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M72 Fusion proteins in nanocapsules enhance BCG efficacy against bovine tuberculosis in a mouse model

Mycobacterium bovis is the causative pathogen of bovine tuberculosis (bTB), a disease that affects cattle and other mammals, including humans. Currently, there is no efficient vaccine against bTB, underscoring the need for novel immunization strategies. The M72 fusion protein, composed of three poly...

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Autores principales: Blanco, Federico Carlos, Onnainty, Renée, Marini, María Rocío, Klepp, Laura Ines, Garcia, Elizabeth Andrea, Vazquez, Cristina Lourdes, Canal, Ana María, Granero, Gladys, Bigi, Fabiana
Formato: info:ar-repo/semantics/artículo
Lenguaje:Inglés
Publicado: MDPI 2025
Materias:
Mycobacterium bovis
Mice
Vaccines
Chitosan
Bovine Tuberculosis
Nanocapsules
Ratón
Vacuna
Quitosano
Tuberculosis Bovina
Nanocápsula
Acceso en línea:http://hdl.handle.net/20.500.12123/22703
https://www.mdpi.com/2076-0817/14/6/592
https://doi.org/10.3390/pathogens14060592
Sumario:Mycobacterium bovis is the causative pathogen of bovine tuberculosis (bTB), a disease that affects cattle and other mammals, including humans. Currently, there is no efficient vaccine against bTB, underscoring the need for novel immunization strategies. The M72 fusion protein, composed of three polypeptides derived from Mycobacterium tuberculosis and M. bovis, has demonstrated protective efficacy against M. tuberculosis in clinical trials when combined with the AS01E adjuvant. Given the established efficacy of nanocapsule formulations as vaccine delivery systems, this study evaluated a novel immunization strategy combining BCG with either full-length M72 or a truncated M72 fused to a streptococcal albumin-binding domain (ABDsM72). Both antigens were encapsulated in chitosan/alginate nanocapsules and assessed in a murine M. bovis challenge model. Priming with BCG followed by an M72 boost significantly improved splenic protection compared to BCG alone, but it did not enhance pulmonary protection. Notably, boosting with ABDsM72 further increased the proportion of CD4+KLRG1-CXCR3+ T cells in the lungs of M. bovis-challenged mice, a key correlate of protective immunity. These findings demonstrate that chitosan/alginate-encapsulated antigens enhance BCG-induced immunity, supporting their potential as next-generation vaccine candidates for bTB control.

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