Longitudinal assessment of an ELISPOT test for Mycobacterium tuberculosis infection

Very little longitudinal information is available regarding the performance of T cell-based tests for Mycobacterium tuberculosis infection. To address this deficiency, we conducted a longitudinal assessment of the enzyme-linked immunosorbent spot test (ELISPOT) test in comparison to the standard tub...

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Veröffentlicht in:PLoS medicine 2007-06, Vol.4 (6), p.e192-e192
Hauptverfasser: Hill, Philip C, Brookes, Roger H, Fox, Annette, Jackson-Sillah, Dolly, Jeffries, David J, Lugos, Moses D, Donkor, Simon A, Adetifa, Ifedayo M, de Jong, Bouke C, Aiken, Alex M, Adegbola, Richard A, McAdam, Keith P
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container_end_page e192
container_issue 6
container_start_page e192
container_title PLoS medicine
container_volume 4
creator Hill, Philip C
Brookes, Roger H
Fox, Annette
Jackson-Sillah, Dolly
Jeffries, David J
Lugos, Moses D
Donkor, Simon A
Adetifa, Ifedayo M
de Jong, Bouke C
Aiken, Alex M
Adegbola, Richard A
McAdam, Keith P
description Very little longitudinal information is available regarding the performance of T cell-based tests for Mycobacterium tuberculosis infection. To address this deficiency, we conducted a longitudinal assessment of the enzyme-linked immunosorbent spot test (ELISPOT) test in comparison to the standard tuberculin skin test (TST). In tuberculosis (TB) contacts we repeated ELISPOT tests 3 mo (n = 341) and 18 mo (n = 210) after recruitment and TSTs at 18 mo (n = 130). We evaluated factors for association with conversion and reversion and investigated suspected cases of TB. Of 207 ELISPOT-negative contacts, 51 (24.6%) had 3-mo ELISPOT conversion, which was associated with a positive recruitment TST (odds ratio [OR] 2.2, 95% confidence interval [CI] 1.0-5.0, p = 0.048) and negatively associated with bacillus Calmette-Guérin (BCG) vaccination (OR 0.5, 95% CI 0.2-1.0, p = 0.06). Of 134 contacts, 54 (40.2%) underwent 3-mo ELISPOT reversion, which was less likely in those with a positive recruitment TST (OR 0.3, 95% CI 0.1-0.8, p = 0.014). Between 3 and 18 mo, 35/132 (26.5%) contacts underwent ELISPOT conversion and 28/78 (35.9%) underwent ELISPOT reversion. Of the 210 contacts with complete results, 73 (34.8%) were ELISPOT negative at all three time points; 36 (17.1%) were positive at all three time points. Between recruitment and 18 mo, 20 (27%) contacts had ELISPOT conversion; 37 (50%) had TST conversion, which was associated with a positive recruitment ELISPOT (OR 7.2, 95% CI 1.4-37.1, p = 0.019); 18 (32.7%) underwent ELISPOT reversion; and five (8.9%) underwent TST reversion. Results in 13 contacts diagnosed as having TB were mixed, but suggested higher TST sensitivity. Both ELISPOT conversion and reversion occur after M. tuberculosis exposure. Rapid ELISPOT reversion may reflect M. tuberculosis clearance or transition into dormancy and may contribute to the relatively low reported ELISPOT conversion rate. Therefore, a negative ELISPOT test for M. tuberculosis infection should be interpreted with caution.
doi_str_mv 10.1371/journal.pmed.0040192
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To address this deficiency, we conducted a longitudinal assessment of the enzyme-linked immunosorbent spot test (ELISPOT) test in comparison to the standard tuberculin skin test (TST). In tuberculosis (TB) contacts we repeated ELISPOT tests 3 mo (n = 341) and 18 mo (n = 210) after recruitment and TSTs at 18 mo (n = 130). We evaluated factors for association with conversion and reversion and investigated suspected cases of TB. Of 207 ELISPOT-negative contacts, 51 (24.6%) had 3-mo ELISPOT conversion, which was associated with a positive recruitment TST (odds ratio [OR] 2.2, 95% confidence interval [CI] 1.0-5.0, p = 0.048) and negatively associated with bacillus Calmette-Guérin (BCG) vaccination (OR 0.5, 95% CI 0.2-1.0, p = 0.06). Of 134 contacts, 54 (40.2%) underwent 3-mo ELISPOT reversion, which was less likely in those with a positive recruitment TST (OR 0.3, 95% CI 0.1-0.8, p = 0.014). 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This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited: Hill PC, Brookes RH, Fox A, Jackson-Sillah D, Jeffries DJ, et al. (2007) Longitudinal Assessment of an ELISPOT Test for Mycobacterium tuberculosis Infection. 