.5mf of.1 M Mg and 98.5mf of Tris A buffer (TRIZMA pre-set crystal, ph 7.7, Sigma Chemical Co.,.3275 g +NaCl.715 g +KCl.372 g +3% albumim 5mf+H 2 1m ). After the number of cells was calculated, smear preparations were made from the cell suspension, and stained with May Giemsa. BAL cytology was performed by observing 5 cells, excluding epithelial cells. The absolute numbers of total cells and each BAL cell, and the proportions of each BAL cell were compared in patients with bronchial asthma and those with COB. Total cell number Results Total cell number In BAL fluid was 9.6 X 1 6 in patients with bronchial asthma, and 51 X 1 6 in those with COB. The number of

26 Airway inflammation in asthma total cells in BAL fluid was markedly different between the two obstructive respiratory diseases, and the number was significantly greater in patients with COB than in those with asthma (P<O.OO1) (Fig. 1). Recovery rate at BAL examination was similar between patients with asthma (42.6%) and those with COB (41.4%). 1 9 8 - >< 7 I-l Q).Q 6 3 s:: 5 M.-l Q) u 4 \D.-l I'Cl +J 3 Eo< 2 1 -=,1. Bronchial asthma Fig. 1. Total cell number in bronchoalveolar lavage (BAL) fluid of patients with asthma and of those with chronic obstructive bronchiolitis (COB). The mean total cell number was significantly higher in patients with COB than in those with asthma. Proportions of each SAL cell Chronic obstructive bronchiolitis The proportion of each BAL cell in patients with asthma was 74.8% macrophages, 15.% lymphocytes, 2.6% neutrophils and 7.6% eosinophils. In contrast, the mean proportion of each BAL cell in patients with COB was 21.2% macrophages, 9.4% lymphocytes, 68.7% neutrophils and.7% eosinophils. The proportion of BAL macrophages was significantly higher in patients with asthma than in those with COB (p<o.oo1). In contrast, the proportion of BAL neutrophils was significantly higher in patients with COB than in those with asthma (p<o.oo1). The proportions of lymphocytes and eosinophils in BAL fluid were higher in patients with asthma than in those with COB, however, these differences were not significant (Fig. 2). " "'.,.. 1 9 8 7 6 5 ~ 4 3 2 1 Mac Lym Neut Eos Fig. 2. Proportions of each bronchoalveolar lavage (BAL) cell in patients with asthma (D) and in those with chronic obstructive bronchiolitis (COB) (~). The proportion of BAL macrophages was significantly higher in patients with asthma than in those with COB. In contrast, the proportion of BAL neutrophils was significantly higher in patients with COB than in those with asthma. Mac, macrophages ; Lym, lymphocytes ; Neut, neutrophils ; Eos, eosinophils.

Airway inflammation In asthma 27 Numbers of each SAL cell The absolute number of BAL lymphocytes was significantly greater in patients with COB than in those with asthma (p<.5). The absolute number of BAL neutrophils was markedly increased in patients with COB, which was significantly greater than that in those with asthma (p<o.oo1). The absolute numbers of macrophages and eosisnophils in BAL fluid were not significantly different between the two obstructive respiratory diseases, although the number of BAL eosinophils was greater In patients with asthma compared to those with COB (Table 1). Table 1. Absolute number of bronchoalveolar lavage (BAL) cells In patients with asthma and those with chronic obstructive bronchiolitis No of Number of 91\1. cells (x1-4) Disease patients H~C' Lym Neut Bos Bronchial 28 712 171 3 17 b 62 asthma i:'319 i:265,25 :t:114 Chronic obstruct!ve 872 495 3 ' 372 b ' 32 bronchiolitis t585 t34,37 Mac, BlacrOphageE':; Ly., lymphocytes; Rent, neutrophil!'!; ROB, eoelinophils.. A significant difference between II and a' at p(o.5, and between band b' lit p(o.oof. 1</m1!) (p<o.oo1). The numbers of macrophages and eosinophils in BAL fluid were not significantly different between the two diseases (Fig. 3). :::;... a 1 " 9.. 8 - H... 1... " u 6 ~ SO.c: u Cd 4 -... " 3 2 ".Q 1 z Fig. 3. Mac Lym Neut Eos Numbers of each bronchoalveolar lavage (BAL) cell in patients with asthma ( D ) and in those with chronic obstructive bronchiolitis (COB) (.). The number of lymphocytes and neutrophils were significantly greater in patients with COB than in those with asthma. Mac, macrophages ; Lym, lymphocytes; Neut, neutrophils ; Eos, eosinophils. Discussion The number of each BAL cell per mj! was compared between the two respiratory diseases. The number of BAL lymphocytes was significantly greater in patients with COB (5.39 ± 5.2 X 1 4 / m ) than in those with asthma (2. ± 2.6 X 1 4 / mj!) (p<.2). The BAL neutrophil number in patients with COB was markedly increased (54.8 ± 44.7 X 1 4 / mj!), and this was significantly greater than that in those with asthma (.22 ±.34 X It is well known that bronchial response to allergen is divided into two phages: immediate asthmatic reaction OAR) and late asthmatic reaction (LAR). The IAR is mainly induced by the release of chemical mediators from tissue mast cells (1-5). In contrtast, the LAR has been clarified to be related to inflammatory cell infiltration (16). Thus, airway inflammation is a common feature of asthma (9-12, 17, 18).

