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Follicular Helper T Cells in DiGeorge Syndrome
DiGeorge syndrome is an immunodeficiency characterized by thymic dysplasia resulting in T cell lymphopenia. Most patients suffer from increased susceptibility to infections and heightened prevalence of autoimmune disorders, such as autoimmune thrombocytopenia. B cells in DiGeorge syndrome show impai...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Frontiers Media S.A.
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6065053/ https://www.ncbi.nlm.nih.gov/pubmed/30083170 http://dx.doi.org/10.3389/fimmu.2018.01730 |
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author | Klocperk, Adam Paračková, Zuzana Bloomfield, Markéta Rataj, Michal Pokorný, Jan Unger, Susanne Warnatz, Klaus Šedivá, Anna |
author_facet | Klocperk, Adam Paračková, Zuzana Bloomfield, Markéta Rataj, Michal Pokorný, Jan Unger, Susanne Warnatz, Klaus Šedivá, Anna |
author_sort | Klocperk, Adam |
collection | PubMed |
description | DiGeorge syndrome is an immunodeficiency characterized by thymic dysplasia resulting in T cell lymphopenia. Most patients suffer from increased susceptibility to infections and heightened prevalence of autoimmune disorders, such as autoimmune thrombocytopenia. B cells in DiGeorge syndrome show impaired maturation, with low switched-memory B cells and a wide spectrum of antibody deficiencies or dysgammaglobulinemia, presumably due to impaired germinal center responses. We set out to evaluate circulating follicular helper T cells (cTFHs) in DiGeorge syndrome, as markers of T–B interaction in the germinal centers in a cohort of 17 patients with partial DiGeorge and 21 healthy controls of similar age. cTFHs were characterized as CXCR5(+)CD45RA(−) CD4(+) T cells using flow cytometry. We verify previous findings that the population of memory CD4(+) T cells is relatively increased in diGeorge patients, corresponding to low naïve T cells and impaired T cell production in the thymus. The population of CXCR5(+) memory CD4(+) T cells (cTFHs) was significantly expanded in patients with DiGeorge syndrome, but only healthy controls and not DiGeorge syndrome patients showed gradual increase of CXCR5 expression on cTFHs with age. We did not observe correlation between cTFHs and serum IgG levels or population of switched memory B cells. There was no difference in cTFH numbers between DiGeorge patients with/without thrombocytopenia and with/without allergy. Interestingly, we show strong decline of PD1 expression on cTFHs in the first 5 years of life in DiGeorge patients and healthy controls, and gradual increase of PD1 and ICOS expression on CD4(−) T cells in healthy controls later in life. Thus, here, we show that patients with DiGeorge syndrome have elevated numbers of cTFHs, which, however, do not correlate with autoimmunity, allergy, or production of immunoglobulins. This relative expansion of cTFH cells may be a result of impaired T cell development in patients with thymic dysplasia. |
format | Online Article Text |
id | pubmed-6065053 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-60650532018-08-06 Follicular Helper T Cells in DiGeorge Syndrome Klocperk, Adam Paračková, Zuzana Bloomfield, Markéta Rataj, Michal Pokorný, Jan Unger, Susanne Warnatz, Klaus Šedivá, Anna Front Immunol Immunology DiGeorge syndrome is an immunodeficiency characterized by thymic dysplasia resulting in T cell lymphopenia. Most patients suffer from increased susceptibility to infections and heightened prevalence of autoimmune disorders, such as autoimmune thrombocytopenia. B cells in DiGeorge syndrome show impaired maturation, with low switched-memory B cells and a wide spectrum of antibody deficiencies or dysgammaglobulinemia, presumably due to impaired germinal center responses. We set out to evaluate circulating follicular helper T cells (cTFHs) in DiGeorge syndrome, as markers of T–B interaction in the germinal centers in a cohort of 17 patients with partial DiGeorge and 21 healthy controls of similar age. cTFHs were characterized as CXCR5(+)CD45RA(−) CD4(+) T cells using flow cytometry. We verify previous findings that the population of memory CD4(+) T cells is relatively increased in diGeorge patients, corresponding to low naïve T cells and impaired T cell production in the thymus. The population of CXCR5(+) memory CD4(+) T cells (cTFHs) was significantly expanded in patients with DiGeorge syndrome, but only healthy controls and not DiGeorge syndrome patients showed gradual increase of CXCR5 expression on cTFHs with age. We did not observe correlation between cTFHs and serum IgG levels or population of switched memory B cells. There was no difference in cTFH numbers between DiGeorge patients with/without thrombocytopenia and with/without allergy. Interestingly, we show strong decline of PD1 expression on cTFHs in the first 5 years of life in DiGeorge patients and healthy controls, and gradual increase of PD1 and ICOS expression on CD4(−) T cells in healthy controls later in life. Thus, here, we show that patients with DiGeorge syndrome have elevated numbers of cTFHs, which, however, do not correlate with autoimmunity, allergy, or production of immunoglobulins. This relative expansion of cTFH cells may be a result of impaired T cell development in patients with thymic dysplasia. Frontiers Media S.A. 2018-07-23 /pmc/articles/PMC6065053/ /pubmed/30083170 http://dx.doi.org/10.3389/fimmu.2018.01730 Text en Copyright © 2018 Klocperk, Paračková, Bloomfield, Rataj, Pokorný, Unger, Warnatz and Šedivá. https://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Immunology Klocperk, Adam Paračková, Zuzana Bloomfield, Markéta Rataj, Michal Pokorný, Jan Unger, Susanne Warnatz, Klaus Šedivá, Anna Follicular Helper T Cells in DiGeorge Syndrome |
title | Follicular Helper T Cells in DiGeorge Syndrome |
title_full | Follicular Helper T Cells in DiGeorge Syndrome |
title_fullStr | Follicular Helper T Cells in DiGeorge Syndrome |
title_full_unstemmed | Follicular Helper T Cells in DiGeorge Syndrome |
title_short | Follicular Helper T Cells in DiGeorge Syndrome |
title_sort | follicular helper t cells in digeorge syndrome |
topic | Immunology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6065053/ https://www.ncbi.nlm.nih.gov/pubmed/30083170 http://dx.doi.org/10.3389/fimmu.2018.01730 |
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