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To address this deficiency, we conducted a longitudinal assessment of the enzyme-linked immunosorbent spot test (ELISPOT) test in comparison to the standard tuberculin skin test (TST). In tuberculosis (TB) contacts we repeated ELISPOT tests 3 mo (n = 341) and 18 mo (n = 210) after recruitment and TSTs at 18 mo (n = 130). We evaluated factors for association with conversion and reversion and investigated suspected cases of TB. Of 207 ELISPOT-negative contacts, 51 (24.6%) had 3-mo ELISPOT conversion, which was associated with a positive recruitment TST (odds ratio [OR] 2.2, 95% confidence interval [CI] 1.0-5.0, p = 0.048) and negatively associated with bacillus Calmette-Guérin (BCG) vaccination (OR 0.5, 95% CI 0.2-1.0, p = 0.06). Of 134 contacts, 54 (40.2%) underwent 3-mo ELISPOT reversion, which was less likely in those with a positive recruitment TST (OR 0.3, 95% CI 0.1-0.8, p = 0.014). Between 3 and 18 mo, 35/132 (26.5%) contacts underwent ELISPOT conversion and 28/78 (35.9%) underwent ELISPOT reversion. Of the 210 contacts with complete results, 73 (34.8%) were ELISPOT negative at all three time points; 36 (17.1%) were positive at all three time points. Between recruitment and 18 mo, 20 (27%) contacts had ELISPOT conversion; 37 (50%) had TST conversion, which was associated with a positive recruitment ELISPOT (OR 7.2, 95% CI 1.4-37.1, p = 0.019); 18 (32.7%) underwent ELISPOT reversion; and five (8.9%) underwent TST reversion. Results in 13 contacts diagnosed as having TB were mixed, but suggested higher TST sensitivity. Both ELISPOT conversion and reversion occur after M. tuberculosis exposure. Rapid ELISPOT reversion may reflect M. tuberculosis clearance or transition into dormancy and may contribute to the relatively low reported ELISPOT conversion rate. Therefore, a negative ELISPOT test for M. tuberculosis infection should be interpreted with caution.</description><subject>Adolescent</subject><subject>Adult</subject><subject>Aged</subject><subject>Antigens, Bacterial - immunology</subject><subject>Bacteria</subject><subject>Bacterial infections</subject><subject>Bacterial Proteins - immunology</subject><subject>Cohort Studies</subject><subject>Comparative analysis</subject><subject>Confidence intervals</subject><subject>Contact Tracing</subject><subject>Databases, Factual</subject><subject>DNA, Bacterial - genetics</subject><subject>Enzyme-Linked Immunosorbent Assay</subject><subject>Enzymes</subject><subject>False Negative Reactions</subject><subject>Female</subject><subject>Follow-Up Studies</subject><subject>Gambia - epidemiology</subject><subject>Genetic aspects</subject><subject>Humans</subject><subject>Immune system</subject><subject>Immunology</subject><subject>Immunology and allergy</subject><subject>Infections</subject><subject>Infectious Diseases</subject><subject>Interferon-gamma - analysis</subject><subject>Male</subject><subject>Medicine in Developing Countries</subject><subject>Middle Aged</subject><subject>Mycobacterium tuberculosis - immunology</subject><subject>Mycobacterium tuberculosis - isolation &amp; purification</subject><subject>Predictive Value of Tests</subject><subject>Public Health</subject><subject>Public Health and Epidemiology</subject><subject>Reproducibility of Results</subject><subject>Respiratory Medicine</subject><subject>Sensitivity and Specificity</subject><subject>Skin</subject><subject>Sputum - microbiology</subject><subject>T-Lymphocytes - immunology</subject><subject>T-Lymphocytes - metabolism</subject><subject>Time Factors</subject><subject>Tuberculin Test</subject><subject>Tuberculosis</subject><subject>Tuberculosis - diagnosis</subject><subject>Tuberculosis - epidemiology</subject><subject>Tuberculosis - immunology</subject><subject>Tuberculosis - microbiology</subject><issn>1549-1676</issn><issn>1549-1277</issn><issn>1549-1676</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2007</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><sourceid>BENPR</sourceid><sourceid>DOA</sourceid><recordid>eNqVk1-L1DAUxYso7rr6DUQLwoIPMyZp_vVFWJZVB0ZHnNXXkKRpJ0PbjEkq7rc341SdyjwofWhJfvecm5PeLHsKwRwWDL7ausH3sp3vOlPNAcAAluhedg4JLmeQMnr_6PssexTCFgBUghI8zM4gIxRjzs6z9dL1jY1DZZNWLkMwIXSmj7mrc9nnN8vF-uPqNo8mxLx2Pn9_p52SOhpvhy6PgzJeD60LNuS2r42O1vWPswe1bIN5Mr4vss9vbm6v382Wq7eL66vlTLMCx1lVmFoCUjKkSImBVKyqNMKQVIpDigutJC0kxhWBpjAIQW1KWBBYl0BKyoviInt-0N2lBsSYRxAQcQ5KxglPxOJAVE5uxc7bTvo74aQVPxecb4T00erWCKZqSqVKvrzCDCClMAGAElQDihjau70e3QaVItcpJC_bieh0p7cb0bhvAvLUNmRJ4HIU8O7rkAIVnQ3atK3sjRuCoBwSkI6ZwBd_gafPNjtQjUztp_BdctWN6U0yd72pbVq-gpSWnDNIEz8_waenMp3VJwteTgoSE8332MghBLFYf_oP9sO_s6svU_byiN0Y2cZNcO2w_83CFMQHUHsXgjf174uBQOzn5VeGYj8vYpyXVPbs-FL_FI0DUvwA7ZgPMA</recordid><startdate>20070601</startdate><enddate>20070601</enddate><creator>Hill, Philip C</creator><creator>Brookes, Roger H</creator><creator>Fox, Annette</creator><creator>Jackson-Sillah, Dolly</creator><creator>Jeffries, David J</creator><creator>Lugos, Moses D</creator><creator>Donkor, Simon A</creator><creator>Adetifa, Ifedayo M</creator><creator>de Jong, Bouke C</creator><creator>Aiken, Alex M</creator><creator>Adegbola, Richard A</creator><creator>McAdam, Keith P</creator><general>Public Library of Science</general><general>Public Library of Science (PLoS)</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>IOV</scope><scope>ISN</scope><scope>ISR</scope><scope>3V.