GET THE APP

Cancer Vaccines Harnessing: Immune System for Prevention and Treatment
Cancer Science & Therapy

Cancer Science & Therapy

ISSN: 1948-5956

Open Access

Opinion - (2025) Volume 17, Issue 1

Cancer Vaccines Harnessing: Immune System for Prevention and Treatment

Milad Ashrafizadeh*
*Correspondence: Milad Ashrafizadeh, Department of General Surgery, Shenzhen University, Shenzhen, Guangdong 518055, China, Email:
1Department of General Surgery, Shenzhen University, Shenzhen, Guangdong 518055, China

Received: 02-Jan-2025, Manuscript No. jcst-25-126796; Editor assigned: 04-Jan-2025, Pre QC No. P-126796; Reviewed: 16-Jan-2025, QC No. Q-126796; Revised: 22-Jan-2025, Manuscript No. R-126796; Published: 29-Jan-2025 , DOI: 10.37421/1948-5956.2025.17.689
Citation: Ashrafizadeh, Milad. “Cancer Vaccines Harnessing: Immune System for Prevention and Treatment.” J Cancer Sci Ther 17 (2025): 689.
Copyright: © 2025 Ashrafizadeh M. This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.

Introduction

Cancer vaccines work on a different concept than conventional vaccinations, which are designed to prevent infectious illnesses. They encourage the immune system to identify and target cancer cells in particular. When the immune system is working at its best, it can discriminate between cells that are dangerous, such as malignant ones, and those that are healthy. Nevertheless, cancer cells frequently avoid immune system recognition or inhibit its reaction, enabling them to spread uncontrolled. Although there are many different types of cancer vaccines, they usually fall into two groups therapeutic and preventative (prophylactic) vaccinations [1,2].

Conversely, therapeutic cancer vaccinations are intended for those who have already received a cancer diagnosis. These vaccinations work as a supplement to traditional therapies like radiation therapy, chemotherapy, and surgery by encouraging the immune system to identify and combat cancer cells [3].

The way cancer vaccines work is by using the immune system's capacity to recognize and destroy aberrant cells. The innate immune system and the adaptive immune system are the two primary parts of the immune response to cancer. A quick, all-around protection against foreign invaders is offered by the innate immune system. Innate immune cells, including natural killer cells and macrophages, can be drawn to the tumor site by signals released by cancer cells. By encouraging the activation and recruitment of these innate immune cells, cancer vaccines may improve this process [4].

A highly focused and specialized subset of immunity, the adaptive immune system includes both T and B cells. T cells are activated and trained to detect certain antigens on cancer cells using cancer vaccinations. Molecules known as antigens cause an immunological reaction. Many efforts for cancer vaccines rely on tumor-specific antigens, like altered proteins. Numerous vaccines against cancer are being developed, each with a different strategy for stimulating the immune system. The short chains of amino acids (peptides) used in these vaccinations are sourced from antigens unique to tumors. By exposing the immune system to these peptides, the vaccination seeks to activate T cells to identify and combat cancer cells that exhibit the same antigens. In order to elicit an immune response, whole cell vaccines employ whole cancer cells, either living or inactivated. These cells can be allogeneic (derived from a different source) or autologous (derived from the patient's own tumor). By exposing the immune system to a wide variety of tumor antigens, whole cell vaccines raise the possibility of a successful reaction [5]. Vaccines based on DNA or RNA injects genetic material into the body that codes for antigens unique to tumors. Once within cells, this genetic material triggers an immune response by telling the cell to create the antigen. This method is flexible and enables the addition of many antigens.

Description

Neoantigen vaccines, another name for personalized cancer vaccinations, capitalize on the distinct genetic alterations found in each person's cancer cells. Researchers can find neoantigens antigens that result from mutations by sequencing the patient's tumor DNA. Then, vaccines are designed to elicit an immune response against these particular neoantigens, possibly providing a highly individualized and successful therapeutic approach. Combination therapies, which mix cancer vaccines with other immunotherapies or conventional treatments, are being investigated by researchers more and more. Combining immune checkpoint inhibitors, which maximize the effectiveness of the immune system, with a cancer vaccination, for example, has demonstrated promise in improving treatment outcomes.

