- Open Access
TNFα-blockade stabilizes local airway hyperresponsiveness during TLR-induced exacerbations in murine model of asthma
© Starkhammar et al. 2016
- Received: 5 March 2015
- Accepted: 9 October 2015
- Published: 22 October 2015
Viral infections are a common cause of asthma exacerbation. These maladies are sometimes complicated by bacterial infections. Toll-like receptors (TLRs) are in the forefront of our microbial defence, with TLR3 responding to viral and TLR4 to bacterial stimulation. The present study was designed to evaluate the effect of concomitant TLR3 and TLR4 stimulation in a murine model of allergic asthma.
BALB/c mice were stimulated intranasally with a combination of poly(I:C) and LPS activating TLR3 and TLR4, respectively. This resulted in the development of airway hyperresponsiveness (AHR) in the proximal part of the lung, along with signs of neutrophilic inflammation. Analysis of the bronchioalveolar lavage fluid (BALF) revealed a marked increase in TNFα. In contrast, the allergic airway inflammation induced by ovalbumin administration to sensitized mice caused AHR in the whole lung along with an increase in eosinophils and lymphocytes in the BALF and lung.
When poly(I:C) + LPS were given to mice with an ongoing allergic airway inflammation induced by ovalbumin, the AHR was further increased in the peripheral lung and neutrophils appeared together with eosinophils and lymphocytes in the BALF and lung. Treatment with the TNFα-blocking antibody infliximab blunted the AHR increase, without affecting the cells influx in BALF.
To conclude; a combined TLR3- and TLR4-stimulation, representing a concomitant viral and bacterial infection, causes an AHR that is further exaggerated during an ongoing allergic inflammation. The airway stabilizing effect of infliximab indicates the possible future use of TNFα blockade in treatment of microbial induced exacerbations of allergic asthma.
- Airway mechanics
- Innate immunity
- Viral infection
- Bacterial infection
Viral infections, such as respiratory syncytial virus (RSV) and human rhinovirus (HRV) are believed to be the primary cause of asthmatic exacerbations in adults [1, 2]. Haemophilius influenzae and Moraxella cattarhalis are bacteria known to play an opportunistic role following respiratory viral infections, with their own ability to trigger exacerbations . Moreover, especially Haemophilius influenza is frequently found together with RSV and HRV . Thus, combined bacterial and viral infestations are not an uncommon problem in asthma.
Pattern recognition receptors (PRRs) is an umbrella term for several receptor families all with their specific ability to recognizing various microbes, initiating an innate host defence reaction [5, 6]. The Toll-like receptors (TLRs) are the most well characterized PRR family comprised of 10 members (13 in mice) . TLR3 are known to identify viruses like RSV and HRV, whereas TLR4 recognizes bacteria like Haemophilius influenza. During experimental conditions poly(I:C) and LPS, ligands for TLR3 and TLR4, can be used to mimic the innate immune effects of viruses (i.e. RSV/HRV) and bacteria (i.e. Haemophilius influenza), respectively.
As a consequence of respiratory infections patients with allergic asthma generally suffer from prolonged and more severe symptoms than patients without established allergy [7, 8]. The mechanistic interplay between on-going allergy inflammation, microbial infections and TLR activation is complex and still poorly understood. Airway hyperresponsiveness (AHR) is closely related to the asthmatic exacerbation [2, 9]. In the present study AHR was evaluated in ovalbumin (OVA) mouse model of allergic asthma. The effect of a combined TLR3 and TLR4 activation was studied by adding poly(I:C) and LPS together once daily during four consecutive day, just after the mice had completed their sensitization protocol. The purpose was to mimic the situation when asthmatic subjects with an allergic airway inflammation are exposed to a concomitant viral and bacterial infection for a time period representing occasional infection. In addition to changes in AHR, alterations in the local respiratory tract cell and mediator composition were assessed in bronchioalveolar lavage fluid (BALF). Special attention was given to the role of TNFα which has been implicated in many aspects of airway pathology in asthma . In the present study infliximab, a well-established TNFα antibody was used to investigate the involvement of TNFα in AHR.
Female BALB/c mice (approximately 20 g, 8–12 weeks old) were obtained from Charles River (Sulzfeld, Germany). The mice were housed in plastic cages with adsorbent bedding material in a conventional animal house with 12-hours dark/light cycles. Water and pelleted food were provided ad libitum. All animal procedures were approved by the regional committee of animal experimentation ethics (Stockholm norra djurförsöksetiska nämnd).
