TY - JOUR
T1 - Cytomegalovirus infection is a risk factor for tuberculosis disease in infants
AU - Müller, Julius
AU - Tanner, Rachel
AU - Matsumiya, Magali
AU - Snowden, Margaret A.
AU - Landry, Bernard
AU - Satti, Iman
AU - Harris, Stephanie A.
AU - O'Shea, Matthew K.
AU - Stockdale, Lisa
AU - Marsay, Leanne
AU - Chomka, Agnieszka
AU - Harrington-Kandt, Rachel
AU - Thomas, Zita Rose Manjaly
AU - Naranbhai, Vivek
AU - Stylianou, Elena
AU - Mbandi, Stanley Kimbung
AU - Hatherill, Mark
AU - Hussey, Gregory
AU - Mahomed, Hassan
AU - Tameris, Michele
AU - Bruce McClain, J.
AU - Evans, Thomas G.
AU - Hanekom, Willem A.
AU - Scriba, Thomas J.
AU - McShane, Helen
AU - Fletcher, Helen A.
N1 - Funding Information:
We thank study participants and their families, the community of Cape Winelands East district, and South African Tuberculosis Vaccine Initiative (SATVI) personnel. This work was funded by Aeras and The Wellcome Trust with support from the European Commission within the 7th framework program (FP7) NEWT-BVAC (grant no. HEALTH-F3-2009-241745) and by the European Commission within Horizon2020 TBVAC2020 (grant no. H2020 PHC-643381). HM was a Wellcome Trust Senior Clinical Research Fellow.
Publisher Copyright:
© 2019, Müller et al.
PY - 2019/12/5
Y1 - 2019/12/5
N2 - Immune activation is associated with increased risk of tuberculosis (TB) disease in infants. We performed a case-control analysis to identify drivers of immune activation and disease risk. Among 49 infants who developed TB disease over the first 2 years of life, and 129 healthy matched controls, we found the cytomegalovirus-stimulated (CMV-stimulated) IFN- response to be associated with CD8+ T cell activation (Spearman's rho, P = 6 × 10 8). A CMV-specific IFN- response was also associated with increased risk of developing TB disease (conditional logistic regression; P = 0.043; OR, 2.2; 95% CI, 1.02 4.83) and shorter time to TB diagnosis (Log Rank Mantel-Cox, P = 0.037). CMV+ infants who developed TB disease had lower expression of NK cell associated gene signatures and a lower frequency of CD3 CD4 CD8 lymphocytes. We identified transcriptional signatures predictive of TB disease risk among CMV ELISpot positive (area under the receiver operating characteristic [AUROC], 0.98, accuracy, 92.57%) and negative (AUROC, 0.9; accuracy, 79.3%) infants; the CMV signature was validated in an independent infant study (AUROC, 0.71; accuracy, 63.9%). A 16-gene signature that previously identified adolescents at risk of developing TB disease did not accurately classify case and control infants in this study. Understanding the microbial drivers of T cell activation, such as CMV, could guide new strategies for prevention of TB disease in infants.
AB - Immune activation is associated with increased risk of tuberculosis (TB) disease in infants. We performed a case-control analysis to identify drivers of immune activation and disease risk. Among 49 infants who developed TB disease over the first 2 years of life, and 129 healthy matched controls, we found the cytomegalovirus-stimulated (CMV-stimulated) IFN- response to be associated with CD8+ T cell activation (Spearman's rho, P = 6 × 10 8). A CMV-specific IFN- response was also associated with increased risk of developing TB disease (conditional logistic regression; P = 0.043; OR, 2.2; 95% CI, 1.02 4.83) and shorter time to TB diagnosis (Log Rank Mantel-Cox, P = 0.037). CMV+ infants who developed TB disease had lower expression of NK cell associated gene signatures and a lower frequency of CD3 CD4 CD8 lymphocytes. We identified transcriptional signatures predictive of TB disease risk among CMV ELISpot positive (area under the receiver operating characteristic [AUROC], 0.98, accuracy, 92.57%) and negative (AUROC, 0.9; accuracy, 79.3%) infants; the CMV signature was validated in an independent infant study (AUROC, 0.71; accuracy, 63.9%). A 16-gene signature that previously identified adolescents at risk of developing TB disease did not accurately classify case and control infants in this study. Understanding the microbial drivers of T cell activation, such as CMV, could guide new strategies for prevention of TB disease in infants.
UR - https://www.scopus.com/pages/publications/85076674335
U2 - 10.1172/jci.insight.130090
DO - 10.1172/jci.insight.130090
M3 - Article
C2 - 31697647
AN - SCOPUS:85076674335
SN - 2379-3708
VL - 4
JO - JCI Insight
JF - JCI Insight
IS - 23
M1 - e130090
ER -