IDO1 Protein Is Expressed in Diagnostic Biopsies from Both Follicular and Transformed Follicular Patients

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Standard

IDO1 Protein Is Expressed in Diagnostic Biopsies from Both Follicular and Transformed Follicular Patients. / Enemark, Marie Beck Hairing; Sørensen, Emma Frasez; Hybel, Trine Engelbrecht; Andersen, Maja Dam; Madsen, Charlotte; Lauridsen, Kristina Lystlund; Honoré, Bent; d’Amore, Francesco; Plesner, Trine Lindhardt; Hamilton-Dutoit, Stephen Jacques; Ludvigsen, Maja.

I: International Journal of Molecular Sciences, Bind 24, Nr. 8, 7314, 2023.

Publikation: Bidrag til tidsskriftTidsskriftartikelForskningfagfællebedømt

Harvard

Enemark, MBH, Sørensen, EF, Hybel, TE, Andersen, MD, Madsen, C, Lauridsen, KL, Honoré, B, d’Amore, F, Plesner, TL, Hamilton-Dutoit, SJ & Ludvigsen, M 2023, 'IDO1 Protein Is Expressed in Diagnostic Biopsies from Both Follicular and Transformed Follicular Patients', International Journal of Molecular Sciences, bind 24, nr. 8, 7314. https://doi.org/10.3390/ijms24087314

APA

Enemark, M. B. H., Sørensen, E. F., Hybel, T. E., Andersen, M. D., Madsen, C., Lauridsen, K. L., Honoré, B., d’Amore, F., Plesner, T. L., Hamilton-Dutoit, S. J., & Ludvigsen, M. (2023). IDO1 Protein Is Expressed in Diagnostic Biopsies from Both Follicular and Transformed Follicular Patients. International Journal of Molecular Sciences, 24(8), [7314]. https://doi.org/10.3390/ijms24087314

Vancouver

Enemark MBH, Sørensen EF, Hybel TE, Andersen MD, Madsen C, Lauridsen KL o.a. IDO1 Protein Is Expressed in Diagnostic Biopsies from Both Follicular and Transformed Follicular Patients. International Journal of Molecular Sciences. 2023;24(8). 7314. https://doi.org/10.3390/ijms24087314

Author

Enemark, Marie Beck Hairing ; Sørensen, Emma Frasez ; Hybel, Trine Engelbrecht ; Andersen, Maja Dam ; Madsen, Charlotte ; Lauridsen, Kristina Lystlund ; Honoré, Bent ; d’Amore, Francesco ; Plesner, Trine Lindhardt ; Hamilton-Dutoit, Stephen Jacques ; Ludvigsen, Maja. / IDO1 Protein Is Expressed in Diagnostic Biopsies from Both Follicular and Transformed Follicular Patients. I: International Journal of Molecular Sciences. 2023 ; Bind 24, Nr. 8.

Bibtex

@article{0ebae375cf704b0cae29ab5f9ae38e19,
title = "IDO1 Protein Is Expressed in Diagnostic Biopsies from Both Follicular and Transformed Follicular Patients",
abstract = "Follicular lymphoma (FL) is a lymphoid neoplasia characterized by an indolent clinical nature. Despite generally favorable prognoses, early progression and histological transformation (HT) to a more aggressive lymphoma histology remain the leading causes of death among FL patients. To provide a basis for possible novel treatment options, we set out to evaluate the expression levels of indoleamine 2,3-dioxygenase 1 (IDO1), an immunoinhibitory checkpoint molecule, in follicular and transformed follicular biopsies. The expression levels of IDO1 were assessed using immunohistochemical staining and digital image analysis in lymphoma biopsies from 33 FL patients without subsequent HT (non-transforming FL, nt-FL) and 20 patients with subsequent HT (subsequently transforming FL, st-FL) as well as in paired high-grade biopsies from the time of HT (transformed FL, tFL). Despite no statistical difference in IDO1 expression levels seen between the groups, all diagnostic and transformed lymphomas exhibited positive expression, indicating its possible role in novel treatment regimens. In addition, IDO1 expression revealed a positive correlation with another immune checkpoint inhibitor, namely programmed death 1 (PD-1). In summary, we report IDO1 expression in all cases of FL and tFL, which provides the grounds for future investigations of anti-IDO1 therapy as a possible treatment for FL patients.",
keywords = "follicular lymphoma, histological transformation, indoleamine 2,3-dioxygenase",
author = "Enemark, {Marie Beck Hairing} and S{\o}rensen, {Emma Frasez} and Hybel, {Trine Engelbrecht} and Andersen, {Maja Dam} and Charlotte Madsen and Lauridsen, {Kristina Lystlund} and Bent Honor{\'e} and Francesco d{\textquoteright}Amore and Plesner, {Trine Lindhardt} and Hamilton-Dutoit, {Stephen Jacques} and Maja Ludvigsen",
note = "Publisher Copyright: {\textcopyright} 2023 by the authors.",
year = "2023",
doi = "10.3390/ijms24087314",
language = "English",
volume = "24",
journal = "International Journal of Molecular Sciences (Online)",
issn = "1661-6596",
publisher = "MDPI AG",
number = "8",

