Epidermal Langerhans cells from mice bearing a granulocyte macrophage-colony stimulating factor-producing mammary tumor display impaired accessory functions

Yong Xie, Mary E. Fernandez, J. Wayne Streilein, Diana M Lopez

Research output: Contribution to journalArticle

4 Citations (Scopus)

Abstract

A progressive depression of delayed type hypersensitivity reactions occurs during development of mammary tumors in BALB/c mice. This tumor constitutively produces prostaglandin E2 (PGE2) and granulocyte-macrophage colony stimulating factor (GM-CSF). Epidermal Langerhans cells were found to have a decreased responsiveness to bacterial superantigen and to defined antigens in tumor-bearing mice, and also showed an impaired ability to induce proliferative responses in syngeneic or allogeneic responder T cells. Flow cytometric analyses revealed that the Langerhans cells of tumor bearers had decreased densities of the Ia molecule on their surfaces. No defects were observed in the potential of keratinocytes from tumor bearers to produce granulocyte-macrophage colony stimulating factor or to support the activation of syngeneic T cells. Incubation of normal Langerhans cells with tumor derived factors depressed their capacity to stimulate T cell syngeneic responses. Addition of indomethacin and anti-prostaglandin E2 did not reverse this depressed activity. These results indicate that epidermal Langerhans cells from tumor-bearing mice possess a functional deficit in acquiring accessory properties in vitro, which cannot be ascribed to a lack of GM-CSF in the local microenvironment or to production of inhibitory cytokines by their keratinocytes. The functional deficit of epidermal Langerhans cells of tumor-bearing mice may account for the depressed delayed hypersensitivity displayed by these mice, and factors elaborated by the tumor may be responsible for the deficiencies observed.

Original languageEnglish
Pages (from-to)9-16
Number of pages8
JournalAnticancer Research
Volume16
Issue number1
StatePublished - Jan 1 1996

Fingerprint

Langerhans Cells
Granulocyte-Macrophage Colony-Stimulating Factor
Breast Neoplasms
Neoplasms
Delayed Hypersensitivity
T-Lymphocytes
Keratinocytes
Dinoprostone
Superantigens
Neoplasm Antigens
Indomethacin
Cytokines

Keywords

  • Accessory functions, or derived factors
  • Epidermal Langerhans cells

ASJC Scopus subject areas

  • Cancer Research
  • Oncology

Cite this

Epidermal Langerhans cells from mice bearing a granulocyte macrophage-colony stimulating factor-producing mammary tumor display impaired accessory functions. / Xie, Yong; Fernandez, Mary E.; Streilein, J. Wayne; Lopez, Diana M.

In: Anticancer Research, Vol. 16, No. 1, 01.01.1996, p. 9-16.

Research output: Contribution to journalArticle

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