Background: A study was undertaken to evaluate Chlamydia pneumoniae chronic infection, other respiratory infections, and functional impairment in patients with chronic bronchitis (stage 1) and to examine chronic C pneumoniae infection, rate of acute exacerbations of chronic bronchitis, and rate of C pneumoniae eradication following antibiotic treatment (stage 2).
Methods: In the stage 1 study respiratory specimens from 42 patients with steady state chronic bronchitis were analysed for Gram staining, sputum culture, and C pneumoniae DNA detection by nested touchdown polymerase chain reaction (PCR). On the basis of the results of stage 1, a second population of 141 consecutive patients with steady state mild to moderate chronic bronchitis (FEV1 ≥50% predicted) was studied. On admission, at regular intervals, and at exacerbation all patients underwent serological testing for C pneumoniae (microimmunofluorescence) and a nested touchdown PCR to detect C pneumoniae DNA was performed on peripheral blood mononuclear cells (PBMCs). Patients were assessed over a 12 month period. Information regarding the previous 12 months was taken from medical records.
Results: Chronic colonisation of the sputum with C pneumoniae was significantly associated with lower FEV1 and greater airway bacterial colonisation. On admission to the stage 2 study, 80 patients were PCR negative and 61 were PCR positive. Over the 2 years a mean (SD) of 1.43 (1.32) acute exacerbations occurred in PCR negative patients and 2.03 (1.21) in PCR positive patients (p<0.01). During the 12 month follow up period 34 PCR positive patients had acute exacerbations and were treated with azithromycin for 6 weeks. Serological evidence of acute C pneumoniae reinfection/reactivation was found in two of the 34 patients. The rate of C pneumoniae DNA clearance from blood following treatment was 29% at follow up.
Conclusion: Chronic colonisation with C pneumoniae is associated with a higher rate of exacerbations of chronic bronchitis. Long term treatment is required to obtain clearance of the organism from the blood.
- Chlamydia pneumoniae
- chronic obstructive pulmonary disease
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Chlamydia pneumoniae has been recognised as a cause of respiratory tract infections and is considered the most common non-viral intracellular human respiratory pathogen.1 It is involved in a wide spectrum of respiratory infections of the upper respiratory tract (pharyngitis, sinusitis and otitis) and lower respiratory tract (acute bronchitis, exacerbations of chronic bronchitis and asthma, community acquired pneumonia) in both immunocompetent and immunocompromised hosts.2
Chronic C pneumoniae infection has been found to be common in chronic bronchitis and could contribute to disease progression by a toxic effect on bronchial epithelial cells, impairing ciliary function, and increasing chronic inflammation via proinflammatory cytokine production. Several studies have provided evidence of this involvement. Blasi et al reported a significantly higher prevalence of the IgG antibody fraction in patients with chronic obstructive pulmonary disease (COPD) than in controls, particularly in those aged over 50 years.3 Moreover, they found an increase in both specific IgG prevalence and geometric mean titre with age, suggesting chronic infection. Another study in hospitalised and non-hospitalised patients with COPD showed a significantly higher IgA seroprevalence in COPD patients than in control subjects.4 The authors also found a correlation between the geometric mean titre of IgA and COPD severity that persisted after controlling for smoking. Some years later the same group studied patients with COPD enrolled in a separate geographical area.5 They determined four different markers of C pneumoniae infection: (1) serum antibodies, (2) sputum antibodies (secretory IgA), (3) sputum polymerase chain reaction (PCR), and (4) circulating immunocomplexes. The authors found a gradient of marker positive patients which increased from mild to severe COPD. The overall prevalence of chronic infection was 71% in patients with severe COPD and 46% in those with mild COPD.
A hypothetical model for the C pneumoniae/chronic bronchitis interaction was discussed in a recent review.6 In this model involvement of C pneumoniae in patients with COPD is characterised by raised serum antibodies and the presence of secretory IgA in sputum, both associated with a Th2 type immune response that may lead to chronic infection.