The mice were anaesthetised (pentobarbital sodium, 90 mg/kg bw given i.p.), put on a heating pad (body temperature, 37 °C), tracheotomised (18-gauge cannula) and connected to the flexivent animal ventilator (Scireq, Montreal, Canada). After ventilation was started, the mice were monitored as described earlier . After a five minutes resting period, methacholine (MCh; Sigma-Aldrich) was injected through the tail vein in increasing doses (0.01, 0.03, 0.1, 0.3, 1, 3 and 10 mg/kg · body weight), in order to induce AHR.
For the first experiments, lung resistance and compliance were measured by assuming a single-compartment linear model and multiple linear regressions at a sinusoidal frequency of 2.5 Hz every eighth breath for 3 min after each injection. For the second experiment, lung mechanics were measured using a forced oscillation technique . The parameters obtained were the Newtonian resistance (R N ), a close approximation of resistance in the conducting airways; tissue resistance (G), which reflects energy dissipation in the lung tissue consisting of airway closure and heterogeneity of airway distribution; and tissue elastance (H), which characterises tissue stiffness and reflects the energy storage within the tissue.
Directly after lung function measurements BALF was collected (1 mL ice cold PBS containing 0.6 mM ethylendiaminetetraacetic acid (EDTA) was lavaged three times in the lung). The fluid was centrifuged at +4 °C, 1200 rpm, for 10 min and the supernatant was stored at −80 °C until use. Lysis buffer (150 mM NH4Cl, 10 mM KHCO3, 0.1 mM EDTA, pH 7.2), was used for 2 min, to lyse the red blood cells, followed by washing in PBS. Total cell number was counted and expressed as cells/ml BALF. Differential cell counts were performed on May-Grünwald/Giemsa stained cytospins, counting a minimum of 300 cells, in a blinded manner.
Measurement of cytokines
Cytokines in BALF were measured using the Cytokine Mouse 20-Plex Panel together with RANTES Mouse Singleplex Bead Kit (Invitrogen Corp., Carlsbad, CA, USA) that were run in a Luminex200 system. The simultaneous immunoassay was carried out according to manufacturer’s instructions.
Lungs were removed and immersed with 4 % buffered formaldehyde. They were then embedded in paraffin, sectioned and stained in haematoxylin and eosin. Histological findings with a focus on inflammatory cells, such as peribronchial/perivascular and parenchymal cell infiltration, were semi-quantitatively graded in a blinded manned as 0 to 4 (zero to abundant cell infiltration) and summed together. The cells were identified according to their morphology in 1000x magnification.
Data were analysed using Graph Pad Prism®, version 5.01, software (GraphPad Software Inc., San Diego, CA, U.S.A.). Results are presented as mean ± standard error of mean (SEM) and n equals’ number of subjects. For comparison of airway reactivity, two-way analysis of variance (ANOVA) was followed by Bonferroni’s Multiple Comparison Test. BALF cell data and lung histology data were analysed with Kruskal-Wallis analysis of variance, followed by Dunn’s test for between group comparisons. A p value of less than 0.05 was considered significant.
Intranasal administration of poly(I:C) + LPS for four consecutive days induces airway hyperresponsiveness with concomitant influx of inflammatory cells and release of a number of inflammatory mediators
TNFα blockade inhibits the poly(I:C) + LPS induced exaggerated airway hyperresponsiveness
TNFα, one of the mediators that was increased after the treatment with poly(I:C) + LPS, was not increased in a previous study when exposing the mice separately to the two TLR agonists with a similar protocol . Thus, to investigate the role for TNFα, further experiments were performed using treatment with infliximab, an antibody against TNFα, administered i.p. one hour before the TLR-agonists were given. With this intervention, the role of TNFα was investigated both in non-allergic conditions and on an established allergic airway inflammation. In order to delineate the localization of the effect both of TLR stimulation and the TNFα action, forced oscillation techniques were used measuring the airway responses both in the conducting airways (R N ) and in the peripheral parts, defined as tissue damping (G) and tissue elastance (H).
As predicted, ovalbumin sensitization and challenge caused an AHR in both the proximal (Fig. 3d) and distal parts of the lung (Fig. 3e-f) . When poly(I:C) + LPS was administered after an allergic airway inflammation was established, the treatment did not cause a further increase in AHR in R N . In contrast, the TLR treatment caused a marked increase in AHR in both the distal parameters G and H. This increased effect of the TLRs on G and H on the established allergic airway inflammation was markedly inhibited by infliximab whereas the infliximab treatment did not affect the R N .
