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Vaccine Detail
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SHR3/DMT |
| Vaccine Information |
- Vaccine Name: SHR3/DMT
- Target Pathogen: Mycobacterium tuberculosis
- Target Disease: Tuberculosis
- Type: Subunit vaccine
- Status: Research
- Host Species for Licensed Use: Mouse
- Antigen: SHR3 fusion protein, composed of Rv1626, Rv2866 and Rv1884(Zhang et al., 2024).
- Rv1626
gene engineering:
- Type: Fusion Protein
- Description: use in preparation of fusion protein(Zhang et al., 2024).
- Detailed Gene Information: Click Here.
- relG
gene engineering:
- Type: Fusion Protein
- Description: This is use for preparation of fusion protein(Zhang et al., 2024).
- Detailed Gene Information: Click Here.
- rpfC
gene engineering:
- Type: Fusion Protein
- Description: Use in preparation of fusion protein(Zhang et al., 2024).
- Detailed Gene Information: Click Here.
- Preparation: Recombinant fusion protein expressed in E. coli, purified by Ni-NTA affinity chromatography, dialyzed into phosphate-buffered saline, and formulated with DMT adjuvant as a subunit vaccine(Zhang et al., 2024).
- Immunization Route: subcutaneous injection
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| Host Response |
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Mouse Response
- Host Strain: C57BL/6
- Host age: 6 week old
- Host gender: female
- Vaccination Protocol: Mice were immunized subcutaneously. The BCG+SHR3/DMT group received BCG priming at week 0 followed by two booster doses of SHR3/DMT at 3-week intervals. SHR3/DMT and subunit groups were immunized every 3 weeks over a 9-week period(Zhang et al., 2024).
- Immune Response: Vaccination induced strong antigen-specific Th1-type immune responses characterized by increased IFN-?, TNF-?, and IL-2 secretion from CD4? and CD8? T cells, with low IL-4 levels. The BCG+SHR3/DMT group produced the highest IgG titers and IgG2a/IgG1 ratios (>1), indicating a Th1-dominant response (Zhang et al., 2024).
- Information about this animal model: Mouse Model for TB research
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| References |
Zhang et al., 2024: Zhang Z, Xu L, Wang X, Kong L, Shi Z, Zhong Q, Xu Y, Wang J. Construction and expression of Mycobacterium tuberculosis fusion protein SHR3 and its immunogenicity analysis in combination with various adjuvants. Tuberculosis (Edinburgh, Scotland). 2024; 145; 102480. [PubMed: 38278100].
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