C pneumoniae infection induces secretion of tumour necrosis factor (TNF)-α by monocytes,7 a cytokine involved in the endothelial and epithelial expression of IL-1 and adhesion molecules.8 TNF-α production is induced by C pneumoniae heat shock protein 60 (HSP60) in a concentration and time dependent fashion.9 HSP60 also induces production of matrix metalloproteinases (MMPs) by macrophages, particularly MMP-9.9 Recent observations have contributed to growing evidence of the importance of macrophages and MMPs in the pathogenesis of emphysema.10,11
In addition, C pneumoniae infection activates nuclear factor-κB (NF-κB) which is thought to control the transcriptional initiation of inflammatory genes.12,13 The genes encoding proinflammatory cytokines such as TNF-α and IL-1β, chemokines including IL-8, RANTES, and macrophage chemotactic protein-3, adhesion molecules such as ICAM-1, VCAM-1 and E-selectin, and inflammatory enzymes such as COX-2 have all been shown to depend on NF-κB for their expression. A recent study showed that the level of NF-κB activity is highly correlated with the degree of lung dysfunction and that the kinetics of NF-κB activity are strongly related to the course of the disease in an animal model of asthma.14
Preliminary data on chronic infection with C pneumoniae in patients with COPD and its interaction with host cells indicate that this agent may be responsible for the modulation of the natural history of chronic bronchitis and emphysema. However, a recent paper questioned the influence of C pneumoniae infection—defined by serological analysis—on the decline in lung function.15
We examined the association between C pneumoniae infection, degree of airflow limitation, and rate of acute exacerbations using a combined diagnostic approach for the identification of chronic C pneumoniae infection.
The study was performed in two stages. During the first part (stage 1) we examined the association between C pneumoniae infection and baseline severity of chronic bronchitis. In the second part of the study (stage 2) we prospectively evaluated the rate of acute exacerbations in C pneumoniae positive and negative patients with mild to moderate chronic bronchitis. Patients with suspected bronchiectasis were excluded from the study. Written informed consent was obtained from all patients and the study was approved by the ethical committee of the University of Milan.
Between 1996 and 1997 our pulmonary rehabilitation centre enrolled 42 patients (31 men) of mean (SD) age 62.2 (6.3) years (range 43–78) with steady state chronic bronchitis (mean forced expiratory volume in 1 second (FEV1) 66.3 (19.8)% of predicted value), defined by the absence of an acute exacerbation during the previous 4 weeks.
Patients were assessed over a 12 month period. At least four sputum samples were obtained from each patient at 4 week intervals with the aid of chest physiotherapy under the supervision of trained nurses. Gram staining and culture were carried out on all sputum specimens. Validity of sputum samples was determined by the presence of ≥25 polymorphonuclear leucocytes/field and <10 squamous epithelial cells/field. Culture was considered significant when a pathogen count of ≥106 cfu/ml was obtained. Respiratory specimens were also analysed to detect C pneumoniae DNA by nested touchdown PCR.16
For each patient a serological test for C pneumoniae was performed using a microimmunofluorescence (MIF) test for IgG, IgM, and IgA (Labsystems, Helsinki, Finland). MIF results were classified as follows: past (chronic infection) pattern (≥16 IgG <512, ≥16 IgA <256); acute first infection (IgM ≥16 associated with IgG ≥512, IgA ≥256, or fourfold increase in IgG or IgA titres); reinfection (IgG ≥512, IgA ≥256, or fourfold increase in IgG or IgA titres).
Lung function tests and blood gas analysis were performed in all patients on admission and at each successive visit.
A different population of 141 consecutive patients (100 men) of mean (SD) age 68.2 (7.5) years (range 47–81) with steady state mild to moderate chronic bronchitis (FEV1 73.6 (15.3)% of predicted value) was subsequently studied. On admission all patients underwent a serological test for C pneumoniae using the MIF test as described above. In addition, C pneumoniae DNA detection was performed on peripheral blood mononuclear cells (PBMCs).17 Patients were defined as C pneumoniae positive or C pneumoniae negative on the basis of the PCR results. Lung function tests and blood gas analysis were performed for all patients on admission. Patients were assessed over a 12 month follow up period. Information regarding the previous 12 month period was taken from medical records.
