Repurposing ospemifene for potentiating an antigen-specific immune response

Menopause. 2017 Apr;24(4):437-451. doi: 10.1097/GME.0000000000000776.

Abstract

Objective: Ospemifene, an estrogen receptor agonist/antagonist approved for the treatment of dyspareunia and vaginal dryness in postmenopausal women, has potential new indications as an immune modulator. The overall objective of the present series of preclinical studies was to evaluate the immunomodulatory activity of ospemifene in combination with a peptide cancer vaccine.

Methods: Immune regulating effects, mechanism of action and structure activity relationships of ospemifene and related compounds were evaluated by examining expression of T-cell activating cytokines in vitro, and antigen-specific immune response and cytotoxic T-lymphocyte activity in vivo. The effects of ospemifene (OSP) on the immune response to a peptide cancer vaccine (PV) were evaluated after chronic [control (n = 22); OSP 50 mg/kg (n = 16); PV (n = 6); OSP+PV (n = 11)], intermittent [control (n = 10); OSP 10 and 50 mg/kg (n = 11); PV (n = 11); combination treatment (n = 11 each dose)] and pretreatment [control; OSP 100 mg/kg; PV 100 μg; combination treatment (n = 8 all groups)] ospemifene oral dosing schedules in a total of 317 mixed-sex tumor-bearing and nontumor-bearing mice.

Results: The results showed that ospemifene induced expression of the key TH1 cytokines interferon gamma and interleukin-2 in vitro, which may be mediated by stimulating T-cells through phosphoinositide 3-kinase and calmodulin signaling pathways. In combination with an antigen-specific peptide cancer vaccine, ospemifene increased antigen-specific immune response and increased cytotoxic T-lymphocyte activity in tumor-bearing and nontumor-bearing mice. The pretreatment, intermittent, and chronic dosing schedules of ospemifene activate naive T-cells, modulate antigen-induced tolerance and reduce tumor-associated, pro-inflammatory cytokines, respectively.

Conclusions: Taken together, ospemifene's dose response and schedule-dependent immune modulating activity offers a method of tailoring and augmenting the efficacy of previously failed antigen-specific cancer vaccines for a wide range of malignancies.

Publication types

  • Research Support, Non-U.S. Gov't
  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Animals
  • Antineoplastic Combined Chemotherapy Protocols / immunology
  • Antineoplastic Combined Chemotherapy Protocols / therapeutic use
  • Breast Neoplasms / immunology*
  • Calmodulin / metabolism
  • Cancer Vaccines / administration & dosage
  • Cancer Vaccines / immunology
  • Carcinogenesis
  • Chromones / pharmacology
  • Cytokines / blood*
  • Drug Administration Schedule
  • Drug Repositioning
  • Female
  • Flavonoids / pharmacology
  • Gene Expression / drug effects
  • Humans
  • Immunologic Factors / administration & dosage
  • Immunologic Factors / chemistry
  • Immunologic Factors / immunology
  • Immunologic Factors / pharmacology*
  • Interferon-gamma / blood
  • Interferon-gamma / genetics
  • Interleukin-2 / genetics
  • Jurkat Cells
  • Lung Neoplasms / blood
  • Lung Neoplasms / chemically induced
  • Lung Neoplasms / drug therapy*
  • Lymphocyte Activation / drug effects*
  • Membrane Glycoproteins / administration & dosage
  • Membrane Glycoproteins / immunology
  • Mice
  • Mice, Transgenic
  • Morpholines / pharmacology
  • Mucin-1 / genetics
  • Phosphatidylinositol 3-Kinases / metabolism
  • RNA, Messenger / metabolism
  • Signal Transduction / drug effects
  • Structure-Activity Relationship
  • T-Lymphocytes, Cytotoxic / drug effects*
  • T-Lymphocytes, Regulatory / drug effects
  • Tamoxifen / administration & dosage
  • Tamoxifen / analogs & derivatives*
  • Tamoxifen / chemistry
  • Tamoxifen / immunology
  • Tamoxifen / pharmacology
  • Trifluoperazine / pharmacology

Substances

  • Calmodulin
  • Cancer Vaccines
  • Chromones
  • Cytokines
  • Flavonoids
  • Immunologic Factors
  • Interleukin-2
  • L-BLP25
  • Membrane Glycoproteins
  • Morpholines
  • Mucin-1
  • RNA, Messenger
  • Tamoxifen
  • Trifluoperazine
  • 2-(4-morpholinyl)-8-phenyl-4H-1-benzopyran-4-one
  • Interferon-gamma
  • Ospemifene
  • Phosphatidylinositol 3-Kinases
  • 2-(2-amino-3-methoxyphenyl)-4H-1-benzopyran-4-one