Investigating Vα7.2+/CD161− T Cell and MAIT Cell Profiles Using Flow Cytometry in Healthy Subjects and Subjects with Atopic Dermatitis

This study investigates the roles of mucosal-associated invariant T (MAIT) cells and Vα7.2+/CD161− T cells in skin diseases, focusing on atopic dermatitis. MAIT cells, crucial for bridging innate and adaptive immunity, were analyzed alongside Vα7.2+/CD161− T cells in peripheral blood samples from 14...

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Veröffentlicht in:International journal of molecular sciences Jg. 25; H. 6; S. 3486
Hauptverfasser: Singh, Parvind, Gaspar, Krisztian, Szegedi, Andrea, Sajtos, Laszlo, Barath, Sandor, Hevessy, Zsuzsanna
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Sprache:Englisch
Veröffentlicht: Switzerland MDPI AG 20.03.2024
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Abstract This study investigates the roles of mucosal-associated invariant T (MAIT) cells and Vα7.2+/CD161− T cells in skin diseases, focusing on atopic dermatitis. MAIT cells, crucial for bridging innate and adaptive immunity, were analyzed alongside Vα7.2+/CD161− T cells in peripheral blood samples from 14 atopic dermatitis patients and 10 healthy controls. Flow cytometry and machine learning algorithms were employed for a comprehensive analysis. The results indicate a significant decrease in MAIT cells and CD69 subsets in atopic dermatitis, coupled with elevated CD38 and polyfunctional MAIT cells producing TNFα and Granzyme B (TNFα+/GzB+). Vα7.2+/CD161− T cells in atopic dermatitis exhibited a decrease in CD8 and IFNγ-producing subsets but an increase in CD38 activated and IL-22-producing subsets. These results highlight the distinctive features of MAIT cells and Vα7.2+/CD161− T cells and their different roles in the pathogenesis of atopic dermatitis and provide insights into their potential roles in immune-mediated skin diseases.
AbstractList This study investigates the roles of mucosal-associated invariant T (MAIT) cells and Vα7.2+/CD161− T cells in skin diseases, focusing on atopic dermatitis. MAIT cells, crucial for bridging innate and adaptive immunity, were analyzed alongside Vα7.2+/CD161− T cells in peripheral blood samples from 14 atopic dermatitis patients and 10 healthy controls. Flow cytometry and machine learning algorithms were employed for a comprehensive analysis. The results indicate a significant decrease in MAIT cells and CD69 subsets in atopic dermatitis, coupled with elevated CD38 and polyfunctional MAIT cells producing TNFα and Granzyme B (TNFα+/GzB+). Vα7.2+/CD161− T cells in atopic dermatitis exhibited a decrease in CD8 and IFNγ-producing subsets but an increase in CD38 activated and IL-22-producing subsets. These results highlight the distinctive features of MAIT cells and Vα7.2+/CD161− T cells and their different roles in the pathogenesis of atopic dermatitis and provide insights into their potential roles in immune-mediated skin diseases.
This study investigates the roles of mucosal-associated invariant T (MAIT) cells and Vα7.2+/CD161- T cells in skin diseases, focusing on atopic dermatitis. MAIT cells, crucial for bridging innate and adaptive immunity, were analyzed alongside Vα7.2+/CD161- T cells in peripheral blood samples from 14 atopic dermatitis patients and 10 healthy controls. Flow cytometry and machine learning algorithms were employed for a comprehensive analysis. The results indicate a significant decrease in MAIT cells and CD69 subsets in atopic dermatitis, coupled with elevated CD38 and polyfunctional MAIT cells producing TNFα and Granzyme B (TNFα+/GzB+). Vα7.2+/CD161- T cells in atopic dermatitis exhibited a decrease in CD8 and IFNγ-producing subsets but an increase in CD38 activated and IL-22-producing subsets. These results highlight the distinctive features of MAIT cells and Vα7.2+/CD161- T cells and their different roles in the pathogenesis of atopic dermatitis and provide insights into their potential roles in immune-mediated skin diseases.This study investigates the roles of mucosal-associated invariant T (MAIT) cells and Vα7.2+/CD161- T cells in skin diseases, focusing on atopic dermatitis. MAIT cells, crucial for bridging innate and adaptive immunity, were analyzed alongside Vα7.2+/CD161- T cells in peripheral blood samples from 14 atopic dermatitis patients and 10 healthy controls. Flow cytometry and machine learning algorithms were employed for a comprehensive analysis. The results indicate a significant decrease in MAIT cells and CD69 subsets in atopic dermatitis, coupled with elevated CD38 and polyfunctional MAIT cells producing TNFα and Granzyme B (TNFα+/GzB+). Vα7.2+/CD161- T cells in atopic dermatitis exhibited a decrease in CD8 and IFNγ-producing subsets but an increase in CD38 activated and IL-22-producing subsets. These results highlight the distinctive features of MAIT cells and Vα7.2+/CD161- T cells and their different roles in the pathogenesis of atopic dermatitis and provide insights into their potential roles in immune-mediated skin diseases.
