Analysis of CD8 T cell reactivity to cytomegalovirus using protein‐spanning pools of overlapping pentadecapeptides

• Published in: European journal of immunology Vol. 30; no. 6; pp. 1676 - 1682
• Main Authors: Kern, Florian, Faulhaber, Nicole, Frömmel, Claudia, Khatamzas, Elham, Prösch, Susanna, Schönemann, Constanze, Kretzschmar, Ines, Volkmer‐Engert, Rudolf, Volk, Hans‐Dieter, Reinke, Petra
• Format: Journal Article
• Language: English
• Published: Weinheim WILEY‐VCH Verlag GmbH 01.06.2000
• Subjects: AIDS/HIV; AIE1 protein; Amino Acid Sequence; CD8 antigen; CD8-Positive T-Lymphocytes - immunology; Cytomegalovirus - immunology; Cytomegalovirus Infections - blood; Cytomegalovirus Infections - immunology; g-Interferon; HLA-A1 Antigen - immunology; HLA-A2 Antigen - immunology; HLA-B7 Antigen - immunology; HLA-B8 Antigen - immunology; Human cytomegalovirus; Humans; IE1 protein; Immediate-Early Proteins - immunology; Immediate‐early‐1 protein; Interferon-gamma - biosynthesis; Molecular Sequence Data; pentadecapeptides; Peptide pool; Peptides - immunology; Phosphoproteins - immunology; pp65; Viral Matrix Proteins - immunology; Viral Proteins
• ISSN: 0014-2980; 1521-4141
• DOI: 10.1002/1521-4141(200006)30:6<1676::AID-IMMU1676>3.0.CO;2-V

The frequencies of human cytomegalovirus (HCMV) protein‐specific CD8 T cells, identified by the presence of intracellular IFN‐γ, were measured by flow cytometry following stimulation of freshly isolated peripheral blood mononuclear cells (PBMC) with comprehensive peptide pools. These pools spanned the entire amino acid sequences of the HCMV pp65 and major immediate early (IE‐1) proteins and consisted of 15‐amino acid peptides with at least nine overlaps between neighboring peptides. As a result all potential CD8 T cell epitopes contained in these proteins were provided by the complete pools and, therefore, unlike with single epitopes, testing was independent of donor HLA type. Individual stimulating peptides from the same pools were identified in parallel experiments. Thus we found that our results with the complete pools using PBMC from 26 healthy HCMV‐seropositive donors were 100 % sensitive and specific with respect to predicting the presence of recognized epitopes in the respective proteins. In addition, cells from 15 renal transplant patients were tested with complete pools alone. While our results confirmed our previous contention that HCMV IE‐1 is an important CD8 T cell target, the technical improvement we made in order to address this question has clearly wider implications. Similar pools may be applied to examine the role of proteins from other pathogens, in autoimmune disease or following vaccination.