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Generation of Multivirus-specific T Cells to Prevent/treat Viral Infections after Allogeneic Hematopoietic Stem Cell Transplant
Published on: May 27, 2011
Clonotype analysis of cytomegalovirus-specific cytotoxic T lymphocytes
Nina Babel1, Gordon Brestrich, Lukasz P Gondek
1Experimental Haematology and Hematopoiesis Section, Taussig Cancer Center, Cleveland Clinic Foundation, Cleveland, Ohio, USA. nina.babel@charite.de
Insights
Cytotoxic T lymphocytes (CTLs) controlling human cytomegalovirus (CMV) replication show a focused T cell receptor repertoire. This suggests immunodominant epitopes are key in shaping the clonal response, aiding immunotherapy insights.
Area of Science:
- Immunology
- Virology
- T cell biology
Background:
- Cytotoxic T lymphocytes (CTLs) are crucial for controlling human cytomegalovirus (CMV) replication.
- Previous studies on CTL clonotypic composition were limited by focusing on single peptides and specific HLA contexts.
Purpose of the Study:
- To determine the clonotypic composition of CMV-specific CTLs in kidney transplant recipients and healthy donors.
- To compare CTL responses after stimulation with a whole pp65 peptide pool versus a single immunodominant peptide.
Main Methods:
- Peripheral blood mononuclear cells from HLA-A2, CMV-seropositive individuals were stimulated.
- T cell receptor (TCR) CDR3 regions of CMV-specific CTLs were sequenced.
Main Results:
- CMV-specific CTL responses were monoclonal or oligoclonal, even with whole peptide pool stimulation.
- Dominant CTL clones showed identical CDR3 motifs regardless of stimulation method (single peptide vs. pool).
- Significant interindividual variation in CDR3 sequences was observed, with structural homology in dominant clonotypes.
Conclusions:
- Immunodominant epitopes play a critical role in shaping the clonal T cell receptor repertoire against CMV.
- The focused repertoire suggests a regulatory mechanism for CMV clonal dominance.
- Findings may inform the design and monitoring of adoptive immunotherapy strategies for CMV infections.
Abstract:
Cytotoxic T lymphocytes (CTL) control the replication of human cytomegalovirus (CMV). Previous studies assessed the clonotypic composition of CTL specific for individual immunodominant peptides within a certain HLA context. Such an approach has inherent limitations and may not assess the true clonal CTL response in vivo. Here, the clonotypic composition of CMV-specific CTL was determined in HLA-A2, CMV-seropositive kidney transplant recipients and healthy blood donors after stimulation of peripheral blood mononuclear cells with either a pp65 whole-peptide pool or a single immunodominant peptide. Even after stimulation with the whole peptide pool, CMV-specific CTL remained monoclonal or oligoclonal. Regarding intraindividual variation, the CDR3 motifs of the dominant clones were identical to those observed in CTL generated by the single immunodominant peptide. Sequencing of the CDR3 regions demonstrated significant interindividual variation; however, structural homology was observed for immunodominant clonotypes in three individuals. In conclusion, the highly focused T cell receptor repertoire found after stimulation with either a single immunodominant peptide or a peptide pool demonstrates a pivotal role for immunodominant epitopes in the generation of a clonal repertoire. These results provide new insights into the regulation of CMV clonal dominance and may contribute to the design and monitoring of adoptive immunotherapy.
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