|Home | About | Journals | Submit | Contact Us | Français|
Despite respiratory syncytial virus (RSV) bronchiolitis remaining the most common cause of lower respiratory tract disease in infants worldwide, treatment has progressed little in the past 30 years. The aim of our study was to determine whether post-infection administration of de novo pyrimidine synthesis inhibitors could prevent the reduction in alveolar fluid clearance (AFC) and hypoxemia that occurs at Day 2 after intranasal infection of BALB/c mice with RSV. BALB/c mice were infected intranasally with RSV strain A2. AFC was measured in anesthetized, ventilated mice after instillation of 5% bovine serum albumin into the dependent lung. Post-infection systemic treatment with leflunomide has no effect on AFC. However, when added to the AFC instillate, leflunomide's active metabolite, A77-1726, blocks RSV-mediated inhibition of AFC at Day 2. This block is reversed by uridine (which allows pyrimidine synthesis via the scavenger pathway) and not recapitulated by genistein (which mimics the tyrosine kinase inhibitor effects of A77-1726), indicating that the effect is specific for the de novo pyrimidine synthesis pathway. More importantly, when administered intranasally at Day 1, A77-1726, but not its vehicle dimethyl sulfoxide, maintains its beneficial effect on AFC and lung water content until Day 2. Intranasal instillation of A77-1726 at Day 1 also reduces bronchoalveolar lavage nucleotide levels, lung inflammation, and hypoxemia at Day 2 without impairing viral replication at Day 2 or viral clearance at Day 8. Post-infection intranasal or aerosolized treatment with pyrimidine synthesis inhibitors may provide symptomatic relief from the pathophysiologic sequelae of impaired AFC in children with RSV bronchiolitis.
Herein we show that prophylactic intranasal administration of A77-1726, an agent that decreases UTP levels, prevents the respiratory syncytial virus–induced decrease of alveolar fluid clearance and onset of arterial hypoxemia in mice.
Respiratory syncytial virus (RSV) remains the most common cause of lower respiratory tract infection in infants and children worldwide (1), and recent studies indicate that it has a disease impact comparable to that of nonpandemic influenza A in the elderly (2). However, while infant hospitalization rates for RSV increased 2.4-fold from 1980 to 1996 (3), treatment for infants with moderate to severe RSV bronchiolitis has progressed little in the past 30 years: supplemental oxygen and periodic suctioning to remove excess nasopharyngeal secretions provide clear benefit, but more specific pharmacologic therapies are moderately successful at best (4). The need for new approaches to RSV treatment is therefore paramount.
The interface between the respiratory epithelium and the air is normally bathed by a thin layer of fluid, the airspace lining fluid (ALF). To permit efficient gas exchange in the bronchoalveolar compartment and effective mucociliary clearance in the airways, the depth of this layer must be tightly regulated. Active transport of sodium (Na+) ions from the ALF to the interstitial space by bronchoalveolar epithelial cells is critical to the regulation of ALF thickness (5). Inhibition of active Na+ transport can result in formation of an excessive volume of ALF, impairment of gas exchange (6), narrowing of airway lumens (7), and dilution of the surface-active materials that stabilize small airways (8). The resultant small airway obstruction, which would be exacerbated by any intercurrent inflammatory process, such as that occurring during RSV bronchiolitis, would be predicted to be most severe in infancy and early childhood when airway diameter is lowest.
