NARA Discovery
Article Details
← Back to Search Results
Journal Article

Vaccine strategies for cancer prevention in Lynch syndrome: the potential of dendritic cell-based therapy

Romy N. Kuipers; Mark A. J. Gorris; Cristina Bayó; Tom Hofland; Daniel Benítez Ribas; Georgina Flórez Grau; Nicoline Hoogerbrugge; Joaquin Castillo; Francesc Balaguer; Tanya M. Bisseling; Gerty Schreibelt; I. Jolanda M. de Vries
Familial Cancer · Vol. 25, Issue 2 · 2026

Abstract

Cancer vaccines offer a promising strategy for cancer prevention, particularly in hereditary cancer syndromes such as Lynch syndrome (LS). LS is characterized by a high lifetime risk of developing various malignancies due to defects in DNA mismatch repair, leading to an accumulation of mutations, particularly frameshift insertion/deletions (indels) within microsatellite loci. These indels create shared tumour-specific neoantigens, which are unique to LS and can be recognized by the immune system and trigger cancer cell killing. Importantly, these neoantigens are also present in precancerous lesions, making LS an ideal target for immune-interception strategies aimed at prevention. Over the years, a variety of vaccine designs targeting different antigens along with a range of delivery platforms have been explored for different types of tumours, each with its own advantages and limitations. In this review, we provide an overview of the key antigens and delivery platforms used in cancer preventive vaccine development for LS, evaluate their limited clinical outcomes to date, and explore the future directions of preventive vaccine immunotherapy. A particular focus is placed on the promising potential of dendritic cell vaccination therapy as a future approach in this field.

Bibliographic Information

JournalFamilial Cancer
PublisherSpringer
Publication Date2026-04-22
Publication Year2026
Volume25
Issue2
Document TypeJournal Article
eISSN1573-7292
DOI10.1007/s10689-026-00559-y

Access Information

NARA Access Coverage2001-01-01~Current
Journal Homepagehttps://www.springer.com/journal/10689
Publisher PageOpen Publisher Page
Full-text access depends on NARA's subscribed coverage and institutional access.