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Low-dose radiation potentiates the therapeutic efficacy of folate receptor-targeted hapten therapy.

AbstractPURPOSE:
Human cancers frequently overexpress a high-affinity cell-surface receptor for the vitamin folic acid. Highly immunogenic haptens can be targeted to folate receptor-expressing cell surfaces by administration of folate-hapten conjugates, rendering the decorated tumor cell surfaces more recognizable by the immune system. Treatment of antihapten-immunized mice with folate-hapten constructs results in elimination of moderately sized tumors by the immune system. However, when subcutaneous tumors exceed 300 mm(3) before initiation of therapy, antitumor activity is significantly decreased. In an effort to enhance the efficacy of folate-targeted hapten immunotherapy (FTHI) against large tumors, we explored the combination of targeted hapten immunotherapy with low-dose radiotherapy.
METHODS AND MATERIALS:
Mice bearing 300-mm(3) subcutaneous tumors were treated concurrently with FTHI (500 nmol/kg of folate conjugated to fluorescein isothiocyanate, 20,000 U/dose of interleukin 2, and 25,000 U/dose of interferon alpha) and low-dose radiotherapy (3 Gy/dose focused directly on the desired tumor mass). The efficacy of therapy was evaluated by measuring tumor volume.
RESULTS:
Tumor growth analyses show that radiotherapy synergizes with FTHI in antihapten-immunized mice, thereby allowing for cures of animals bearing tumors greater than 300 mm(3). More importantly, nonirradiated distal tumor masses in animals containing locally irradiated tumors also showed improved response to hapten immunotherapy, suggesting that not all tumor lesions must be identified and irradiated to benefit from the combination therapy.
CONCLUSIONS:
These results suggest that simultaneous treatment with FTHI and radiation therapy can enhance systemic antitumor activity in tumor-bearing mice.
AuthorsEmanuela I Sega, Yingjuan Lu, Michael Ringor, Christopher P Leamon, Philip S Low
JournalInternational journal of radiation oncology, biology, physics (Int J Radiat Oncol Biol Phys) Vol. 71 Issue 2 Pg. 559-66 (Jun 01 2008) ISSN: 0360-3016 [Print] United States
PMID18411004 (Publication Type: Journal Article, Research Support, N.I.H., Extramural, Research Support, Non-U.S. Gov't)
Chemical References
  • Antineoplastic Agents
  • Carrier Proteins
  • Folate Receptors, GPI-Anchored
  • Haptens
  • Interleukin-2
  • Neoplasm Proteins
  • Receptors, Cell Surface
  • Interferon-gamma
  • Folic Acid
  • Fluorescein-5-isothiocyanate
Topics
  • Animals
  • Antineoplastic Agents (therapeutic use)
  • Carrier Proteins (immunology)
  • Combined Modality Therapy (methods)
  • Female
  • Fluorescein-5-isothiocyanate (therapeutic use)
  • Folate Receptors, GPI-Anchored
  • Folic Acid (therapeutic use)
  • Haptens (immunology, therapeutic use)
  • Humans
  • Immunotherapy (methods)
  • Interferon-gamma (therapeutic use)
  • Interleukin-2 (therapeutic use)
  • Mice
  • Mice, Inbred BALB C
  • Neoplasm Proteins (immunology)
  • Radiotherapy (methods)
  • Radiotherapy Dosage
  • Random Allocation
  • Receptors, Cell Surface (immunology)
  • Skin Neoplasms (immunology, pathology, radiotherapy, therapy)
  • Tumor Burden

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