Cytomegalovirus (CMV) Phosphoprotein 65 Makes a Large Contribution to Shaping the T Cell Repertoire in CMV‐Exposed Individuals

Florian Kern(Charité - Universitätsmedizin Berlin), Torsten Bunde(Charité - Universitätsmedizin Berlin), Nicole Faulhaber(Charité - Universitätsmedizin Berlin), Felix Kiecker(Charité - Universitätsmedizin Berlin), Elham Khatamzas(Charité - Universitätsmedizin Berlin), Ina‐Maria Rudawski(Charité - Universitätsmedizin Berlin), Axel Prüß(Charité - Universitätsmedizin Berlin), Jan‐Willem Gratama(Rotterdam University of Applied Sciences), Rudolf Volkmer(Charité - Universitätsmedizin Berlin), Ralf Ewert(Deutsches Herzzentrum der Charité), Petra Reinke(Charité - Universitätsmedizin Berlin), Hans‐Dieter Volk(Charité - Universitätsmedizin Berlin), Louis J. Picker(Oregon Health & Science University)
The Journal of Infectious Diseases
June 15, 2002
Cited by 279

Abstract

Antigen-specific, cytokine flow cytometry was used to analyze the prevalence and frequency of CD4 and CD8 memory T cells specific for the abundantly expressed cytomegalovirus (CMV) phosphoprotein 65 (pp65) in healthy CMV IgG-seropositive individuals. Stimulation of peripheral blood mononuclear cells with peptide pools and individual peptides derived from the pp65 amino acid sequence in 40 donors revealed that 63% of donors had a detectable CD4 T cell response and that 83% of donors had a detectable CD8 T cell response against this protein. The overall frequencies of T cells directed against pp65 were analyzed for 20 donors by stimulation with peptide pools covering the complete pp65 protein and were as high as 2 in 1000 and 9 in 1000 (median) peripheral blood CD4 and CD8 T cells, respectively. In addition, a comparison between CD4 responses to a CMV lysate containing various CMV proteins and pp65-specific responses in 9 donors indicated that pp65 was a dominant target of the CMV-specific CD4 T cell response in some, but not all, donors. Several new T cell epitopes were identified.


Related Papers

No related papers found

Powered by citation graph analysis