TNFα blockade does not inhibit the poly(I:C) + LPS induced exaggerated cellular influx in bronchoalveolar lavage fluid
TNFα blockade does not affect the poly(I:C) + LPS induced increase in inflammatory cell infiltration in lung tissue
The present study showed that intranasal installation of poly(I:C) together with LPS for four days in mice triggered an AHR and airway inflammation with increased influx of macrophages, neutrophils and lymphocytes, and enhanced release of several pro-inflammatory cytokines including TNFα in BALF. These TLR-induced effects were not affected by treatment with the anti-TNF antibody infliximab. In mice with established allergic airway inflammation, characterized by an AHR and an eosinophilic influx in BALF, the administration of poly(I:C) + LPS caused a further increase of AHR in the peripheral lung; tissue damping and tissue elastance. This TLR agonist-induced increase of AHR was blocked by infliximab, but it did not inhibit the additional influx of macrophages, neutrophils and lymphocytes in BALF. Thus, the present study indicates that TNFα causes an AHR in the peripheral lung in allergic inflammatory airways which not is linked to cellular influx in BALF.
Four days intranasal administration of poly(I:C) together with LPS, mimicking an effect of a combined viral and bacterial stimulation during a time period representing occasional infection, caused a marked AHR in mice. In our earlier studies, where these two TLR agonists were given separately in a similar regimen, both of them induced AHR [11, 13]. However, the mean maximal effect on the lung resistance (R L ) was clearly higher for the combination of poly(I:C) together with LPS in this study (4.9 cmH2O.s/ml) compared to the effect when either of the TLR agonist were given alone which did not exceed 3.5 cmH2O.s/ml. Isolated mouse airways, which express both TLR3 and TLR4 in the smooth muscle layer, become hyperreactive when exposed to either poly(I:C) or LPS . In the same study it was shown that when the two TLR agonists were given together this caused a synergistic increase of the hyperreactivity . Thus, it is possible that the combined effect of intranasal challenge with poly(I:C) or LPS cause is due to a direct action of TLR3 and TLR4 on airway smooth muscle layer which causes AHR.
The combined treatment with poly(I:C) and LPS also caused an inflammation shown both by the influx of cells in BALF and lung tissue as well as by the recorded release of inflammatory mediators in the airways. Macrophages, neutrophils and lymphocytes were found to be increased in BALF. As it has previously been shown that poly(I:C) induces lymphocytes and LPS induces neutrophils [11, 13], the increase of both neutrophils and lymphocytes in BALF in the present study suggests additive effects for the TLR agonists. The infiltration in lung was also dominated by neutrophils and lymphocytes. As an additional marked increase in macrophages was found in BALF, this indicates that the response is more than simply summation of effects. When analyzing the release of inflammatory mediators, the same pattern as for the cells appears. Hence, those mediators that were previously found to be increased by poly(I:C) (IL-5, IL-12, CCL2 and CXCL1) and by LPS (CXCL9 and VEGF) [11, 13] were also, with the exception of CXCL1, increased by the combined TLR agonist treatment. In addition, the levels of IL-1α, IL-17, TNFα, CCL3 and CCL5 were only increased when poly(I:C) and LPS were given together. This synergistic effect of poly(I:C) + LPS in causing TNFα secretion has previously been shown in macrophages and osteoclast precursors [15, 16]. As TNFα release is a supposed to be an early event and it can stimulate the induction of various inflammatory genes , it is possible that several of the other mediators are induced due to the effect of TNFα. Thus, it appears that the TLR agonists both induce an effect by themselves and their combined activation causes an interaction that generates further effects.
