Improved diagnosis of extrapulmonary tuberculosis by antigen detection using immunochemistry-based assay. Tehmina Mustafa
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1 Improved diagnosis of extrapulmonary tuberculosis by antigen detection using immunochemistry-based assay Tehmina Mustafa
2 Overview Introduction: extrapulmonary tuberculosis (TB) & diagnostic challenges New diagnostic method Biopsies Fluids Further research plans
3 Burden & distribution of extrapulmonary TB Both, 9% Extrapulmonary, 20% Pleural, 18% Lymphatic, 42% Pulmonary, 71% Other, 13% Bone/joint, 11% Genitourinary, 5% Source: United States, CDC, 2008 Peritoneal, 6% Meningeal, 5%
4 Burden of extrapulmonary TB (2) HIV-TB co-nfection- > 50% extrapulmonary Pediatric TB higher proportion extrapulmonary
5 Is extrapulmonary TB infectious? EPTB /sputum neg TB accounts for 13% of TB transmission (Tostmann, 2008) Transmission from genitourinary TB ( D Agata, 2001)
6 Diagnostic challenges EPTB Clinical criteria without lab: over-diagnosis (~25%) Acid-fast stain/microscopy: detection limit bacilli/ml Culture: detection limit 100 bacilli/ml Histology/cytology differentiation from other granulomatous diseases atypical histological with HIV coinfection PCR based methods: better sensitivity, expensive, PCR machine, sensitive to contamination Serology: not recommended
7 Immunohistochemistry & immunocytochemistry Immunochemistry - more sensitive than acid fast staining- intact bacillary cell-wall is not a prerequisite. Potential to distinguish between different mycobacterial species. Limited studies for use as a diagnostic test probably due to nonavailability of specific antibodies for M.tuberculosis antigens
8 MPT64 antigen In-house rabbit polyclonal antibody for detection of MPT64 antigen: 26-kDa secreted mycobacterial protein specific for the M.tuberculosis complex Distinguish pathogenic from atypical mycobacteria.
9 Material Extrapulmonary TB Lymph nodes Pleura Abdomen CNS Tissue biopsies- pleura, lymph nodes, abdominal TB Cell smears-pleural fluid, ascitic fluid, CSF & lymph node aspirates
10 Diagnostic procedures Acid-fast staing Culture (LJ medium) Immunohistochemistry/immunocytochemistry PCR for IS6110 (specific for M.tuberculosis complex)
11 Positive results of diagnostic procedure in TB and non-tb biopsies
12 Validity of MPT64-IHC as diagnostic test PCR for IS6110 (specific for M.tuberculosis complex) was used as gold standard Tissues Sensitivity Specificity LYMPH GLAND Norway (n=32) Tanzania (n=35) India (n=152 ) ABDOMINAL TB India (n=51) Pleura (HIV-coinfection) South Africa (n=36) (80) (100)
13 M.tuberculosis specific protein MPT64 in TB lymph nodes MPT64 10x 10x 40x
14 M.tuberculosis specific protein MPT64 in TB lymph nodes
15 M.tuberculosis specific protein MPT64 antigen in abdominal TB lesions Intestinal wall Peritoneum
16 Mycobacterial MPT64 antigen in HIV-TB coinfected pleural TB lesions Granulomatous inflammation, n=14 MPT64
17 Mycobacterial MPT64 antigen in HIV-TB coinfected pleural TB lesions- atypical histology H&E stain Acid-fast stain IHC-MPT64 IHC- MPT64
18 Positive results of various diagnostic procedures on fluids & aspirate
19 Immunocytochemical staining of mycobacterial antigen MPT64 CSF Pleural fluid B LN Aspirate Ascitic fluid D
20 Validation of Immunocytochemistry Nested-PCR used as gold standard Sensitivity = 96% Specificity = 96%
21 Conclusion Immunochemistry with a-mpt64 is: rapid, sensitive and specific method for establishing etiological diagnosis of TB unlike PCR, not sensitive to contamination, does not require sofisticated equipment, can be established in a pathology/cytology lab.
22 Further Research To assess the feasibility of implementation and validity of the assay in the routine diagnostic settings To assess improvement in case detection comparing the intervention and control hospitals. To improve the diagnostic capacity and sustain the quality at the TB diagnostic laboratories in low-income settings by training and academic building of the staff. Cost-effectiveness analysis of the assay after implementation at selected hospitals for future scale-up.
23 A hospital implementing WHO endorsed DOTS strategy and a pathology laboratory will be selected from each of the 5 sites; Tanzania, Zanzibar, India, Pakistan,and Norway. 1-3 control from each site (except Norway)
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