- Open Access
Effects of overexpression of IL-10, IL-12, TGF-β and IL-4 on allergen induced change in bronchial responsiveness
© Fu et al. 2006
- Received: 22 November 2005
- Accepted: 08 May 2006
- Published: 08 May 2006
An increasing prevalence of allergic diseases, such as atopic dermatitis, allergic rhinitis and bronchial asthma, has been noted worldwide. Allergic asthma strongly correlates with airway inflammation caused by the unregulated production of cytokines secreted by allergen-specific type-2 T helper (Th2) cells. This study aims to explore the therapeutic effect of the airway gene transfer of IL-12, IL-10 and TGF-β on airway inflammation in a mouse model of allergic asthma.
BALB/c mice were sensitized to ovalbumin (OVA) by intraperitoneal injections with OVA and challenged by nebulized OVA. Different cytokine gene plasmids or non-coding vector plasmids were instilled daily into the trachea up to one day before the inhalatory OVA challenge phase.
Intratracheal administration of IL-10, IL-12 or TGF-β can efficiently inhibit antigen-induced airway hyper-responsiveness and is able to largely significantly lower the number of eosinophils and neutrophils in bronchoalveolar lavage fluid of ovalbumin (OVA) sensitized and challenged mice during the effector phase. Furthermore, the effect of IL-10 plasmids is more remarkable than any other cytokine gene plasmid. On the other hand, local administration of IL-4 gene plasmids before antigen challenge can induce severe airway hyper-responsiveness (AHR) and airway eosinophilia.
Our data demonstrated that anti- inflammatory cytokines, particularly IL-10, have the therapeutic potential for the alleviation of airway inflammation in murine model of asthma.
- Airway Inflammation
- Gene Plasmid
- Airway Eosinophilic Inflammation
Asthma is an immunological disease that has increased dramatically in prevalence over the past two decades. It is characterized by airway hyper-reactivity to a variety of specific and non-specific stimuli, severe chronic airway inflammation with pulmonary eosinophils, mucus hypersecretion, and increased serum IgE levels. Activation of Th2 cells in the respiratory tract is now believed to be responsible, in part, for the pathogenesis of this disease. Th2 cells secreting IL-4, IL-5, and IL-13 have been identified in the airways of asthmatics . Th2 cytokines produced in the respiratory tract, airway eosinophilia, high levels of serum IgE, and mast cell activation [2, 3], are all believed to contribute to the pathological consequences inducing airway hyper-responsiveness (AHR), epithelial damage, and mucus hypersecretion.
Whereas the immunological mechanisms that induce asthma and allergies are relatively well characterized, the specific mechanisms that transpire in vivo to downmodulate Th2 cell-mediated allergic inflammatory responses are not yet clear. The Th1-relatived cytokines, such as IL-12 and IFN-γ, are the candidate cytokines for the treatment of allergic diseases as they downregulate Th2 responses . There is strong evidence regarding the therapeutic effect of Th1 cytokine administration. Using Th1-related cytokine proteins [5–7] and constructed plasmids expressing cytokine genes [8–10], airway inflammation could be decreased. According to our previous study , we also demonstrated that the local transfer of the IL-12 gene to the respiratory tract could modify allergic inflammation and airway hyper-responsiveness (AHR). However, recent studies have shown that not only Th1-related cytokines, but also other anti-inflammatory cytokines, including TGF-β and IL-10, can downregulate Th2 responses and might also play an important role in regulating pulmonary inflammation and asthma [12, 13]. IL-10 and TGF-β, which are pleiotropic cytokines with significant anti-inflammatory and immunosuppressive properties, are key regulators in the maintenance of immunological homeostasis. In humans, relative underproduction of IL-10 by alveolar macrophages and in the sputum of patients with asthma has been reported [14, 15], which suggests an essential role IL-10 in regulating airway inflammation. In addition, TGF-β inhibits the production of proinflammatory cytokines from macrophages, B cells, and T cells and is a potent inhibitor of T cell-mediated immune responses, both in vitro [16, 17] and in vivo [18, 19]. Moreover, TGF-β has been postulated in the mechanism of oral tolerance, which is mediated by regulatory T cells that produce TGF-β preferentially induced at mucosal sites, possibly under the influence of IL-10 and/or IL-4 . Recently, Hansen et al. showed that not only TGF-β-producing T cells  but also IL-10-producing T cells  could abolish AHR and airway inflammation in a murine model of asthma. Thus, not only Th1-related cytokine but also anti-inflammatory cytokines can regulate airway inflammation. However, the different effects between these cytokines on alleviating airway inflammation still need further investigation. The purpose of the current study was to compare the effect of four different cytokine genes plasmid including IL-12, IL-10, and TGF-β on the effector phase of allergen-induced AHR and airway eosinophilic inflammation.
