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Journal of Clinical Microbiology, February 2004, p. 665-669, Vol. 42, No. 2
0095-1137/04/$08.00+0     DOI: 10.1128/JCM.42.2.665-669.2004
Copyright © 2004, American Society for Microbiology. All Rights Reserved.

Association of Presence of Aspergillus Antibodies with Hemoptysis in Patients with Old Tuberculosis or Bronchiectasis but No Radiologically Visible Mycetoma

Chung-ming Chu,¹ Patrick C. Y. Woo,² Ken T. K. Chong,² Wah-shing Leung,¹ Veronica L. Chan,¹ and Kwok-yung Yuen^2,3*

Division of Respiratory Medicine, Department of Medicine, United Christian Hospital,¹ Department of Microbiology, The University of Hong Kong,² HKU-Pasteur Research Centre, Hong Kong³

Received 25 July 2003/ Returned for modification 23 October 2003/ Accepted 8 November 2003

Top Abstract Introduction Materials and Methods Results Discussion References

 
Old tuberculosis and bronchiectasis are the two most important causes of chronic structural changes of lungs in our locality. In the absence of radiologically visible mycetoma, the cause of hemoptysis in these two groups of patients is largely unknown. A 17-month prospective study was carried out to compare the prevalence of Aspergillus fumigatus and Aspergillus flavus antibodies in hemoptysis patients with old tuberculosis or bronchiectasis but no radiologically visible mycetoma (cases, n = 38), hemoptysis patients with other diagnosis (control group 1, n = 29), and patients with old tuberculosis or bronchiectasis but no hemoptysis (control group 2, n = 47) by a recently developed sensitive and specific A. fumigatus and A. flavus antibody assay. There were a significantly larger number of patients with antibody against A. fumigatus or A. flavus among the cases than among the patients in control groups 1 and 2 (P < 0.05 in both comparisons). Molds were not recovered from any of the patients. Among the 10 cases with Aspergillus antibody, eight and two had antibody against A. flavus and A. fumigatus, respectively. We conclude that there was an association between the presence of Aspergillus antibodies and hemoptysis in patients with old tuberculosis or bronchiectasis, suggesting that these patients probably had occult infections caused by the corresponding fungi. Development of serological tests against other Aspergillus species as well as other causes of mycetoma will probably increase the detection of occult mold infections in patients with existing parenchymal lung diseases, and treatment of fungal microinvasion may help to alleviate hemoptysis in these patients with bronchiectasis or old tuberculosis who have Aspergillus antibodies.

Top Abstract Introduction Materials and Methods Results Discussion References

 
Hemoptysis is one of the frequent complications in patients with old tuberculosis or bronchiectasis. It is well known that molds will colonize and proliferate in the lung parenchymal cavities of patients with old tuberculosis, leading to mycetoma formation. Fungal species that have been implicated as causative agents of mycetoma include Aspergillus species, Pseudallescheria boydii, Coccidioides species, Penicillium species, Cladosporium cladosporioides, and Schizophyllum commune, of which the most common are Aspergillus species (4, 9, 11, 13-15, 20). The true incidence of aspergillous mycetoma, or aspergilloma, is unknown, but it has been estimated that it occurs in 11 to 17% of patients with tuberculous cavities (1). The most frequent symptom associated with mycetoma is hemoptysis, which occurs in about 74% of these patients, and the hemoptysis may occasionally be massive and life-threatening. However, the causes of hemoptysis in most cases of hemoptysis complicating old tuberculosis without mycetoma formation are still unknown. As for bronchiectasis, although bronchial artery proliferation has been shown to be associated with hemoptysis, the role of molds in causing hemoptysis in these patients is largely unknown (12).

Recently, we cloned the AFMP1 and AFLMP1 genes, which encode the first antigenic cell wall secretory galactomannoproteins Afmp1p and Aflmp1p, respectively, in Aspergillus fumigatus and Aspergillus flavus, respectively (18, 21). Furthermore, we have shown that serological assays with recombinant Afmp1p are sensitive and specific for the diagnosis of aspergilloma (3, 17). Clinical evaluation revealed that the assay was 100% sensitive for patients with aspergilloma caused by A. fumigatus, and no false-positive results were found for serum samples from 80 healthy blood donors, six patients with typhoid fever, four patients with melioidosis, 20 patients with penicilliosis marneffei, five patients with candidiasis, and four patients with cryptococcosis, indicating a high specificity of the test.

