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Citations to this article

Human MAIT cells exit peripheral tissues and recirculate via lymph in steady state conditions
Valentin Voillet, … , Michael R. Betts, Martin Prlic
Valentin Voillet, … , Michael R. Betts, Martin Prlic
Published April 5, 2018
Citation Information: JCI Insight. 2018;3(7):e98487. https://doi.org/10.1172/jci.insight.98487.
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Research Article Immunology

Human MAIT cells exit peripheral tissues and recirculate via lymph in steady state conditions

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Abstract

Mucosal-associated invariant T cells (MAIT cells) recognize bacterial metabolites as antigen and are found in blood and tissues, where they are poised to contribute to barrier immunity. Recent data demonstrate that MAIT cells located in mucosal barrier tissues are functionally distinct from their blood counterparts, but the relationship and circulation of MAIT cells between blood and different tissue compartments remains poorly understood. Previous studies raised the possibility that MAIT cells do not leave tissue and may either be retained or undergo apoptosis. To directly address if human MAIT cells exit tissues, we collected human donor–matched thoracic duct lymph and blood and analyzed MAIT cell phenotype, transcriptome, and T cell receptor (TCR) diversity by flow cytometry and RNA sequencing. We found that MAIT cells were present in the lymph, despite being largely CCR7– in the blood, thus indicating that MAIT cells in the lymph migrated from tissues and were capable of exiting tissues to recirculate. Importantly, MAIT cells in the lymph and blood had highly overlapping clonotype usage but distinct transcriptome signatures, indicative of differential activation states.

Authors

Valentin Voillet, Marcus Buggert, Chloe K. Slichter, Julia D. Berkson, Florian Mair, Mary M. Addison, Yoav Dori, Gregory Nadolski, Maxim G. Itkin, Raphael Gottardo, Michael R. Betts, Martin Prlic

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Total citations by year

Year: 2025 2024 2023 2022 2021 2020 2019 2018 Total
Citations: 4 1 7 6 8 8 8 1 43
Citation information
This citation data is accumulated from CrossRef, which receives citation information from participating publishers, including this journal. Not all publishers participate in CrossRef, so this information is not comprehensive. Additionally, data may not reflect the most current citations to this article, and the data may differ from citation information available from other sources (for example, Google Scholar, Web of Science, and Scopus).

Citations to this article in year 2020 (8)

Title and authors Publication Year
MAIT Cells in Barrier Tissues: Lessons from Immediate Neighbors
A Amini, D Pang, CP Hackstein, P Klenerman
Frontiers in immunology 2020
Immunobiology and immunotherapy of HCC: spotlight on innate and innate-like immune cells
B Ruf, B Heinrich, TF Greten
Cellular and Molecular Immunology 2020
Differential Skewing of Circulating MR1-Restricted and γδ T Cells in Human Psoriasis Vulgaris
V Plužarić, M Štefanić, M Mihalj, MT Levak, I Muršić, L Glavaš-Obrovac, M Petrek, P Balogh, S Tokić
Frontiers in immunology 2020
Defining T Cell Tissue Residency in Humans: Implications for HIV Pathogenesis and Vaccine Design
BL Shacklett, AL Ferre, BE Kiniry
Current HIV/AIDS Reports 2020
MR1-restricted T cells: the new dawn of cancer immunotherapy
Z Wang, M Wang, J Chen, L Zhang, L Zhang, L Yu
Bioscience Reports 2020
Inflammatory Cytokines Induce Sustained CTLA-4 Cell Surface Expression on Human MAIT Cells
JD Berkson, CK Slichter, HA DeBerg, MA Delaney, AS Woodward-Davis, NJ Maurice, Y Lwo, A Ko, J Hsu, YW Chiu, PS Linsley, D Dixon, M Prlic
ImmunoHorizons 2020
Understanding the Role of Mucosal-Associated Invariant T-Cells in Non-human Primate Models of HIV Infection
IM Barber-Axthelm, SJ Kent, JA Juno
Frontiers in immunology 2020
The identity of human tissue-emigrant CD8+ T cells
Buggert M, Vella LA, Nguyen S, Wu V, Chen Z, Sekine T, Perez-Potti A, Maldini CR, Manne S, Darko S, Ransier A, Kuri-Cervantes L, Japp AS, Brody IB, Ivarsson MA, Gorin JB, Rivera-Ballesteros O, Hertwig L, Antel JP, Johnson ME, Okoye A, Picker L, Vahedi G, Sparrelid E, Llewellyn-Lacey S, Gostick E, Sandberg J, Björkström N, Bar-Or A, Dori Y, Naji A, Canaday DH, Laufer TM, Wells AD, Price DA, Frank I, Douek DC, Wherry EJ, Itkin MG, Betts MR
Cell 2020

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