}

RIS

TY - JOUR

T1 - IDO1 Protein Is Expressed in Diagnostic Biopsies from Both Follicular and Transformed Follicular Patients

AU - Enemark, Marie Beck Hairing

AU - Sørensen, Emma Frasez

AU - Hybel, Trine Engelbrecht

AU - Andersen, Maja Dam

AU - Madsen, Charlotte

AU - Lauridsen, Kristina Lystlund

AU - Honoré, Bent

AU - d’Amore, Francesco

AU - Plesner, Trine Lindhardt

AU - Hamilton-Dutoit, Stephen Jacques

AU - Ludvigsen, Maja

N1 - Publisher Copyright: © 2023 by the authors.

PY - 2023

Y1 - 2023

N2 - Follicular lymphoma (FL) is a lymphoid neoplasia characterized by an indolent clinical nature. Despite generally favorable prognoses, early progression and histological transformation (HT) to a more aggressive lymphoma histology remain the leading causes of death among FL patients. To provide a basis for possible novel treatment options, we set out to evaluate the expression levels of indoleamine 2,3-dioxygenase 1 (IDO1), an immunoinhibitory checkpoint molecule, in follicular and transformed follicular biopsies. The expression levels of IDO1 were assessed using immunohistochemical staining and digital image analysis in lymphoma biopsies from 33 FL patients without subsequent HT (non-transforming FL, nt-FL) and 20 patients with subsequent HT (subsequently transforming FL, st-FL) as well as in paired high-grade biopsies from the time of HT (transformed FL, tFL). Despite no statistical difference in IDO1 expression levels seen between the groups, all diagnostic and transformed lymphomas exhibited positive expression, indicating its possible role in novel treatment regimens. In addition, IDO1 expression revealed a positive correlation with another immune checkpoint inhibitor, namely programmed death 1 (PD-1). In summary, we report IDO1 expression in all cases of FL and tFL, which provides the grounds for future investigations of anti-IDO1 therapy as a possible treatment for FL patients.

AB - Follicular lymphoma (FL) is a lymphoid neoplasia characterized by an indolent clinical nature. Despite generally favorable prognoses, early progression and histological transformation (HT) to a more aggressive lymphoma histology remain the leading causes of death among FL patients. To provide a basis for possible novel treatment options, we set out to evaluate the expression levels of indoleamine 2,3-dioxygenase 1 (IDO1), an immunoinhibitory checkpoint molecule, in follicular and transformed follicular biopsies. The expression levels of IDO1 were assessed using immunohistochemical staining and digital image analysis in lymphoma biopsies from 33 FL patients without subsequent HT (non-transforming FL, nt-FL) and 20 patients with subsequent HT (subsequently transforming FL, st-FL) as well as in paired high-grade biopsies from the time of HT (transformed FL, tFL). Despite no statistical difference in IDO1 expression levels seen between the groups, all diagnostic and transformed lymphomas exhibited positive expression, indicating its possible role in novel treatment regimens. In addition, IDO1 expression revealed a positive correlation with another immune checkpoint inhibitor, namely programmed death 1 (PD-1). In summary, we report IDO1 expression in all cases of FL and tFL, which provides the grounds for future investigations of anti-IDO1 therapy as a possible treatment for FL patients.

KW - follicular lymphoma

KW - histological transformation

KW - indoleamine 2,3-dioxygenase

UR - http://www.scopus.com/inward/record.url?scp=85156209031&partnerID=8YFLogxK

U2 - 10.3390/ijms24087314

DO - 10.3390/ijms24087314

M3 - Journal article

C2 - 37108483

AN - SCOPUS:85156209031

VL - 24

JO - International Journal of Molecular Sciences (Online)

JF - International Journal of Molecular Sciences (Online)

SN - 1661-6596

IS - 8

M1 - 7314

ER -

ID: 369361161