In this study, with the help of these antibody assays and mold cultures of bronchoalveolar lavage specimens, we compared the prevalence of A. fumigatus and A. flavus antibodies in patients with hemoptysis complicating old tuberculosis or bronchiectasis but no radiologically apparent mycetoma formation on high-resolution computed tomography (HRCT) scan, those with hemoptysis due to other causes, and those with old tuberculosis or bronchiectasis but without hemoptysis. The role of molds in causing occult microinvasion and hemoptysis in patients with existing structural abnormalities of the lung parenchyma is also discussed.

Top Abstract Introduction Materials and Methods Results Discussion References

 
Patients, study design, and inclusion criteria. The study protocol was reviewed and approved by the Hospital Ethics Committee. Patients presenting to the Department of Medicine & Geriatrics of the United Christian Hospital in Hong Kong with hemoptysis as the predominant symptom in a 17-month period (June 2001 to October 2002) were recruited to the study. Clinical details were recorded on a standard form. Complete blood counts, liver and renal function tests, and coagulation studies were performed. Serum antineutrophil cytoplasmic antibodies were checked for diagnosis of pulmonary hemorrhage associated with vasculitis. Sputum specimens were collected for bacterial, fungal, and mycobacterial cultures and cytological examination for malignant cells. Chest radiographs were taken and examined by a thoracic radiologist. Patients who had an obvious diagnosis at this stage (e.g., active tuberculosis) without further need for bronchoscopy and HRCT of the thorax were excluded from the study.

All patients finally included in the study were subject to fiber optic bronchoscopic examination and HRCT of the thorax. Bronchial washes were obtained from the segment corresponding to the abnormal areas on radiographs and were sent for bacterial, fungal, and mycobacterial cultures. Bronchial and transbronchial biopsy specimens were obtained as appropriate. HRCT of the thorax was examined by a thoracic radiologist, and the presence of bronchiectasis and lesions suggestive of mycetoma were noted. Blood was collected for A. fumigatus and A. flavus antibody detection.

The final diagnosis was reached after analysis of the clinical, laboratory, and radiological findings. Patients with a final diagnosis of allergic bronchopulmonary aspergillosis and mycetoma were excluded from the final statistical analysis. Allergic bronchopulmonary aspergillosis is defined by a history of asthma, circulating blood eosinophilia of more than 1,000 eosinophils/ml, immediate cutaneous reactivity to Aspergillus skin test antigen, precipitating antibodies against Aspergillus antigen, elevated total serum immunoglobulin E concentration, history of recurrent pulmonary infiltrates, and central bronchiectasis. Mycetoma is defined by the presence of a mobile mass within an existing cavity (air crescent sign) on HRCT, with or without culture of mold from respiratory tract specimens.

The patients with a final diagnosis of hemoptysis complicating bronchiectasis or old tuberculosis were considered cases, and those with any other diagnosis for their hemoptysis were considered controls (control group 1). A case of old tuberculosis was defined by a history of tuberculosis with a documented completed course of antituberculous treatment and a documented bacteriological cure and/or a chest radiograph or HRCT of the thorax showing fibrocalcified or cavitary lesions that had been stable over time. A case of bronchiectasis was defined by compatible clinical features with HRCT showing bronchial dilation, bronchial wall thickening, lack of normal bronchial tapering, or air-fluid levels in distended bronchi.

During the same study period, another group of patients followed up in the same department for old tuberculosis or bronchiectasis but without a history of hemoptysis were also recruited (control group 2). Blood was collected for A. fumigatus and A. flavus antibody detection, but bronchoscopic examinations were not performed with these patients as they did not have hemoptysis.

Detection of antibody against A. fumigatus and A. flavus. Detection of antibody against Afmp1p of A. fumigatus and Aflmp1p of A. flavus was performed by enzyme-linked immunosorbent assays (ELISAs), with positive results confirmed by Western blot assay (3, 17, 18). For the ELISA, each well of an immunoplate (Nunc, Roskilde, Denmark) was coated with 0.5 ng of purified glutathione S-transferase (GST)-Afmp1p or GST-Aflmp1p protein for 12 h and then blocked in phosphate-buffered saline with 2% bovine serum albumin. One hundred microliters of patient serum at 1:3,000 dilution was added to the wells of the recombinant protein-coated plates in a total volume of 100 µl and incubated at 37°C for 2 h. After washing with washing buffer (phosphate-buffered saline with 2% bovine serum albumin) three times, 100 µl of 1:10,000-diluted horseradish peroxidase-conjugated goat anti-human antibody (Zymed, S. San Francisco, Calif.) was added to the wells and incubated at 37°C for 30 min. After washing with washing buffer three times, 100 µl of 3,3',5,5'-tetramethylbenzidine single solution (Zymed) was added to each well and incubated at room temperature for 15 min. One hundred microliters of 0.3 M H₂SO₄ was added, and the absorbance at 405 nm of each well was measured. Each sample was tested in duplicate, and the mean absorbance for each serum was calculated.

