Combination effect of regulatory T-cell depletion and ionizing radiation in mouse models of lung and colon cancer

Int J Radiat Oncol Biol Phys. 2015 Jun 1;92(2):390-8. doi: 10.1016/j.ijrobp.2015.01.011. Epub 2015 Mar 5.

Abstract

Purpose: To investigate the potential of low-dose cyclophosphamide (LD-CTX) and anti-CD25 antibody to prevent activation of regulatory T cells (Tregs) during radiation therapy.

Methods and materials: We used LD-CTX and anti-CD25 monoclonal antibody as a means to inhibit Tregs and improve the therapeutic effect of radiation in a mouse model of lung and colon cancer. Mice were irradiated on the tumor mass of the right leg and treated with LD-CTX and anti-CD25 antibody once per week for 3 weeks.

Results: Combined treatment of LD-CTX or anti-CD25 antibody with radiation significantly decreased Tregs in the spleen and tumor compared with control and irradiation only in both lung and colon cancer. Combinatorial treatments resulted in a significant increase in the effector T cells, longer survival rate, and suppressed irradiated and distal nonirradiated tumor growth. Specifically, the combinatorial treatment of LD-CTX with radiation resulted in outstanding regression of local and distant tumors in colon cancer, and almost all mice in this group survived until the end of the study.

Conclusions: Our results suggest that Treg depletion strategies may enhance radiation-mediated antitumor immunity and further improve outcomes after radiation therapy.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Antineoplastic Agents, Alkylating / administration & dosage*
  • Colonic Neoplasms / immunology
  • Colonic Neoplasms / mortality
  • Colonic Neoplasms / radiotherapy*
  • Combined Modality Therapy
  • Cyclophosphamide / administration & dosage*
  • Immunosuppressive Agents / administration & dosage*
  • Interleukin-2 Receptor alpha Subunit / antagonists & inhibitors*
  • Lung Neoplasms / immunology
  • Lung Neoplasms / mortality
  • Lung Neoplasms / radiotherapy*
  • Male
  • Mice
  • Mice, Inbred BALB C
  • T-Lymphocytes, Regulatory / drug effects*
  • T-Lymphocytes, Regulatory / radiation effects*

Substances

  • Antineoplastic Agents, Alkylating
  • Immunosuppressive Agents
  • Interleukin-2 Receptor alpha Subunit
  • Cyclophosphamide