Quantitative B-lymphocyte deficiency and increased TCRγδ T-lymphocytes in acute infectious spondylodiscitis

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Standard

Quantitative B-lymphocyte deficiency and increased TCRγδ T-lymphocytes in acute infectious spondylodiscitis. / Haugaard, Anna K; Marquart, Hanne V; Kolte, Lilian; Ryder, Lars Peter; Kehrer, Michala; Krogstrup, Maria; Dragsted, Ulrik B; Dahl, Benny; Gjørup, Ida E; Andersen, Åse B; Garred, Peter; Nielsen, Susanne D.

In: Scientific Reports, Vol. 8, 15174, 2018.

Research output: Contribution to journalJournal articleResearchpeer-review

Harvard

Haugaard, AK, Marquart, HV, Kolte, L, Ryder, LP, Kehrer, M, Krogstrup, M, Dragsted, UB, Dahl, B, Gjørup, IE, Andersen, ÅB, Garred, P & Nielsen, SD 2018, 'Quantitative B-lymphocyte deficiency and increased TCRγδ T-lymphocytes in acute infectious spondylodiscitis', Scientific Reports, vol. 8, 15174. https://doi.org/10.1038/s41598-018-33318-w

APA

Haugaard, A. K., Marquart, H. V., Kolte, L., Ryder, L. P., Kehrer, M., Krogstrup, M., Dragsted, U. B., Dahl, B., Gjørup, I. E., Andersen, Å. B., Garred, P., & Nielsen, S. D. (2018). Quantitative B-lymphocyte deficiency and increased TCRγδ T-lymphocytes in acute infectious spondylodiscitis. Scientific Reports, 8, [15174]. https://doi.org/10.1038/s41598-018-33318-w

Vancouver

Haugaard AK, Marquart HV, Kolte L, Ryder LP, Kehrer M, Krogstrup M et al. Quantitative B-lymphocyte deficiency and increased TCRγδ T-lymphocytes in acute infectious spondylodiscitis. Scientific Reports. 2018;8. 15174. https://doi.org/10.1038/s41598-018-33318-w

Author

Haugaard, Anna K ; Marquart, Hanne V ; Kolte, Lilian ; Ryder, Lars Peter ; Kehrer, Michala ; Krogstrup, Maria ; Dragsted, Ulrik B ; Dahl, Benny ; Gjørup, Ida E ; Andersen, Åse B ; Garred, Peter ; Nielsen, Susanne D. / Quantitative B-lymphocyte deficiency and increased TCRγδ T-lymphocytes in acute infectious spondylodiscitis. In: Scientific Reports. 2018 ; Vol. 8.

Bibtex

@article{452c8f0f0b5a4f89b9e25f6c0015fcf4,
title = "Quantitative B-lymphocyte deficiency and increased TCRγδ T-lymphocytes in acute infectious spondylodiscitis",
abstract = "Acute infectious spondylodiscitis (AIS) is a serious infection of the spine with rising incidence and a mortality of 3-6%. The role of the immune system in AIS is largely unknown. We performed extensive B and T-lymphocyte phenotyping in patients with AIS at diagnosis and after treatment cessation. In this prospective multicentre study, flow cytometric analysis of T and B-lymphocyte subsets was performed in 35 patients at diagnosis and 3 months after treatment cessation. We additionally analysed levels of immunoglobulins and IgG subclasses, serum level and genetic variants of mannose-binding lectin, and somatic hypermutation. A total of 22 (61%) patients had B-lymphocytes below reference limit at baseline, persisting in 7 (30%) patients at follow-up. We found a lower proportion of CD19 + CD27 + IgD+ marginal zone B-lymphocytes and a higher proportion of γδ+ T-lymphocyte receptors compared with controls at both time points. Immunoglobulin levels were elevated at baseline compared to follow-up, and not associated with absolute B-lymphocyte count. In conclusion, a large proportion of AIS patients presented with profound B-lymphocyte deficiency, only partly reversible at follow-up. Identification of immune dysfunction related to AIS may allow for future targeted therapeutic interventions to restore host immunity.",
author = "Haugaard, {Anna K} and Marquart, {Hanne V} and Lilian Kolte and Ryder, {Lars Peter} and Michala Kehrer and Maria Krogstrup and Dragsted, {Ulrik B} and Benny Dahl and Gj{\o}rup, {Ida E} and Andersen, {{\AA}se B} and Peter Garred and Nielsen, {Susanne D}",
year = "2018",
doi = "10.1038/s41598-018-33318-w",
language = "English",
volume = "8",
journal = "Scientific Reports",
issn = "2045-2322",
publisher = "nature publishing group",

