1. A simple and efficient method for the monitoring of antigen-specific T cell responses using peptide pool arrays in a modified ELISpot assay
- Author
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Kathrin U. Jansen, Mcclements William L, Michael P. Neeper, Su Wang, Timothy W Tobery, Xin-Min Wang, and Michael J. Caulfield
- Subjects
CD4-Positive T-Lymphocytes ,Cellular immunity ,T cell ,Papillomavirus E7 Proteins ,Immunology ,Epitopes, T-Lymphocyte ,Enzyme-Linked Immunosorbent Assay ,Biology ,CD8-Positive T-Lymphocytes ,Epitope ,Interferon-gamma ,Mice ,Immune system ,medicine ,Immunology and Allergy ,Cytotoxic T cell ,Animals ,Humans ,Oncogene Proteins ,Mice, Inbred BALB C ,ELISPOT ,Oncogene Proteins, Viral ,Virology ,Cell biology ,Epitope mapping ,medicine.anatomical_structure ,Immunologic Techniques ,Capsid Proteins ,Peptides ,CD8 ,Epitope Mapping - Abstract
In this study, we describe a simple and efficient method for both the monitoring of antigen-specific CD4 and CD8 T cell responses as well as the identification of novel CD4 and CD8 T cell epitopes using a modified ELISpot assay and pools of 20mer peptides. We have demonstrated that pools containing as many as 64 20mer peptides may be used to screen for CD4 and CD8 T cell responses to HPV16 L1, E1, and E7 in mice. Using arrays of pools of overlapping 20mer peptides, we have identified novel CD4 and CD8 epitopes in both HPV16L1 and HPV16E1 which are presented in Balb/c mice. We have further shown that the use of 20mer peptides is equivalent to using minimal 9mer epitopes for the stimulation of CD8 T cell responses in our assay. While our experiments are conducted in mice, the use of peptide pool arrays allows for the identification of epitope-specific responses using far fewer cells than is required for testing a panel of overlapping peptides individually, making this strategy particularly useful in clinical settings where immune cells may be limiting.
- Published
- 2001