It is reported that eosinophils are so important in the asthma, because the toxic products in its granules were proven to directly damage lung tissue . Amongst eosinophil-active chemoattractants, eotaxin has also been demonstrated to selectively induce eosinophil recruitment to the airway undergoing allergic reaction [24, 25]. In addition, both leukotriene B4 (LTB4) and prostaglandin E2 (PGE2) are potent pro- inflammatory mediators and are involved in several inflammatory diseases . In this current study, we have compared the levels of eotaxin, LTB4 and PGE2 in the BALF to investigate the role of cytokine gene in regulating the production of these inflammatory mediators and try to address possible mechanisms for the effect of different cytokine genes.
Female BALB/c mice were obtained from and maintained at the Animal Center of the College of Medicine of National Taiwan University. Animals were used between 6 and 10 weeks of age and were age-matched within each experiment. The animal study protocol was approved by the committee of College of Medicine, National Taiwan University.
Plasmids and preparation of lipid-plasmid DNA complexes
For the construction of plasmid DNA encoding murine IL-10 or TGF-β, the cDNA for murine IL-10, or TGF-β was cloned by reverse transcription- polymerase chain reaction (RT-PCR) from normal mouse spleen cells, using primers based on the published cytokine sequence. The cDNA was sequenced and in vitro expression was confirmed by enzyme-linked immunosorbent assay (ELISA) and bioassay (data not shown). The cytokine gene expression vector utilized the human cytomegalovirus (CMV) immediate-early promoter and the simian virus 40 (SV40) polyadenylation sequence. The vector without a gene insert (empty vector) served as a control for in vivo gene delivery studies.
The construction of pscIL-12 vectors has been described previously . Briefly, a linker of 54-bp in length in the pscIL-12 plasmids connected the p40 and p35 subunits of the murine IL-12 gene. The p40 and p35 subunits were obtained by polymerase chain reaction (PCR) from the BLpSV35 and BLpSV40 plasmids. Recombinant PCR, using the p40 and P35 PCR products as the DNA templates and the Sal I-containing and the Bam HI-containing primers as such primers, generated the single- chain IL-12 genes. The resulting recombinant PCR fragments were cloned at the Sal I and Bam HI sites of the pCMV vector. Plasmid DNA was subsequently introduced into the Escherichia coli DH5α by transformation. The plasmids were purified using EndoFree plasmid kits (QIAGEN, Valencia, CA) and suitable for gene therapy.
For intra-tracheal delivery, lipid-DNA complexes were prepared by combining 15 μl lipofectAMINE (Life Technologies, Gaithersburg, MD), per 10 μg of plasmid DNA at a final volume of 15 μl in PBS. The expression of cytokine plasmid in pulmonary tissues was determined by the cytokine ELISA of BALF collected 48 hr post- injection [data not shown, ].
Administration of DNA-lipid complexes
Intra-tracheal administration was accomplished by the use of a No. 23 steel gavage tube and a 1.0-ml syringe. Animals were anesthetized (pentobarbital sodium salt, Tokyo Chemical Industry, Tokyo, Japan, 10 mg/ml solution, 0.005 ml/g body weight) prior to intra-tracheal injection and placed in dorsal recumbence on an inclined board. The gavage tube was directed into the proximal trachea, and then the lipid-DNA solution was slowly injected. Proper positioning of the tube was assured by visualization of movement of the fluid meniscus and by palpation of the gavage tube moving across the tracheal rings. A volume of 30 μl lipid-DNA mixture was injected intra-tracheally, such that each mouse received 10 μg of plasmid DNA. This technique works well without involving any surgical procedure and allows the aspirated material to spread over the whole lung.
Administration of cytokine plasmid into allergen-sensitized mice
In order to test varying doses of each a single dose of a cytokine gene, some mice received 2.5 μg IL-10 gene plasmid liposome complex (p-IL-10-low) or 20 μg IL-10 gene plasmid liposome complex (p-IL-10-hi). In the cytokine gene combination experiment, some mice received 10 μg IL-10 gene plasmid plus 10 μg single-chain IL-12 gene plasmid at a final volume of 30 μl DNA-liposome complex (pIL-10 + pscIL-12).
