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tuberculosis vaccine (Mw) (Immuvac / Cadi05 / Sepsivac)

✓ Approved

Cadila Pharmaceuticals Ltd. · Cell-based Therapies · Cell-based Therapies

What is tuberculosis vaccine (Mw)?

tuberculosis vaccine (Mw) is a cell-based therapies developed by Cadila Pharmaceuticals Ltd.. It is approved for therapeutic indications via injectable (others) or intradermal injection.

Drug Profile

Brand NamesImmuvac, Cadi05, Sepsivac
CompanyCadila Pharmaceuticals Ltd.
Drug ClassCell-based Therapies, Vaccine
RouteInjectable (Others), Intradermal Injection
StatusApproved

Therapeutic Indications

tuberculosis vaccine (Mw) is developed for 10 unique indications across 2 therapeutic areas.

Therapeutic AreaConditionPhase
Infections and infestationsLeprosy✓ Approved
Neoplasms benign, malignant and unspecified (incl cysts and polyps)Non-small cell lung cancer stage IV✓ Approved
Infections and infestationsSepsis✓ Approved
Neoplasms benign, malignant and unspecified (incl cysts and polyps)Non-small cell lung cancer metastatic✓ Approved
Infections and infestationsSystemic infection✓ Approved

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Related Research Articles

PubMedClinical case reports2026-09-20

Intestinal Perforation Caused by Intestinal Tuberculosis of a Nepalese Man Living in a Low Tuberculosis-Burden Country: A Case Report.

Matsushita Shunya S, Kanata Kei K, Matsushita Shoma S, Ito Yutaro Y et al.

Intestinal tuberculosis generally presents with chronic symptoms. However, in our case, the patient experienced rapid progression from intestinal obstruction to perforation. Even in low-burden countries, intestinal tuberculosis should be considered when patients from high-burden countries present with abdominal symptoms and characteristic computed tomography findings.

PubMedCurrent health sciences journal2026-09-20

Cutaneous Tuberculosis in a 22-Day-Old Neonate:A Diagnostic Challenge and Case Report.

Imran Arisha A, Shah Syeda Wareesha Fareeduddin SWF, Shah Syed Abdul Rafayuddin SAR, Rafique Muhammad M et al.

Cutaneous tuberculosis (CTB) is a rare extrapulmonary manifestation of tuberculosis, particularly in neonates. Its diagnosis is often challenging due to non-specific presentations that can mimic common conditions. We report the case of a 22-day-old male neonate who presented to the emergency room with fever and a scalp swelling following a reported fall from bed. Initial assessment suggested a subcutaneous abscess. The patient did not respond to multiple courses of intravenous antibiotics. A blood culture grew Burkholderia species, but targeted therapy also failed. Incision and drainage were performed, and pus GeneXpert testing was positive for Mycobacterium tuberculosis, despite a negative tuberculin skin test and clear chest X-ray. A final diagnosis of cutaneous tuberculosis (tuberculous chancre) was established. Anti-tuberculosis therapy (ATT) was initiated, leading to the complete resolution of the swelling and full recovery. This case underscores the diagnostic challenges of neonatal CTB. It highlights the importance of considering tuberculosis in the differential diagnosis of non-resolving abscesses in infants, especially in endemic areas, and demonstrates the critical role of molecular diagnostics like GeneXpert in achieving a timely diagnosis.

PubMedAdvances in virology2026-09-20

Comparative Sequence Analysis of the Envelope Gene of Kyasanur Forest Disease Virus Vaccine Strain With Currently Circulating Field Strains.

Kaje Keerthi K, Marinaik Chandranaik B CB, Gomes Amitha Reena AR, Rizwan Apsana A et al.

The present study was undertaken with the objective of performing comparative sequence analysis of the envelope (E) gene of Kyasanur forest disease virus (KFDV) vaccine strain P9605 with the circulating field strains. The study was taken up as the currently used KFDV vaccine strain, KFDV P9605, was isolated in the 1960s. For this study, we designed two sets of primers targeting the complete amplification of the E gene of KFDV. The sequencing was performed by the Sanger method, and the deduced sequence of the vaccine virus was deposited in GenBank with accession number PX067005. This sequence obtained for the vaccine virus was aligned and compared with sequences of GenBank-deposited circulating field strains. We also performed comparative sequence analysis of the Kyasanur forest disease (KFD) vaccine seed virus having passaged twice in mouse brain with the vaccine seed virus passaged six times in mouse brain to investigate whether multiple passages in mouse brain will lead to genetic mutation in the immunologically important E gene. The phylogenetic analysis revealed seven amino acid mutations in the field strains at positions A123T, S158N, D178E, D239N, A313S, M429I, and G479A when compared with the vaccine strain. We did not find any mutations at the critical fusogenic segment (residues 98-113) in the E gene of currently circulating field strains compared to the vaccine seed virus. The study found no genetic variations in the E gene of the KFD virus passed two times and passed six times in mouse brain. We performed SWISS-MODEL homology modeling, AlphaFold protein analysis, and Ramachandran plot analysis to study the E protein structures and stability. The observations made in this study suggest slow evolutionary drift and conserved structural stability of the envelope gene of KFDV ever since its emergence 7 decades ago; however, the functional implications of these amino acid substitutions need further studies on their roles in viral infectivity, transmission, and impact on immunity.

PubMedFood science & nutrition2026-09-20

Developing an Analytical Framework for the Molecular Weight Analysis of Fish-Derived Collagen Peptides in Beverages: A Multi-Method Comparative Study.

