Mouse B cells engineered to express an anti-HPV antibody elicit anti-tumor T cell responses.
Transplantation of engineered B cells has demonstrated efficacy in HIV disease models. B cell engineering may also be utilized for the treatment of cancer. Recent studies have highlighted that B cell activity is associated with favorable clinical outcomes in oncology. In mice, polyclonal B cells have been shown to elicit anti-cancer responses. As a potential novel cell therapy, we demonstrate that engineering B cells to target a tumor-associated antigen enhances polyclonal anti-tumor responses. We observe that engineered B cells expressing an anti-HPV B cell receptor internalize the antigen, enabling subsequent activation of oncoantigen-specific T cells. Secreted antibodies from engineered B cells form immune complexes, which are taken up by antigen-presenting cells to further promote T cell activation. Engineered B cells hold promise as novel, multi-modal cell therapies and open new avenues in solid tumor targeting.
Authors
- Alessio D. Nahmad (ORCID: https://orcid.org/0000-0001-6104-577X)
- Guy Biber
- Leah N. Klapper
- Moshe Bracha
- Yael Katz
- Adi Barzel
- Roy Avraham (ORCID: https://orcid.org/0000-0002-3010-3372)
- Yaron Vagima (ORCID: https://orcid.org/0000-0003-2147-6342)
- Natalie Zelikson (ORCID: https://orcid.org/0009-0006-6323-6389)
- Shmuel Hess
- S. Shavit
- Débora Rosa Bublik
Institutions
- Israel Institute for Biological Research (IL)
- Tel Aviv University (IL)
- Samueli Institute (US)
Publication Details
- Journal
- PubMed
- Published
- 2025-01-01
- DOI
- https://doi.org/10.3389/fimmu.2025.1613879
- Citations
- 1
- Primary Topic
- Immunotherapy and Immune Responses
- Type
- article
- Field-Weighted Citation Impact
- 0.80