- Research article
- Open Access
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Serum markers in interstitial pneumonia with and without Pneumocystis jiroveciicolonization: a prospective study
© Shimizu et al; licensee BioMed Central Ltd. 2009
- Received: 28 October 2008
- Accepted: 22 April 2009
- Published: 22 April 2009
In patients with chronic respiratory disease, Pneumocystis jirovecii (P. jirovecii) colonization is observed, and may influence disease progression and systemic inflammation. Pneumocystis pneumonia causes interstitial changes, so making a diagnosis of PCP in patients who have interstitial pneumonia (IP) with P. jirovecii colonization is sometimes difficult based on radiography.
This study investigated the prevalence of P. jirovecii colonization in IP patients and assessed pulmonary injury due to P. jirovecii colonization by measurement of serum markers (KL-6, SP-A, SP-D, and (1→3) β-D-glucan (β-D-glucan)) and the peripheral lymphocyte counts, prospectively. A total of 75 patients with idiopathic pulmonary fibrosis (n = 29), collagen vascular-related interstitial pneumonia (n = 19), chronic bronchitis or pneumonia (n = 20), and Pneumocystis pneumonia (n = 7) were enrolled in this prospective study. P. jirovecii DNA was detected in sputum samples, while serum markers and the lymphocyte count were measured in the peripheral blood.
IP patients (idiopathic pulmonary fibrosis and collagen vascular-related IP) who received oral corticosteroids had a high prevalence of P. jirovecii colonization (23.3%). In IP patients, oral corticosteroid therapy was a significant risk factor for P. jirovecii colonization (P < 0.05). Serum markers did not show differences between IP patients with and without P. jirovecii colonization. The β-D-glucan level and lymphocyte count differed between patients with Pneumocystis pneumonia or P. jirovecii colonization.
Serum levels of KL-6, SP-A, SP-D, and β-D-glucan were not useful for detecting P. jirovecii colonization in IP patients. However, the serum β-D-glucan level and lymphocyte count were useful for distinguishing P. jirovecii colonization from pneumocystis pneumonia in IP patients.
- Idiopathic Pulmonary Fibrosis
- Interstitial Pneumonia
- Pneumocystis Pneumonia
- Mixed Connective Tissue Disease
- Usual Interstitial Pneumonia
Pneumocystis jirovecii (P. jirovecii) is a fungus, and a high prevalence of P. jirovecii colonization has been reported among non-human immunodeficiency virus (HIV)-infected immunocompetent patients with primary respiratory disease [1–3]. Interstitial pneumonia (IP) is also associated with a high colonization rate of P. jirovecii . The mortality rate of patients with acute exacerbation of IP is 78% after hospital admission . After acute exacerbation of IP occurs in IP patient with P. jirovecii colonization, it is difficult to distinguish IP associated with Pneumocystis pneumonia (PCP) from IP without PCP based on the clinical and radiological features. When P. jirovecii is detected in sputum or bronchoalveolar lavage (BAL) fluid from IP patients with exacerbation, the clinician has to determine whether the patient has infection or colonization by P. jirovecii, and whether treatment should include sulfamethoxazole/trimethoprim (ST). Serum levels of KL-6 , surfactant protein A (SP-A), and surfactant protein D (SP-D) are used as markers of active IP . KL-6 is an epithelial mucin and also membrane glycoprotein classified as cluster 9. KL-6 is more prominent in injured type II pneumocytes, and leaked into blood flow [6, 8]. SP-A and SP-D are calcium-dependent lectins, and prominently produced by type II pneumocytes and Clara cells in injured lung . PCP infection leads the accumulation of neutrophils and CD8 lymphocytes, and elicits the inflammatory mediator of macrophage inflammatory protein (MIP)-2, interleukin (IL)-8, and tumor necrosis factor (TNF)-α [10, 11]. Mechansims of elevation of serum markers in PCP are thought that these mediators induce type II pneumocytes damages or hyperplasia, and this affects the elevations of KL-6, SP-A and SP-D on serum levels. Although elevation of serum levels of KL-6 and SP-A are reported in PCP, while elevation of the serum (1→3) β-D-glucan (β-D-glucan) level has been reported as a marker of PCP [12, 13], whether these markers are affected by P. jirovecii colonization has not yet been investigated in IP patients. In the present study, we prospectively examined colonization by P. jirovecii in IP patients, including those with idiopathic pulmonary fibrosis (IPF) or collagen vascular disease-related interstitial pneumonia (CVD), and also examined P. jirovecii in patients with chronic bronchitis or pneumonia (CB/Pneumonia). Furthermore, we compared the levels of these serum markers between IP patients with or without P. jirovecii colonization to determine whether the markers were affected by colonization.
