4.7 Article

Effects of Pregnancy and Isoniazid Preventive Therapy on Mycobacterium tuberculosis Interferon Gamma Response Assays in Women With HIV

期刊

CLINICAL INFECTIOUS DISEASES
卷 73, 期 9, 页码 E3555-E3562

出版社

OXFORD UNIV PRESS INC
DOI: 10.1093/cid/ciaa1083

关键词

latent tuberculosis infection; interferon gamma response assays; pregnancy; HIV infection; isoniazid preventive therapy

资金

  1. National Institute of Allergy and Infectious Diseases (NIAID) of the National Institutes of Health (NIH) [UM1AI068632, UM1AI068616, UM1AI106716]
  2. Eunice Kennedy Shriver National Institute of Child Health and Human Development (NICHD) of the National Institutes of Health (NIH) [UM1AI068632, UM1AI068616, UM1AI106716]
  3. National Institute of Mental Health (NIMH) of the National Institutes of Health (NIH) [UM1AI068632, UM1AI068616, UM1AI106716]
  4. NICHD [HHSN275201800001I]
  5. NIH [AI110527, AI077505, UM1AI069465, R01HD081929]

向作者/读者索取更多资源

This study found that immune suppression during pregnancy may lead to decreased QuantiFERON-gold-in-tube (QGIT) positivity for latent tuberculosis infection (LTBI) due to reduced interferon gamma responses. Tuberculin skin test (TST) was less affected by pregnancy and had lower positivity compared to QGIT. Isoniazid preventive therapy (IPT) was associated with loss of QGIT positivity, suggesting potential clinical implications that need further investigation.
Background. Pregnancy is accompanied by immune suppression. We hypothesized that Mycobacterium tuberculosis-specific inflammatory responses used to identify latent tuberculosis infection (LTBI) lose positivity during pregnancy. We also hypothesized that isoniazid preventive therapy (IPT) may revert LTBI diagnoses because of its sterilizing activity. Methods. 944 women with human immunodeficiency virus infection (HIV) participating in a randomized, double-blind, placebo-controlled study comparing 28 weeks of IPT antepartum versus postpartum, were tested by QuantiFERON-gold-in-tube (QGIT) antepartum and by QGIT and tuberculin skin test (TST) at delivery and postpartum. Serial QGIT positivity was assessed by logistic regression using generalized estimating equations. Results. From entry to delivery, 68 (24%) of 284 QGIT-positive women reverted to QGIT-negative or indeterminate. Of these, 42 (62%) recovered QGIT positivity postpartum. The loss of QGIT positivity during pregnancy was explained by decreased interferon gamma (IFN.) production in response to TB antigen and/or mitogen. At delivery, LTBI was identified by QGIT in 205 women and by TST in 113 women. Corresponding numbers postpartum were 229 and 122 women. QGIT and TST kappa agreement coefficients were 0.4 and 0.5, respectively. Among QGIT-positive women antepartum or at delivery, 34 (12%) reverted to QGIT-negative after IPT. There were no differences between women who initiated IPT antepartum or postpartum. Conclusions. Decreased IFN. responses in pregnancy reduced QGIT positivity, suggesting that this test cannot reliably rule out LTBI during pregnancy. TST was less affected by pregnancy, but had lower positivity compared to QGIT at all time points. IPT was associated with loss of QGIT positivity, the potential clinical consequences of which need to be investigated.

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