Moderately severe RSV bronchiolitis is commonly associated with signs of respiratory distress, and admission decisions are often based upon clinical evidence of hypoxemia (4). The underlying causes of hypoxemia in RSV bronchiolitis have not been determined, but its presence must perforce indicate either hypoventilation of the bronchoalveolar compartment (as a result perhaps of airway obstruction by fluid secretions, mucus, inflammatory infiltrates, or necrotic cell debris), an abnormal alveolar ventilation–perfusion ratio, and/or diminished respiratory membrane diffusion. Our previous findings suggest that bronchoalveolar edema, occurring as a consequence of reduced active Na+ transport by the respiratory epithelium, may be an unrecognized component of RSV disease that plays a role in development of hypoxemia, either by impairing alveolar gas exchange or by contributing to obstruction of small airways (9). We have found that infection of BALB/c mice with RSV significantly impairs alveolar fluid clearance (AFC), an in vivo measure of active Na+ transport in the whole lung, at early time points after infection (by 43% from mock-infected values at Day 2) (10). This decrease in AFC is mediated by de novo synthesized UTP acting on P2Y purinergic receptors, and is rapidly reversed by addition to the AFC instillate of agents that degrade UTP, but not ATP (9, 10). Our studies also demonstrated that RSV-mediated nucleotide release, AFC inhibition, and physiologic sequelae thereof can be prevented by pretreatment of mice with the de novo pyrimidine synthesis inhibitor leflunomide (9). These findings suggested that inhibitors of de novo pyrimidine synthesis, while not being antiviral, might be useful in alleviating symptoms of RSV bronchiolitis. However, as a consequence of its poor pharmacodynamic profile (11), leflunomide is only effective in abrogating effects of RSV on AFC when given as a systemic pretreatment regimen. This renders it less valuable as a potential therapy for RSV bronchiolitis. The aim of the current study was to determine whether post-infection treatment with the active metabolite of leflunomide, A77-1726, could produce similar beneficial effects on AFC, lung edema, and hypoxemia in a murine model of RSV infection. Some of the results of these studies have previously been reported in the form of abstracts (12–14).
Preparation of viral stocks and intranasal infection of 8- to 12-week-old pathogen-free BALB/c mice of either sex with RSV strain A2 (106 plaque-forming units in 100 μl) were performed as previously described (10). All mouse procedures were approved by the UAB and OSU Institutional Animal Care and Use Committees.
Leflunomide, A77-1726, genistein, and amiloride were reconstituted in dimethyl sulfoxide (DMSO), aliquoted, and stored frozen. Uridine was reconstituted in sterile normal saline. All reagents were from Sigma-Aldrich (St. Louis, MO).
AFC was measured as previously described (10). Briefly, mice were anesthetized with diazepam (1.75 mg/100 g, intraperitoneally; Abbott Laboratories, Abbott Park, IL) followed 6 minutes later by ketamine (45 mg/100 g, intraperitoneally) and were placed on a heating pad (Braintree Scientific, Cambridge, MA). The trachea was exposed and cannulated with a trimmed 18-gauge intravenous catheter, which was then connected to a mouse respirator (model 687; Harvard Apparatus, Holliston, MA). Mice were paralyzed with pancuronium bromide (0.04 mg, intraperitoneally; Gensia Pharmaceuticals, Irvine, CA) and ventilated with 100% O2 with a 200-μl tidal volume (8–10 ml/kg body wt) at 160 breaths/minute. Once stable anesthesia was obtained, mice were positioned in the left decubitus position, and 300 μl of isosmolar NaCl containing 5% fatty acid–free bovine serum albumin was instilled via the tracheal cannula, followed by 100 μl of room air to clear dead space. After instillation, mice were ventilated for a 30-minute period, then the alveolar fluid was aspirated. AFC was calculated from the ratio between the protein concentration of the instillate before instillation and of the alveolar sample at 30 minutes.
All reagents were added to the AFC instillate from stock solutions directly before instillation, in a minimal volume of solvent (1–10 μl/ml). Previous studies have demonstrated that mock infection has no effect on AFC or other measured lung parameters, and that measured declines in AFC are not a consequence of instillate dilution by intrapulmonary edema fluid, but require replication-competent virus (10). No sex difference in AFC rate has been found in BALB/c mice.
Mice were lightly anesthetized. One hundred microliters of saline, containing 0.5 μl A77-1726 in DMSO, was administered dropwise, via both nares, at Day 1 after RSV infection. Control animals received an equal volume of saline + DMSO. Mice were placed in lateral recumbency, allowed to recover, and returned to their cage.
SpO2 was measured in conscious mice using the MouseOx system (Starr Life Sciences Corp., Allison Park, PA), in accordance with manufacturer's instructions. To ensure accurate sensor placement, SpO2 data points were excluded from analysis if one of the four measured parameters (SpO2, pulse rate, pulse distension, and respiratory rate) received an error code during measurement. Data were collected for a minimum of 10 s (150 data points) per sample. Arterial Po2 was estimated from SpO2 using the Ventworld interactive oxyhemoglobin dissociation curve tool (http://www.ventworld.com/resources/oxydisso/oxydisso.html), assuming a normal blood pH and arterial Pco2.
