# Novel Multistage Subunit Mycobacterium tuberculosis Nanoparticle Vaccine Confers Protection Against Experimental Infection in Prophylactic and Therapeutic Regimens

**Authors:** Amir I. Tukhvatulin, Alina S. Dzharullaeva, Daria V. Vasina, Mikhail V. Fursov, Fatima M. Izhaeva, Denis A. Kleymenov, Dmitry N. Shcherbinin, Nikita B. Polyakov, Andrey I. Solovyev, Vladimir G. Zhukhovitsky, Alla S. Zhitkevich, Ilya V. Gordeychuk, Anna M. Litvinova, Victor A. Manuylov, Vasiliy D. Potapov, Artem P. Tkachuk, Vladimir A. Gushchin, Denis Y. Logunov, Alexander L. Gintsburg

PMC · DOI: 10.3390/vaccines14010005 · Vaccines · 2025-12-19

## TL;DR

A new tuberculosis vaccine using nanoparticles and multiple antigens shows strong protection in animal models when used both preventively and therapeutically.

## Contribution

A novel multistage subunit TB vaccine with combined antigens and adjuvants in nanoparticles is shown to confer protection in experimental models.

## Key findings

- The vaccine induced a mixed Th1/Th17 immune response and sustained IgG and IgA production.
- It provided prophylactic protection in mice and guinea pigs after BCG priming.
- The vaccine was also effective in a therapeutic setting in a murine infection model.

## Abstract

Background/Objectives: Tuberculosis (TB) remains the leading cause of death from a single infectious agent worldwide. In line with the World Health Organization’s (WHO) goal to end TB by 2035, the rapid development and clinical implementation of new, effective vaccines is urgently needed. To support global TB control efforts, we developed a novel candidate subunit multistage vaccine. Methods: This vaccine incorporates multiple Mycobacterium tuberculosis antigens expressed during both dormant and active stages of infection, fused into a single recombinant protein (ESAT6-CFP10-Ag85A-Rv2660c-Rv1813c). The antigen was encapsulated in biodegradable poly(D,L-lactide-co-glycolide) (PLGA) nanoparticles along with the pattern recognition receptor (PRR) agonists monophosphoryl lipid A (MPLA) and muramyl dipeptide (MDP), which function as adjuvants. Results: Using a mixed intramuscular/nasal prime-boost regimen, the vaccine elicited a mixed Th1/Th17 cell-mediated immune response, as well as a robust humoral response characterized by sustained systemic IgG (lasting at least one year) and prominent local secretory IgA. The vaccine demonstrated protective efficacy as a prophylactic booster following BCG priming in both murine and guinea pig models and was also effective in a therapeutic setting in a murine infection model. Conclusions: The results of this study provide empirical evidence that multistage tuberculosis vaccines represent a promising strategy for achieving global TB control.

## Linked entities

- **Proteins:** esxA (ESAT-6 protein EsxA), esxB (ESAT-6-like protein EsxB), ag85A (diacylglycerol acyltransferase/mycolyltransferase Ag85A), Rv2660c (hypothetical protein), Rv1813c (hypothetical protein), DPEP1 (dipeptidase 1)
- **Chemicals:** monophosphoryl lipid A (PubChem CID 24978548), muramyl dipeptide (PubChem CID 451714)
- **Diseases:** Tuberculosis (MONDO:0018076)
- **Species:** Mus musculus (taxon 10090), Cavia porcellus (taxon 10141)

## Full-text entities

- **Diseases:** death (MESH:D003643), infectious (MESH:D003141), TB (MESH:D014376), Infection (MESH:D007239)
- **Chemicals:** MPLA (MESH:C048436), MDP (MESH:D000119), PLGA (MESH:D000077182)
- **Species:** Mycobacterium tuberculosis (species) [taxon 1773], Bacillus sp. CG (species) [taxon 1196795], Mus musculus (house mouse, species) [taxon 10090], Cavia porcellus (domestic guinea pig, species) [taxon 10141]

## Full text

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## Figures

6 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12846566/full.md

## References

80 references — full list in the complete paper: https://tomesphere.com/paper/PMC12846566/full.md

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Source: https://tomesphere.com/paper/PMC12846566