</scope><scope>7TK</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BENPR</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>K9.</scope><scope>M0S</scope><scope>M1P</scope><scope>PIMPY</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>7X8</scope><scope>5PM</scope><scope>DOA</scope><scope>CZK</scope></search><sort><creationdate>20070601</creationdate><title>Longitudinal assessment of an ELISPOT test for Mycobacterium tuberculosis infection</title><author>Hill, Philip C ; 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To address this deficiency, we conducted a longitudinal assessment of the enzyme-linked immunosorbent spot test (ELISPOT) test in comparison to the standard tuberculin skin test (TST). In tuberculosis (TB) contacts we repeated ELISPOT tests 3 mo (n = 341) and 18 mo (n = 210) after recruitment and TSTs at 18 mo (n = 130). We evaluated factors for association with conversion and reversion and investigated suspected cases of TB. Of 207 ELISPOT-negative contacts, 51 (24.6%) had 3-mo ELISPOT conversion, which was associated with a positive recruitment TST (odds ratio [OR] 2.2, 95% confidence interval [CI] 1.0-5.0, p = 0.048) and negatively associated with bacillus Calmette-Guérin (BCG) vaccination (OR 0.5, 95% CI 0.2-1.0, p = 0.06). Of 134 contacts, 54 (40.2%) underwent 3-mo ELISPOT reversion, which was less likely in those with a positive recruitment TST (OR 0.3, 95% CI 0.1-0.8, p = 0.014). Between 3 and 18 mo, 35/132 (26.5%) contacts underwent ELISPOT conversion and 28/78 (35.9%) underwent ELISPOT reversion. Of the 210 contacts with complete results, 73 (34.8%) were ELISPOT negative at all three time points; 36 (17.1%) were positive at all three time points. Between recruitment and 18 mo, 20 (27%) contacts had ELISPOT conversion; 37 (50%) had TST conversion, which was associated with a positive recruitment ELISPOT (OR 7.2, 95% CI 1.4-37.1, p = 0.019); 18 (32.7%) underwent ELISPOT reversion; and five (8.9%) underwent TST reversion. Results in 13 contacts diagnosed as having TB were mixed, but suggested higher TST sensitivity. Both ELISPOT conversion and reversion occur after M. tuberculosis exposure. Rapid ELISPOT reversion may reflect M. tuberculosis clearance or transition into dormancy and may contribute to the relatively low reported ELISPOT conversion rate. Therefore, a negative ELISPOT test for M. tuberculosis infection should be interpreted with caution.</abstract><cop>United States</cop><pub>Public Library of Science</pub><pmid>17564487</pmid><doi>10.1371/journal.pmed.0040192</doi><tpages>10</tpages><oa>free_for_read</oa></addata></record>
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source MEDLINE; DOAJ Directory of Open Access Journals; Elektronische Zeitschriftenbibliothek - Frei zugängliche E-Journals; PubMed Central; Public Library of Science (PLoS)
subjects Adolescent
Adult
Aged
Antigens, Bacterial - immunology
Bacteria
Bacterial infections
Bacterial Proteins - immunology
Cohort Studies
Comparative analysis
Confidence intervals
Contact Tracing
Databases, Factual
DNA, Bacterial - genetics
Enzyme-Linked Immunosorbent Assay
Enzymes
False Negative Reactions
Female
Follow-Up Studies
Gambia - epidemiology
Genetic aspects
Humans
Immune system
Immunology
Immunology and allergy
Infections
Infectious Diseases
Interferon-gamma - analysis
Male
Medicine in Developing Countries
Middle Aged
Mycobacterium tuberculosis - immunology
Mycobacterium tuberculosis - isolation & purification
Predictive Value of Tests
Public Health
Public Health and Epidemiology
Reproducibility of Results
Respiratory Medicine
Sensitivity and Specificity
Skin
Sputum - microbiology
T-Lymphocytes - immunology
T-Lymphocytes - metabolism
Time Factors
Tuberculin Test
Tuberculosis
Tuberculosis - diagnosis
Tuberculosis - epidemiology
Tuberculosis - immunology
Tuberculosis - microbiology
title Longitudinal assessment of an ELISPOT test for Mycobacterium tuberculosis infection
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