Mice were anesthetized using the same regimen as for AFC studies. Total lung resistance was measured in mice undergoing mechanical ventilation at 150 breaths per minute on a computer-controlled piston ventilator (flexiVent; Scireq Scientific Respiratory Equipment Inc., Montreal, PQ, Canada), with 3 cm H2O PEEP, as previously described (15). R was recorded after performance of two TLC maneuvers to standardize volume history and administration of normal saline by Aeroneb nebulizer. Data were analyzed using the single compartment model. Female mice only were used in these studies, since male mice exhibit exaggerated AHR responses to methacholine (MCH) (16).
Descriptive statistics were calculated using Instat software (GraphPad, San Diego, CA). Differences between group means were analyzed by ANOVA, with Tukey-Kramer multiple comparison post-tests. All data values are presented as mean ± SEM.
Previously, we had shown that, in the BALB/c mouse model, pretreatment with the dihydro-orotate dehydrogenase inhibitor leflunomide by oral gavage for 7 d blocked RSV-mediated inhibition of AFC at Day 2 after infection (when AFC is most impaired) (9). However, we have found in subsequent studies that post-infection gavage with leflunomide at Day 1 had no beneficial effect on AFC at Day 2 (mean AFC rate 20.5 ± 2.3% in leflunomide-treated mice, n = 15, versus 21.4 ± 1.2% in untreated animals, n = 19, 34.2 ± 1.1% in uninfected animals, n = 10). AFC rates in uninfected mice and at Day 2 in the current study are comparable to those that we have reported previously using this model (9, 10).
We hypothesized that the lack of effect of post-infection leflunomide treatment at Day 1 on AFC at Day 2 was a result of the need for its metabolism to an active form, and of poor bioavailability in the lungs after a single dose (since 90% of the drug remains bound to plasma proteins ). We therefore decided to investigate the effects of intrapulmonary administration of the active metabolite of leflunomide, A77-1726, on AFC after RSV infection. In agreement with our hypothesis, addition of 25 μM A77-1726 to the AFC instillate resulted in complete blockade of RSV-induced suppression of AFC at Day 2 and returned AFC to control levels (Table 1). A77-1726 also restored normal amiloride sensitivity to AFC at Day 2: amiloride reduced AFC by 56% in the presence of A77-1726 at Day 2, while our previous studies (10) have shown that amiloride reduces AFC by 61% in uninfected mice and has no effect on AFC at Day 2 in untreated, RSV-infected mice.
Dihydro-orotate dehydrogenase inhibitors such as A77-1726 also have nonspecific tyrosine kinase inhibitory activity (19). However, the beneficial effect of A77-1726 on AFC at Day 2 was not replicated by the broad-spectrum tyrosine kinase inhibitor genistein, even at a concentration of 25 μM (Table 1), which is far greater than that which has been shown previously to be effective at tyrosine kinase blockade in a rat AFC model (1 μM) (20). Furthermore, blockade of RSV-mediated AFC inhibition by A77-1726 was reversed by concomitant addition of 10 μM uridine to the instillate, which allows pyrimidine synthesis via a salvage pathway, indicating the A77-1726 block is specific to the de novo pyrimidine synthesis pathway. Uridine alone had no effect on AFC in RSV-infected mice.
Since topical, post-infection treatment with A77-1726 appeared effective in blocking RSV-mediated inhibition of AFC at Day 2 after infection, we wished to determine whether A77-1726 might provide prolonged therapeutic benefit. When A77-1726 (10–50 μM, but not 1 μM, in DMSO) was administered intranasally at Day 1 after infection, its blocking effect on RSV-induced inhibition of AFC persisted for at least 24 hours: AFC remained at control levels at Day2, even in the absence of further addition of A77-1726 to the AFC instillate (Figure 1A). In contrast, administration of an equivalent volume of DMSO in saline (100 μl of 5 μl/ml solution) alone intranasally at Day 1 had no beneficial effect on AFC at Day 2. However, in spite of this ability to restore normal AFC to RSV-infected mice, intranasal treatment with 10 or 50 μM A77-1726 did decrease AFC in uninfected mice 24 hours later, by 19% and 34%, respectively (Figure 1B). This effect is comparable to that which we observed previously after treatment of uninfected mice with leflunomide (9).
