Neoantigen vaccine platforms in clinical development: understanding the future of personalized immunotherapy.


Journal

Expert opinion on investigational drugs
ISSN: 1744-7658
Titre abrégé: Expert Opin Investig Drugs
Pays: England
ID NLM: 9434197

Informations de publication

Date de publication:
May 2021
Historique:
pubmed: 2 3 2021
medline: 24 6 2021
entrez: 1 3 2021
Statut: ppublish

Résumé

Derived from genetic alterations, cancer neoantigens are proteins with novel amino acid sequences that can be recognized by the immune system. Recent evidence demonstrates that cancer neoantigens represent important targets of cancer immunotherapy. The goal of cancer neoantigen vaccines is to induce neoantigen-specific immune responses and antitumor immunity, while minimizing the potential for autoimmune toxicity. Advances in sequencing technologies, neoantigen prediction ?algorithms,? and other technologies have dramatically improved the ability to identify and prioritize cancer neoantigens. These advances have generated considerable enthusiasm for ?the ?development of neoantigen vaccines. Several neoantigen vaccine platforms are currently being evaluated in early phase clinical trials including the synthetic long peptide (SLP), RNA, dendritic cell (DC), and DNA vaccine platforms. In this review, we describe, evaluate the mechanism(s) of action, compare the advantages and disadvantages, and summarize early clinical experience with each vaccine platform. We provide perspectives on the future directions of the neoantigen vaccine field. All data are derived from PubMed and ClinicalTrials search updated in October 2020. Although the initial clinical experience is promising, significant challenges to the success of neoantigen vaccines include limitations in neoantigen identification and the need to successfully target the immunosuppressive tumor microenvironment.

Identifiants

pubmed: 33641576
doi: 10.1080/13543784.2021.1896702
pmc: PMC8327784
mid: NIHMS1679237
doi:

Substances chimiques

Antigens, Neoplasm 0
Cancer Vaccines 0

Types de publication

Journal Article Review

Langues

eng

Sous-ensembles de citation

IM

Pagination

529-541

Subventions

Organisme : NCI NIH HHS
ID : P30 CA091842
Pays : United States
Organisme : NCI NIH HHS
ID : P50 CA196510
Pays : United States
Organisme : NCI NIH HHS
ID : R01 CA240983
Pays : United States

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Auteurs

Suangson Supabphol (S)

Department of Surgery, Washington University School of Medicine, St Louis, MO, USA.
The Center of Excellence in Systems Biology, Faculty of Medicine, Chulalongkorn University, Bangkok, Thailand.

Lijin Li (L)

Department of Surgery, Washington University School of Medicine, St Louis, MO, USA.

S Peter Goedegebuure (SP)

Department of Surgery, Washington University School of Medicine, St Louis, MO, USA.
The Alvin J. Siteman Cancer Center at Barnes-Jewish Hospital and Washington University School of Medicine, St Louis, MO, USA.

William E Gillanders (WE)

Department of Surgery, Washington University School of Medicine, St Louis, MO, USA.
The Alvin J. Siteman Cancer Center at Barnes-Jewish Hospital and Washington University School of Medicine, St Louis, MO, USA.

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