Literature DB >> 33708202

Frequencies of CD8 and DN MAIT Cells Among Children Diagnosed With Type 1 Diabetes Are Similar to Age-Matched Controls.

Robert Z Harms1, Katie R Ostlund1, Monina Cabrera2,3, Earline Edwards2,3, Victoria B Smith4, Lynette M Smith5, Nora Sarvetnick1,6.   

Abstract

Mucosal-associated invariant T (MAIT) cells have been implicated in various forms of autoimmunity, including type 1 diabetes (T1D). Here, we tested the hypothesis that CD8 and double negative (DN) MAIT cell frequencies were altered among diagnosed T1D subjects compared to controls. To do this, we analyzed cryopreserved peripheral blood mononuclear cells (PBMCs) from age-matched T1D and control children using flow cytometry. We observed that CD8 and DN MAIT cell frequencies were similarly abundant between the two groups. We tested for associations between MAIT cell frequency and T1D-associated parameters, which could reveal a pathogenic role for MAIT cells in the absence of changes in frequency. We found no significant associations between CD8 and DN MAIT cell frequency and levels of islet cell autoantibodies (ICA), glutamate decarboxylase 65 (GAD65) autoantibodies, zinc transporter 8 (ZNT8) autoantibodies, and insulinoma antigen 2 (IA-2) autoantibodies. Furthermore, CD8 and DN MAIT cell frequencies were not significantly associated with time since diagnosis, c-peptide levels, HbA1c, and BMI. As we have examined this cohort for multiple soluble factors previously, we tested for associations between relevant factors and MAIT cell frequency. These could help to explain the broad range of MAIT frequencies we observed and/or indicate disease-associated processes. Although we found nothing disease-specific, we observed that levels of IL-7, IL-18, 25 (OH) vitamin D, and the ratio of vitamin D binding protein to 25 (OH) vitamin D were all associated with MAIT cell frequency. Finally, previous cytomegalovirus infection was associated with reduced CD8 and DN MAIT cells. From this evaluation, we found no connections between CD8 and DN MAIT cells and children with T1D. However, we did observe several intrinsic and extrinsic factors that could influence peripheral MAIT cell abundance among all children. These factors may be worth consideration in future experimental design.
Copyright © 2021 Harms, Ostlund, Cabrera, Edwards, Smith, Smith and Sarvetnick.

Entities:  

Keywords:  autoantibodies; human cytomegalovirus; interleukin 18; interleukin 7; mucosal associated invariant T cells; type 1 diabetes; vitamin D

Mesh:

Substances:

Year:  2021        PMID: 33708202      PMCID: PMC7940386          DOI: 10.3389/fimmu.2021.604157

Source DB:  PubMed          Journal:  Front Immunol        ISSN: 1664-3224            Impact factor:   7.561


  61 in total

1.  Multiple autoantibodies as predictors of Type 1 diabetes in a general population.

Authors:  N K Maclaren; M S Lan; D Schatz; J Malone; A L Notkins; J Krischer
Journal:  Diabetologia       Date:  2003-06-11       Impact factor: 10.122

2.  Vitamin D treatment modulates immune activation in cystic fibrosis.

Authors:  T Pincikova; D Paquin-Proulx; J K Sandberg; M Flodström-Tullberg; L Hjelte
Journal:  Clin Exp Immunol       Date:  2017-05-24       Impact factor: 4.330

3.  IL-7 licenses activation of human liver intrasinusoidal mucosal-associated invariant T cells.

Authors:  Xin-Zi Tang; Juandy Jo; Anthony T Tan; Elena Sandalova; Adeline Chia; Kai Chah Tan; Kang Hoe Lee; Adam J Gehring; Gennaro De Libero; Antonio Bertoletti
Journal:  J Immunol       Date:  2013-02-27       Impact factor: 5.422

4.  Feasibility of screening for T1D and celiac disease in a pediatric clinic setting.

Authors:  Patricia D Gesualdo; Kimberly A Bautista; Kathleen C Waugh; Liping Yu; Jill M Norris; Marian J Rewers; Judith Baxter
Journal:  Pediatr Diabetes       Date:  2015-08-06       Impact factor: 4.866

5.  Immunologic activity in the small intestinal mucosa of pediatric patients with type 1 diabetes.

Authors:  Mia Westerholm-Ormio; Outi Vaarala; Päivi Pihkala; Jorma Ilonen; Erkki Savilahti
Journal:  Diabetes       Date:  2003-09       Impact factor: 9.461

6.  Human mucosal-associated invariant T cells contribute to antiviral influenza immunity via IL-18-dependent activation.

Authors:  Liyen Loh; Zhongfang Wang; Sneha Sant; Marios Koutsakos; Sinthujan Jegaskanda; Alexandra J Corbett; Ligong Liu; David P Fairlie; Jane Crowe; Jamie Rossjohn; Jianqing Xu; Peter C Doherty; James McCluskey; Katherine Kedzierska
Journal:  Proc Natl Acad Sci U S A       Date:  2016-08-19       Impact factor: 11.205

7.  Mucosal-associated invariant T cell-rich congenic mouse strain allows functional evaluation.

Authors:  Yue Cui; Katarzyna Franciszkiewicz; Yvonne K Mburu; Stanislas Mondot; Lionel Le Bourhis; Virginie Premel; Emmanuel Martin; Alexandra Kachaner; Livine Duban; Molly A Ingersoll; Sylvie Rabot; Jean Jaubert; Jean-Pierre De Villartay; Claire Soudais; Olivier Lantz
Journal:  J Clin Invest       Date:  2015-10-12       Impact factor: 14.808

8.  Mucosal-associated invariant T-cells are severely reduced and exhausted in humans with chronic HBV infection.

Authors:  Wenyong Huang; Wenjing He; Xiaomin Shi; Qianyu Ye; Xiaoshun He; Lang Dou; Yifang Gao
Journal:  J Viral Hepat       Date:  2020-06-22       Impact factor: 3.728

9.  On the etiology of type 1 diabetes: a new animal model signifying a decisive role for bacteria eliciting an adverse innate immunity response.

Authors:  Stella Korsgren; Ylva Molin; Kaija Salmela; Torbjörn Lundgren; Asa Melhus; Olle Korsgren
Journal:  Am J Pathol       Date:  2012-09-01       Impact factor: 4.307

10.  Analysis of stem-cell-like properties of human CD161++IL-18Rα+ memory CD8+ T cells.

Authors:  Simone H C Havenith; Si La Yong; Sian M Henson; Berber Piet; Mirza M Idu; Sven D Koch; René E Jonkers; Natasja A M Kragten; Arne N Akbar; René A W van Lier; Ineke J M ten Berge
Journal:  Int Immunol       Date:  2012-07-26       Impact factor: 4.823

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.