Drug Database
TU

tuberculosis vaccine

✓ Approved

SK Chemicals · 细胞治疗 · 细胞治疗

什么是 tuberculosis vaccine?

tuberculosis vaccine 是一种细胞治疗,由SK Chemicals研发。该药已获批,用于治疗相关适应症,给药途径:Injectable (Others)、Intradermal Injection。

药物档案

公司SK Chemicals
药物类别细胞治疗, 疫苗
给药途径Injectable (Others), Intradermal Injection
状态Approved

相关研究文献

PubMedBMC microbiology2026-10-26

Prevalence of pulmonary tuberculosis and associated factors among suspected tuberculosis patients attending Halaba Kulito General Hospital, Ethiopia: cross-sectional study.

Mesele Derso Wale DW, Ayele Gizachew G, Gashaw Birku B, Fekadu Bisrat B et al.

Pulmonary tuberculosis remains the leading cause of mortality worldwide from a single infectious agent. This is more pronounced in resource-limited settings like Ethiopia, where HIV co-infection is more common. This study aimed to assess the prevalence of pulmonary tuberculosis and its associated factors among suspected pulmonary tuberculosis patients attending Halaba Kulito General Hospital. A hospital-based cross-sectional study was conducted from October 27 to December 27, 2025, at Halaba Kulito General Hospital. Sputum samples were collected and analyzed using GeneXpert MTB/RIF assay following standard operating procedures. Descriptive statistics, bivariable, and multivariable logistic regression analyses were performed to assess factors associated with pulmonary tuberculosis, with statistical significance set at a p-value < 0.05 at a 95% confidence level. The prevalence of pulmonary tuberculosis among the study participants was 8.0% (13/163; 95% CI 4.3-13.3%). HIV seropositivity (AOR = 6.683, 95% CI = 1.286-34.727) and alcohol consumption (AOR = 3.773, 95% CI = 1.047-13.593) were independently associated with pulmonary tuberculosis. This study found a non-negligible prevalence of pulmonary tuberculosis among the study population. HIV seropositivity and alcohol consumption were significantly associated with pulmonary tuberculosis. These findings support the need for integrated tuberculosis and HIV services and consideration of alcohol-use assessment within tuberculosis screening and prevention activities.

PMID 42928105
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PubMedIranian journal of biotechnology2026-10-26

Engineered ESAT-6 Linear Epitopes in Tuberculosis: An Interesting Immunologic Signal, but Diagnostic Efficacy Still Needs Clinical Validation.

Shadbash Piruz P

PMID 42928731
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PubMedJournal of medical case reports2026-10-26

Post-tubercular bronchopleural fistula with tension hydropneumothorax: a rare case and its management and diagnostic challenges in a low-income country: a case report.

Wakoya Amanuel Dagabas AD, Negash Ayto Addisu AA, Assefa Fitsum Negusse FN

A bronchopleural fistula (BPF) accompanied by tension hydropneumothorax is a rare but potentially life-threatening complication of tuberculosis, posing significant diagnostic and treatment challenges. Effective management requires a multidisciplinary approach, particularly when there are additional concurrent infections involved. A 28-year-old Black Ethiopian male with no significant past medical history presented to the emergency department with a 1-week exacerbation of shortness of breath, alongside a 2-month history of productive cough, weight loss, and night sweats. He was diagnosed with tuberculosis via GeneXpert testing and subsequently bronchopleural fistula complicated by hydropneumothorax with imaging. Management consisted of chest tube drainage, intravenous antibiotic therapy, and standard first-line antitubercular treatment. The patient showed significant improvement and was discharged in stable condition. This case highlights a rare complication of cavitary tuberculosis and demonstrates that bronchopleural fistula can be successfully managed with nonsurgical approaches, resulting in clinical recovery and lung re-expansion, while also providing insights into diagnostic and management strategies.

PMID 42928330
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PubMedCancer discovery2026-10-26

First mRNA Cancer Vaccine Succeeds in Phase III Trial.

Adding the mRNA-based individualized neoantigen vaccine intismeran autogene to the PD-1 inhibitor pembrolizumab following surgery for melanoma reduced the risk of disease recurrence or death by 42%, according to the results of the phase III INTerpath-0001 trial. The data were presented at the ESMO Congress 2026, held October 23-27, in Madrid, Spain.

PMID 42929716
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PubMedAnimal health research reviews2026-10-26

Innovative vaccine strategies for sustainable control and eradication of peste des petits ruminants virus.

Bello Muhammad Bashir MB, Hameed Sodiq A SA, Abdullahi Adama Musa AM, Lawal Nafi'u N et al.

PMID 42929676
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PubMedIranian journal of biotechnology2026-10-26

Genome-Wide DNA Methylation Analysis Reveals Immune Genes in Tuberculosis with Potential Relevance for Host-Directed Interventions.

Shahzad Hira H, Mujtaba Mariam Ahmed MA, Fatima Khazina K, Javed Muhammad Ishaq MI et al.

Growing evidence suggests that Mycobacterium tuberculosis (M. tb) infection manipulates the host's epigenetic landscape to evade the immune responses and establish a disease phenotype. Among these epigenetic changes, DNA methylation has emerged as a key mechanism that influences the host immune response, playing a crucial role in either controlling the infection or contributing to disease pathogenesis. M. tb and other pathogens can alter the host's epigenetic landscape to weaken immune defenses and facilitate infection. In this study we aimed to investigate differential DNA methylation patterns in Tuberculosis (TB) phenotypes i.e., Active, Latent, Cured and healthy controls. In this study, we investigated genome-wide DNA methylation patterns via Infinium Methylation EPIC array in a total of eight M. tb-exposed patients with two biological replicates in each clinical group: active tuberculosis (TB, n=2), latent TB (n=2), therapy-cleared (cured) TB (n=2) and uninfected controls (n=2). Genes linked to hypermethylated promoters were further analyzed through gene ontology (GO) and biological pathways analyses (DAVID). Motif enrichment analysis was performed using differentially methylated regions (DMRs) (>300bp) and promotor CpG site methylation was correlated with corresponding gene expression profile. Our study identified a repressed immune signature in active TB patients, characterized by hypermethylated genes such as IFNA2, IFNA6, TNFRSF19, IL2, IL21 and TGFβ2 etc. This hypermethylation persists even in cured individuals, despite M. tb clearance and was further reinforced by qPCR analysis showing downregulated expression of hypermethylated genes IFNA2 and IFNA6 in active TB compared to latent and control subjects. Key pathways affected include those associated with tuberculosis, phagosome function, JAK/STAT pathway and cytokine receptors during active M. tb infection, with these effects continuing post-clearance (cured phenotype). Enriched transcription factor motifs within DMRs included ZBTB14, E2F1, and NRF1. Our findings reveal that M. tb infection is marked by a DNA hypermethylation signature linked to key immune-related genes, driving a repressed immune response and active disease manifestation. This epigenetic signature remains even after M. tb is cleared, suggesting long-term alterations in immune regulation. While preliminary, this methylation signatures once validated in larger cohorts highlight the potential for developing early epigenetic markers to help distinguish active TB from other clinical states or to monitor post-treatment immune recovery.

PMID 42928845
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