Feng Mengmeng M, Li Yali Y, Luo Yongkang Y, Jiang Yanfei Y et al.

Accurate determination of the molecular weight of collagen peptides is crucial for quality control in functional beverages. Current national and industry standard methods for peptide powders face challenges of matrix interference and insufficient comparability when applied to complex beverage systems. In this study, three mainstream chromatographic methods were systematically evaluated for their suitability, reproducibility, and consistency in determining the molecular weight (MW) of fish-derived collagen peptides in beverages. An analytical framework was established by identifying and removing interference peaks from non-peptide excipients, followed by systematic comparison of linear and cubic fitting models. All three methods exhibited good reproducibility. After interference peak removal, the peptide profiles of the beverages were highly consistent with those of pure peptide powder. Cubic fitting reduced inter-method differences, with relative standard deviation (RSD) values below 5% in the bioactive < 1 kDa range. The framework was further validated through beverage formulation optimization, demonstrating compatibility between functional ingredient quality control and sensory flavor adjustability. The proposed approach provides a practical solution for industry quality control and cross-laboratory data comparability of collagen peptide beverages.

PubMedFrontiers in cellular and infection microbiology2026-09-19

Macrophage states and polarization during Mycobacterium tuberculosis infection: mechanisms, granuloma adaptation, and host-directed therapeutic opportunities.

Xu Minglong M, Peng Zhangli Z

Tuberculosis is a chronic infectious disease caused by Mycobacterium tuberculosis (Mtb). As primary host cells targeted by Mtb, macrophages play central roles in both innate and adaptive immunity. Accumulating evidence indicates that macrophage polarization is a key determinant of tuberculosis pathogenesis. In response to diverse microenvironmental cues, macrophages adopt functionally distinct polarization states, ranging from pro-inflammatory, microbicidal programs (M1-like) to anti-inflammatory, tissue-reparative programs (M2-like). These states differentially shape tuberculosis progression. Defining the remodeling of these context-dependent macrophage states is therefore critical for understanding Mtb infection, granuloma formation, and disease outcomes, as well as for guiding the development of next-generation vaccines, immunotherapies, and host-directed interventions. This Review synthesizes the molecular mechanisms underlying macrophage polarization during Mtb infection, integrates the bidirectional regulatory networks between pathogen-derived and host-derived factors, and highlights their roles in immune evasion, granuloma biology, and emerging therapeutic strategies in tuberculosis.

PubMedEClinicalMedicine2026-09-19

Effectiveness of the 2025-2026 seasonal influenza vaccine among U.S. veterans: an observational study.

Xie Yan Y, Choi Taeyoung T, Al-Aly Ziyad Z

Annual vaccination is the primary strategy for preventing adverse clinical outcomes associated with seasonal influenza, but vaccine effectiveness varies by season with the degree of antigenic match and the predominant circulating subtype. The 2025-2026 season has been dominated by a newly emerged, antigenically distinct influenza A(H3N2) subclade K that arose after the vaccine strain was selected, raising concern about a vaccine mismatch and reduced effectiveness. Contemporary, season-specific evidence on effectiveness against clinically important outcomes is needed. We used U.S. Department of Veterans Affairs (VA) electronic health records to emulate a series of 24 sequential 7-day target trials among VA users with an in-person primary care visit between September 15, 2025, and February 28, 2026, comparing those who did and did not receive a seasonal influenza vaccine at the visit. The final analytic cohort comprised 1,401,492 participant-trials (526,350 vaccinated and 875,142 unvaccinated). Exposure was defined as receipt of the 2025-2026 seasonal influenza vaccine on the date of an eligible primary care visit, compared with no seasonal influenza vaccination at that visit or during follow-up. The primary outcome was a composite of seasonal influenza-associated emergency department visit or hospitalization. Individual components were also evaluated. Vaccine effectiveness (VE), defined as 1 minus the risk ratio, was estimated as the per-protocol effect among vaccinated participants using discrete-time survival models with inverse-probability-of-treatment and inverse-probability-of-censoring weighting. Marginal cumulative risks, and risk differences (RDs) per 10,000 persons, together with risk ratios, were estimated. Compared with no vaccination, receipt of the 2025-2026 vaccine was associated with a lower risk of the composite outcome (VE, 21.95%; 95% CI, 16.08%-27.65%; RD per 10,000 persons, -4.94; 95% CI, -6.49 to -3.47), influenza-associated emergency department visits (VE, 22.25%; 95% CI, 16.38%-27.94%; RD, -5.01; 95% CI, -6.55 to -3.53), and influenza-associated hospitalizations (VE, 31.84%; 95% CI, 14.77%-46.27%; RD, -1.08; 95% CI, -1.82 to -0.44). Vaccination was associated with lower risk of the composite outcome across prespecified subgroups defined by age (≤65 and >65 years) and immunocompromised status. Results were consistent across multiple sensitivity analyses, and negative outcome controls (all-cause hospitalization and all-cause death within 14 days) showed no association with vaccination. In analyses applying the same design to the 2024-2025 season, vaccine effectiveness was lower in 2025-2026 than in 2024-2025 for every outcome (composite, 21.95% vs 32.15%; approximately 30% lower in relative terms). The 2025-2026 seasonal influenza vaccine was associated with reductions in influenza-associated emergency department visits and hospitalizations, but its effectiveness was lower than in the immediately preceding season. These findings provide contemporary, season-specific evidence supporting the continued use of seasonal influenza vaccination to prevent clinically important influenza outcomes. U.S. Department of Veterans Affairs.

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