HER2/neu-Based Peptide Vaccination-Pulsed with B-Cell Epitope Induced Efficient Prophylactic and Therapeutic Antitumor Activities in TUBO Breast Cancer Mice Model Article Swipe
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· 2021
· Open Access
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· DOI: https://doi.org/10.3390/cancers13194958
Breast cancer is the most common invasive cancer diagnosed among women. A cancer vaccine has been recognized as a form of immunotherapy with a prominent position in the prevention and treatment of breast cancer. The majority of current breast cancer vaccination strategies aim to stimulate antitumor T-cell responses of the HER2/neu oncogene, which is abnormally expressed in breast cancer cells. However, the role of the B-cell humoral response is often underappreciated in the cancer vaccine design. We have advanced this idea by elucidating the role of B-cells in cancer vaccination by designing a chimeric antigenic peptide possessing both cytotoxic T lymphocytes (GP2) and B-cell (P4) peptide epitopes derived from HER2/neu. The chimeric peptide (GP2–P4) was further conjugated to a carrier protein (KLH), forming a KLH–GP2–P4 conjugate. The immunogenicity of KLH–GP2–P4 was compared with KLH–GP2 (lacking the B-cell epitope) in BALB/c mice. Mice immunized with KLH–GP2–P4 elicited more potent antigen-specific neutralizing antibodies against syngeneic TUBO cells (cancer cell line overexpressing HER2/neu) that was governed by a balanced Th1/Th2 polarization in comparison to KLH–GP2. Subsequently, these immune responses led to greater inhibition of tumor growth and longer survival in TUBO tumor-bearing mice in both prophylactic and therapeutic challenge experiments. Overall, our data demonstrated that the B-cell epitope has a profound effect in orchestrating an efficacious antitumor immunity. Thus, a multi-epitope peptide vaccine encompassing cytotoxic T-lymphocytes, T-helper and B-cell epitopes represents a promising strategy in developing cancer vaccines with a preventive and therapeutic modality for the effective management of breast cancer.
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- Type
- article
- Language
- en
- Landing Page
- https://doi.org/10.3390/cancers13194958
- https://www.mdpi.com/2072-6694/13/19/4958/pdf?version=1633771142
- OA Status
- gold
- Cited By
- 21
- References
- 49
- Related Works
- 10
- OpenAlex ID
- https://openalex.org/W3201743683
Raw OpenAlex JSON
- OpenAlex ID
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https://openalex.org/W3201743683Canonical identifier for this work in OpenAlex
- DOI
-
https://doi.org/10.3390/cancers13194958Digital Object Identifier
- Title
-
HER2/neu-Based Peptide Vaccination-Pulsed with B-Cell Epitope Induced Efficient Prophylactic and Therapeutic Antitumor Activities in TUBO Breast Cancer Mice ModelWork title
- Type
-
articleOpenAlex work type
- Language
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enPrimary language
- Publication year
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2021Year of publication
- Publication date
-
2021-10-01Full publication date if available
- Authors
-
Muhammad Luqman Nordin, Abdin Shakirin Mohamad Norpi, Pei Yuen Ng, Khatijah Yusoff, Nadiah Abu, Kue Peng Lim, Fazren AzmiList of authors in order
- Landing page
-
https://doi.org/10.3390/cancers13194958Publisher landing page
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https://www.mdpi.com/2072-6694/13/19/4958/pdf?version=1633771142Direct link to full text PDF
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YesWhether a free full text is available
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-
goldOpen access status per OpenAlex
- OA URL
-
https://www.mdpi.com/2072-6694/13/19/4958/pdf?version=1633771142Direct OA link when available
- Concepts
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Epitope, Cytotoxic T cell, Cancer vaccine, Immunogenicity, Immunotherapy, Cancer, Peptide vaccine, Immunology, Antigen, Breast cancer, Immune system, Cancer research, T cell, Cancer immunotherapy, Vaccination, Medicine, Biology, Internal medicine, In vitro, BiochemistryTop concepts (fields/topics) attached by OpenAlex
- Cited by
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21Total citation count in OpenAlex
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2025: 7, 2024: 4, 2023: 6, 2022: 4Per-year citation counts (last 5 years)
- References (count)
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49Number of works referenced by this work
- Related works (count)
-
10Other works algorithmically related by OpenAlex
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