Perspective - (2025) Volume 10, Issue 1
Personalized Immunotherapy: A New Era of Cancer Treatment
Hensel Stepan*
*Correspondence:
Hensel Stepan, Department of Infection Control, University of Stanford, Stanford, CA 94305,
USA,
Email:
Department of Infection Control, University of Stanford, Stanford, CA 94305, USA
Received: 29-Jan-2025, Manuscript No. jidm-25-162496;
Editor assigned: 31-Jan-2025, Pre QC No. P-162496;
Reviewed: 12-Feb-2025, QC No. Q-162496;
Revised: 19-Feb-2025, Manuscript No. R-162496;
Published:
26-Feb-2025
, DOI: 10.37421/2576-1420.2025.10.383
Citation: Stepan, Hensel. "Personalized Immunotherapy: A New Era of Cancer Treatment." J Infect Dis Med 10 (2025): 383.
Copyright: © 2025 Stepan H. 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 treatment has long relied on traditional approaches such as surgery,
chemotherapy and radiation therapy. However, these treatments often come with significant side effects and may not be effective for all patients. The advent of personalized
immunotherapy has ushered in a new era of
cancer care, offering targeted and customized solutions that enhance the body's natural defense mechanisms to combat
cancer more effectively. Personalized
immunotherapy involves tailoring treatments based on a patientâ??s unique genetic, molecular and immune system profile [1]. This approach enables oncologists to develop highly specific therapies that maximize effectiveness while minimizing adverse reactions. Key strategies in personalized
immunotherapy include immune checkpoint inhibitors,
cancer vaccines, adoptive T-cell therapy and monoclonal antibodies. These innovative treatments work by either boosting the immune systemâ??s ability to recognize and destroy
cancer cells or by directly targeting tumor-specific markers [2]. One of the most promising aspects of personalized
immunotherapy is its ability to adapt to the evolving nature of cancer. Unlike traditional therapies, which may struggle against treatment-resistant mutations,
immunotherapy leverages the immune system's memory and adaptability to provide long-term protection.
Description
Moreover, advances in biomarker analysis and artificial intelligence are further refining treatment selection, ensuring that each patient receives the most effective therapy based on their specific cancer profile. A groundbreaking development in this field is the use of Chimeric Antigen Receptor (CAR) T-cell therapy, which involves genetically modifying a patientâ??s own T-cells to recognize and attack cancer cells. CAR-T therapy has shown remarkable success in treating blood cancers such as leukemia and lymphoma, leading to significant remission rates in many patients. Researchers are now working to expand its application to solid tumors, which pose additional challenges due to their complex tumor microenvironment and ability to suppress immune responses [3]. Another area of rapid advancement is cancer vaccines. Unlike traditional preventive vaccines, therapeutic cancer vaccines are designed to stimulate the immune system to target existing tumors. These vaccines work by introducing tumor-associated antigens that prime the immune system to recognize and attack cancer cells.
Recent studies on mRNA-based cancer vaccines, inspired by COVID-19 vaccine technology, have shown encouraging results, particularly for melanoma and pancreatic cancer. Despite its revolutionary potential, personalized immunotherapy also presents challenges. High costs, complex manufacturing processes and the need for extensive genetic testing can limit accessibility. Furthermore, while many patients respond positively, some cancers develop mechanisms to evade immune detection, necessitating ongoing research and combination therapies to enhance efficacy. The potential for immune-related adverse effects, such as cytokine release syndrome and autoimmune reactions, also requires careful monitoring and management by healthcare professionals [4,5]. The future of personalized immunotherapy looks promising, with emerging technologies such as CRISPR-based gene editing and neoantigen-targeted therapies pushing the boundaries of what is possible.
Conclusion
Scientists are exploring the role of the gut microbiome in modulating immune responses, which could lead to innovative treatment strategies that optimize the effectiveness of immunotherapy. Additionally, integrating big data and
artificial intelligence in
oncology is expected to improve patient stratification, enabling more precise predictions of treatment outcomes. As research in
immunotherapy continues to evolve, it is becoming clear that this approach represents a paradigm shift in
cancer treatment. By leveraging the bodyâ??s own immune system to fight
cancer more effectively, personalized
immunotherapy is not only improving survival rates but also enhancing patients' quality of life. With ongoing advancements in science and technology, this revolutionary treatment approach has the potential to transform
cancer care and offer new hope to patients worldwide.
Acknowledgement
None.
Conflict of Interest
None.
References
- Mineo, Giangaspare, F. Ciccarese, C. Modolon and Maria Paola Landini, et al. “Post-ARDS pulmonary fibrosis in patients with H1N1 pneumonia: Role of follow-up CT.” Radiol Med117 (2012): 185.
Google Scholar Cross Ref Indexed at
- Gudowska-Sawczuk, Monika and Barbara Mroczko. “Free light chains as a novel diagnostic biomarker of immune system abnormalities in multiple sclerosis and HIV infection.” Biomed Res Int 2019 (2019).
Google Scholar Cross Ref Indexed at
- Diener, T. O. “Potato spindle tuber “virus”: IV. A replicating, low molecular weight RNA.” Virol 45 (1971): 411-428.
Google Scholar Cross Ref Indexed at
- Bartsch, Yannic, Xin Tong, Jaweon Kang and María José Avendaño, et al. “Preserved omicron spike specific antibody binding and Fc-recognition across COVID-19 vaccine platforms.” Medrxiv(2021).
Google Scholar Cross Ref
- Wei, Shuang, Ruiling Bian, Ida Bagus Andika and Erbo Niu, et al. “Symptomatic plant viroid infections in phytopathogenic fungi.” Proc Natl Acad Sci116 (2019): 13042-13050.
Google Scholar Cross Ref Indexed at