Measurement of airway hyper-responsivenes
Airway responsiveness was measured as a change in function after challenge with aerosolized mechacholine (Mch) in conscious, spontaneously breathing animals by barometric plethysmography (Buxco, Troy, NY) as described in the literature . Pressure differences were measured between the main chamber of the plethysmograph, containing the animal and a reference chamber (box pressure signal). Mice were challenged with aerosolized saline (for the baseline measurement) or Mch (6.25 to 50 mg/ml) for three minutes and readings were taken and averaged for three minutes after nebulization. The Penh value for each minute was recorded and after the third recorded value, the average Penh value was divided by the Penh of normal saline and was presented as a relative percentage increase of Penh.
Analysis of bronchoalveolar lavage (BAL) fluid and lung histology
At 48 hours after the last aerosol exposure, all groups of mice were bled from the retro-orbital venous plexus and terminated. The lungs were immediately lavaged via the tracheal cannula with 3 × 1 ml of HBSS, free of ionized calcium and magnesium. The lavage fluid was centrifuged at 400 × g for 10 minutes at 4°C. After washing, the cells were resuspended in 1 ml HBSS, and total cells counts were determined by counting in a hemocytometer. Cyto- centrifuged preparations were stained with Liu's stain for different cell counts. A minimum of 200 cells were counted and classified as macrophages, lymphocytes, neutrophils, and eosinophils, based on standard morphological criteria.
After the lavage, the lungs were immediately removed and fixed in 10% neutral- buffered formalin, routinely processed, and embedded in paraffin wax. Five-micrometer sections were prepared and stained with hematoxylin and eosin (H&E).
Eotaxin level in bronchoalveolar lavage
The concentration of eotaxin was assayed with an ELISA kit (R&D Systems Inc., Minneapolis, MN) according to the manufacturer's instructions. Briefly, the bronchoalveolar lavage of each condition was added to wells precoated over- night at 4°C with anti-eotaxin antibody. After two hours of incubation, the plates were washed and biotin-conjugated antibody was added. After two more hours at room temperature, HRP-avidin was then added, and the OD (at 450 nm) values were converted to concentrations of chemokine in the BALF. The sensitivity of this assay was 1.9 pg/ml for eotaxin.
Measurement of cytokines
Quantifications of IL-10, IL-12, and TGF-β in the BAL fluids were evaluated using commercially available ELISA kits (Duoset, R & D, Minneapolis, MN, USA). Briefly, the BAL fluids were added to wells pre-coated over night at 4°C with anti-cytokine Ab. After 2 hours of incubation, the plates were washed and biotin-conjugated Ab was added. After two more hours at room temperature, HRP-avidin was added to each well. The substrate tetramethylbenzidine was then added and the OD (at 450 nm) values were converted to concentrations of cytokines in the BAL fluids. The sensitivity of this assay was 31.3 pg/ml for IL-10, IL-12 and TGF-β.
Quantification of PGE2 and LTB4
PGE2 or LTB4 levels in the BALF were determined using the PGE2 enzyme immunoassay kit or LTB4 enzyme immunoassay kit (Assay Designs, Inc., Ann Arbor, MI) according to the manufacturer's instructions. The detection limits for PGE2 and LTB4 are 39 and 47 pg/ml, respectively.
Data are expressed as the mean ± SEM for each group. The statistical significance of the differences between various treatment groups was assessed with the Mann-Whitney U test for non-parametric data.
The effect of different cytokine genes on methacholine-induced increase in AHR and airway eosinophilia
To further assay the cytokine levels in BAL fluids (BALFs) of mice received cytokine genes treatment. BALFs collected from control and cytokine gene-treated mice were analyzed with sandwich-ELISA. The results showed that the level of IL-12 (365.0 ± 111.9 pg/ml vs. 85.7 ± 16.1 pg/ml), IL-10 (453.6 ± 99.2 pg/ml vs. 66.4 ± 22.6 pg/ml) and TGF-β (1110.6 ± 47.2 pg/ml vs. 166.0 ± 25.5 pg/ml) increased in individual cytokine gene delivered mice compared to the control mice respectively.
