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Insights into cancer vaccines




Current Frontier of Cancer Vaccines
How cancer vaccines work
Breast cancer cancer vaccine
How proteomics and virology are used together

Due to the recent surge in virology and vaccine production due to the COVID-19 pandemic, healthcare professionals are even more dependent on this new technique. One prominent example is the use of a relatively new technique in the field of oncology, the “cancer vaccine,” which was first adopted only 20 years ago. This is often preferred over traditional methods such as chemotherapy and radiation therapy because of its more accurate targeting. In addition to this benefit, these vaccines provide preventative measures, such as those created against carcinogenic viruses such as HPV and HBV, and proactive measures if the patient in question has already been diagnosed with late-stage cancer. Can be adopted.

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Current Frontier of Cancer Vaccines

The three most prominent forms of cancer vaccines are the live intravesical BCG vaccine, the sipulecel-T, and the T-VEC vaccine. When introduced into the body, each exhibits unique kinetics and targets abnormally expressed proteins. A notable example of an aberrant protein could be a new antigen that has the ability to exchange across various cancer cell lines and results in a harmful antigen cascade.

The Bacillus of Calmette and Guerin (BCG) strain of Mycobacterium Bovis is used as an attenuated cancer vaccine and is enhanced by a high colony turnover and subsequent serial dilution assay. The Sipuleucel-T vaccine (developed by Dendreon Corporation) has been used to treat asymptomatic metastatic prostate cancer, made possible after 10 years of immunological research and 13 years of clinical trials.

Representing the first approved cancer vaccine, this treatment has a good risk-to-benefit ratio and is easy to use in combination with other more aggressive treatments. Finally, the Tarimogene laherpalepbeck (T-VEC) vaccine melanoma Skin cancer that has spread to lymph nodes and soft tissues.

How cancer vaccines work

Cancer vaccines play a role in stimulating the long-term immune response evoked by host T cells. This treatment is in the early stages compared to more traditional treatments and is therefore used in C57BL / 6 mice, Sprague-Dawley rats, and other mouse models. This is performed to test its properties within the tumor microenvironment and its properties of immunosuppression. The tumor microenvironment is composed of many components, including immunosuppressive markers, extracellular matrix changes, and solubility factors. All of these alter the metastatic potential of tumors and, as a result, are major targets for cancer vaccines.

What is a cancer vaccine?

DeMaria PJ et al. In a treatise written by, we see 10 driver mutations tested for immunogenicity. These mutations resulted in a new antigen, a protein formed on cancer cells rather than normal host cells. These cells are major targets because they can be targets for the CD4 + and CD8 + T cell receptors, and inhibition of these new antigens does not jeopardize the health and biochemistry of normal cells. .. In addition to these targets, inhibition of CD169 + (sialic acid receptor) through these cancer vaccines appears to stimulate a specific amount of T cell response.This has been demonstrated in relation to anti-melanoma antigen In human leukocytes and transgenic mice.

Breast cancer cancer vaccine

These cancer vaccines are often offered in combination with other immunotherapies and treatments to effectively target the disease based on the mutation / stage of the cancer. Such designer therapies can be found in the Mayo Clinic Phase 2 clinical trials in patients with triple-negative breast cancer. By targeting the folic acid receptor αFOLR1 Metastatic breast cancerAs a result, downregulation of the resulting protein progressed, leading to a decrease in tumor growth. They have also been used to treat ductal carcinoma in situ, which is a precancerous form of breast cancer.

Image Credits: CI Photos /

Image Credits: CI Photos /

How proteomics and virology are used together

Many strategies have been adopted to achieve increased tumor antigen recognition and reduced immune tolerance, all using vaccineology (if unaffected). Tumor antigens are now injected into patients, giving them a stronger immune response produced by non-pathogenic viruses.

Tumor-related lymphocytes are biopsied and can be amplified in vitro by a variety of elongation techniques. The resulting protein is then reinjected into the patient to enhance the immune response through recognition. This same method can be performed with idiotype antibodies, which share a characteristic binding specificity and structure, and then can be applied directly to cancer cells and heavier masses.


While this new technology is becoming more and more prominent now, there are many hurdles to overcome and other technologies are still in sight. Most recently, the necessary advances have been made to genotype rapidly developing tumors. This is a necessary process when trying to assay relevant biomarkers and parts of a drug target. Our approach to finding defined antigens in all tumors was unsuccessful until the recent discovery of new antigens. This target has not yet received a sufficient amount of research.

Therefore, the vaccine used must be very patient-specific and requires time and resources to achieve. Finally, these vaccines employ aggressive taxation on the body’s immune system, which can lead to the depletion of T cells in the body.

All of these restrictions have been addressed using checkpoint blockade. If we want to normalize the implementation of these vaccines, we need a more complete understanding of the cancer and immune cycle. Until then, a variety of other therapeutic approaches have been used.


  • Apostolopoulos V. (2019). Cancer vaccines: research and application. cancer11 (8), 1041.
  • DeJager R, Guinan P, Lamm D, Khana O, Brosman S, DeKernion J, et al. Long-term completion. (2021) In-situ remission of bladder cancer by intravesical TICE bacillus Carmet Guerlain. Urology 1991; 38: 507-513.
  • Zhang Zheying, Lu Manman, Qin Yu, Gao Wuji, Tao Li, Su Wei, Zhong Jiateng. (2021) New antigen: A new breakthrough in tumor immunotherapy. Immunology Frontier (12) 1664-3224 10.3389 / fimmu.2021.672356
  • Zhang, Z., Liu, S., Zhang, B., Qiao, L., Zhang, Y. , & Zhang, Y. (2020) T cell dysfunction and malaise in cancer..Frontier of Cellular and Developmental Biology8, 17.
  • Sipuleucel-T: APC 8015, APC-8015, Prostate Cancer Vaccine-Dendreon. Drag RD.. 2006; 7 (3): 197-101. Doi: 10.2165 / 00126839-200607030-00006. PMID: 16752945.
  • Kalli, KR, Block, MS, Kasi, PM, Erskine, CL, Hobday, TJ, Dietz, A., Padley, D., Gustafson, MP, Shreeder, B., Puglisi-Knutson, D., Visscher, DW, Mangskau, TK, Wilson, G., and Knutson, KL (2018). The folic acid receptor alpha peptide vaccine produces immunity in patients with breast and ovarian cancer. Clinical Cancer Research: Official Journal of the American Association for Cancer Research24 (13), 3014-3025.
  • Butterfield LH. Cancer vaccine. BMJ.. April 22, 2015; 350: h988. Doi: 10.1136 / bmj.h988. PMID: 25904595; PMCID: PMC4707521.

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