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Depletion of human regulatory T cells (Treg) and antigen-specific immune responses to cancer vaccines.

Publication ,  Journal Article
Clay, TM; Hobeika, A; Osada, T; Serra, D; Niedzwiecki, D; Lyerly, HK; Morse, MA
Published in: J Clin Oncol
May 20, 2008

3010 Background: CD4+CD25+FoxP3+ regulatory T cells (Treg) limit antigen-specific immune responses and are a cause of suppressed anticancer immunity. Conversely, depletion of Treg leads to immune enhancement. The immunotoxin denileukin diftitox which selectively targets lymphocytes expressing CD25 may deplete FoxP3+ Treg. METHODS: We evaluated the proliferative potential of PBMC to various antigens in vitro following exposure to denileukin diftitox. We then performed a pilot study in which patients with advanced CEA expressing malignancies, being immunized with autologous dendritic cells modified with a fowlpox vector encoding CEA (rF-CEA(6D)-TRICOM), received denileukin diftitox 18 mcg/kg, once, 4 days before the immunizations began, or 9 mcg/kg prior to each of the 4 immunizations. ELISPOT, cytokine flow cytometry, and ELISA were used to measure the T cell and antibody response. RESULTS: In vitro, escalating doses of denileukin diftitox depleted FoxP3+ Treg, decreased Treg function in vitro, and enhanced antigen-specific T cell responses. In the pilot study (n=15), denileukin diftitox was associated with a 74 ± 6% decrease in Treg in those receiving multiple doses, but not in those receiving a single dose. An earlier peak in the vaccine-induced CEA-specific T cell responses, and significant levels (>0.5%) of circulating CD8+ and CD4+ CEA-specific T cells were also seen in the multiple dose group. Conversely, a single dose of denileukin diftitox enhanced anti-CEA, but not antifowlpox vector, antibody responses. Multiple doses abolished the anti-CEA antibody response. CONCLUSIONS: These results indicate the potential for combining Treg depletion with anticancer vaccines to enhance tumor antigen specific immune responses. No significant financial relationships to disclose.

Duke Scholars

Published In

J Clin Oncol

EISSN

1527-7755

Publication Date

May 20, 2008

Volume

26

Issue

15_suppl

Start / End Page

3010

Location

United States

Related Subject Headings

  • Oncology & Carcinogenesis
  • 3211 Oncology and carcinogenesis
  • 1112 Oncology and Carcinogenesis
  • 1103 Clinical Sciences
 

Citation

APA
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ICMJE
MLA
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Clay, T. M., Hobeika, A., Osada, T., Serra, D., Niedzwiecki, D., Lyerly, H. K., & Morse, M. A. (2008). Depletion of human regulatory T cells (Treg) and antigen-specific immune responses to cancer vaccines. J Clin Oncol, 26(15_suppl), 3010.
Clay, T. M., A. Hobeika, T. Osada, D. Serra, D. Niedzwiecki, H. K. Lyerly, and M. A. Morse. “Depletion of human regulatory T cells (Treg) and antigen-specific immune responses to cancer vaccines.J Clin Oncol 26, no. 15_suppl (May 20, 2008): 3010.
Clay TM, Hobeika A, Osada T, Serra D, Niedzwiecki D, Lyerly HK, et al. Depletion of human regulatory T cells (Treg) and antigen-specific immune responses to cancer vaccines. J Clin Oncol. 2008 May 20;26(15_suppl):3010.
Clay, T. M., et al. “Depletion of human regulatory T cells (Treg) and antigen-specific immune responses to cancer vaccines.J Clin Oncol, vol. 26, no. 15_suppl, May 2008, p. 3010.
Clay TM, Hobeika A, Osada T, Serra D, Niedzwiecki D, Lyerly HK, Morse MA. Depletion of human regulatory T cells (Treg) and antigen-specific immune responses to cancer vaccines. J Clin Oncol. 2008 May 20;26(15_suppl):3010.

Published In

J Clin Oncol

EISSN

1527-7755

Publication Date

May 20, 2008

Volume

26

Issue

15_suppl

Start / End Page

3010

Location

United States

Related Subject Headings

  • Oncology & Carcinogenesis
  • 3211 Oncology and carcinogenesis
  • 1112 Oncology and Carcinogenesis
  • 1103 Clinical Sciences