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Updated: Aug 11, 2026

An Immunohistopathologic Study to Profile the Folate Receptor Beta Macrophage and Vascular Immune Microenvironment in Giant Cell Arteritis
Published on: February 8, 2019
Folate-mediated targeting of T cells to tumors
Edward J Roy1, Ute Gawlick, Brent A Orr
1Neuroscience Program, University of Illinois at Urbana-Champaign, Urbana, IL 61801, USA.
Abstract:
Recently various strategies have been developed to exploit in a clinical setting the well established finding that T cells can specifically recognize and destroy tumor cells. Several independent approaches to the targeting of T cells against cancer have been explored, including the use of bispecific antibodies (anti-T cell/anti-tumor cell) to redirect T cells, vaccines to induce tumor-reactive T cells, and adoptive transfer of ex vivo activated, tumor-reactive T cells. In this review, we focus on studies in which high-affinity folate receptors (FRs) on tumor cells have served as targets for redirecting or enhancing the effectiveness of activated T cells. Bispecific antibody conjugates of folate and antibodies to the T cell receptor (TCR) complex can generate tumor-reactive T cell responses. The development of folate/antibody conjugates specific for the T cell co-stimulatory molecule CD28 could yield activated T cells that recognize endogenous peptide-major histocompatibility complex (MHC) antigens on tumor cells. Finally, we discuss a less investigated area in which high-affinity FRs on macrophages, or other antigen presenting cells (APCs), may provide opportunities in the design of tumor-antigen-specific vaccines.
Insights
This review explores using folate receptors (FRs) to target T cells for cancer therapy. Strategies include bispecific antibodies and vaccines to enhance T cell-mediated tumor destruction.
Area of Science:
- Immunology
- Oncology
- Molecular Biology
Background:
- T cells can specifically recognize and destroy tumor cells.
- Various strategies are being developed to leverage this for clinical cancer treatment.
- High-affinity folate receptors (FRs) are present on tumor cells.
Purpose of the Study:
- To review strategies targeting cancer using T cells directed by folate receptors.
- To explore the use of bispecific antibodies and vaccines involving FRs.
- To discuss the potential of FRs on antigen-presenting cells for vaccine design.
Main Methods:
- Review of studies utilizing bispecific antibodies (anti-T cell/anti-tumor cell).
- Exploration of vaccines designed to induce tumor-reactive T cells.
- Discussion of adoptive T cell transfer strategies.
- Focus on folate receptor-targeted approaches.
Main Results:
- Bispecific antibody conjugates of folate and T cell receptor (TCR) antibodies can generate tumor-reactive T cell responses.
- Folate/antibody conjugates targeting CD28 may enhance T cell recognition of tumor antigens.
- High-affinity FRs on antigen-presenting cells (APCs) offer potential for tumor-antigen-specific vaccines.
Conclusions:
- Folate receptors represent a promising target for enhancing T cell-mediated cancer immunotherapy.
- Bispecific antibodies and novel vaccine designs utilizing FRs show potential for clinical application.
- Targeting FRs on APCs could lead to new vaccine strategies against cancer.
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