28 Airway inflammation in asthma In the present study, clinical significance of airway inflammation in bronchial asthma was evaluated in relation to inflammatory process in chronic obstructive bronchiolitis (COB). The total cell number in the BAL fluid was considerably small in patients with asthma compared to the number in those with COB. The results suggest that airway inflammation in bronchial asthma is not so intensive as that in COB. Regarding the proportion of BAL cells, the proportion of BAL macrophages was significantly higher in patients with asthma than in those with COB. However, the absolute number of BAL macrophages was not significantly different between the two obstructive respiratory diseases. The proportion of BAL lymphocytes was higher in patients with asthma than in those with COB, although this difference was not significant. In contrast, the absolute number of BAL lymphocytes was signifiicantly greater in patients with COB than in those with asthma. The proportion and the numbe of BAL neutrophils were markedly increased in patients with COB, and this increase was significantly higher than that in patients with asthma. An increase in eosinophil number in the peripheral blood and local allergic reaction site is one of the characteristics of bronchial asthma. In this study, the proportion and the number of BAL eosinophils were greater in patients with asthma than in those with COB. However, the difference was not significant between them: this may be due to the reason that BAL examination was performed in asthma patients when they were free of attacks. References 1. Ishizaka T : Analysis of triggering events m mast cells for immunoglobulin E mediated histamine release. J Immunol 67 : 9-96, 1981. Allergy Clin 2. Tanizaki Y, Komagoe H, Morinaga H, Kitani H, Goda Y, Kimura I: Allergen- and anti-ige-induced histamine release from whole blood. Int Arch Allergy Appl Immunol 73: 141-145, 1984. 3. Tanizaki Y, Komagoe H, Sudo M, Morinaga H, Kitani Y, Goda Y, Tada S, Takahashi K, Kimura I: IgE-mediated histamine release from whole blood in atopic asthmatics. Jpn J Allergol 32 : 179 183, 1983. 4. Burrows B, Martinez F, Halonen H, Barbee RA, Cline MG : Association of asthma with serum IgE levels and skin-test reactivity to allergen. New Eng J Med 32 : 271-277, 1989. 5. Tollerud DJ, O'Connor GT, Sparrow D, Weiss ST: Asthma, hay fever, and phlegm production associated with distinct patterns of allergy skin test reactivity, eosinophilia, and serum IgE levels. The normative aging study. Am Rev Respir Dis 144 : 776-871, 1991.. 6. Nadel JA : Inflammation and asthma. J Allergy Clin Immunol 73 : 651-653, 1984. 7. Pauwels R : The relationship between airway inflammation and bronchial hyperresponsivenes Clin Exp Allergy 19 : 395-398, 1989. 8. Holgate ST, Djukanovic R, Wilson J, Roche WR, Howarth PH : Inflammatory process and bronchial hyperresponsiveness. Clin Exp Allergy 21 : 3-36, 1991. 9. Beasley RM, Roche WR, Holgate ST : Cellular events in the bronchi in mild asthma after bronchial provocation. Am Rev Respir Dis 139: 86-817, 1989. 1. Kelly CA, Ward C, Stenton CS, Bird G,

Airway inflammation in asthma 29 Hendrick DJ, Walters EH : Numbers and activity of inflammatory cell III bronchoalveolar lavage in asthma, and their relationship to airway responsiveness. Thorax 43 : 684-692, 1988. 11. Wardlaw AJ, Kay AB : The role of the eosinophil in the pathogenesis of asthma. Allergy 42 : 321-335, 1987. 12. Kirby JG, Hargreave FE, Gleich GJ, O'Byrne DM : Bronchoalveolar cell profiles of asthmatic and nonasthmatic subjects. Am Rev Respir Dis 136 : 379-383, 1987. 13. American Thoracic Society : Chronic bronchitis, asthma, and pulmonary emphysema. Am Rev Respir Dis 85 : 762-768, 1962. 14. Tanizaki Y, Sudo M, Kitani H, Kawauchi K, Mifune T, Takeyama H, Kohi F, Tada S, Takahashi K, Kimura I : Characteristics of cell components III bronchoalveolar lavage fluid (BALF) in patients with bronchial asthma classified by clinical symptoms. Jpn J Allergol 39 : 75-81, 199. 15. Tanizaki Y, Kitani H, Okazaki M, Mifune T, Mitsunobu F, Ochi K, Harada H : Cellular composition of fluid in the airways of patients with house dust sensitive asthma, classified by clinical symptoms. Jpn J Med 31 : 333-338, 16. demonchy SGR, Kauffman HF, Venge F, Koefer GH, Sluiter HJ, Jansen HM, devries E : Bronchoalveolar eosinophilia during allergen-induced late asthmatic reaction. Am Rev Respir Dis 131 : 373-376, 1985. 17. Kelly CA, Stenton SC, Ward C, Bird G, Hendrick DJ, Walters EH : Lymphocyte subsets in bronchoalveolar lavage fluid from stable asthmatics, and their correlations with bronchial responsiveness. Clin Exp Allergy 19 : 169-175, 1989. 18. Walker C, Kaegi MK, Braun P, Blaser K : Activated T cells and eosinophilia in bronchoalveolar lavages from subjects with asthma correlated with disease severity.j Allergy Clin Immunol 88 : 935-942, 1991.