A total of 75 patients were enrolled in this prospective study. The IPF group (n = 29, men/women = 18/11, age = 64.7 ± 10.2 years) included 22 patients with usual interstitial pneumonia (UIP) and 7 patients with non-specific interstitial pneumonia (NSIP). The CVD group (n = 19, men/women = 10/9, age = 63.6 ± 7.8 years) included 11 patients with rheumatoid arthritis, 3 with polymyositis, 2 with polyarteritis nodosa, 1 with dermatomyositis, 1 with mixed connective tissue disease, and 1 with Sjögren syndrome. The CB/Pneumonia group (n = 20) included 10 men and 10 women aged 66.8 ± 9.5 years. The PCP group (n = 7, men/women = 4/3, age = 61.6 ± 10.8 years) included 1 patient with ulcerative colitis, 3 with lung cancer, 1 with adrenal deficiency, 1 with human immunodeficiency virus, and 1 with polymyositis. The numbers of patients who received the oral corticosteroid therapy were 11 patients in UIP, 5 patients in NSIP, 14 patients in CVD and 1 patient in PCP. The diagnosis of IPF was made by using the American Thoracic Society/European Respiratory Society (ATS/ERS) International Multidisciplinary Consensus Classification of Idiopathic Interstitial Pneumonias . PCP was diagnosed from the detection of P. jirovecii DNA in sputum or BAL by PCR, typical radiographic features, typical symptoms , and the course of chest symptoms and pulmonary changes on CT or chest radiographs. A diagnosis of P. jirovecii colonization was based on the detection of P. jirovecii DNA in induced sputum by PCR, no changes of chest X-ray films or chest CT scans for two months, no change of oxygen saturation for two months, no past or current PCP infection or HIV infection, no treatment with ST for PCP, and no clinical signs of PCP . Patients receiving oral corticosteroids at doses above 5 mg/day were defined as the IP patients on corticosteroid therapy. This study was conducted according to the guidelines of the Declaration of Helsinki and approved by institutional review board. All of the patients are given written informed consent.
Induced sputum samples were collected after inhalation of ultrasonically nebulized hypertonic saline. Sputum samples were subjected to PCR according to the method of Wakefield et al [17, 18] using AmpliTaq DNA polymerase (Roche Diagnostics, Switzerland) and a PJ-2000 thermal cycler (Perkin Elmer, U.S.A). A peripheral blood sample was collected, and the lymphocyte count, CD4 T cell count, and serum KL-6 level were measured as described previously . SP-A and SP-D were measured by using the SP-A test Kokusai F kit (Sysmex, Japan) and SP-D Yamasa EIA kit (Yamasa, Japan), respectively [7, 20]. β-D-glucan was measured by the β-D-glucan test (Wako, Japan) based on a kinetic turbidmetric assay .
Categorical data were compared by using the chi-squared test or Fisher's exact test. The significance of differences between groups was calculated by Dunnet's test after the Kruskal-Wallis test. The relation of oral corticosteroid therapy (odds ratio) to P. jirovecii colonization was calculated by using the chi-squared test for comparison between IP patients receiving oral corticosteroids and those not on corticosteroid therapy. The significance of differences between IP patients on oral corticosteroid therapy with P. jirovecii colonization and IP patients on corticosteroid therapy without P. jirovecii colonization was calculated by the Man-Whitney test. Statistical significance was defined as P <0.05.
