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Invest. Ophthalmol. Vis. Sci. · Sep 2009
Activated CD11b+ CD15+ granulocytes increase in the blood of patients with uveal melanoma.
- Kyle C McKenna, Kelly M Beatty, Richard A Bilonick, Lynn Schoenfield, Kira L Lathrop, and Arun D Singh.
- Department of Ophthalmology, University of Pittsburgh, Pittsburgh, Pennsylvania 15213, USA. mckennakc@upmc.edu
- Invest. Ophthalmol. Vis. Sci. 2009 Sep 1; 50 (9): 4295-303.
PurposeTo determine whether activated CD11b(+) CD15(+) granulocytes increase in the blood of patients with uveal melanoma.MethodsPeripheral blood mononuclear cells (PBMCs) were isolated by density gradient centrifugation from the blood of patients with primary choroidal/ciliochoroidal uveal melanomas (six women, four men; age range, 46-91 years) and healthy control donors (14 women, 10 men; age range, 50-81 years). The expression of CD15 and CD68 on CD11b(+) myeloid cells within PBMCs and primary uveal melanomas was evaluated by flow cytometry. CD3zeta chain expression by CD3epsilon(+) T cells in PBMCs and within primary uveal melanomas was measured as an indirect indication of T-cell function.ResultsThe percentage of CD11b(+) cells in PBMCs of patients with uveal melanoma increased 1.8-fold in comparison to healthy donors and comprised three subsets: CD68 negative CD15(+) granulocytes, which increased 4.1-fold; CD68(-) CD15(-) cells, which increased threefold; and CD68(+) CD15(low) cells, which were unchanged. A significant (2.7-fold) reduction in CD3zeta chain expression on CD3epsilon(+) T cells, a marker of T-cell dysfunction, was observed in PBMCs of patients with uveal melanoma in comparison with healthy control subjects and correlated significantly with the percentage of CD11b(+) cells in PBMCs. CD3zeta chain expression on T cells within primary tumors was equivalent to CD3zeta expression in PBMCs of the same patient in four of five patients analyzed.ConclusionsActivated CD11b(+) CD15(+) granulocytes expand in the blood of patients with uveal melanoma and may contribute to immune evasion by ocular tumors by inhibiting T-cell function via decreasing CD3zeta chain expression.
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