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Antigen Selection Shapes the T-cell Repertoire in Chronic Lymphocytic Leukemia
Ctr Res & Technol Hellas, Inst Appl Biosci, Thessaloniki, Greece..
Ist Sci San Raffaele, Div Mol Oncol, Milan, Italy.;Ist Sci San Raffaele, Dept Oncohematol, Milan, Italy.;Fdn Ctr San Raffaele, Milan, Italy..
Ctr Res & Technol Hellas, Inst Appl Biosci, Thessaloniki, Greece..
Ctr Res & Technol Hellas, Inst Appl Biosci, Thessaloniki, Greece.;G Papanicolaou Hosp, Dept Hematol, Thessaloniki, Greece.;G Papanicolaou Hosp, HCT Unit, Thessaloniki, Greece..
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2016 (English)In: Clinical Cancer Research, ISSN 1078-0432, E-ISSN 1557-3265, Vol. 22, no 1, 167-174 p.Article in journal (Refereed) PublishedText
Abstract [en]

Purpose: The role of antigen(s) in shaping the T-cell repertoire in chronic lymphocytic leukemia, although relevant for understanding malignant cell interactions with cognate T cells, is largely unexplored. Experimental Design: Here we profiled the T-cell receptor beta chain gene repertoire in 58 chronic lymphocytic leukemia patients, focusing on cases assigned to well-characterized subsets with stereotyped clonotypic B-cell receptor immunoglobulins, therefore those cases most evidently selected by antigen (subsets #1, #2, and #4). Results: Remarkable repertoire skewing and oligoclonality were observed, and differences between subsets were noted regarding both T-cell receptor b chain gene usage and the extent of clonality, with subset #2 being the least oligoclonal. Longitudinal analysis of subset #4 cases revealed that although the repertoire may fluctuate over time, certain clonotypes persist, thus alluding to persistent antigenic stimulation. Shared ("stereotyped") clonotypes were found between different patients, reflecting selection by common antigenic elements. Cross-comparison of our dataset with public databases showed that some T-cell clonotypes may have expanded secondary to common viral infections; however, the majority of clonotypes proved to be disease-specific. Conclusions: Overall, the T-cell receptor b chain repertoire in chronic lymphocytic leukemia is likely shaped by antigen selection and the implicated antigenic elements may concern epitopes that also select the malignant B-cell progenitors or, more intriguingly, chronic lymphocytic leukemia-derived epitopes.

Place, publisher, year, edition, pages
2016. Vol. 22, no 1, 167-174 p.
National Category
Cancer and Oncology
URN: urn:nbn:se:uu:diva-274905DOI: 10.1158/1078-0432.CCR-14-3017ISI: 000367550300020PubMedID: 26338994OAI: oai:DiVA.org:uu-274905DiVA: diva2:899852
EU, European Research CouncilSwedish Research CouncilSwedish Cancer SocietyGlaxoSmithKline (GSK)
Available from: 2016-02-02 Created: 2016-01-26 Last updated: 2016-02-02Bibliographically approved

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