# Pediatric Tuberculosis: Unraveling Immunity, Clinical Complexities, and Resource-Driven Disparities in the Pursuit of Prevention

**Authors:** Daniel Mashiach, Justin Shon, Raquel Mashiach, Gregory Ayzenberg, Osnat Barazani, Andre Aabedi, Vishwanath Venketaraman

PMC · DOI: 10.3390/vaccines14020119 · Vaccines · 2026-01-27

## TL;DR

This paper reviews the challenges of pediatric tuberculosis, focusing on immune responses, diagnostic difficulties, and prevention strategies in low-resource settings.

## Contribution

The paper provides a comprehensive synthesis of pediatric TB pathogenesis, risk factors, and prevention strategies, emphasizing the need for equitable interventions.

## Key findings

- Children under five face disproportionately high TB mortality due to delayed diagnosis and limited treatment access.
- Multidrug-resistant TB is rising in low-resource regions, highlighting gaps in current control strategies.
- BCG vaccination remains crucial for preventing severe pediatric TB, though its effectiveness varies by context.

## Abstract

Pediatric tuberculosis (TB) remains a critically underrecognized contributor to global childhood morbidity and mortality, with the highest burden concentrated in low-resource settings. Although children comprise a minority of overall TB cases, mortality is disproportionately high, particularly among those under five years of age, driven largely by delayed diagnosis, inadequate linkage to care, and limited access to effective treatment. The continued rise of pediatric multidrug-resistant TB (MDR-TB), especially in regions with low sociodemographic development, further highlights persistent gaps in current control strategies. This review synthesizes key aspects of pediatric TB pathogenesis and host immune responses that predispose young children to rapid disease progression and severe outcomes, including immune immaturity and paucibacillary infection. We summarize pulmonary and extrapulmonary disease manifestations and identify populations at heightened risk, including children with HIV, malnutrition, type 1 diabetes mellitus, and congenital or treatment-related immunosuppression. Ongoing challenges in diagnosis and treatment are discussed, including limitations of existing microbiologic and immunologic tests, specimen collection constraints, regimen toxicity, and barriers to adherence. Prevention remains central to reducing pediatric TB mortality. We highlight the sustained importance of bacille Calmette–Guérin (BCG) vaccination in preventing severe disease and death, the context-dependent variability in vaccine effectiveness, and the structural and socioeconomic determinants of vaccine coverage. We conclude that integrating equitable vaccine delivery, scalable preventive therapy, and child-adapted diagnostic strategies is essential to meaningfully reduce the global pediatric TB burden.

## Linked entities

- **Diseases:** tuberculosis (MONDO:0018076), multidrug-resistant TB (MONDO:0005861), type 1 diabetes mellitus (MONDO:0005147)

## Full-text entities

- **Genes:** CD4 (CD4 molecule) [NCBI Gene 920] {aka CD4mut, IMD79, Leu-3, OKT4D, T4}, IL12B (interleukin 12B) [NCBI Gene 3593] {aka CLMF, CLMF2, IL-12B, IMD28, IMD29, NKSF}, IFNG (interferon gamma) [NCBI Gene 3458] {aka IFG, IFI, IMD69}, TNF (tumor necrosis factor) [NCBI Gene 7124] {aka DIF, IMD127, TNF-alpha, TNFA, TNFSF2, TNLG1F}, IL6 (interleukin 6) [NCBI Gene 3569] {aka BSF-2, BSF2, CDF, HGF, HSF, IFN-beta-2}, IL1B (interleukin 1 beta) [NCBI Gene 3553] {aka IL-1, IL1-BETA, IL1F2, IL1beta}, CD8A (CD8 subunit alpha) [NCBI Gene 925] {aka CD8, CD8alpha, IMD116, Leu2, p32}, GNLY (granulysin) [NCBI Gene 10578] {aka D2S69E, LAG-2, LAG2, NKG5, TLA519}
- **Diseases:** miliary disease (MESH:D000071071), hypersensitivity (MESH:D004342), pneumonia (MESH:D011014), diminished appetite (MESH:D001068), hilar and mediastinal lymphadenopathy (MESH:D008477), granuloma (MESH:D006099), M. tuberculosis Infection (MESH:D014376), T1DM (MESH:D003922), osteomyelitis (MESH:D010019), chronic granulomatous disease (MESH:D006105), weight gain (MESH:D015430), raised intracranial pressure (MESH:D019586), rash (MESH:D005076), lymphadenopathy (MESH:D008206), type 2 diabetes (MESH:D003924), renal impairment (MESH:D007674), splenomegaly (MESH:D013163), cerebrovascular infarction (MESH:D007238), acute malnutrition (MESH:D000067011), tissue damage (MESH:D017695), coma (MESH:D003128), vomiting (MESH:D014839), lymphadenitis (MESH:D008199), BCG disease (MESH:D001176), Infectious Diseases (MESH:D003141), cranial nerve palsies (MESH:D003389), hydrocephalus (MESH:D006849), Genetic disorders (MESH:D030342), metabolic disorders (MESH:D008659), tuberculoma (MESH:D014375), seizures (MESH:D012640), airway obstruction (MESH:D000402), HIV (MESH:D015658), TB meningitis (MESH:D014390), Primary immunodeficiencies (MESH:D000081207), fever (MESH:D005334), death (MESH:D003643), Undernutrition (MESH:D044342), altered consciousness (MESH:D003244), phlyctenular conjunctivitis (MESH:D003231), MDR-TB (MESH:D018088), hepatomegaly (MESH:D006529), viral (MESH:D014777), inflammation (MESH:D007249), collapse of the lungs (MESH:D001261), injury to (MESH:D014947), erythema nodosum (MESH:D004893), SDI (MESH:C566784), hyperglycemia (MESH:D006943), respiratory and gastrointestinal complaints (MESH:D012818), toxicities (MESH:D064420), juvenile idiopathic arthritis (MESH:D001171), weight loss (MESH:D015431), cough (MESH:D003371), neck stiffness (MESH:D006258), LTBI (MESH:D055985), anorexia (MESH:D000855), meningismus (MESH:D008580), mycobacterial disease (MESH:C564468), EPTB (MESH:D000092225)
- **Chemicals:** ethionamide (MESH:D005000), E (MESH:D004540), methotrexate (MESH:D008727), Z (MESH:C000597310), rifamycin (MESH:C023808), H (MESH:D006859), pretomanid (MESH:C410767), aminoglycoside (MESH:D000617), pyrazinamide (MESH:D011718), rifapentine (MESH:C018421), isoniazid (MESH:D007538), HRZE (-), fluoroquinolone (MESH:D024841), rifampicin (MESH:D012293), R (MESH:D001120), linezolid (MESH:D000069349), bedaquiline (MESH:C493870), ethambutol (MESH:D004977)
- **Species:** Mycobacterium tuberculosis complex (species group) [taxon 77643], Mycobacterium tuberculosis variant africanum (biotype) [taxon 33894], Human immunodeficiency virus 1 (no rank) [taxon 11676], Mycobacterium tuberculosis variant bovis (biotype) [taxon 1765], Bacillus sp. CG (species) [taxon 1196795], Mycobacterium canetti (species) [taxon 78331], Mycobacterium tuberculosis variant pinnipedii (biotype) [taxon 194542], Homo sapiens (human, species) [taxon 9606], Mycobacterium tuberculosis (species) [taxon 1773]

## Full text

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## Figures

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## References

114 references — full list in the complete paper: https://tomesphere.com/paper/PMC12945030/full.md

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Source: https://tomesphere.com/paper/PMC12945030