The expanded double negative T cell populations of a patient with ALPS are not clonally related to CD4+ or to CD8+ T cells: BRIEF DEFINITE REPORT
Abstract
The autoimmune lymphoproliferative syndrome (ALPS) is characterized by non-malignant lymphoproliferation and signs of autoimmunity. A hallmark of ALPS are high amounts of circulating CD3+/CD4-/CD8- double negative T-lymphocytes (DN T cells). The origin of these cells remains elusive. To investigate the relationships of DN T cells and the single positive T cell populations (CD4+ and CD8+), we analyzed by spectratyping the complementarity determining regions 3 (CDR3) of the T cell receptors in sorted "single positive" (CD4+, CD8+) and DN T cells in a patient with ALPS type 1a. We observed signs for clonal expansion in all three T cell subpopulations. Strong and weak clonal expansions were to be seen in 16 and 14 for DN, 6 and 12 for CD8+, and 1 and 5 for CD4 + T cells, respectively. Most importantly, 24 out of 30 aberrant peaks in the spectratype histograms of the DN T cells where unique for this population and were not to be detected in the histograms of the single positive T cells. In contrast to published data, we conclude that expanded DN T cell populations in ALPS are not generally derived from expanded CD3+/CD4+ or CD3+/CD8+ populations.
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Two unrelated HEM1-deficient patients displayed persistently elevated proportions of αβ double-negative T cells.
“Two unrelated patients displayed persistently elevated proportions of αβ double-negative T (DNT) cells, an interesting comparison to the hallmark expansion of DNTs in autoimmune lymphoproliferative syndrome [8, 31, 32].”
From HEM1 Actin Immunodysregulatory Disorder: Genotypes, Phenotypes, and Future Directions (2022) · cites this paper as [31]
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HEM1 Actin Immunodysregulatory Disorder: Genotypes, Phenotypes, and Future Directions
Cook, S., Lenardo, M. J., & Freeman, A. F. (2022) · Journal of Clinical Immunology · doi:10.1007/s10875-022-01327-0 · Cited by 24 · see citing works
- Authors
- Arnold, M., Gaipl, U., Brunner, J., Spriewald, B., Herrmann, M., & Haas, J. P.
- Affiliations
- Universitätsklinikum Erlangen (DE)
- Universität Innsbruck (AT)
- Universität Greifswald (DE)
- Venue
- Autoimmunity
- Publisher
- Informa UK Limited
- Published
- 2007-01
- Volume
- 40
- Issue
- 4
- Pages
- 299-301
- ISSN
- 0891-6934 (ISSN-L)
- 1607-842X
- OpenAlex
- W2123547670
- Cited by
- 16
- References
- 0
- Citations by year
- 2024: 1 · 2023: 1 · 2022: 1 · 2019: 1 · 2018: 1 · 2016: 1 · 2015: 1 · 2014: 1 · 2012: 3
- FWCI
- 0.49
- Type
- journal article
- Language
- en
- Open access
- closed
- Locations
- Autoimmunity (publishedVersion)
- PubMed (publishedVersion)
- Funders
- Bundesministerium für Bildung und Forschung
- Topics
- Life Sciences › Immunology and Microbiology › Immunology › T-cell and B-cell Immunology
- Life Sciences › Immunology and Microbiology › Immunology › Immunodeficiency and Autoimmune Disorders
- Health Sciences › Medicine › Pathology and Forensic Medicine › Lymphoma Diagnosis and Treatment
- Keywords
- autoimmune lymphoproliferative syndrome, double-negative T cells, CD4+ T cells, CD8+ T cells, clonal expansion, T cell receptor CDR3, T cell origin, lymphoproliferation
- MeSH terms
- Adult, Autoimmune Diseases, Humans, Lymphoproliferative Disorders, Male, Receptors, Antigen, T-Cell, Syndrome, CD4-Positive T-Lymphocytes, CD3 Complex, CD8-Positive T-Lymphocytes
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