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Experimental Melanoma Immunotherapy Model Using Tumor Vaccination with a Hematopoietic Cytokine
Published on: February 24, 2023
Recombinant BCG-Ag85A enhances antitumor immunity and controls melanoma progression through multimodal immune
Suzana Lemke Lanius1, Bruna Silveira Pacheco1, Fernanda Severo Sabedra Sousa1
1Molecular and Cellular Oncology Research Group, Cancer Biotechnology Laboratory, Postgraduate Program in Biotechnology, Technological Development Center, Federal University of Pelotas, Pelotas, RS, 96010900, Brazil.
Abstract:
Melanoma is an aggressive form of skin cancer characterized by high metastatic potential and increasing incidence and mortality worldwide. Although significant advances have been achieved with immune checkpoint inhibitors and targeted therapies, effective preventive and long-term therapeutic strategies remain limited. Bacillus Calmette-Guérin (BCG), widely used in bladder cancer immunotherapy, exhibits potent immunostimulatory properties and has emerged as a promising platform for recombinant cancer vaccines. Among the candidate antigens, Antigen 85A (Ag85A), derived from Mycobacterium bovis, is notable for its strong immunogenicity and ability to induce robust Th1-mediated cellular immune responses. In this study, recombinant BCG strains overexpressing efficacy was evaluated in melanoma models in vitro and in vivo. Gene expression analysis by RT-qPCR revealed that rBCG-Ag85A induced systemic immune activation, characterized by increased Il1B and Trl4 expression in splenocytes. In tumor tissues, rBCG-Ag85A significantly upregulated genes associated with apoptosis (Bax, Bcl2), oxidative stress (Sod1, Cat), inflammatory and immune signaling pathways (Tlr4, Nfkb, Il12, Il1b, Casp1), and modulation of pathways involved in cellular metabolism (Mtor) indicating enhanced modulation of the tumor microenvironment. Functionally, these molecular and immunological effects were associated with reduced tumor progression, slower tumor growth, and improved survival in B16F10 melanoma-bearing mice. Collectively, these findings demonstrate that rBCG-Ag85A promotes multifaceted antitumor activity through the modulation of apoptosis, inflammation and oxidative stress-related gene expression, highlighting its potential as a promising prophylactic vaccine strategy to prevent cutaneous malignant melanoma and supporting future studies aimed at elucidating the immune cell populations involved and optimizing combinatorial therapeutic approaches.
Insights
This study shows that a modified Bacillus Calmette-Guérin (BCG) vaccine expressing Antigen 85A (Ag85A) effectively combats melanoma. The recombinant BCG-Ag85A vaccine reduced tumor growth and improved survival in mice by modulating immune responses and the tumor microenvironment.
Area of Science:
- Immunology
- Oncology
- Vaccinology
Background:
- Melanoma is an aggressive skin cancer with limited effective preventive strategies.
- Bacillus Calmette-Guérin (BCG) is a potent immunostimulant and a platform for cancer vaccines.
- Antigen 85A (Ag85A) from Mycobacterium bovis is highly immunogenic and induces Th1 responses.
Purpose of the Study:
- To evaluate the efficacy of a recombinant BCG strain overexpressing Ag85A (rBCG-Ag85A) in melanoma models.
- To investigate the molecular mechanisms underlying the antitumor activity of rBCG-Ag85A.
Main Methods:
- In vitro and in vivo evaluation of rBCG-Ag85A in melanoma models.
- Gene expression analysis (RT-qPCR) of splenocytes and tumor tissues.
- Assessment of tumor progression, growth, and survival in mice.
Main Results:
- rBCG-Ag85A induced systemic immune activation (increased Il1B, Tlr4 expression).
- Upregulation of apoptosis, oxidative stress, and inflammatory genes in tumor tissues.
- Significant reduction in tumor progression, slower tumor growth, and improved survival in mice.
Conclusions:
- rBCG-Ag85A demonstrates multifaceted antitumor activity against melanoma.
- The vaccine modulates apoptosis, inflammation, and oxidative stress-related gene expression.
- rBCG-Ag85A holds promise as a prophylactic vaccine strategy for cutaneous malignant melanoma.
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