4.2 Article

Immunotherapy with autologous, human dendritic cells transfected with carcinoembryonic antigen mRNA

Journal

CANCER INVESTIGATION
Volume 21, Issue 3, Pages 341-349

Publisher

TAYLOR & FRANCIS INC
DOI: 10.1081/CNV-120018224

Keywords

dendritic cells; immunotherapy; CEA; hepatic metastases

Categories

Funding

  1. DIVISION OF BASIC SCIENCES - NCI [Z01BC010597] Funding Source: NIH RePORTER
  2. NATIONAL CANCER INSTITUTE [R01CA075472, P01CA078673] Funding Source: NIH RePORTER
  3. NATIONAL CENTER FOR RESEARCH RESOURCES [M01RR000030] Funding Source: NIH RePORTER
  4. NCI NIH HHS [P01-CA78673-01, R01-CA75472-01] Funding Source: Medline
  5. NCRR NIH HHS [M01RR00030] Funding Source: Medline

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Immunizations with dendritic cells (DC) transfected with RNA encoding tumor antigens induce potent tumor antigen-specific immune responses in vitro and in murine models. We performed a phase I study of patients with advanced carcinoembryonic antigen (CEA)-expressing malignancies followed by a phase II study of patients with resected hepatic metastases of colon cancer to assess safety and feasibility of administering autologous DC loaded with CEA mRNA. The immunizations were well tolerated. Of the 24 evaluable patients in the dose-escalation phase, there was I complete response (by tumor marker), 2 minor responses, 3 with stable disease, and 18 with progressive disease. In the phase II study, 9 of 13 patients have relapsed at a median of 122 days. Evidence of an immunologic response was demonstrated in biopsies of DC injection sites and peripheral blood of selected patients. We conclude that it is feasible and safe to administer mRNA-loaded DC to patients with advanced malignancies.

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