Clinical Utility of a Commercial LAM-ELISA Assay for TB Diagnosis in HIV-Infected Patients Using Urine and Sputum Samples

被引:110
作者
Dheda, Keertan [1 ,2 ,3 ,5 ]
Davids, Virginia [1 ,2 ]
Lenders, Laura [1 ,2 ]
Roberts, Teri [3 ]
Meldau, Richard [1 ,2 ]
Ling, Daphne [7 ]
Brunet, Laurence [7 ]
Smit, Richard van Zyl [1 ,2 ]
Peter, Jonathan [1 ,2 ]
Green, Clare [5 ]
Badri, Motasim [4 ]
Sechi, Leonardo [8 ]
Sharma, Surendra [9 ]
Hoelscher, Michael [11 ]
Dawson, Rodney [1 ,2 ]
Whitelaw, Andrew [10 ]
Blackburn, Jonathan [3 ,6 ]
Pai, Madhukar [7 ]
Zumla, Alimuddin [5 ]
机构
[1] Univ Cape Town, Dept Med, Div Pulmonol & Clin Immunol, Lung Infect & Immun Unit, ZA-7925 Cape Town, South Africa
[2] Univ Cape Town, Dept Med, UCT Lung Inst, ZA-7925 Cape Town, South Africa
[3] Univ Cape Town, Inst Infect Dis & Mol Med, ZA-7925 Cape Town, South Africa
[4] Univ Cape Town, Dept Med, Clin Res Support Unit, ZA-7925 Cape Town, South Africa
[5] UCL, Sch Med, Dept Infect, Ctr Infect Dis & Int Hlth, London W1N 8AA, England
[6] Univ Cape Town, Div Med Biochem, ZA-7925 Cape Town, South Africa
[7] McGill Univ, Dept Epidemiol Biostat & Occupat Hlth, Montreal, PQ, Canada
[8] Univ Sardinia, Dipartimento Sci Biomed, Sassari, Italy
[9] All India Inst Med Sci, Dept Med, Div Pulm Crit Care & Sleep Med, New Delhi 110029, India
[10] Univ Cape Town, Div Med Microbiol, ZA-7925 Cape Town, South Africa
[11] Klinikum Univ Munich, Dept Infect Dis & Trop Med, Munich, Germany
基金
英国医学研究理事会; 加拿大健康研究院; 欧盟第七框架计划;
关键词
MYCOBACTERIAL LIPOARABINOMANNAN; ACTIVE TUBERCULOSIS; BURDEN; TECHNOLOGIES;
D O I
10.1371/journal.pone.0009848
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Background: The accurate diagnosis of TB in HIV-infected patients, particularly with advanced immunosuppression, is difficult. Recent studies indicate that a lipoarabinomannan (LAM) assay (Clearview-TB (R)-ELISA) may have some utility for the diagnosis of TB in HIV-infected patients; however, the precise subgroup that may benefit from this technology requires clarification. The utility of LAM in sputum samples has, hitherto, not been evaluated. Methods: LAM was measured in sputum and urine samples obtained from 500 consecutively recruited ambulant patients, with suspected TB, from 2 primary care clinics in South Africa. Culture positivity for M. tuberculosis was used as the reference standard for TB diagnosis. Results: Of 440 evaluable patients 120/387 (31%) were HIV-infected. Urine-LAM positivity was associated with HIV positivity (p = 0.007) and test sensitivity, although low, was significantly higher in HIV-infected compared to uninfected patients (21% versus 6%; p<0.001), and also in HIV-infected participants with a CD4 <200 versus <200 cells/mm(3) (37% versus 0%; p = 0.003). Urine-LAM remained highly specific in all 3 subgroups (95%-100%). 25% of smear-negative but culture-positive HIV-infected patients with a CD4 <200 cells/mm(3) were positive for urine-LAM. Sputum-LAM had good sensitivity (86%) but poor specificity (15%) likely due to test cross-reactivity with several mouth-residing organisms including actinomycetes and nocardia species. Conclusions: These preliminary data indicate that in a high burden primary care setting the diagnostic usefulness of urine-LAM is limited, as a rule-in test, to a specific patient subgroup i.e. smear-negative HIV-infected TB patients with a CD4 count <200 cells/mm(3), who would otherwise have required further investigation. However, even in this group sensitivity was modest. Future and adequately powered studies in a primary care setting should now specifically target patients with suspected TB who have advanced HIV infection.
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