EBV and CMV as possible pathogens in patients presenting with interstitial lung disease
M. P. D. Deege, S. F. T. Thijsen, R. Luderer, J. W. A. Rossen, A. M. V. Loon, J. M. H. V. Gorp, A. W. J. Bossink (Utrecht, Netherlands)
Source: Annual Congress 2006 - Virus-induced respiratory tract infection
Session: Virus-induced respiratory tract infection
Session type: Oral Presentation
Number: 967
Disease area: Interstitial lung diseases
Abstract Introduction Interstitial lung abnormalities may be due to a wide range of disorders. Medical work-up including a bronchoalveolar lavage (BAL) not always results in a diagnosis. To elucidate a possible role of herpes virus in the pathogenesis of interstitial lung abnormalities, Epstein-Barr (EBV) and Cytomegalovirus (CMV) viral loads were determined in BAL fluid and serum. Methods In this prospective study, 33 patients with new interstitial lung abnormalities, who underwent a BAL were included. In most cases matching serum was obtained. BAL fluids and sera were analysed for the presence of EBV- and CMV-DNA using real-time EBV- and CMV-PCR. EBV and CMV serology was carried out on available specimens. Results Seventeen (52%) out of 33 BAL specimens contained EBV DNA (median 3043, range 183-4,000,000 geq/mL). From 25 of 33 patients serum was available. In 6 (46%) out of 13 patients with an EBV positive BAL fluid, EBV DNA was present in serum (median 427, range 70-2,098 geq/mL). EBV DNA was not detectable in the sera (0/12) of patients with an EBV negative BAL fluid (p=0.015). CMV DNA was detectable in 5 out of 31 (16%) BAL specimens (median 1,725, range 163-2,800,435 geq/mL). In 3 out of these 5 (60%) serum CMV PCR was positive (median 677, range 296-4,474 geq/mL). CMV DNA was not detected in serum (0/19) of patients with a CMV negative BAL result (p=0.005). Conclusions 1. EBV is detectable in BAL fluid in a remarkable number of cases presenting with interstitial lung disease, whereas CMV seems to play a much less prominent role. 2. Systemic reactivation, reflected by positive PCR results in serum, of both EBV or CMV infection was only seen in patients with EBV- or CMV-PCR positive BAL fluids.
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M. P. D. Deege, S. F. T. Thijsen, R. Luderer, J. W. A. Rossen, A. M. V. Loon, J. M. H. V. Gorp, A. W. J. Bossink (Utrecht, Netherlands). EBV and CMV as possible pathogens in patients presenting with interstitial lung disease. Eur Respir J 2006; 28: Suppl. 50, 967
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