Although clinical studies using antibodies against TNFα to treat asthma has shown variable , the initial clinical studies using TNFα-antibodies showed improved effect specifically on AHR [10, 19]. Interestingly, a subgroup of severe asthmatic patients also suffering from rhinosinuitis responded very well to anti-TNFα treatment . To evaluate the importance of the TLR-induced effect by TNFα on the development of AHR in this study, the mice were treated with the TNFα antibody infliximab during the four days of intranasal administration of poly(I:C) + LPS. In these experiments a forced oscillation technique was used to localize which parts of the airway were affected. As in the first experiment, the combination of the TLR agonists induced AHR. However this was found to be localized in the conducting airways (R N ) and not in the peripheral tissue damping (G) and tissue elastance (H). Previous experiments also investigating the pulmonary resistance using a forced oscillation technique showed the same pattern for the TLR9-agonist CpG oligodeoxy-nucleotide 2006 which only caused an increase of R N with no effect on G and H . As the conductive airways is the part of the lung that contain smooth muscle cells it further strengthen the suggestion above that the TLR-agonists given in non-allergic healthy conditions cause a hypercontractile smooth muscle a poly(I:C) + LPS [14, 22] which is responsible for the AHR. However, the effects by the dual TLR stimulation on R N , the cellular influx in BALF and infiltration of cells in the lung were not affected by infliximab indicating that TNFα has only a minor effect on smooth muscle and cellular trafficking in this model.
The sensitization and challenge of OVA also induced an AHR which at R N was similar to that induced by the administration of poly(I:C) + LPS but it caused a higher AHR in both the peripheral parameters. This level of AHR was observed five days after the last OVA challenge, indicating a persistent allergic airway inflammation as described previously [13, 21]. When poly(I:C) + LPS were given for four days on an established allergic inflammation, the AHR was further increased as measured by both the peripheral parameters G and H but the TLR-agonists did not affect the conducting airways (R N ). An increase in lung resistance has been shown in response to both poly(I:C) and LPS when they were given separately on a similar allergic airway inflammation . However comparison of the level of response is not possible as the effect in different compartments of the lung was not determined in that study. It has been shown that when G and H increase in a similar manner it depends on airway closure  which is a major component of hyperresponsiveness in allergically inflamed airways . One important factor for airway closure is the production of surfactant which has shown to be decreased by both viral  and TLR4 activation . Thus, the increase of the combined response to TLR3 and TLR4 suggests that there may be a specific effect of combined viral and bacterial infection on peripheral dysfunction of the lung during allergic conditions. Considering that there is a substantial amount of evidence that inflammation of the small airways contributes to the clinical expression of asthma , the markedly difference of AHR caused by TLR activation during allergic (peripheral) and non-allergic (central) may be one reason for the severity for asthmatic subjects during infections.
When infliximab was given on the established allergic inflammation one hour before the TLR-agonist administration the increased peripheral AHR was markedly reduced, without any effect on the influx of cells in the BALF or the infiltration of cells in lung. These results indicate that TNFα has a specific effect on the peripheral AHR, which has been suggested to be dependent on heterogeneous airway closure due to protein interference with surfactant . Through the separation of the lung mechanics it could be shown that the response on R N of TLR-stimulation on non-provoked airways differed from the responses when the TLR-agonists were given on an established allergic airway inflammation. The reason may be that the latter condition induces a resistance close to the maximal capacity of this parameter. On the other hand, that the TLR-agonist-induced increase of AHR in the peripheral parameters was caused by TNFα may be of specific importance since airway closure is linked to excessive bronchoconstriction , recurrent exacerbations  and asthma severity . It is possible that several other inflammatory mediators also are reduced secondary to the reduction of TNFα. The interpretation is further complicated by the effects TNFα by itself has on the airways . It is also important to keep in mind that secondary stimulus like IL-1β  can be directly linked to TNFα.
To summarize, a combined TLR3- and TLR4-stimulation, representing a concomitant viral and bacterial infection, caused an AHR that was further exaggerated during an on-going allergic inflammation. It is likely that there is a synergistic interplay between the two innate receptor subtypes that contributes to the worsening of the situation for the mice as reflected in an increased AHR and elevated levels of a multitude of BALF mediators. It is interesting to notice that the TLR-induced increase of AHR in our model was dampened when the mice were treated with infliximab suggesting a pivot role for TNFα in microbial induced exacerbation of allergic asthma. The outcome of previous attempts to use various TNFα blocking agents in asthma has been meagre . Most of these drug evolutions have been dealing with asthma from a more general perspective, and it could be that the role of TNFα is of specific importance only during the circumstances reflected in the present set up. It should be stated that the experimental set-up in this study was performed to define the action of TNF during infection and not to investigate the effect as add-on therapy for asthmatic subjects exposed to infections. Hence, further studies needs to outline whether it might be a future for specific anti-TNFα trials focusing on exacerbations of allergic asthma.
