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Systematic review links diabetes to impaired immune control of tuberculosis pathogenesis across 81 studiesDiabetes changes how the body fights tuberculosis infection in humans and animals

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Key Takeaway
Note that diabetes is associated with impaired immune control of tuberculosis pathogenesis.

This systematic review synthesizes evidence from 81 eligible studies involving animal models, human participants, or combined approaches to examine the immunological mechanisms through which diabetes mellitus alters tuberculosis pathogenesis. The scope covers innate and adaptive immune responses, cytokine signalling, granuloma structure and function, and control of Mycobacterium tuberculosis (Mtb). The authors note that distinct immune profiles emerged between TB disease with diabetes and latent TB infection with diabetes.

Key synthesized findings indicate an association between diabetes and broad dysregulation of innate and adaptive immune responses, altered cytokine signalling, and impaired granuloma structure and function. Additionally, diabetes is associated with reduced control of Mycobacterium tuberculosis (Mtb). The review also highlights that pre-diabetes and intermediate hyperglycaemia compromise TB immunity and contribute to disease progression.

The authors acknowledge that heterogeneity in immune profiles was explained by differences in study design, metabolic status, and disease stage. Safety data, including adverse events and tolerability, were not reported. The certainty of the evidence and specific causal inferences were not reported. Practice relevance suggests that earlier metabolic optimisation and host-directed therapeutic strategies could be explored as potential approaches to improve outcomes in this growing high-risk TB-DM population.

When diabetes and tuberculosis meet, the body's defense system often fails. A new review looked at 81 different studies involving both humans and animals to understand exactly how this happens. The findings are clear: diabetes causes a broad disruption in the immune responses needed to fight tuberculosis. It also changes how the body sends chemical signals to stop the infection and damages the protective structures that usually contain the bacteria.

The research found that people with diabetes have distinct immune profiles compared to those without the disease. Even pre-diabetes and high blood sugar levels can compromise immunity and help the tuberculosis bacteria progress. This means the condition is not just a background factor but a direct driver of worse outcomes.

However, the picture is complex. Differences in how studies were designed and the specific stage of the disease made it hard to draw one single conclusion. While the link is strong, more work is needed to find the best ways to treat this growing group of patients who face both conditions.

What this means for you:
Diabetes weakens immune defenses and makes tuberculosis harder to control.

Study Details

Study typeMeta analysis
EvidenceLevel 1
PublishedApr 2026
View Original Abstract ↓
Tuberculosis (TB) remains a leading cause of infectious disease mortality worldwide, and the rising prevalence of diabetes mellitus (DM) represents a major obstacle to TB control. DM increases susceptibility to TB, worsens disease severity, delays treatment response, and is associated with poorer outcomes, largely through disruption of host immunity. We conducted a systematic review of studies published between 1974 and May 31, 2023 that examined immunological mechanisms through which DM alters TB pathogenesis. In total, 81 eligible studies involving animal models, human participants, or combined approaches were identified and synthesised across different stages of TB. Across studies, DM was associated with broad dysregulation of innate and adaptive immune responses, altered cytokine signalling, impaired granuloma structure and function, and reduced control of Mycobacterium tuberculosis (Mtb). Distinct immune profiles emerged between TB disease with DM and latent TB infection with DM, with heterogeneity partly explained by differences in study design, metabolic status, and disease stage. Importantly, emerging evidence indicates that pre-diabetes and intermediate hyperglycaemia may also compromise TB immunity and contribute to disease progression. Our findings highlight DM as a key immunometabolic modifier of TB pathogenesis. They also suggest that earlier metabolic optimisation and host-directed therapeutic strategies could be explored as potential approaches to improve outcomes in this growing high-risk TB-DM population. https://www.crd.york.ac.uk/PROSPERO/, identifier CRD42023431040.
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