Folate receptor α: a storied past and promising future in immunotherapy.

Guy T Clifton, Alan K Sears, Kevin S Clive, Jarrod P Holmes, Elizabeth A Mittendorf, Constantine G Ioannides, Sathibalan Ponniah, George E Peoples

Journal: Human vaccines 2011;7(2):183-90

PMID: 21321484

Abstract

Folate receptor alpha (FR α) is a membrane-bound transport protein with several features which make it an attractive target for cancer immunotherapy. FR α is largely shielded from the immune system in normal tissue but exposed while expressed on a variety of malignancies; it is functionally active in cancer pathogenesis; and it is immunogenic. A variety of different immunotherapeutic methods targeting FR α are being explored to treat cancer. Passive immunotherapy includes monoclonal antibodies, antibodies modified to deliver treatments, and modified T cell therapy. Active immunotherapy has focused on using FR α to increase the immunogenicity of cancer or to generate active FR α-directed immunity through a range of vaccination techniques. We will review the rationale behind targeting immunotherapy to FR α and cover the various techniques designed to do this. Folate receptor alpha (FRα) is a unique tumor-associated antigen (TAA) with many characteristics that make it an attractive target for immunotherapy in cancer. Many different immunotherapeutic modalities utilizing FRα are being explored to treat cancer. The research is in various stages: some are just beyond conception, others have been tried and abandoned, and others still are progressing through human clinical trials. This review will cover immunotherapeutic methods, both active and passive, that target FRα.

Address: Department of Surgery, General Surgery Service, Brooke Army Medical Center, Ft. Sam Houston, TX, USA.

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