We would like to acknowledge the support from the Swedish Medical Research Council, the Swedish Heart-Lung foundation, Konsul Th C Berghs research foundation, the Stockholm County Council Research Funds (ALF), Karolinska Institutet, the ChAMP project, COST BM1201, the Swedish Society of Medicine and the Centre for Allergy Research at Karolinska Institutet.
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- Kurai D, Saraya T, Ishii H, Takizawa H. Virus-induced exacerbations in asthma and COPD. Front Microbiol. 2013;4:293.View ArticlePubMedPubMed CentralGoogle Scholar
- Busse WW, Lemanske Jr RF, Gern JE. Role of viral respiratory infections in asthma and asthma exacerbations. Lancet. 2010;376:826–34.View ArticlePubMedPubMed CentralGoogle Scholar
- Kraft M. The role of bacterial infections in asthma. Clin Chest Med. 2000;21:301–13.View ArticlePubMedGoogle Scholar
- van den Bergh MR, Biesbroek G, Rossen JW, de Steenhuijsen Piters WA, Bosch AA, van Gils EJ, et al. Associations between pathogens in the upper respiratory tract of young children: interplay between viruses and bacteria. PLoS One. 2012;7:e47711.View ArticlePubMedPubMed CentralGoogle Scholar
- Kumar H, Kawai T, Akira S. Pathogen recognition by the innate immune system. Int Rev Immunol. 2011;30:16–34.View ArticlePubMedGoogle Scholar
- Gon Y. Toll-like receptors and airway inflammation. Allergol Int. 2008;57:33–7.View ArticlePubMedGoogle Scholar
- Corne JM, Marshall C, Smith S, Schreiber J, Sanderson G, Holgate ST, et al. Frequency, severity, and duration of rhinovirus infections in asthmatic and non-asthmatic individuals: a longitudinal cohort study. Lancet. 2002;359:831–4.View ArticlePubMedGoogle Scholar
- Olenec JP, Kim WK, Lee WM, Vang F, Pappas TE, Salazar LE, et al. Weekly monitoring of children with asthma for infections and illness during common cold seasons. J Allergy Clin Immunol. 2010;125:1001–1006 e1001.View ArticlePubMedPubMed CentralGoogle Scholar
- Micillo E, Bianco A, D’Auria D, Mazzarella G, Abbate GF. Respiratory infections and asthma. Allergy. 2000;55 Suppl 61:42–5.View ArticlePubMedGoogle Scholar
- Berry MA, Hargadon B, Shelley M, Parker D, Shaw DE, Green RH, et al. Evidence of a role of tumor necrosis factor alpha in refractory asthma. N Engl J Med. 2006;354:697–708.View ArticlePubMedGoogle Scholar
- Starkhammar M, Kumlien Georen S, Swedin L, Dahlen SE, Adner M, Cardell LO. Intranasal administration of poly(I:C) and LPS in BALB/c mice induces airway hyperresponsiveness and inflammation via different pathways. PLoS One. 2012;7:e32110.View ArticlePubMedPubMed CentralGoogle Scholar
- Swedin L, Ellis R, Kemi C, Ryrfeldt A, Inman M, Dahlen SE, et al. Comparison of aerosol and intranasal challenge in a mouse model of allergic airway inflammation and hyperresponsiveness. Int Arch Allergy Immunol. 2010;153:249–58.View ArticlePubMedGoogle Scholar
- Starkhammar M, Larsson O, Kumlien Georen S, Leino M, Dahlen SE, Adner M, et al. Toll-like receptor ligands LPS and poly (I:C) exacerbate airway hyperresponsiveness in a model of airway allergy in mice, independently of inflammation. PLoS One. 2014;9:e104114.View ArticlePubMedPubMed CentralGoogle Scholar
- Bachar O, Adner M, Uddman R, Cardell LO. Toll-like receptor stimulation induces airway hyper-responsiveness to bradykinin, an effect mediated by JNK and NF-kappa B signaling pathways. Eur J Immunol. 2004;34:1196–207.View ArticlePubMedGoogle Scholar
- Bagchi A, Herrup EA, Warren HS, Trigilio J, Shin HS, Valentine C, et al. MyD88-dependent and MyD88-independent pathways in synergy, priming, and tolerance between TLR agonists. J Immunol. 2007;178:1164–71.View ArticlePubMedGoogle Scholar
