Simultaneous measurement of antigen-stimulated interleukin-1β and gamma interferon production enhances test sensitivity for the detection of Mycobacterium bovis infection in cattle

Clinical and Vaccine Immunology

Volumn 17, Issue 12, 2010, Pages 1946-1951

  Jones, Gareth J ^a   Pirson, Chris ^a   Hewinson, R Glyn ^a   Vordermeier, H Martin ^a  

^a VETERINARY LABORATORIES AGENCY   (United Kingdom)

Author keywords

[No Author keywords available]

Indexed keywords

ANTIGEN; EARLY SECRETORY ANTIGENIC TARGET 6; GAMMA INTERFERON; INTERLEUKIN 10; INTERLEUKIN 12; INTERLEUKIN 1BETA; INTERLEUKIN 4; MACROPHAGE INFLAMMATORY PROTEIN 1BETA; TUMOR NECROSIS FACTOR ALPHA;

ARTICLE; BACTERIUM DETECTION; BOVINE TUBERCULOSIS; CATTLE; CONTROLLED STUDY; CYTOKINE PRODUCTION; DIAGNOSTIC PROCEDURE; MYCOBACTERIUM BOVIS; NONHUMAN; PRIORITY JOURNAL; RECEIVER OPERATING CHARACTERISTIC; SENSITIVITY AND SPECIFICITY;

ANIMALS; ANTIGENS, BACTERIAL; BACTERIAL PROTEINS; BACTERIOLOGICAL TECHNIQUES; BLOOD; CATTLE; CELLS, CULTURED; IMMUNOASSAY; INTERFERON-GAMMA; INTERLEUKIN-1BETA; MYCOBACTERIUM BOVIS; ROC CURVE; SENSITIVITY AND SPECIFICITY; TUBERCULIN; TUBERCULOSIS, BOVINE; TUMOR NECROSIS FACTOR-ALPHA;

EID: 78649875896     PISSN: 15566811     EISSN: 1556679X     Source Type: Journal    
DOI: 10.1128/CVI.00377-10     Document Type: Article

References (26)

