2B4(CD244)-mediated activation of NK cells reduces metastases of B16F10 melanoma in mice.

Abstract:

BACKGROUND:Natural killer (NK) cells are a third population of lymphocytes that can kill certain tumor cells. This killing is regulated by signals received through activating and inhibitory receptors. 2B4 (CD244), a member of the CD2 subset of Immunoglobulin superfamily, was identified as an activating receptor on NK cells. Interaction of 2B4 with its ligand CD48 or anti-2B4 mAb stimulates NK cell cytolytic function as well as production of INF-gamma. MATERIALS AND METHODS:A murine tumor model was used to study the in vivo role of 2B4. 2B4 and CD48 were activated in vivo by injecting anti-2B4 and anti-CD48 monoclonal antibodies. RESULTS:Activation of 2B4 or CD48 resulted in a five-fold reduction in tumor metastasis. IFN-gamma knockout mice had a two-fold increase in metastasis as compared to wild-type after 2B4 activation. CONCLUSION:Activation of 2B4 and CD48 reduces metastasis of B16F10 melanoma cells and this anti-tumor effect involves both cytolytic function and cytokine production.

journal_name

Anticancer Res

journal_title

Anticancer research

authors

Johnson LA,Vaidya SV,Goldfarb RH,Mathew PA

subject

Has Abstract

pub_date

2003-09-01 00:00:00

pages

3651-5

issue

5A

eissn

0250-7005

issn

1791-7530

journal_volume

23

pub_type

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