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Journal article

QuantiFERON conversion following tuberculin administration is common in HIV infection and relates to baseline response.

Abstract:

Background

HIV-1 infection impairs tuberculosis (TB) specific immune responses affecting the diagnosis of latent TB. We aimed to (1) determine the proportion of HIV-1-infected adults with a negative QuantiFERON®-TB Gold in-tube (QFT-GIT) and Tuberculin skin testing (TST) that convert to QFT-GIT positive following TST, and (2) evaluate the relationship between conversion and baseline QFT-GIT results.

Methods

HIV-1 infected adults being screened for a TB vaccine study in South Africa underwent QFT-GIT followed by TST. As per protocol, QFT-GIT was repeated if randomization was delayed allowing for evaluation of TST boosting in a proportion of participants.

Results

Of the 22 HIV-1 infected, TST and QFT-GIT negative adults (median CD4 477/mm^3 IQR 439–621) who had QFT-GIT repeated after median 62 days (IQR 49–70), 40.9 % (95 % CI 18.6–63.2 %) converted. Converters had a significantly greater increase in the background subtracted TB antigen response (TBAg-Nil–all units IU/mL) following TST, 0.82 (IQR 0.39–1.28) vs 0.03 (IQR−0.05–0.06),p= 0.0001. Those who converted also had a significantly higher baseline TBAg-Nil 0.21(IQR 0.17–0.26) vs 0.02(IQR 0.01–0.07),p= 0.002. Converters did not differ with regard to CD4 count or ART status. ROC analysis showed a baseline cut off of 0.15 correctly classified 86.4 % of converters with 88.9 % sensitivity.

Conclusions

Our findings support the possibility that there are 2 distinct groups in an HIV-1 infected population with negative QFT-GIT and TST; a true negative group and a group showing evidence of a weak Mtb specific immune response that boosts significantly following TST resulting in conversion of the test result that may represent false negatives. Further evaluation of whether a lower cut off may improve sensitivity of QFT-GIT in this population is warranted.

Publication status:
Published
Peer review status:
Peer reviewed

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Publisher copy:
10.1186/s12879-016-1875-6

Authors


More by this author
Institution:
University of Oxford
Division:
MSD
Department:
RDM
Sub department:
RDM Clinical Laboratory Sciences
Role:
Author


Publisher:
BioMed Central
Journal:
BMC Infectious Diseases More from this journal
Volume:
16
Issue:
1
Pages:
545
Publication date:
2016-10-01
Acceptance date:
2016-09-27
DOI:
ISSN:
1471-2334
Pmid:
27717329


Language:
English
Keywords:
Pubs id:
pubs:652354
UUID:
uuid:e06df011-b35e-43b6-be7b-acefffec800a
Local pid:
pubs:652354
Source identifiers:
652354
Deposit date:
2016-10-13

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