» Articles » PMID: 33679703

Cancer Vaccines: Adjuvant Potency, Importance of Age, Lifestyle, and Treatments

Overview
Journal Front Immunol
Date 2021 Mar 8
PMID 33679703
Citations 48
Authors
Affiliations
Soon will be listed here.
Abstract

Although the discovery and characterization of multiple tumor antigens have sparked the development of many antigen/derived cancer vaccines, many are poorly immunogenic and thus, lack clinical efficacy. Adjuvants are therefore incorporated into vaccine formulations to trigger strong and long-lasting immune responses. Adjuvants have generally been classified into two categories: those that 'depot' antigens (e.g. mineral salts such as aluminum hydroxide, emulsions, liposomes) and those that act as immunostimulants (Toll Like Receptor agonists, saponins, cytokines). In addition, several novel technologies using vector-based delivery of antigens have been used. Unfortunately, the immune system declines with age, a phenomenon known as immunosenescence, and this is characterized by functional changes in both innate and adaptive cellular immunity systems as well as in lymph node architecture. While many of the immune functions decline over time, others paradoxically increase. Indeed, aging is known to be associated with a low level of chronic inflammation-inflamm-aging. Given that the median age of cancer diagnosis is 66 years and that immunotherapeutic interventions such as cancer vaccines are currently given in combination with or after other forms of treatments which themselves have immune-modulating potential such as surgery, chemotherapy and radiotherapy, the choice of adjuvants requires careful consideration in order to achieve the maximum immune response in a compromised environment. In addition, more clinical trials need to be performed to carefully assess how less conventional form of immune adjuvants, such as exercise, diet and psychological care which have all be shown to influence immune responses can be incorporated to improve the efficacy of cancer vaccines. In this review, adjuvants will be discussed with respect to the above-mentioned important elements.

Citing Articles

Iterative selection of lipid nanoparticle vaccine adjuvants for rapid elicitation of tumoricidal CD8⁺ T cells.

Luo Y, Zhou S, Song Y, Huang W, Wilding G, Jablonski J Bioact Mater. 2025; 48:189-199.

PMID: 40046011 PMC: 11880734. DOI: 10.1016/j.bioactmat.2025.01.028.


Targeting murine metastatic cancers with cholera toxin A1-adjuvanted peptide vaccines.

Paul S, Kaya M, Johnsson O, Grauers Wiktorin H, Tornell A, Arabpour M Hum Vaccin Immunother. 2025; 21(1):2455240.

PMID: 39848921 PMC: 11760229. DOI: 10.1080/21645515.2025.2455240.


Grapefruit-Derived Vesicles Loaded with Recombinant HSP70 Activate Antitumor Immunity in Colon Cancer In Vitro and In Vivo.

Garaeva L, Komarova E, Emelianova S, Putevich E, Konevega A, Margulis B Biomedicines. 2025; 12(12.

PMID: 39767665 PMC: 11674020. DOI: 10.3390/biomedicines12122759.


Targeting immunosenescence for improved tumor immunotherapy.

Liu Z, Zuo L, Zhou Z, Liu S, Ba Y, Zuo A MedComm (2020). 2024; 5(11):e777.

PMID: 39473905 PMC: 11518697. DOI: 10.1002/mco2.777.


Bioinformatics design of a peptide vaccine containing sarcoma antigen NY-SAR-35 epitopes against breast cancer and evaluation of its immunological function in BALB/c mouse model.

Samman N, Mohabatkar H, Behbahani M, Ganjlikhani Hakemi M PLoS One. 2024; 19(6):e0306117.

PMID: 38923980 PMC: 11207152. DOI: 10.1371/journal.pone.0306117.


References
1.
Sridharan A, Esposo M, Kaushal K, Tay J, Osann K, Agrawal S . Age-associated impaired plasmacytoid dendritic cell functions lead to decreased CD4 and CD8 T cell immunity. Age (Dordr). 2010; 33(3):363-76. PMC: 3168606. DOI: 10.1007/s11357-010-9191-3. View

2.
Liu H, Tu Z, Feng F, Shi H, Chen K, Xu X . Virosome, a hybrid vehicle for efficient and safe drug delivery and its emerging application in cancer treatment. Acta Pharm. 2015; 65(2):105-16. DOI: 10.1515/acph-2015-0019. View

3.
Berinstein N, Karkada M, Morse M, Nemunaitis J, Chatta G, Kaufman H . First-in-man application of a novel therapeutic cancer vaccine formulation with the capacity to induce multi-functional T cell responses in ovarian, breast and prostate cancer patients. J Transl Med. 2012; 10:156. PMC: 3479010. DOI: 10.1186/1479-5876-10-156. View

4.
Shariat S, Badiee A, Jalali S, Mansourian M, Yazdani M, Mortazavi S . P5 HER2/neu-derived peptide conjugated to liposomes containing MPL adjuvant as an effective prophylactic vaccine formulation for breast cancer. Cancer Lett. 2014; 355(1):54-60. DOI: 10.1016/j.canlet.2014.09.016. View

5.
Dreno B, Thompson J, Smithers B, Santinami M, Jouary T, Gutzmer R . MAGE-A3 immunotherapeutic as adjuvant therapy for patients with resected, MAGE-A3-positive, stage III melanoma (DERMA): a double-blind, randomised, placebo-controlled, phase 3 trial. Lancet Oncol. 2018; 19(7):916-929. DOI: 10.1016/S1470-2045(18)30254-7. View