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Impact of Intermediate Hyperglycemia and Diabetes on Immune Dysfunction in Tuberculosis.

Authors :
Eckold, Clare
Kumar, Vinod
Weiner, January
Alisjahbana, Bachti
Riza, Anca-Lelia
Ronacher, Katharina
Coronel, Jorge
Kerry-Barnard, Sarah
Malherbe, Stephanus T
Kleynhans, Leanie
Stanley, Kim
Ruslami, Rovina
Ioana, Mihai
Ugarte-Gil, Cesar
Walzl, Gerhard
Crevel, Reinout van
Wijmenga, Cisca
Critchley, Julia A
Dockrell, Hazel M
Cliff, Jacqueline M
Source :
Clinical Infectious Diseases. Jan2021, Vol. 72 Issue 1, p69-78. 10p.
Publication Year :
2021

Abstract

Background People with diabetes have an increased risk of developing active tuberculosis (TB) and are more likely to have poor TB-treatment outcomes, which may impact on control of TB as the prevalence of diabetes is increasing worldwide. Blood transcriptomes are altered in patients with active TB relative to healthy individuals. The effects of diabetes and intermediate hyperglycemia (IH) on this transcriptomic signature were investigated to enhance understanding of immunological susceptibility in diabetes-TB comorbidity. Methods Whole blood samples were collected from active TB patients with diabetes (glycated hemoglobin [HbA1c] ≥6.5%) or IH (HbA1c = 5.7% to <6.5%), TB-only patients, and healthy controls in 4 countries: South Africa, Romania, Indonesia, and Peru. Differential blood gene expression was determined by RNA-seq (n = 249). Results Diabetes increased the magnitude of gene expression change in the host transcriptome in TB, notably showing an increase in genes associated with innate inflammatory and decrease in adaptive immune responses. Strikingly, patients with IH and TB exhibited blood transcriptomes much more similar to patients with diabetes-TB than to patients with only TB. Both diabetes-TB and IH-TB patients had a decreased type I interferon response relative to TB-only patients. Conclusions Comorbidity in individuals with both TB and diabetes is associated with altered transcriptomes, with an expected enhanced inflammation in the presence of both conditions, but also reduced type I interferon responses in comorbid patients, suggesting an unexpected uncoupling of the TB transcriptome phenotype. These immunological dysfunctions are also present in individuals with IH, showing that altered immunity to TB may also be present in this group. The TB disease outcomes in individuals with IH diagnosed with TB should be investigated further. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
10584838
Volume :
72
Issue :
1
Database :
Academic Search Index
Journal :
Clinical Infectious Diseases
Publication Type :
Academic Journal
Accession number :
148277754
Full Text :
https://doi.org/10.1093/cid/ciaa751