The rate of P. jirovecii colonization on pulmonary diseases
Serum marker levels and lymphocytes count in pulmonary diseases
P. jirovecii colonization occurs in patients with chronic respiratory disease, even in the absence of HIV infection . The P. jirovecii colonization rate is 15.5% in pregnant women  and 10% to 40% in chronic obstructive disease (COPD) patients [1, 24, 25]. In the present study, IP patients who received oral corticosteroid therapy had a high P. jirovecii colonization rate of 23.3%. Oral steroid therapy was a statistical risk factor for P. jirovecii colonization. Furthermore, the serum β-D-glucan level and the lymphocyte count were useful to distinguish IP with P. jirovecii colonization patients from PCP patients, while serum SP-A, SP-D, and KL-6 levels were not useful. These serum markers were not affected by P. jirovecii colonization.
β-D-glucan is a major component of the P. jirovecii cyst wall . Infection is established by adhesion of the trophic form of Pneumocystis to the alveolar epithelium, where it proliferates . One of the reasons for the different levels of β-D-glucan in PCP and P. jirovecii colonization was considered to be Pneumocystis proliferation. Cyst wall β-D-glucan is partly responsible for the inflammatory response in the lung [28, 29]. SP-A and SP-D levels were reported to be affected by PCP infection via inflammatory mediators [10, 11] or reported to influence on PCP infection, and to play a role in host defenses against P. jirovecii [30–32]. Based on these reports, we examined serum KL-6, SP-A, and SP-D levels in IP patients with or without P. jirovecii colonization on oral corticosteroids. Our results indicated that these markers did not show any difference between IP patients with and without P. jirovecii colonization, suggesting that KL-6, SP-A, and SP-D levels were not affected by P. jirovecii colonization in IP patients. Although there has been a report that P. jirovecii colonization plays a role in systemic inflammation in COPD patients , we did not examine the effect of P. jirovecii on other cytokines or on disease progression. To determine the effect of P. jirovecii colonization on serum markers, it would be necessary to compare the changes of each marker when new P. jirovecii colonization occurs in a patient. Since present study did not show the affect of P. jirovecii colonization on serum markers of KL-6, SP-A and SP-D, we could not determine the value of prophylaxis with ST for IP patients with P. jirovecii colonization against pulmonary injury. There are unsolved problems regarding droplet transmission of P. jirovecii and the existence of drug-resistant organisms associated with prophylaxis of ST. Further analysis will be needed to determine the efficacy of ST prophylaxis for IP patients with P. jirovecii colonization on oral corticosteroid therapy.
Recently, quantification of P. jirovecii DNA by real-time PCR targeting the heat shock protein 70 gene was reported to be useful for discrimination between colonization and infection with this organism . When P. jirovecii is detected in sputum or bronchoalveolar lavage (BAL) fluid from a patient with exacerbation of IP, the clinician has to determine whether a patient has infection or colonization. To make a diagnosis of PCP, real-time PCR of the HSP 70 gene might be used in the clinical setting.
In conclusion, serum markers (KL-6, SP-A, and SP-D) were not higher in IP patients with P. jirovecii colonization than in those without colonization. IP patients receiving oral corticosteroid therapy had a high prevalence of P. jirovecii colonization, and oral corticosteroids are a risk factor for colonization. When patients develop exacerbation of IP, to diagnosis PCP or P. jirovecii colonization, it seems to be useful to know in advance whether the patient is a carrier of P. jirovecii, and to also examine the serum β-D-glucan level and the peripheral lymphocyte count.
The authors thank medical staffs of Gunma University and Jobu hospital for their expert assistance.
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