Protective Immunity Against Lung Infection Induced by a DNA Plasmid Vaccine Carrying Gene Inhibits Dissemination in BALB/c Mice
Overview
Chemistry
Molecular Biology
Affiliations
(), a zoonotic pathogen, poses a potential threat to public health security and the development of animal husbandry. Vaccine-based preventative measures for infectious diseases have a promising landscape. DNA vaccines, with many advantages, have become one of the dominant candidate strategies in preventing and controlling the chlamydial infection. Our previous study showed that CPSIT_p7 protein is an effective candidate for a vaccine against . Thus, this study evaluated the protective immunity of pcDNA3.1(+)/CPSIT_p7 against infection in BALB/c mice. We found that pcDNA3.1(+)/CPSIT_p7 can induce strong humoral and cellular immune responses. The IFN-γ and IL-6 levels in the infected lungs of mice immunized with pcDNA3.1(+)/CPSIT_p7 reduced substantially. In addition, the pcDNA3.1(+)/CPSIT_p7 vaccine diminished pulmonary pathological lesions and reduced the load in the lungs of infected mice. It is worth noting that pcDNA3.1(+)/CPSIT_p7 suppressed dissemination in BALB/c mice. In a word, these results demonstrate that the pcDNA3.1(+)/CPSIT_p7 DNA vaccine has good immunogenicity and immunity protection effectiveness against infection in BALB/c mice, especially pulmonary infection, and provides essential practical experience and insights for the development of a DNA vaccine against chlamydial infection.
Profile of vaccine research: A bibliometric analysis.
Wang X, Wang Q, Gao Y, Jiang L, Tang L Hum Vaccin Immunother. 2025; 21(1):2459459.
PMID: 39906958 PMC: 11801346. DOI: 10.1080/21645515.2025.2459459.