1. Boom, W. H. 1996. The role of T-cell subsets in Mycobacterium tuberculosis infection. Infect. Agents Dis. 5:73-81.
2. Chegou, N. N., G. F. Black, M. Kidd, P. D. van Helden, and G. Walzl. 2009. Host markers in QuantiFERON supernatants differentiate active TB from latent TB infection: preliminary report. BMC Pulm. Med. 9:21.
3. Coad, M., D. Clifford, S. G. Rhodes, R. G. Hewinson, H. M. Vordermeier, and A. O. Whelan. 2010. Repeat tuberculin skin testing leads to desensitisation in naturally infected tuberculous cattle which is associated with elevated interleukin-10 and decreased interleukin-1β responses. Vet. Res. 41:14.
4. Cooper, A. M., D. K. Dalton, T. A. Stewart, J. P. Griffin, D. G. Russell, and I. M. Orme. 1993. Disseminated tuberculosis in interferon gamma gene-disrupted mice. J. Exp. Med. 178:2243-2247.
5. Cosivi, O., J. M. Grange, C. J. Daborn, M. C. Raviglione, T. Fujikura, D. Cousins, R. A. Robinson, H. F. Huchzermeyer, I. de Kantor, and F. X. Meslin. 1998. Zoonotic tuberculosis due to Mycobacterium bovis in developing countries. Emerg. Infect. Dis. 4:59-70.
6. de la Rua-Domenech, R., A. T. Goodchild, H. M. Vordermeier, R. G. Hewinson, K. H. Christiansen, and R. S. Clifton-Hadley. 2006. Ante mortem diagnosis of tuberculosis in cattle: a review of the tuberculin tests, gamma-interferon assay and other ancillary diagnostic techniques. Res. Vet. Sci. 81:190-210.
7. Denis, M., and B. M. Buddle. 2008. Bovine dendritic cells are more permissive for Mycobacterium bovis replication than macrophages, but release more IL-12 and induce better immune T-cell proliferation. Immunol. Cell Biol. 86:185-191.
8. Fremond, C. M., D. Togbe, E. Doz, S. Rose, V. Vasseur, I. Maillet, M. Jacobs, B. Ryffel, and V. F. Quesniaux. 2007. IL-1 receptor-mediated signal is an essential component of MyD88-dependent innate response to Mycobacterium tuberculosis infection. J. Immunol. 179:1178-1189.
9. Grange, J. M. 2001. Mycobacterium bovis infection in human beings. Tuberculosis (Edinb.) 81:71-77.
10. Hernandez-Pando, R., H. Orozco, K. Arriaga, A. Sampieri, J. Larriva-Sahd, and V. Madrid-Marina. 1997. Analysis of the local kinetics and localization of interleukin-1α, tumour necrosis factor-α and transforming growth factor-β, during the course of experimental pulmonary tuberculosis. Immunology 90:607-617.
11. Juffermans, N. P., S. Florquin, L. Camoglio, A. Verbon, A. H. Kolk, P. Speelman, S. J. van Deventer, and T. van Der Poll. 2000. Interleukin-1 signaling is essential for host defense during murine pulmonary tuberculosis. J. Infect. Dis. 182:902-908.
12. Kazwala, R. R., C. J. Daborn, J. M. Sharp, D. M. Kambarage, S. F. Jiwa, and N. A. Mbembati. 2001. Isolation of Mycobacterium bovis from human cases of cervical adenitis in Tanzania: a cause for concern? Int. J. Tuberc. Lung Dis. 5:87-91.
13. Koo, I. C., C. Wang, S. Raghavan, J. H. Morisaki, J. S. Cox, and E. J. Brown. 2008. ESX-1-dependent cytolysis in lysosome secretion and inflammasome activation during mycobacterial infection. Cell. Microbiol. 10:1866-1878.
14. Kurenuma, T., I. Kawamura, H. Hara, R. Uchiyama, S. Daim, S. R. Dewamitta, S. Sakai, K. Tsuchiya, T. Nomura, and M. Mitsuyama. 2009. The RD1 locus in the Mycobacterium tuberculosis genome contributes to activation of caspase-1 via induction of potassium ion efflux in infected macrophages. Infect. Immun. 77:3992-4001.
15. Masters, S. L., L. A. Mielke, A. L. Cornish, C. E. Sutton, J. O'Donnell, L. H. Cengia, A. W. Roberts, I. P. Wicks, K. H. Mills, and B. A. Croker. 2010. Regulation of interleukin-1β by interferon-γ is species specific, limited by suppressor of cytokine signalling 1 and influences interleukin-17 production. EMBO Rep. 11:640-646.
16. Mayer-Barber, K. D., D. L. Barber, K. Shenderov, S. D. White, M. S. Wilson, A. Cheever, D. Kugler, S. Hieny, P. Caspar, G. Nunez, D. Schlueter, R. A. Flavell, F. S. Sutterwala, and A. Sher. 2010. Caspase-1 independent IL-1β production is critical for host resistance to Mycobacterium tuberculosis and does not require TLR signaling in vivo. J. Immunol. 184:3326-3330.
17. Mishra, B. B., P. Moura-Alves, A. Sonawane, N. Hacohen, G. Griffiths, L. F. Moita, and E. Anes. 2010. Mycobacterium tuberculosis protein ESAT-6 is a potent activator of the NLRP3/ASC inflammasome. Cell. Microbiol. 12:1046-1063.
18. Orme, I. M., and A. M. Cooper. 1999. Cytokine/chemokine cascades in immunity to tuberculosis. Immunol. Today 20:307-312.
19. Raices, R. M., Y. Kannan, A. Sarkar, V. Bellamkonda-Athmaram, and M. D. Wewers. 2008. A synergistic role for IL-1β and TNFα in monocyte-derived IFNγ inducing activity. Cytokine 44:234-241.
20. Rodwell, T. C., M. Moore, K. S. Moser, S. K. Brodine, and S. A. Strathdee. 2008. Tuberculosis from Mycobacterium bovis in binational communities, United States. Emerg. Infect. Dis. 14:909-916.
21. Sidders, B., C. Pirson, P. J. Hogarth, R. G. Hewinson, N. G. Stoker, H. M. Vordermeier, and K. Ewer. 2008. Screening of highly expressed mycobacterial genes identifies Rv3615c as a useful differential diagnostic antigen for the Mycobacterium tuberculosis complex. Infect. Immun. 76:3932-3939.
22. Thacker, T. C., M. V. Palmer, and W. R. Waters. 2007. Associations between cytokine gene expression and pathology in Mycobacterium bovis infected cattle. Vet. Immunol. Immunopathol. 119:204-213.
23. Vordermeier, H. M., A. Whelan, P. J. Cockle, L. Farrant, N. Palmer, and R. G. Hewinson. 2001. Use of synthetic peptides derived from the antigens ESAT-6 and CFP-10 for differential diagnosis of bovine tuberculosis in cattle. Clin. Diagn. Lab. Immunol. 8:571-578.
24. Wallis, R. S., M. Amir-Tahmasseb, and J. J. Ellner. 1990. Induction of interleukin 1 and tumor necrosis factor by mycobacterial proteins: the monocyte Western blot. Proc. Natl. Acad. Sci. U. S. A. 87:3348-3352.
25. Waters, W. R., M. V. Palmer, D. L. Whipple, M. P. Carlson, and B. J. Nonnecke. 2003. Diagnostic implications of antigen-induced gamma interferon, nitric oxide, and tumor necrosis factor alpha production by peripheral blood mononuclear cells from Mycobacterium bovis-infected cattle. Clin. Diagn. Lab. Immunol. 10:960-966.
26. Wood, P. R., and S. L. Jones. 2001. BOVIGAM: an in vitro cellular diagnostic test for bovine tuberculosis. Tuberculosis (Edinb.) 81:147-155.