Trial watch: Adoptive cell transfer for anticancer immunotherapy

Fernando Aranda, Erika Vacchelli, Florine Obrist, Alexander Eggermont, Jérôme Galon, Wolf Hervé Fridman, Isabelle Cremer, Eric Tartour, Laurence Zitvogel, Guido Kroemer, Lorenzo Galluzzi

Research output: Contribution to journalReview articlepeer-review

49 Citations (Scopus)

Abstract

The expression "adoptive cell transfer" (ACT) is commonly employed to indicate an immunotherapeutic regimen involving the isolation of autologous blood-borne or tumorinfiltrating lymphocytes, their selection/expansion/activation ex vivo, and their reinfusion into the patient, most often in the context of lymphodepleting pre-conditioning and in combination with immunostimulatory treatments. Optionally, the cellular material for ACT is genetically manipulated before expansion to (1) target specific tumor-associated antigens; (2) endogenously express immunostimulatory molecules; and/or (3) persist for long periods upon reinfusion. Consistent efforts have been dedicated at the amelioration of this immunotherapeutic regimen throughout the past decade, resulting in the establishment of ever more efficient and safer ACT protocols. Accordingly, the number of clinical trials testing ACT in oncological indications does not cease to increase. In this Trial Watch, we summarize recent developments in this exciting area of research, covering both high-impact studies that have been published during the last 12 months and clinical trials that have been launched in the same period to evaluate the safety and therapeutic potential of ACT in cancer patients.

Original languageEnglish
Article numbere28344
JournalOncoImmunology
Volume3
Issue number5
DOIs
Publication statusPublished - 2014
Externally publishedYes

Keywords

  • CD19
  • Chimeric antigen receptor
  • Cytokine-induced killer cells
  • Interleukin-2
  • Peripheral blood lymphocytes

Fingerprint

Dive into the research topics of 'Trial watch: Adoptive cell transfer for anticancer immunotherapy'. Together they form a unique fingerprint.

Cite this