Acute exacerbations were defined by the Winnipeg I criteria.18 During the observation period patients were contacted by telephone periodically and all subjects were instructed to report to the outpatient clinics if an exacerbation occurred. At the first acute exacerbation C pneumoniae DNA positive patients were treated with azithromycin for a total of 6 weeks (0.5 g daily for 3 days on 3 successive weeks followed by a single dose of 1 g/week for 3 weeks). At the onset of an exacerbation all patients performed sputum culture, MIF C pneumoniae serology, C pneumoniae DNA detection on PBMCs, blood gas analysis and lung function testing, all of which were repeated 1 week later. During the following 2 weeks the patients were contacted by telephone to ascertain compliance with treatment and adverse events. Successive visits were performed at weeks 4 and 7 (end of treatment). A first follow up examination was performed approximately 2 months (72 (9) days) after the end of treatment.
Analysis of data
Data were analysed using the SPSS statistical package. Homogeneity analysis was performed using the ANOVA F-test for parametric data and a χ2 test for non-parametric data. Wilcoxon’s rank sum test and median test were applied for comparison of exacerbations between PCR positive and negative groups.
Of the 42 patients enrolled, those whose respiratory samples were C pneumoniae DNA PCR positive (n=16) had a significantly greater number of pathogens on sputum culture than PCR negative patients (n=26, table 1). In addition, PCR positivity for C pneumoniae was significantly more common in chronic bronchitis patients with greater functional impairment (table 2).
On admission 80 of the 141 patients were C pneumoniae PCR negative and 61 were PCR positive on PBMCs. No significant differences in age, sex, smoking habits, and FEV1 were observed between PCR negative and positive subjects. Correlation between serological and PCR results is shown in table 3.
Over the 2 year observation period a mean (SD) of 1.43 (1.32) acute exacerbations occurred in PCR negative patients and 2.03 (1.21) in PCR positive patients (p=0.0021, Wilcoxon’s rank sum test; p<0.01 median test (χ2 = 7.947)). Thirty four of the 61 PCR positive patients with an exacerbation agreed to treatment with azithromycin for 6 weeks. Serological evidence of acute C pneumoniae reinfection/reactivation was found in two of the 34 patients. The geometric mean C pneumoniae IgG titre between admission and follow up decreased from 128 (4.8) to 77.5 (4.5), p<0.0001, and the geometric mean IgA titre between admission and follow up varied from 17 (2.25) to 16.5 (3.1), p=NS.
Clearance of C pneumoniae from the blood following treatment with azithromycin was achieved in 20 of the 34 patients (59%) at the end of treatment and in 10 (29%) at follow up, as assessed by PBMC PCR. Figure 1 shows variations in the rate of C pneumoniae PBMC PCR positivity during the study period.
In patients with COPD the relevance of chronic infection may be twofold: persistence of micro-organisms in the respiratory tract may facilitate access of different pathogens to the lower airways, and longstanding infection might trigger what is traditionally described as the vicious circle of chronic bronchitis. According to this hypothesis, infection may play an aetiological role in the development of the disease and act as a worsening factor. Epithelial damage, impairment of defence mechanisms, and an increase in the inflammatory and oxidative burden within the airways may all accelerate the functional and anatomical deterioration associated with the disease.
The possibility of chronic colonisation with C pneumoniae in patients with COPD, first suggested on the basis of serological evidence, has recently been further supported by electron microscopic and immunohistochemical identification of the organism in diseased airways.19,20
The first stage of this study indicates that patients with chronic bronchitis with chronic C pneumoniae infection have a higher rate of airway microbial colonisation. This may be because persistence of this intracellular organism in the airways favours ongoing inflammatory processes, dampens the immune response, and depresses mucociliary function.12–13,21 Moreover, we found that the probability of chronic colonisation with C pneumoniae is significantly associated with lung function, as shown by the increased rate of C pneumoniae positivity in patients with more severe functional impairment.