For the Western blot assays, recombinant Afmp1p and Aflmp1p samples were run on sodium dodecyl sulfate-10% polyacrylamide gels and electroblotted onto nitrocellulose membranes (Bio-Rad, Hercules, Calif.). The blots were cut into strips and the strips were incubated with patient sera diluted 1:500. Antigen-antibody interaction was detected with the ECL fluorescence kit (Amersham Life Science, Buckinghamshire, United Kingdom).

Statistical analysis. Comparison was made between the characteristics of cases and those of control groups 1 and 2. Comparisons of continuous variables were performed with a one-way analysis of variance test, and post hoc analyses were performed with Bonferroni's correction. A Mann-Whitney test and chi-square test were used for nonparametric and categorical variables, respectively. Comparison was also made between the characteristics of cases positive for antibody and those negative for antibody against A. fumigatus or A. flavus. A P of <0.05 was considered statistically significant.

Top Abstract Introduction Materials and Methods Results Discussion References

 
A total of 125 patients were recruited into the study. One patient had allergic bronchopulmonary aspergillosis and 10 had mycetoma and were therefore excluded, leaving 114 patients in the final analysis (mean age = 63.5 years, male/female ratio = 82:32). Thirty-eight patients (33.3%) were cases, with 9 (7.9%) and 29 (25.4%) having final diagnoses of old tuberculosis and bronchiectasis, respectively. Twenty-nine patients (25.4%) were in control group 1, with the breakdown of their diagnoses depicted in Table 1. Forty-seven patients (41.2%) were in control group 2, with 17 (14.9%) bronchiectasis and 30 (26.3%) old tuberculosis diagnoses.

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TABLE 1. Diagnosis of patients in the case and control groups

A comparison of the characteristics of patients with hemoptysis who had bronchiectasis or old tuberculous cavities (cases) and the two control groups is shown in Table 2. Cases had significantly larger number of patients with histories of hemoptysis, significantly larger hemoptysis blood volume, significantly larger number of patients with positive bacterial growth in their bronchial washing specimens, and significantly larger number of patients with antibody against A. fumigatus or A. flavus than patients in control group 1 (P < 0.05 in all four comparisons). Furthermore, cases also had a significantly larger number of patients with antibody against A. fumigatus or A. flavus than patients in control group 2 (P < 0.05). Molds were recovered from none of the patients.

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TABLE 2. Comparison of characteristics of patients with hemoptysis who had bronchiectasis or old tuberculous cavities (cases) and those with other diagnoses (control group 1) and bronchiectasis or old tuberculous cavities without hemoptysis (control group 2)

Since positive bacterial growth could be a confounding factor in the statistical analysis, further analysis was performed after removal of data for cases and controls with positive bacterial growth in their bronchial washing specimens (14 from cases and 4 from control group 1). In this subset analysis, 8 out of the 24 patients in the cases but only 1 out of the 25 patients in control group 1 had antibody against A. fumigatus or A. flavus (P < 0.01), indicating that the presence of Aspergillus antibodies is independently associated with bronchiectasis or old tuberculosis in patients with hemoptysis.

The characteristics of patients with hemoptysis who had bronchiectasis or old tuberculous cavities (cases) positive for antibodies against A. fumigatus or A. flavus are shown in Table 3. The median age was 64.5 years (range, 46 to 78 years). The male/female ratio was 6:4. The median number of hemoptysis episodes in the past was one (range, 0 to 6). The median volume of hemoptysis blood was 200 (range, 10 to 1,000) ml. Seven (70%) and three (30%) cases had bronchiectasis and old tuberculosis, respectively. Eight (80%) and two (20%) cases had antibody against A. flavus and A. fumigatus, respectively (Fig. 1).