Treatment of mice with 50 μM A77-1726 by intranasal instillation at Day 1 after infection restored normal lung wet:dry weight ratios at Day 2 (Figure 2), but had no significant effect on lung water content in mock-infected mice (mean wet:dry weight ratio 4.54 ± 0.05 in A77-1726–treated mice, versus 4.67 ± 0.03 in untreated animals, n = 8 for both groups). In contrast, intranasal treatment with an equivalent volume of DMSO in saline (100 μl of 5 μl/ml solution) at Day 1 had no beneficial effect on wet:dry weight ratios at Day 2.
Previously, we demonstrated that RSV infection resulted in a doubling of bronchoalveolar lavage (BAL) UTP and ATP levels at Day 2 (9). Intranasal treatment with 50 μM A77–1726 at Day 1 after infection returned BAL UTP and ATP content at Day 2 to levels comparable to those in untreated, uninfected mice (Figures 3A and 3B). These findings are consistent with the observation that de novo purine and pyrimidine synthesis pathways are usually concordantly regulated (reviewed in Ref. 21). Interestingly, despite causing mild suppression of AFC in uninfected mice 24 hours later, intranasal treatment of uninfected mice with A77-1726 had no stimulatory effect on BAL nucleotide content. This differs from our previous finding after treatment of uninfected mice with leflunomide, when suppression of AFC was associated with elevated BAL nucleotide levels (9).
RSV had a very significant overall effect on peripheral blood oxygen saturation (SpO2) in conscious mice over the 8-d infection period (P < 0.0005 by ANOVA), and impairment of AFC at Day 2 was temporally associated with a statistically significant (P < 0.05, by Tukey-Kramer post-test) reduction (1.95%) in SpO2 (Figure 4). This corresponds to a decline in arterial Po2 from 82 to 71 mm Hg. No change in either respiratory rate or heart rate was detected at any time after infection (data not shown). Treatment of mice with 50 μM A77-1726 by intranasal instillation at Day 1 prevented the decline in SpO2 readings seen in untreated, RSV-infected, conscious mice at Day 2, but had no significant effect on SpO2 at later time points after infection. Mean SpO2 values in A77-1726–treated RSV-infected mice at Day 2 were significantly higher than in untreated animals. In contrast, intranasal treatment with an equivalent volume of DMSO in saline at Day 1 had no beneficial effect on SpO2 at d2. Finally, intranasal treatment of uninfected mice with 10 μM A77–1726 did not result in hypoxemia 24 hours later (mean SpO2 96.25 ± 0.3%, n = 10), despite causing a 19% decrease in AFC.
Infection with RSV resulted in a significant increase in baseline airway resistance at Day 2, but not at other time points after infection (Figure 5). Increased airway resistance at Day 2 was reversed by intranasal administration of 50 μM A77-1726 at Day 1.
Post-infection intranasal treatment with 50 μM A77-1726 had a very limited effect on BAL cytokine and chemokine responses after RSV infection (Table 2). Interestingly, treatment with the A77-1726 vehicle DMSO at Day 1 had some proinflammatory effects (induction of BAL IL-1β and TNF-α at Day 2, and of TNF-α at Day 4). These proinflammatory effects of the vehicle at Day 2 were abrogated by A77-1726 itself, resulting in normalization of IL-1β levels and complete suppression of TNF-α. However, the anti-inflammatory effect of A77-1726 on TNF-α did not persist until Day 4. Intranasal A77-1726 treatment at Day 1 also significantly reduced BAL keratinocyte cytokine (KC) (murine homolog of CXCL8) chemokine levels at Day 2 after RSV infection, but not later time points. However, DMSO treatment had a similar effect. Some limited suppression of CCL3 (MIP-1α) was seen after A77-1726 treatment, but only at Day 8. Neither DMSO nor A77-1726 treatment had any effect on BAL IFN-γ or CCL5 (RANTES) levels at any time point after infection. A77-1726 treatment had no significant effect on the minimal levels of proinflammatory cytokines and chemokines detectable in BAL fluid from mock-infected mice.