Similar to our previous study , local administration of single- chain IL-12 gene plasmids exerted the therapeutic effect in OVA-induced asthma model as in the Der p 1-induced asthma model. Further, administration of TGF-β gene plasmids and IL-10 gene plasmids has also been found to inhibit the increase in airway responsiveness to methacholine after aerosol challenge in OVA-sensitized mice when compared with that of the mock vector-only group.
We also examined whether the level of OVA-specific serum antibodies were affected by the treatment of different cytokine gene plasmids (data not shown). Ovalbumin-sensitized mice had increased total serum IgE concentrations and produced OVA-specific IgE and IgG1 antibodies after airway challenge with OVA. However, only low levels of OVA-specific IgG2a were detected in serum. Intra-tracheal administration of mock vector DNA did not change OVA-specific antibody levels. The OVA-specific IgE concentrations were also increased, but the increase was not significant. Furthermore, administration of scIL-12, IL-10, or TGF-β plasmid DNA did not significantly change OVA-specific IgE, IgG1, or IgG2a levels in serum.
The effect of different cytokine gene plasmids on eotaxin and leukotriene B4 (LTB4) levels in BAL fluid
LTB4 and PGE2 are potent eicosanoid lipid mediators that are involved in numerous homeostatic biological functions and inflammation . The interaction between eicosanoid may represent means to regulate the release of inflammatory mediators, and may be important for the regulation of cell functions and inflammatory disorders, such as allergic asthma. Previous studies have reported that PGE2 could enhance the production of endogenous IL-10, which inhibits LTB4 production. In this study, the levels of LTB4 and PGE2 in the BAL fluid were also determined after administration of different cytokine gene plasmid. The level of LTB4 and PGE2 in BAL fluid did not show a significant difference among groups treated with different cytokine gene plasmids. However, LTB4 concentrations in the BAL fluid of the IL-10 gene-treated group was obviously lower than that of vector-only treated group (p = 0.085). This result was proven that IL-10 gene plasmid could decrease the production of LTB4 as previous study.
Dose-dependent effect of IL-10 gene plasmid in the suppression of AHR and airway eosinophilic inflammation in OVA-sensitized mice
Combination effect of IL-10 and IL-12 gene plasmid in the suppression of AHR and airway eosinophilic inflammation in OVA-sensitized mice
Allergic diseases are characterized by the presence of Th2 cells and related cytokines, such as interleukin-4 (IL-4), IL-5, IL-9, and IL-13 with the subsequent development of eosinophils infiltration and chronic inflammation. Although the immunologic mechanisms that induce asthma and allergic diseases are relatively well characterized, the specific mechanisms that transpire in vivo to down-modulate Th2-mediated allergic inflammatory responses are yet to be clarified. However, blocking the release or effects of pro-inflammatory cytokines in allergic asthma has provided the basis for the development of novel treatments . In this study, we employed a liposome-mediated genetic transfer approach to examine the therapeutic efficacy of the local pulmonary delivery of various cytokine gene plasmids in the same murine model of asthma in OVA-sensitized mice.
First, we demonstrated that intra-tracheal delivery with scIL-12 plasmid; TGF-β plasmid or IL-10 plasmid could suppress Ag-induced eosinophilic airway inflammation and airway hyper- responsiveness during Ag challenge, an effector phase of the immune response (Fig. 1 and 2). On the other hand, administration of IL-4 plasmid enhanced the severity of airway inflammation.
It is complex in the control of allergic inflammation and asthma, which are involving several different mechanisms and several different cell types and cytokines. Nevertheless, several studies have demonstrated that IL-12 protein can decrease allergen-specific IgE and eosinophils infiltration in a mouse model of airway inflammation [5, 6, 9, 31]. Previous studies have shown that intravenous injection of single chain IL-12 DNA plasmids mixed with liposome achieved the highest protein expression in the lungs and can alleviate airway hyper-responsiveness in an animal model of asthma . Furthermore, the local IL-12 gene transfer to the lung before the tracheal allergen challenge resulted in a remarked decrease in IL-5 levels and a similarly marked increase in IFN-γ, this being consistent with a shift from a Th2 to a Th1 profile . The results of our present study also support the finding that intra-tracheal delivery of IL-12 encoding DNA plasmids can decrease eosinophils infiltration in a murine model of airway inflammation.