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TABLE 3. Characteristics of cases positive for antibodies against Aspergillus fumigatus or Aspergillus flavus

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FIG. 1. Western blot analysis of purified Aflmp1p of A. flavus (A) and Afmp1p of A. fumigatus (B). The lane numbers correspond to the patient numbers in Table 3. Strong antigen-antibody interaction was detected with the sera of eight patients against Aflmp1p (lanes 1, 2, 3, 4, 6, 7, 8, and 9) (A) and those of two patients against Afmp1p (lanes 5 and 10) (B).

A comparison of the characteristics of cases that were positive and negative for antibodies against A. fumigatus or A. flavus is shown in Table 4. Cases that were positive for antibodies against A. fumigatus or A. flavus had significantly lower hemoglobin levels and significantly higher erythrocyte sedimentation rates.

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TABLE 4. Comparison of cases positive and negative for antibodies against Aspergillus fumigatus or Aspergillus flavus

Top Abstract Introduction Materials and Methods Results Discussion References

 
Old tuberculosis and bronchiectasis are the two most important causes of chronic structural changes in lungs in our locality. Since one of the most important causes of bronchiectasis in our locality is old tuberculosis, it is often difficult to distinguish between the two categories, and there is significant overlap between the two groups of patients. In this study, we demonstrated that the prevalence of A. fumigatus and A. flavus antibodies in patients presenting with hemoptysis who had old tuberculosis or bronchiectasis without radiologically visible mycetoma formation was significantly higher than those with hemoptysis due to other causes. Because of the possibility that the difference was due just to the association of Aspergillus infections with old tuberculosis and bronchiectasis but was not related to hemoptysis, another group of controls, patients with old tuberculosis or bronchiectasis without hemoptysis (control group 2), was selected. It was also demonstrated that the presence of Aspergillus antibodies in patients with old tuberculosis or bronchiectasis with hemoptysis was significantly higher than in those without hemoptysis, indicating that the presence of Aspergillus antibodies was associated with hemoptysis in patients with old tuberculosis or bronchiectasis.

As for fungal culture, despite the presence of antibodies, Aspergillus species were not recovered from any of the respiratory tract specimens collected from the patients. In fact, among the 10 patients with mycetoma that we excluded from the study, only three had positive mold cultures, one with A. fumigatus and two with A. flavus. This is in line with the low rate of positive culture of only about 40% in patients with mycetoma reported in another study (10). Due to the very small lesions of less than 5 mm that were not detected by computed tomography scans, a very small amount of fungal shedding, and the possibility of the presence of cells in a viable but nonculturable state, it is not surprising that none of the cases yielded positive mold culture results.

We speculate that Aspergillus species causes hemoptysis in patients with old tuberculosis or bronchiectasis without mycetoma formation through microinvasion of the damaged respiratory epithelium. It has been demonstrated that A. fumigatus secretes fumagillin, a chemical that inhibits angiogenesis (7). Similarly, Aspergillus clavatus secretes cytochalasin E, which is a potent and selective inhibitor of capillary endothelial cell proliferation in an experimental model (16). On the other hand, it has been shown that in patients with aspergillomas, the levels of vascular endothelial growth factor (VEGF) in serum were raised, and the level was related to the area of lung involvement, PaO₂ level, and the presence of hemoptysis (8). Furthermore, the expression of VEGF was high in alveolar macrophages in the lesion of aspergillomas, and VEGF expression in macrophages was induced by hypoxia and lactate and its expression promoted angiogenesis and increased vascular permeability (5, 19).

We speculate that the immediate surrounding of an aspergilloma is rendered ischemic by substances like fumagillin and cytochalasin E, enhancing necrosis and inflammation. Subsequent recruitment of alveolar macrophages into this hypoxic environment induces the macrophage to express VEGF, which enhances angiogenesis around the aspergilloma. Thus, it is conceivable that Aspergillus species might set foot on damaged respiratory epithelium in bronchiectasis and old tuberculous cavities and that the interplay between antiangiogenic factors secreted by the Aspergillus species and VEGF secreted by alveolar macrophages promote necrosis and hypervascularity around the infected areas. In the present study, the patients with confirmed diagnoses of bronchiectasis or old tuberculosis with Aspergillus antibody tended to bleed significantly. The definition of massive hemoptysis has ranged from 100 to 1,000 ml in 24 h (6). If one takes 100 ml as the cutoff, 7 out of the 10 patients with bronchiectasis or old tuberculosis and Aspergillus antibody had massive hemoptysis. This is also supported by the fact that the seropositive cases had significantly lower hemoglobin levels, and they showed a trend to bleed more than the seronegative patients.