Post-infection intranasal treatment of mice with 50 μM A77-1726 also resulted in a significant reduction in BAL total cell counts at Day 2 (Figure 6A), although numbers remained elevated above those in uninfected mice. The decline in BAL cellularity was primarily due to a drop in BAL alveolar macrophages—no significant changes in BAL neutrophil or lymphocyte counts were observed after intranasal A77-1726 treatment (Figure 6B).
Treatment of mice with DMSO or 50 μM A77-1726 by intranasal instillation at Day 1 had no effect on viral growth at any time point after infection (Figure 7). Moreover, unlike with leflunomide treatment (10), viral replication was not prolonged to Day 8—replication of RSV was undetectable at Day 8 in untreated, intranasal DMSO-treated, and intranasal A77-1726–treated animals.
Bronchiolitis results in estimated hospitalization rates of 30 per 1,000 children younger than 1 year old in the United States and Europe (22), and RSV remains its most common underlying cause (23). There is much controversy regarding the best approach to treatment of RSV bronchiolitis (24). β-adrenergic agonists are frequently prescribed, primarily as bronchodilators, but there is little conclusive evidence that they are effective (25), and recent studies suggest that RSV may induce insensitivity to their actions (26). Likewise, systemic corticosteroids (27) and ribavirin (28) appear to provide no clinical benefit in children with bronchiolitis. Finally, trials of surfactant, immunoglobulins, heliox, vitamin A, interferon, and erythropoietin in the ICU setting have been inconclusive (29). Only supportive care (supplemental oxygen, suctioning, and parenteral fluid replacement) appears beneficial (4). In these circumstances, new and effective approaches to therapy are urgently needed.
Previously, we had shown that we could prevent RSV-mediated nucleotide release, AFC inhibition, and the physiologic sequelae thereof, including hypoxemia, by systemic pretreatment of BALB/c mice with leflunomide (an inhibitor of de novo pyrimidine synthesis) for 7 days (9). However, we found that, as a consequence of its poor pharmacodynamic profile (11), leflunomide is completely ineffective in abrogating effects of RSV on AFC when given after infection. In contrast, its active metabolite, A77-1726, was effective as both a topical treatment (added to the AFC instillate) and as an intranasal pretreatment (administered at Day 1 after infection) in blocking RSV-mediated inhibition of AFC at Day 2.
Results of our previous studies with leflunomide had suggested that UTP release from the respiratory epithelium is limited by UTP availability in cells: the pool of UTP that is normally available for release is small, and primarily derived from de novo pyrimidine synthesis (9). The effects of A77-1726 on AFC, when this drug is added directly to the AFC instillate at Day 2, tend to support this contention. For RSV-mediated inhibition of AFC to be blocked so rapidly under these conditions, the extracellular UTP that is activating P2Y receptors must be derived from continuous de novo synthesis, since the uridine salvage pathway is not sensitive to inhibition by A77-1726. Furthermore, this result suggests that the half-life of extracellular UTP is very short and that maintenance of the elevated extracellular steady-state UTP concentrations required to inhibit AFC necessitates a constant efflux of newly synthesized intracellular UTP: if the extracellular UTP that mediates AFC inhibition has a prolonged half-life in the bronchoalveolar space, or were derived from an intracellular pool independent of active de novo pyrimidine synthesis (either a storage pool, or one resulting from salvage synthesis), then there would be sufficient UTP to mediate AFC inhibition for at least the duration of the AFC measurement (30 min) and topical A77-1726 would have no effect. Indeed, previous in vitro studies have demonstrated that UTP and ATP are rapidly degraded by ectonucleotidases at the respiratory mucosal surface (30), which supports our contention that continuous de novo nucleotide synthesis is necessary to maintain AFC inhibition.
