Detection of M-tuberculosis DNA in sarcoidosis: Correlation with T-cell response

Citation
M. Grosser et al., Detection of M-tuberculosis DNA in sarcoidosis: Correlation with T-cell response, LAB INV, 79(7), 1999, pp. 775-784
Citations number
43
Categorie Soggetti
Medical Research General Topics
Journal title
LABORATORY INVESTIGATION
ISSN journal
00236837 → ACNP
Volume
79
Issue
7
Year of publication
1999
Pages
775 - 784
Database
ISI
SICI code
0023-6837(199907)79:7<775:DOMDIS>2.0.ZU;2-G
Abstract
The pathogenetic role of Mycobacterium tuberculosis (M. tuberculosis) in tu berculosis is well defined, whereas its role in sarcoidosis is controversia l. In sarcoidosis, activation of T-helper cells is observed, which is compa rable to tuberculosis. The aim of this study was first to investigate wheth er M. tuberculosis DNA could be retrospectively detected in samples of pati ents with clinically verified sarcoidosis by polymerase chain reaction (PCR ) and second, to analyze the relationship between M. tuberculosis DNA posit ive samples and T-cell response in sarcoidosis patients. Formalin fixed par affin-embedded lung tissues or cell sediments of bronchoalveolar lavage, re spectively, from 65 patients with sarcoidosis and lung tissues from 40 tube rculosis patients were investigated by means of different PCR assays in com parison to control samples. The primers used were derived from insertion se quence IS 986/6110 specific for the M. tuberculosis complex (123 bp PCR) an d from the gene encoding the 38 kDa protein antigen b (419 bp PCR). The 123 bp assay yielded a specificity of 97% and a sensitivity of 95%. In contras t, the 419 bp PCR method showed a lower sensitivity of only 8% likely becau se of possible DNA degradation during fixation and embedding procedures of the tissue and the fact that this PCR uses a single copy element as target. We amplified the M. tuberculosis complex specific 123 bp fragment in 64% o f samples from sarcoidosis patients. The specificity of PCR products in the se cases was confirmed by DNA sequencing. Interestingly in the M. tuberculo sis positive sarcoidoses, we found increased serum levels of soluble interl eukin-2 receptor in correlation to the sarcoidosis stages (p < 0.05). In co nclusion, the determination of M. tuberculosis by PCR alone does not permit a differentiation between sarcoidosis and tuberculosis. However these resu lts support the contention that M. tuberculosis may play a pathogenetic rol e at least in the part of sarcoidosis patients with elevated interleukin-2 receptor values.