In Western countries, A. fumigatus is the most important Aspergillus species that causes invasive aspergillosis and aspergilloma. On the other hand, A. flavus is the most common one associated with human disease in our locality and in other Asian countries (2, 22). In our previous study, we demonstrated that A. flavus is responsible for causing 38% whereas A. fumigatus is responsible for causing only 19% of invasive mold diseases in bone marrow transplant recipients. This is in line with the observation in the present study, in that 80% of the seropositive patients had antibody against A. flavus, whereas only 20% of them had antibody against A. fumigatus. In fact, in the 10 patients with mycetoma diagnosed in the period of the study, four of them were positive for A. flavus antibody, but only two were positive for A. fumigatus antibody.

Development of serological tests against other Aspergillus species as well as other causes of mycetoma will probably increase the detection of occult mold infections in patients with preexisting parenchymal lung diseases. We have demonstrated that Aspergillus antibody assays are highly sensitive and specific for the diagnosis of aspergilloma. However, only 6 of the 10 patients with mycetoma diagnosed in the period of the study had antibody against A. fumigatus or A. flavus. Furthermore, we have also demonstrated that 28% of the invasive mold diseases in our bone marrow transplant recipients were caused by Aspergillus species other than A. fumigatus and A. flavus (22). It is therefore logical to assume that the remaining four patients with mycetoma were infected by Aspergillus species other than A. fumigatus or A. flavus or other molds such as P. boydii and Penicillium species (4, 9, 11, 13-15, 20). We speculate that about six to seven out of the 37 patients with bronchiectasis or old tuberculosis should be positive for antibody against other Aspergillus species or other molds.

Treatment of fungal microinvasion may help to alleviate the hemoptysis in these patients with bronchiectasis or old tuberculosis who had Aspergillus antibody. Massive hemoptysis in patients with bronchiectasis or old tuberculosis can be life-threatening and is a condition dreaded by patients and clinicians alike. Due to their marginal respiratory functions, these patients are often poor surgical candidates for resection of the diseased lung segments affected by bronchiectasis and inactive tuberculosis. Bronchial arterial embolization may afford palliation in some patients, but new collateral formation and rebleeding may occur in the long run (6). As mold microinvasion may be the cause of hemoptysis in these patients, further studies with antifungal therapy may open up a new avenue of treatment for some of these patients with hemoptysis complicating bronchiectasis or old tuberculosis.

 
This work was partly supported by Research Grant Council grant HKU 7388/00 M, AIDS Trust Fund (MSS 083), University Development Fund, and Committee of Research and Conference Grant, University of Hong Kong.

We thank King-man Chan and Andy S. P. Leung for technical help.

 
* Corresponding author. Mailing address: Department of Microbiology, The University of Hong Kong, University Pathology Building, Queen Mary Hospital, Hong Kong. Phone: (852) 28554892. Fax: (852) 28551241. E-mail: hkumicro{at}hkucc.hku.hk.

Top Abstract Introduction Materials and Methods Results Discussion References

 

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Journal of Clinical Microbiology, February 2004, p. 665-669, Vol. 42, No. 2
0095-1137/04/$08.00+0     DOI: 10.1128/JCM.42.2.665-669.2004
Copyright © 2004, American Society for Microbiology. All Rights Reserved.

This article has been cited by other articles:

• Chong, K. T. K., Woo, P. C. Y., Lau, S. K. P., Huang, Y., Yuen, K.-y. (2004). AFMP2 Encodes a Novel Immunogenic Protein of the Antigenic Mannoprotein Superfamily in Aspergillus fumigatus. J. Clin. Microbiol. 42: 2287-2291 [Abstract] [Full Text]  

This Article Abstract Full Text (PDF) Alert me when this article is cited Alert me if a correction is posted Services Similar articles in this journal Similar articles in PubMed Alert me to new issues of the journal Download to citation manager Reprints and Permissions Copyright Information Books from ASM Press MicrobeWorld Citing Articles Citing Articles via HighWire Citing Articles via Google Scholar Google Scholar Articles by Chu, C.-m. Articles by Yuen, K.-y. Search for Related Content PubMed PubMed Citation Articles by Chu, C.-m. Articles by Yuen, K.-y.