}

RIS

TY - JOUR

T1 - Quantitative B-lymphocyte deficiency and increased TCRγδ T-lymphocytes in acute infectious spondylodiscitis

AU - Haugaard, Anna K

AU - Marquart, Hanne V

AU - Kolte, Lilian

AU - Ryder, Lars Peter

AU - Kehrer, Michala

AU - Krogstrup, Maria

AU - Dragsted, Ulrik B

AU - Dahl, Benny

AU - Gjørup, Ida E

AU - Andersen, Åse B

AU - Garred, Peter

AU - Nielsen, Susanne D

PY - 2018

Y1 - 2018

N2 - Acute infectious spondylodiscitis (AIS) is a serious infection of the spine with rising incidence and a mortality of 3-6%. The role of the immune system in AIS is largely unknown. We performed extensive B and T-lymphocyte phenotyping in patients with AIS at diagnosis and after treatment cessation. In this prospective multicentre study, flow cytometric analysis of T and B-lymphocyte subsets was performed in 35 patients at diagnosis and 3 months after treatment cessation. We additionally analysed levels of immunoglobulins and IgG subclasses, serum level and genetic variants of mannose-binding lectin, and somatic hypermutation. A total of 22 (61%) patients had B-lymphocytes below reference limit at baseline, persisting in 7 (30%) patients at follow-up. We found a lower proportion of CD19 + CD27 + IgD+ marginal zone B-lymphocytes and a higher proportion of γδ+ T-lymphocyte receptors compared with controls at both time points. Immunoglobulin levels were elevated at baseline compared to follow-up, and not associated with absolute B-lymphocyte count. In conclusion, a large proportion of AIS patients presented with profound B-lymphocyte deficiency, only partly reversible at follow-up. Identification of immune dysfunction related to AIS may allow for future targeted therapeutic interventions to restore host immunity.

AB - Acute infectious spondylodiscitis (AIS) is a serious infection of the spine with rising incidence and a mortality of 3-6%. The role of the immune system in AIS is largely unknown. We performed extensive B and T-lymphocyte phenotyping in patients with AIS at diagnosis and after treatment cessation. In this prospective multicentre study, flow cytometric analysis of T and B-lymphocyte subsets was performed in 35 patients at diagnosis and 3 months after treatment cessation. We additionally analysed levels of immunoglobulins and IgG subclasses, serum level and genetic variants of mannose-binding lectin, and somatic hypermutation. A total of 22 (61%) patients had B-lymphocytes below reference limit at baseline, persisting in 7 (30%) patients at follow-up. We found a lower proportion of CD19 + CD27 + IgD+ marginal zone B-lymphocytes and a higher proportion of γδ+ T-lymphocyte receptors compared with controls at both time points. Immunoglobulin levels were elevated at baseline compared to follow-up, and not associated with absolute B-lymphocyte count. In conclusion, a large proportion of AIS patients presented with profound B-lymphocyte deficiency, only partly reversible at follow-up. Identification of immune dysfunction related to AIS may allow for future targeted therapeutic interventions to restore host immunity.

U2 - 10.1038/s41598-018-33318-w

DO - 10.1038/s41598-018-33318-w

M3 - Journal article

C2 - 30310085

VL - 8

JO - Scientific Reports

JF - Scientific Reports

SN - 2045-2322

M1 - 15174

ER -

ID: 218085642