Both TGF-β and IL-10 are pleiotropic cytokine with significant anti-inflammatory and immuno-modulatory properties. Thus, we investigated the suppressive effect of these two cytokines in modulating pulmonary inflammation and asthma. TGF-β is a key immunoregulatory factor in the development of unresponsiveness to antigens in the gastrointestinal tract. TGF-β inhibits the production of proinflammatory cytokines from macrophages, B cells, and T cells, and is a potent inhibitor of T cell-mediated immune responses both in vitro [17, 18] and in vivo [19, 20]. Administration of TGF-β diminishes the severity of autoimmune diseases, such as collagen-induced arthritis , allergic encephalomyelitis (EAE) , and experimental colitis , and neutralization of TGF-β adversely affects the course of the diseases. Hansen and his colleagues  have demonstrated that CD4+ T helper cells engineered to produce TGF-β1 in the respiratory mucosa can indeed reverse allergen-induced airway hyper-reactivity and inflammation. TGF-β- secreting T cells, called Th3 cells, have been shown to play a regulatory role at mucosal sites- e.g., in the induction of oral tolerance . In addition, TGF-β- secreting T cells might also play a significant role in modulating allergic inflammation . However, TGF-β is also a potent inducer of myofibroblasts and collagen synthesis. It has been reported that eosinophils might produce TGF-β to prevent allergen-induced AHR in late phase . In our study, the result has shown that administration of TGF-β plasmid in OVA-sensitized and challenged mice can decrease airway hyper-reactivity, eosinophilia and neutrophilia. In conclusion, TGF-β may plays a role in immuno-regulation, wound healing, and to shorten the inflammatory response when it is applied in the treatment of allergen-induced asthma.
IL-10 can down-regulate cytokine production not only from Th1 cells  but also from Th2 cells . Borish et al.  reported that asthmatics had a comparatively decreased ability to produce IL-10 by BALF cells and mononuclear cells. These associations led to the speculation that constitutive expression of IL-10 in the airway might contribute to maintain the normal state of allergen nonresponsiveness. However, the role of IL-10 in regulating Th2-mediated diseases such as asthma is controversial. Some reports have indicated that IL-10-deficient mice exhibit exaggerated eosinophilic airway inflammation provoked by a systemic sensitization to Ag and local inhalation of Ag [39, 40], whereas another report indicated that IL-10-deficient mice show diminished eosinophilic airway inflammation . Indeed, IL-10 is required for the development of AHR and administration of IL-10 enhanced AHR, though it reduces eosinophilia . The overall physiologic effect of IL-10 is to decrease inflammation. It accomplishes this role primarily by down-regulating synthesis of a number of cytokines, both Th1- and Th2-associated. The result of our study has shown that administration of IL-10 plasmids in OVA-sensitized and challenged mice can decrease airway hyper-reactivity, including eosinophilia and neutrophilia. These results support the concept that IL-10 plays a regulatory role in allergic asthma. As suggested by the effect of IL-10 on airway eosinophilia, IL-10 appears to play a role in regulating eosinophils recruitment. Our findings of a regulatory role for IL-10 in asthma are strongly consistent with the idea that IL-10 production mediates Ag-specific tolerance that protects against allergic diseases and airway inflammation. For example, regulatory T cells producing IL-10 are thought to develop after successful bee venom-specific immunotherapy  and during T-cell tolerance induced with respiratory exposure to antigen [44, 45].
Subsequently, we also compared the level of inflammatory mediators in BALF of OVA- sensitized mice among different cytokine gene plasmid treated groups. Amongst eosinophil-active chemoattractants, eotaxin has also been demonstrated to selectively induce eosinophil recruitment to the airway undergoing allergic reaction [46, 47]. Eotaxin is expressed in many different tissues, and may therefore regulate allergen-induced homing of eosinophils to the site of inflammation. In current study, we found that eotaxin levels in BAL fluid were significantly decreased by treatment with IL-10 or TGF-β encoding vector. It is possible that IL-10 and TGF-β can suppress OVA-induced airway eosinophils recruitment directly by down-regulating the production of eotaxin. Although, the eotaxin level in BALF was not so markedly reduced in the group of IL-12 gene plasmid treated mice (Fig. 5). However, it has been reported that IL-12 in regulating eosinophil function by increasing eosinophil apoptosis. On the other hand, we should consider whether the dose of IL-12 gene plasmid affects the efficiency of IL-12 gene plasmid in the inhibiting the airway inflammation.