We have previously shown that infection of mice with RSV resulted in mild hypoxemia in conscious mice at Day 2, which was reversible following pretreatment with leflunomide (9). However, because of the very rapid pulse rate of the mouse, we were only able to measure mean O2 saturation values from arterial and venous blood (SmO2), which therefore appear low (85%) relative to true SpO2 values (95%) even in uninfected mice. In the current study, we used the newly available MouseOx system, which can accurately measure true SpO2, in addition to other physiologic parameters, in conscious mice at a 15-Hz sampling rate. Moreover, the associated software allows accurate sensor placement, since error codes are displayed when arterial pulse signals do not conform to the software algorithm, so that erroneous data may be excluded. To our knowledge, our study is the first to be published using this system. We found that infection with RSV is associated with a significant reduction in SpO2 at Day 2 only, which is when AFC is most impaired (by 43% from mock-infected values). The lack of decline in SpO2 at Day 4 suggests that the degree of AFC impairment at this time point (21%) is insufficient to result in detectable hypoxemia. Indeed, we were similarly unable to detect hypoxemia in uninfected mice 24 hours after intranasal treatment with 10 μM A77-1726, which causes a comparable decline in AFC (19%).
The time course of effect of RSV on SpO2 described herein was almost identical to that which we reported previously for SmO2 (9), and results of the two techniques were very strongly correlated (P < 0.0005), confirming the validity of our earlier findings. Interestingly, van Schaik and coworkers (31) previously reported an early peak in respiratory rate at Day 1 to Day 2 after RSV infection, measured by whole-body plethysmography, although they also found a second period of tachypnea at Day 6, which they associated with the onset of the specific immune response to infection. We found no hypoxemia at Day 6 and no tachypnea at any time point after infection, although this latter finding may be a consequence of the greater animal handling required for SpO2 measurement versus plethysmography, which may have artificially altered respiratory rates. Nevertheless, our findings are supported by the observation of Welliver and colleagues (32) that in human patients, severity of hypoxemia during RSV infection is poorly correlated to T cell cytokine levels.
Although the observed decrease in mean SpO2 at Day 2 in RSV-infected mice appears small (2%), this nevertheless corresponds to a decline in arterial Po2 of 10 mm Hg. Moreover, an SpO2 of 94%, which is greater than the mean value observed in our study at Day 2 (93.5%), has also been suggested as a lower acceptable limit for bronchiolitis outpatient therapy (33), and has been defined by some authors as indicative of hypoxemia (34). In one recent study, an SpO2 below 95% was found to be highly predictive of admission to the pediatric ICU in full-term infants with bronchiolitis that lack other underlying illnesses (35). Most importantly, the limited hypoxemia observed in conscious mice at Day 2 could be prevented by intranasal A77-1726 treatment at Day 1, as we had previously shown for leflunomide pretreatment (9). This finding further supports our hypothesis that hypoxemia during RSV bronchiolitis may result from nucleotide-mediated impairment of AFC. Furthermore, intranasal A77-1726 treatment had no detrimental effect on SpO2 at later time points after infection.
Unlike systemic leflunomide treatment (9), intranasal A77-1726 treatment at Day 1 had only a limited suppressive effect on the intrapulmonary proinflammatory cytokine/chemokine response at Day 2, since it induced significant reductions only in BAL KC and TNF-α levels. However, a comparable suppressive effect on BAL KC levels was also noted after intranasal DMSO treatment at Day 1, suggesting that the reduction in BAL KC levels at Day 2 after intranasal A77 treatment at Day 1 is an effect of the vehicle rather than the drug itself. DMSO has previously been shown to suppress IL-8 production by RSV-infected A549 cells, as a consequence of its antioxidant properties (36). While the suppressive effect of A77 treatment on BAL TNF-α levels was not replicated by DMSO alone, our previous studies demonstrated that leflunomide's effect on RSV-induced AFC inhibition was reversed by uridine, but its effect on BAL TNF-α levels was not (9). Taken together, these findings suggest that the beneficial effect of A77-1726 treatment on AFC in RSV infection is not a consequence of its immunosuppressive effects, but instead results from its inhibitory effect on de novo pyrimidine synthesis.