In order to clarify whether chronic C pneumoniae infection may contribute to disease progression from mild to severe functional impairment, we performed a second stage study on patients with mild to moderate COPD. Data from the this study show that the presence of chronic C pneumoniae infection, as assessed by PCR on peripheral blood monocytes, in patients with chronic bronchitis is associated with a greater propensity to develop acute exacerbations. Our group has previously shown that the rate of C pneumoniae DNA identification is similar in biopsy specimens (vascular and bronchial) and PBMCs, which suggests that blood PCR may be a useful tool for identifying patients with chronic C pneumoniae infection.17,22
C pneumoniae DNA positive patients who developed exacerbations were started on a prolonged (6 weeks) course of treatment with azithromycin. This antibiotic has a high level of intracellular accumulation and has been shown to be effective against C pneumoniae. Serial PCR testing on PBMCs from patients with an exacerbation of chronic bronchitis showed transient clearing of C pneumoniae from the blood. At the end of the 6 week treatment period clearance of C pneumoniae was observed in 20 of 34 patients (59%). Approximately 2 months later the rate of clearance had decreased to 29%. The persistence of C pneumoniae in the blood following treatment is not attributable to reinfection since no serological evidence consistent with acute infection was observed. We suggest that the treatment was insufficient to eradicate the organism completely and that the subsequent increase in the rate of infection may be due to new release of the organism into the bloodstream. On the other hand, we feel that the cases in which bacterial clearance occurred should be attributed to the effect of antibiotic treatment since spontaneous clearance seems unlikely, given that all of the 34 patients with C pneumoniae DNA detection in PBMCs on admission were persistently PCR positive on visit 1 after 111.8 (67.5) days.
As in previous studies,17 our results show a low degree of correlation between C pneumoniae serology and PBMC PCR. A greater degree of correlation was observed combining IgG and IgA titres. Furthermore, following treatment we observed a significant fall in the geometric mean IgG titre but the IgA titre was unchanged. Considering the limited half life of IgA antibodies in the organism, persistent titres probably indicate ongoing C pneumoniae antigen release. Antibiotic treatment, delivered over a 6 week period, may therefore achieve bacterial clearance from the blood rather than systemic eradication. Whether the observed reduction in the bacterial burden is sufficient to alter the natural history of the disease deserves further investigation. On the other hand, as in other intracellular chronic infections such as Mycobacterium tuberculosis, complete eradication probably requires prolonged treatment periods and/or combination therapy.
One of the limitations of the present study is associated with the methodological problems regarding standardisation of both the diagnostic techniques (MIF and PCR) used for detection of C pneumoniae.23,24 A meeting was recently convened by the Centers for Disease Control and Prevention and the Laboratory Centre for Disease Control to provide recommendations for standardised approaches to C pneumoniae diagnostic testing.25 MIF is recommended as the only reliable serological test available in commercial kits, and standardised definitions for “acute” and “past” infection are proposed. These definitions are in line with those used throughout our study. With regard to PCR techniques, although no assay has been commercially standardised or cleared by the FDA, the above mentioned paper identifies four PCR protocols (including the nested touchdown PCR used in our study) that have been validated for sensitivity and specificity in two or more outside laboratories, possess a level of detection of ≤1 inclusion forming units, and whose specificity has been tested against other Chlamydia species as well as other prokaryotic and eukaryotic DNA. Furthermore, in this study the researchers conducting PCR assays and interpreting the results were blinded to patient status (sputum culture positivity, functional impairment, exacerbation rate) and to the results of MIF testing. In a previous study our group performed PCR testing twice in all patients and in 28 of 30 cases the results were in agreement in terms of C pneumoniae DNA detection, indicating that the technique is highly reproducible.26 In addition, a recent paper has shown that detection of C pneumoniae in circulating monocytes by PCR is reproducible and correlates with the results of other detection techniques such as immunoelectron microscopy and culture.27
Peripheral blood mononuclear cell PCR for C pneumoniae is probably a useful tool in identifying chronic C pneumoniae infection and in monitoring bacterial clearance following treatment. In addition, IgA titres may be usefully combined with PCR results in defining chronic C pneumoniae infection.
The results of our study indicate a possible role for C pneumoniae chronic infection in disease progression in patients with COPD. Further confirmation in large scale trials is needed.
This study was partially supported by an unrestricted grant from Pfizer Italia S.p.A., by MURST ex-40% (9906242433-028), and IRCCS Ospedale Maggiore Milano (260/02/1998).
↵* The following members of the CIAC Study Group participated in this study: C Arosio, C Dotti, L Fagetti, M Forloni, A Grugnetti, D Lattuada, N Morelli, C Papetti, C Pravettoni, Institute of Respiratory Diseases, University of Milan, IRCCS Ospedale Maggiore Milano, Italy; G Graziadei, G G Torgano, C Canetta, Department of Emergency Medicine, IRCCS Ospedale Maggiore Milano, Italy; P A Santus, Respiratory Unit, Institute of Lung Disease Ospedale San Paolo, University of Milan, Italy.
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