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Granzyme B ELISPOT assay for ex vivo measurements of T cell immunity
Authors:Rininsland F H  Helms T  Asaad R J  Boehm B O  Tary-Lehmann M
Affiliation:

a Institute of Pathology, School of Medicine, Case Western Reserve University, 10900 Euclid Ave., BRB 928, Cleveland, OH 44106, USA

b Department of Infectious Disease, Case Western Reserve University, Cleveland, OH 44106, USA

c Section of Endocrinology, University Hospitals of Ulm, 89081 Ulm, Germany

Abstract:A major goal in immunodiagnostics has been the development of assay systems that can measure CD8+ T cell immunity in humans, directly ex vivo, at high resolution, and with high throughput. We established granzyme B (grB) enzyme-linked immunospot assay (ELISPOT) in conjunction with image analysis to this end. Using grB transfected and untransfected Chinese hamster ovary (CHO) cells and T cell lines, we show that the antibody pair utilized was grB-specific and that only activated T cells secrete grB. GrB release began within 4 h after antigen stimulation and stopped within 40 h. Side-by-side comparison showed grB ELISPOT assays to have a higher resolution than classic chromium-release assays in terms of signal-to-noise ratio. The linearity of the relation of the number of CD8+ effector T cells plated to grB spots detected suggests that grB ELISPOT assays measure the frequencies of grB-secreting cells directly. Reactivity to HIV peptides was seen in grB ELISPOT assays of freshly isolated PBMC from HIV patients, consistent with the detection of peptide-specific memory cells. The higher resolution and lower labor and material investment should make grB ELISPOT assays an attractive alternative to chromium-release assays in monitoring the clonal sizes of specific CD8 memory cells in vivo.
Keywords:ELISPOT   Granzyme B   Cytotoxic T cells   Memory   Peptide-specificity
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