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This Article Full Text Full Text (PDF) All Versions of this Article: 11/4/357    most recent 15228517-2008-111v1 Alert me when this article is cited Alert me if a correction is posted Citation Map Services Similar articles in this journal Similar articles in PubMed Alert me to new issues of the journal Download to citation manager Citing Articles Citing Articles via Web of Science (1) Citing Articles via Google Scholar Google Scholar Articles by Bryant, N. L. Articles by Lamb, L. S. Search for Related Content PubMed PubMed Citation Social Bookmarking                   What's this?

Characterization and immunotherapeutic potential of T-cells in patients with glioblastoma

Departments of Pediatrics (N.L.B., L.S.L.), Medicine (C.S.-C., S.M., R.D.L., L.S.L.), Surgery (G.Y.G., J.M.M.), and Neurology (L.B.N.), School of Medicine, University of Alabama at Birmingham, Birmingham, AL, USA

Address correspondence to Lawrence S. Lamb, Jr., Suite 541, Tinsley Harrison Tower, 1530 Third Ave. South, Birmingham, AL 35294, USA (lawrence.lamb{at}ccc.uab.edu).

Classical immunotherapeutic approaches to glioblastoma multiforme (GBM) have shown mixed results, and therapies focused on innate lymphocyte activity against GBM have not been rigorously evaluated. We examined peripheral blood lymphocyte phenotype, T-cell number, mitogenic response, and cytotoxicity against GBM cell lines and primary tumor explants from GBM patients at selected time points prior to and during GBM therapy. Healthy volunteers served as controls and were grouped by age. T-cell infiltration of tumors from these patients was assessed by staining for CD3 and T-cell receptor . Our findings revealed no differences in counts of mean absolute T-cells, T-cell subsets CD3⁺CD4⁺ and CD3⁺CD8⁺, and natural killer cells from healthy volunteers and patients prior to and immediately after GBM resection. In contrast, T-cell counts and mitogen-stimulated proliferative response of T-cells were markedly decreased prior to GBM resection and throughout therapy. Expanded/activated T-cells from both patients and healthy volunteers kill GBM cell lines D54, U373, and U251, as well as primary GBM, without cytotoxicity to primary astrocyte cultures. Perivascular T-cell accumulation was noted in paraffin sections, but no organized T-cell invasion of the tumor parenchyma was seen. Taken together, these data suggest that T-cell depletion and impaired function occur prior to or concurrent with the growth of the tumor. The significant cytotoxicity of expanded/activated T-cells from both healthy controls and selected patients against primary GBM explants may open a previously unexplored approach to cellular immunotherapy of GBM.

Key Words: T-cells • glioblastoma multiforme • immunotherapy • innate immunity

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