GMMA decorated with mucin 1 Tn/STn mimetics elicit specific antibodies response and inhibit tumor growth

Carbohydrate-based therapeutic vaccines are actively pursued as targeted immunotherapy to treat cancer. Aberrant glycosylation is indeed of paramount importance in tumors, leading to the formation of "neo-epitopes", known as tumor-associated carbohydrate antigens (TACAs), crucial in cancer onset, development and spread. Accordingly, the over-simplified mucin-type O-glycans Tn and STn have been confirmed among the most promising candidates for the development of cancer vaccines. In this work, we first propose genetically manipulated bacteria outer membrane vesicles (OMVs), namely GMMA, as a vaccine formulation platform to display glycan antigens. GMMA were glycosylated with multiple copies of structurally locked Tn mimetic or STn mimetic as cancer vaccine prototypes. These constructs, in non-adjuvanted formulations, showed sounding immunogenic properties in vivo and impressive efficacy in a mouse model of aggressive triple-negative breast cancer. This example of tailor-made therapeutic vaccine might revolutionize the approach to cancer therapy.

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Publication Details

Journal
npj Vaccines
Published
2025-04-15
DOI
https://doi.org/10.1038/s41541-025-01127-8
Citations
3
Primary Topic
Glycosylation and Glycoproteins Research
Type
article
Field-Weighted Citation Impact
2.42

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article

GMMA decorated with mucin 1 Tn/STn mimetics elicit specific antibodies response and inhibit tumor growth

Elena Palmieri, Renata Grifantini, Cristina Tinti, Andrea Sodini et al.
3 citations
npj Vaccines
Glycosylation and Glycoproteins Research
2.42
article

GMMA decorated with mucin 1 Tn/STn mimetics elicit specific antibodies response and inhibit tumor growth

Elena Palmieri, Renata Grifantini, Cristina Tinti, Andrea Sodini, Antonella Rosa, Francesco Papi, Marco Rossi, Cristina Nativi, Francesca Micoli, Chiara Cordiglieri, Marco Fragai, Francesco Berti, Silvia Valensin, Elisa Pesce
article en
3 citations

Abstract

Carbohydrate-based therapeutic vaccines are actively pursued as targeted immunotherapy to treat cancer. Aberrant glycosylation is indeed of paramount importance in tumors, leading to the formation of "neo-epitopes", known as tumor-associated carbohydrate antigens (TACAs), crucial in cancer onset, development and spread. Accordingly, the over-simplified mucin-type O-glycans Tn and STn have been confirmed among the most promising candidates for the development of cancer vaccines. In this work, we first propose genetically manipulated bacteria outer membrane vesicles (OMVs), namely GMMA, as a vaccine formulation platform to display glycan antigens. GMMA were glycosylated with multiple copies of structurally locked Tn mimetic or STn mimetic as cancer vaccine prototypes. These constructs, in non-adjuvanted formulations, showed sounding immunogenic properties in vivo and impressive efficacy in a mouse model of aggressive triple-negative breast cancer. This example of tailor-made therapeutic vaccine might revolutionize the approach to cancer therapy.

npj VaccinesVol. 10(1)
GlaxoSmithKline (France) (FR), Toscana Life Sciences (IT), Check Point (Israel) (IL), Interuniversity Consortium for Magnetic Resonance (IT), Istituto Nazionale Genetica Molecolare (IT), Global Vaccines (United States) (US), University of Florence (IT)
Dipartimenti di Eccellenza, Associazione Italiana per la Ricerca sul Cancro
Zero hunger
Openalex Percentile: Top 12%
Glycosylation and Glycoproteins Research
2.42
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