Moreover, we also detected the level of inflammatory mediators in the BALF to determine the effect of these cytokine-encoding vectors. Both leukotriene B4 (LTB4) and prostaglandin E2 (PGE2) are potent pro- inflammatory mediator, which are involved in several inflammatory diseases . LTB4 is a potent neutrophil chemoattractant that enhances neutrophil-endothelial interactions and stimulates neutrophil activation . LTB4 may contribute to airway narrowing by producing local edema and increasing mucus secretion. The overproduction of LTB4 plays an important role in the pathogenesis of asthma and acute lung injury . On the other hand, the general consensus is that PGs, in particular PGE2, act to shift the immune response toward a type 2 cytokine profile [50, 51]. Moreover, this lipid mediator can also up-regulate IgE production, and consequently support the development of type 2 cytokine- associated inflammatory disorder. However, there is evidence for a broncho- protective role for PGE2 in asthma [52, 53]. In recent study, Harizi et al.  also demonstrated that PGE2 could inhibit the production of LTB4 from dendritic cells via IL-10 dependent mechanism. It is not clear whether PGE2 synthesis in airway diseases can play a deleterious or a beneficial role. The result of our study indicates that IL-10 can significantly decrease the level of LTB4 in the BALF, but other cytokine gene plasmids may not show a similar effect (Fig. 5). In contrast, all the cytokines together do not have any effect on the level of PGE2 in the BALF (data not shown). Our results may support that IL-10 could inhibit the recruitment of neutrophils by reducing the production of LTB4 (Fig. 3).
Further, we have examined varying doses of IL-10 gene plasmid to test the therapeutic efficiency of this asthma animal model (Fig. 6). It has been reported that instillation of IL-10 protein into the lung could suppress eosinophilic inflammation [55, 56]. However, the half-lives of recombinant cytokines are very short and the suppressive effect is weak. In current study, in vivo IL-10 gene delivery can efficiently suppress airway eosinophilia (Fig. 3). In addition, we also demonstrated that IL-10 gene plasmid had a strong immuno-modulating effect in the suppressing Ag-induced eosinophilic inflammation and AHR in a dose-dependent manner (Fig. 6).
As IL-10 is a multi-potent immunosuppressive cytokine, it could exhibit various effects on many resident cells and inflammatory cells, such as endothelial cells, monocytes/macrophages, lymphocytes, and mast cells [57, 58]. It has been also reported that IL-10 can inhibits Th1cytokine production via the suppression of IL-12 synthesis in accessory cells . Thus, we combined 2 plasmids (IL-10 and IL-12) to treat OVA-sensitized mice (Fig. 7). Our results showed that in vivo delivery of IL-10 or IL-12 gene alone could efficiently inhibit AHR and airway eosinophilic inflammation. However, combination of IL-10 and IL-12 gene therapy did not exert the syngenic effect in the modulating airway inflammation. It may imply that IL-10 and IL-12 have some antagonistic effect in the local inflammatory site. In addition, the regulating mechanisms of IL-10 and IL-12 for the suppression of experimental asthma are totally different. In the recent study of Nakagome K et al., they pointed that IL-10 gene delivery can suppress lung APC functions and the subsequent Th2 response . IL-10 could reduce the recruitment of eosinophils into the lung by modulating the expression of VCAM-1 on endothelial cells  and decreasing the secreting level of eotaxin (in this paper). Thus, IL-10 gene delivery could be more effective in the treatment of local airway inflammation.
Cytokine directed therapies for asthma
a. IFN-γ producing T cells increased;
b. Reduced IL-4 & IL-5 secretion
a. Down-regulating synthesis of both Th1- & Th2- cytokines
b. Reduced both eosinophilia & neutrophilia
a. Th1 skewed response;
b. specific IgE/IgG reduced;
5, 9, 11
Combined IL-12 and IL-18 induce IFN-γ release
Immuno- regulation, wound healing, and to shorten the inflammatory response
Intra-tracheal administration of TGF-β, IL-10 or IL-12 gene plasmids can efficiently inhibit antigen-induced airway hyper-responsiveness and significantly lower the number of eosinophils and neutrophils in bronchoalveolar lavage fluid of ovalbumin (OVA) sensitized mice during the effector phase. Our data demonstrated that anti- inflammatory cytokines, particularly IL-10, have the therapeutic potential for the alleviation of airway inflammation in murine model of asthma.
This study was supported by the National Science Council.
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