Intranasal A77-1726 treatment at Day 1 also blocks the increase in BAL alveolar macrophage counts in response to infection at Day 2, although it has no effect on BAL lymphocyte or neutrophil responses to RSV. Previously, we had found that continuation of leflunomide treatment to Day 8 after infection resulted in impaired leukocyte recruitment to the airspaces and histopathologic evidence of trapping of leukocytes around major blood vessels (9). These data suggest that either nucleotides themselves, or the cytokines and chemokines that they induce, may be important for recruitment of alveolar macrophages to the lung in the early phase of RSV infection. Interestingly, nucleotides have been shown to promote monocyte chemotaxis (37), and our findings may reflect this role. Taken together, the alteration in pulmonary humoral and cellular responses to RSV infection observed after inhibition of de novo pyrimidine synthesis suggest that nucleotides may play a significant role in the initiation of the immune response to RSV infection (although this alteration may be partially attributed to the tyrosine kinase inhibitory activity of these drugs ). Nevertheless, irrespective of the underlying mechanism, the immunosuppressive activity of A77-1726 may be an additional beneficial property of this drug, since an elevated nasal lavage or lung level of CXCL8, which intranasal A77-1726 reduces, may be an indicator of increased disease severity in children with RSV (38, 39).
Our previous studies had demonstrated that the inhibitory effect of RSV on AFC requires active viral replication (10), and the beneficial effect of A77-1726 on AFC at Day 2 might therefore simply result from an antiviral activity. However, neither intranasal A77-1726 treatment nor intranasal DMSO treatment at Day 1 had any effect on viral replication kinetics in mouse lungs. The beneficial effect of A77-1726 on basal and amiloride-sensitive AFC at Day 2 is not therefore simply a consequence of inhibition of viral replication, but is rather a specific modulatory effect on epithelial cell function. Moreover, unlike leflunomide therapy, intranasal A77-1726 treatment at Day 1 does not prolong viral replication to Day 8. This finding suggests that, despite any immunosuppressive effects, this treatment does not impede normal antiviral clearance mechanisms.
In conclusion, our studies indicate that post-infection intranasal therapy with an inhibitor of de novo pyrimidine synthesis can have a prolonged beneficial effect on the pathophysiologic consequences of RSV infection in the BALB/c mouse model—intranasal A77–1726 treatment at Day 1 after RSV infection is able to restore normal AFC and alleviate lung edema 24 hours later, thereby helping to counter the development of hypoxemia, without impairing clearance of RSV from the lung in the long term. Post-infection intranasal or aerosolized therapy with pyrimidine synthesis inhibitors may therefore have the potential to provide symptomatic relief from the pathophysiologic sequelae of impaired AFC in children with severe RSV disease. To our knowledge, this is the first report of an effective post-infection therapy for hypoxemia in RSV bronchiolitis in the murine model, other than supplemental oxygen.
The authors acknowledge the excellent technical assistance of Glenda C. Davis and Zachary Traylor.
This work was supported by PHS grants HL-31197, HL-51173 (to S.M.), and RR-17626 (to I.D.).
Originally Published in Press as DOI: 10.1165/rcmb.2007-0142OC on May 31, 2007
Conflict of Interest Statement: I.C.D., W.M.S., and S.M. have been granted US Provisional Patent Application #60/573558: “Methods for using pyrimidine synthesis inhibitors to increase airway epithelial cell fluid uptake.” (Filed May 21, 2004; Inventors: Dr. Ian C Davis, Dr. Wayne Sullender and Dr. Sadis Matalon) which converted to International PCT application (#PCT/US2005/017939);May 2005. I.C.D. has received $500 in consultancy fees from Inspire Pharamaceuticals for advising on licensing issues related to this patent. S.M. received $1000 as an honorarium from Inspire Pharmaceuticals for a seminar delivered at Inspire. S.M. was the principal investigator for a grant from Inspire Pharmaceuticals, entitled: “Assessment of a novel P2Y receptor antagonist in preventing RSV induced injury to the Alveolar epithelium in vivo” (07/15/2006–07/15/2007; $130,000, direct costs). W.M.S. and I.C.D. acted as a co-investigator and consultant, respectively. None of the experiments and results presented in this paper were funded from this grant. None of the other authors has a financial relationship with a commercial entity that has an interest in the subject of this manuscript.