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Updated: Feb 5, 2026

Protective Efficacy and Pulmonary Immune Response Following Subcutaneous and Intranasal BCG Administration in Mice
Published on: September 19, 2016
Mycobacterium indicus pranii protein MIP_05962 induces Th1 cell mediated immune response in mice
Ashish Sharma1, Mohd Saqib2, Javaid A Sheikh3
1Kusuma School of Biological Science, Indian Institute of Technology, Hauz Khas, New Delhi, 110016, India.
Abstract:
Utility of Mycobacterium indicus pranii (MIP) as a multistage vaccine against mycobacterial infections demands identification of its protective antigens. We explored antigenicity and immunogenicity of a candidate protein MIP_05962 that depicts homology to HSP18 of M. leprae and antigen1 of Mycobacterium tuberculosis. This protein elicited substantial antibody response in immunized mice along with modulation of cellular immune response towards protective Th1 type. Both CD4+ and CD8+ subsets from immunized mice produced hallmark protective cytokines, IFN-γ, TNF-α and IL-2. This protein also enhanced the CD4+ effector memory that could act as first line of defence during infections. These results point to MIP_05962 as a protective antigen that contributes, in conjunction with others, to the protective immunity of this live vaccine candidate.
Insights
Mycobacterium indicus pranii (MIP) vaccine
Area of Science:
- Immunology
- Vaccinology
- Mycobacterial research
Background:
- The live Mycobacterium indicus pranii (MIP) vaccine shows promise against mycobacterial infections.
- Identifying specific protective antigens within MIP is crucial for understanding its efficacy.
Purpose of the Study:
- To investigate the antigenicity and immunogenicity of the MIP_05962 protein.
- To assess its potential as a protective antigen in mycobacterial infections.
Main Methods:
- The study examined the protein MIP_05962, homologous to HSP18 and antigen1 from M. leprae and M. tuberculosis, respectively.
- Immunogenicity was assessed in mice, analyzing antibody responses, cellular immune modulation, cytokine production (IFN-γ, TNF-α, IL-2), and CD4+ effector memory.
Main Results:
- MIP_05962 induced significant antibody production in immunized mice.
- It modulated cellular immunity towards a protective Th1-type response.
- Both CD4+ and CD8+ T cells produced key protective cytokines, and CD4+ effector memory was enhanced.
Conclusions:
- MIP_05962 demonstrates significant antigenicity and immunogenicity.
- It shows potential as a protective antigen contributing to MIP's vaccine efficacy.
- Further research can leverage these findings for improved mycobacterial vaccines.
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