This study investigates the roles of mucosal-associated invariant T (MAIT) cells and Vα7.2 /CD161 T cells in skin diseases, focusing on atopic dermatitis. MAIT cells, crucial for bridging innate and adaptive immunity, were analyzed alongside Vα7.2 /CD161 T cells in peripheral blood samples from 14 atopic dermatitis patients and 10 healthy controls. Flow cytometry and machine learning algorithms were employed for a comprehensive analysis. The results indicate a significant decrease in MAIT cells and CD69 subsets in atopic dermatitis, coupled with elevated CD38 and polyfunctional MAIT cells producing TNFα and Granzyme B (TNFα /GzB ). Vα7.2 /CD161 T cells in atopic dermatitis exhibited a decrease in CD8 and IFNγ-producing subsets but an increase in CD38 activated and IL-22-producing subsets. These results highlight the distinctive features of MAIT cells and Vα7.2 /CD161 T cells and their different roles in the pathogenesis of atopic dermatitis and provide insights into their potential roles in immune-mediated skin diseases.
This study investigates the roles of mucosal-associated invariant T (MAIT) cells and Vα7.2[sup.+]/CD161[sup.−] T cells in skin diseases, focusing on atopic dermatitis. MAIT cells, crucial for bridging innate and adaptive immunity, were analyzed alongside Vα7.2[sup.+]/CD161[sup.−] T cells in peripheral blood samples from 14 atopic dermatitis patients and 10 healthy controls. Flow cytometry and machine learning algorithms were employed for a comprehensive analysis. The results indicate a significant decrease in MAIT cells and CD69 subsets in atopic dermatitis, coupled with elevated CD38 and polyfunctional MAIT cells producing TNFα and Granzyme B (TNFα[sup.+]/GzB[sup.+]). Vα7.2[sup.+]/CD161[sup.−] T cells in atopic dermatitis exhibited a decrease in CD8 and IFNγ-producing subsets but an increase in CD38 activated and IL-22-producing subsets. These results highlight the distinctive features of MAIT cells and Vα7.2[sup.+]/CD161[sup.−] T cells and their different roles in the pathogenesis of atopic dermatitis and provide insights into their potential roles in immune-mediated skin diseases.
Audience Academic
Author Gaspar, Krisztian
Sajtos, Laszlo
Szegedi, Andrea
Singh, Parvind
Barath, Sandor
Hevessy, Zsuzsanna
AuthorAffiliation 2 Department of Dermatology and Venereology, Faculty of Medicine, University of Debrecen, 4032 Debrecen, Hungary; gaspar.krisztian@med.unideb.hu (K.G.); aszegedi@med.unideb.hu (A.S.); sajtos.laszlo@med.unideb.hu (L.S.)
1 Department of Laboratory Medicine, Faculty of Medicine, University of Debrecen, 4032 Debrecen, Hungary; parvind.singh@med.unideb.hu (P.S.); barath.sandor@med.unideb.hu (S.B.)
AuthorAffiliation_xml – name: 2 Department of Dermatology and Venereology, Faculty of Medicine, University of Debrecen, 4032 Debrecen, Hungary; gaspar.krisztian@med.unideb.hu (K.G.); aszegedi@med.unideb.hu (A.S.); sajtos.laszlo@med.unideb.hu (L.S.)
– name: 1 Department of Laboratory Medicine, Faculty of Medicine, University of Debrecen, 4032 Debrecen, Hungary; parvind.singh@med.unideb.hu (P.S.); barath.sandor@med.unideb.hu (S.B.)
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BackLink https://www.ncbi.nlm.nih.gov/pubmed/38542456$$D View this record in MEDLINE/PubMed
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CitedBy_id crossref_primary_10_1093_jimmun_vkaf226
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crossref_primary_10_1016_j_jneuroim_2025_578551
crossref_primary_10_1002_cyto_a_24951
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Issue 6
Keywords atopic dermatitis
dimensionality reduction
flow cytometry
unsupervised clustering
Vα7.2+/CD161− T cells
MAIT cells
Language English
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These authors contributed equally to this work.
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Snippet This study investigates the roles of mucosal-associated invariant T (MAIT) cells and Vα7.2+/CD161− T cells in skin diseases, focusing on atopic dermatitis....
This study investigates the roles of mucosal-associated invariant T (MAIT) cells and Vα7.2 /CD161 T cells in skin diseases, focusing on atopic dermatitis. MAIT...
This study investigates the roles of mucosal-associated invariant T (MAIT) cells and Vα7.2[sup.+]/CD161[sup.−] T cells in skin diseases, focusing on atopic...
This study investigates the roles of mucosal-associated invariant T (MAIT) cells and Vα7.2+/CD161- T cells in skin diseases, focusing on atopic dermatitis....
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SubjectTerms Antigens
Atopic dermatitis
B cells
Dendritic cells
Dermatitis
Dermatitis, Atopic
Development and progression
Disease
Ethylenediaminetetraacetic acid
Flow Cytometry
Healthy Volunteers
Humans
Inflammation
Investigations
Lymphocytes
Medical equipment and supplies industry
Medical test kit industry
Mucosal-Associated Invariant T Cells
Pathogenesis
Skin
T cell receptors
T cells
Tumor Necrosis Factor-alpha
Tumor necrosis factor-TNF
Title Investigating Vα7.2+/CD161− T Cell and MAIT Cell Profiles Using Flow Cytometry in Healthy Subjects and Subjects with Atopic Dermatitis
URI https://www.ncbi.nlm.nih.gov/pubmed/38542456
https://www.proquest.com/docview/3003119671
https://www.proquest.com/docview/3014007974
https://pubmed.ncbi.nlm.nih.gov/PMC10970526
Volume 25
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