- Krisher T, Bar-Shavit Z. Regulation of osteoclastogenesis by integrated signals from toll-like receptors. J Cell Biochem. 2014;115:2146–54.View ArticlePubMedGoogle Scholar
- Chen G, Goeddel DV. TNF-R1 signaling: a beautiful pathway. Science. 2002;296:1634–5.View ArticlePubMedGoogle Scholar
- Matera MG, Calzetta L, Cazzola M. TNF-alpha inhibitors in asthma and COPD: we must not throw the baby out with the bath water. Pulm Pharmacol Ther. 2010;23:121–8.View ArticlePubMedGoogle Scholar
- Howarth PH, Babu KS, Arshad HS, Lau L, Buckley M, McConnell W, et al. Tumour necrosis factor (TNFalpha) as a novel therapeutic target in symptomatic corticosteroid dependent asthma. Thorax. 2005;60:1012–8.View ArticlePubMedPubMed CentralGoogle Scholar
- Wenzel SE, Barnes PJ, Bleecker ER, Bousquet J, Busse W, Dahlén SE, et al. T03 Asthma Investigators. Am J Respir Crit Care Med. 2009;179:549–58.View ArticlePubMedGoogle Scholar
- Adner M, Starkhammar M, Georen SK, Dahlen SE, Cardell LO. Toll-like receptor (TLR) 7 decreases and TLR9 increases the airway responses in mice with established allergic inflammation. Eur J Pharmacol. 2013;718:544–51.View ArticlePubMedGoogle Scholar
- Safholm J, Lovdahl C, Swedin L, Boels PJ, Dahlen SE, Arner A, et al. Inflammation-induced airway smooth muscle responsiveness is strain dependent in mice. Pulm Pharmacol Ther. 2011;24(4):361–6.View ArticlePubMedGoogle Scholar
- Backus-Hazzard GS, Howden R, Kleeberger SR. Genetic susceptibility to ozone-induced lung inflammation in animal models of asthma. Curr Opin Allergy Clin Immunol. 2004;4:349–53.View ArticlePubMedGoogle Scholar
- Lundblad LK, Thompson-Figueroa J, Allen GB, Rinaldi L, Norton RJ, Irvin CG, et al. Airway hyperresponsiveness in allergically inflamed mice: the role of airway closure. Am J Respir Crit Care Med. 2007;175:768–74.View ArticlePubMedPubMed CentralGoogle Scholar
- Krishnan S, Halonen M, Welliver RC. Innate immune responses in respiratory syncytial virus infections. Viral Immunol. 2004;17:220–33.View ArticlePubMedGoogle Scholar
- Glasser SW, Maxfield MD, Ruetschilling TL, Akinbi HT, Baatz JE, Kitzmiller JA, et al. Persistence of LPS-induced lung inflammation in surfactant protein-C-deficient mice. Am J Respir Cell Mol Biol. 2013;49:845–54.View ArticlePubMedPubMed CentralGoogle Scholar
- van den Berge M, ten Hacken NH, Cohen J, Douma WR, Postma DS. Small airway disease in asthma and COPD: clinical implications. Chest. 2011;139:412–23.View ArticlePubMedGoogle Scholar
- Kaminsky DA. Peripheral lung mechanics in asthma: exploring the outer limits. Pulm Pharmacol Ther. 2011;24:199–202.View ArticlePubMedGoogle Scholar
- Gibbons WJ, Sharma A, Lougheed D, Macklem PT. Detection of excessive bronchoconstriction in asthma. Am J Respir Crit Care Med. 1996;153:582–9.View ArticlePubMedGoogle Scholar
- in’t Veen JC, Beekman AJ, Bel EH, Sterk PJ. Recurrent exacerbations in severe asthma are associated with enhanced airway closure during stable episodes. Am J Respir Crit Care Med. 2000;161:1902–6.View ArticleGoogle Scholar
- Sorkness RL, Bleecker ER, Busse WW, Calhoun WJ, Castro M, Chung KF, et al. Lung function in adults with stable but severe asthma: air trapping and incomplete reversal of obstruction with bronchodilation. J Appl Physiol (1985). 2008;104:394–403.View ArticleGoogle Scholar
- Bachar O, Adner M, Cardell LO. Toll-like receptor activation in airway smooth muscle: dual actions via separate MAPK pathways. Am J Physiol. 2006;291:L322–3.Google Scholar
- Zhang Y, Adner M, Cardell LO. IL-1beta-induced transcriptional up-regulation of bradykinin B1 and B2 receptors in murine airways. Am J Respir Cell Mol Biol. 2007;36:697–705.View ArticlePubMedGoogle Scholar