Heterogeneity, or the existence of several cell populations inside a tumor, is a characteristic of cancer. It is still very difficult to create a vaccination that targets every pertinent antigen across this variability. Developing effective vaccinations is made more difficult by the development of resistant cell populations and tumor progression. Cancer cells use a variety of tactics, such as downregulating antigen presentation or producing immune checkpoint molecules, to avoid detection by the immune system. The efficacy of cancer vaccinations may be restricted by these factors. Research on combining vaccinations with substances that interfere with various evasion tactics is ongoing. It is crucial to guarantee the safety of cancer vaccinations. When developing vaccines, it's critical to strike the correct balance between promoting a strong immune response and preventing damage to healthy tissues. There are logistical issues with the manufacture, distribution, and storage of cancer vaccines. Furthermore, the expense of creating and producing customized cancer vaccines in particular presents financial challenges as well as patient access concerns. The use of neoantigen vaccinations is anticipated to increase as genetic profiling becomes more widely available and technology develops. These customized vaccinations may be able to target the distinct features of each patient's cancer, opening the door to more specialized and efficient therapies.

It is anticipated that the use of cancer vaccines in conjunction with other immunotherapies or conventional medicines would increase. Targeting several facets of the immune response and the tumor microenvironment at once may provide synergistic effects. The immune escape strategies used by cancer cells are being actively studied by researchers. Enhancing the immune response against cancer is the goal of tactics like targeting certain signaling pathways or combining vaccinations with immune checkpoint inhibitors. New avenues for the creation of cancer vaccines have been made possible by the success of mRNA vaccines in infectious illnesses. More efficient and adaptable mRNA-based cancer vaccines might result from ongoing research in this field.

Conclusion

Through the use of the immune system, cancer vaccines provide a revolutionary method of both preventing and treating cancer. The discipline has enormous potential to revolutionize cancer care as long as research and development efforts continue. The variety of strategies, from preventative vaccinations that target certain illnesses to individualized neoantigen vaccines made for each patient, highlights how difficult the fight against cancer is. Even if there are still difficulties, new developments like combinatorial treatments and mRNA technology give hope for overcoming barriers and enhancing the effectiveness of cancer vaccines.

Acknowledgement

None.

Conflict of Interest

None.

References

  1. Blandin, Anne-Florence, Guillaume Renner, Maxime Lehmann and Isabelle Lelong-Rebel, et al. "β1 integrins as therapeutic targets to disrupt hallmarks of cancer." Front Pharmacol 6 (2015): 279.

Google Scholar  Cross Ref Indexed at

  1. Gamerith, Gabriele, Marcel Kloppenburg, Finn Mildner and Arno Amann, et al. "Molecular characteristics of radon associated lung cancer highlights MET alterations." Cancers 14 (2022): 5113.

Google Scholar Cross Ref  Indexed at

  1. Bodén, Embla, Fanny Sveréus, Franziska Olm and Sandra Lindstedt. "A systematic review of Mesenchymal Epithelial Transition factor (MET) and its impact in the development and treatment of non-small-cell lung cancer." Cancers 15 (2023): 3827.

 Google Scholar Cross Ref  Indexed at

  1. Van Herpe, Filip and Eric Van Cutsem. "The role of cMET in gastric cancer—A review of the literature." Cancers 15 (2023): 1976.

Google Scholar  Cross Ref  Indexed at

  1. Qin, Kang, Lingzhi Hong, Jianjun Zhang and Xiuning Le. "MET amplification as a resistance driver to TKI therapies in lung cancer: Clinical challenges and opportunities." Cancers 15 (2023): 612.

Google Scholar  Cross Ref  Indexed at

 

 

Google Scholar citation report
Citations: 5332

Cancer Science & Therapy received 5332 citations as per Google Scholar report

Cancer Science & Therapy peer review process verified at publons

Indexed In

 
arrow_upward arrow_upward