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Ultrasonographic Evaluation of Breast Cancer-related Lymphedema
Published on: January 12, 2017
Evaluation of a Particulate Breast Cancer Vaccine Delivered via Skin
Lipika Chablani1, Suprita A Tawde2, Archana Akalkotkar3
1Department of Pharmaceutical Science, Wegmans School of Pharmacy, St. John Fisher College, 3690 East Ave., Rochester, New York, 14618, USA. lchablani@sjfc.edu.
Abstract:
Breast cancer impacts female population globally and is the second most common cancer for females. With various limitations and adverse effects of current therapies, several immunotherapies are being explored. Development of an effective breast cancer vaccine can be a groundbreaking immunotherapeutic approach. Such approaches are being evaluated by several clinical trials currently. On similar lines, our research study aims to evaluate a particulate breast cancer vaccine delivered via skin. This particulate breast cancer vaccine was prepared by spray drying technique and utilized murine breast cancer whole cell lysate as a source of tumor-associated antigens. The average size of the particulate vaccine was 1.5 μm, which resembled the pathogenic species, thereby assisting in phagocytosis and antigen presentation leading to further activation of the immune response. The particulate vaccine was delivered via skin using commercially available metal microneedles. Methylene blue staining and confocal microscopy were used to visualize the microchannels. The results showed that microneedles created aqueous conduits of 50 ± 10 μm to deliver the microparticulate vaccine to the skin layers. Further, an in vivo comparison of immune response depicted significantly higher concentration of serum IgG, IgG2a, and B and T cell (CD4+ and CD8+) populations in the vaccinated animals than the control animals (p < 0.001). Upon challenge with live murine breast cancer cells, the vaccinated animals showed five times more tumor suppression than the control animals confirming the immune response activation and protection (p < 0.001). This research paves a way for individualized immunotherapy following surgical tumor removal to prolong relapse episodes.
Insights
A novel particulate breast cancer vaccine, delivered via microneedles, effectively stimulates immune responses and significantly suppresses tumor growth in preclinical models, offering a promising new immunotherapy approach.
Area of Science:
- Oncology
- Immunology
- Biotechnology
Background:
- Breast cancer is a leading global health concern for women, with current treatments having limitations.
- Immunotherapy, particularly vaccines, presents a promising alternative for breast cancer treatment.
- Developing effective and accessible breast cancer vaccines is a critical research area.
Purpose of the Study:
- To evaluate a novel particulate breast cancer vaccine delivered intradermally using microneedles.
- To assess the vaccine's ability to elicit a robust immune response.
- To determine the vaccine's efficacy in suppressing breast cancer tumor growth in vivo.
Main Methods:
- A particulate vaccine was prepared using spray drying with murine breast cancer whole cell lysate.
- The vaccine was administered intradermally via metal microneedles, with microchannel visualization using confocal microscopy.
- Immune responses (serum IgG, IgG2a, CD4+, CD8+ cells) and tumor suppression were measured in vaccinated and control mice.
Main Results:
- Microneedles successfully created microchannels for vaccine delivery to skin layers.
- Vaccinated mice showed significantly higher levels of key immune markers (IgG, IgG2a, B and T cells) compared to controls.
- Vaccinated animals exhibited a five-fold increase in tumor suppression after challenge with live breast cancer cells.
Conclusions:
- The particulate breast cancer vaccine delivered via microneedles effectively activates the immune system and provides significant protection against tumor growth.
- This microneedle-delivered vaccine represents a potential advancement in individualized immunotherapy for breast cancer, particularly post-surgical treatment.
- The findings support further investigation into this approach for prolonging relapse-free intervals in breast cancer patients.
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