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Ability of γδ T cells to modulate the Foxp3 T cell response is dependent on adenosine
Author(s) -
Dongchun Liang,
JeongIm Woo,
Hui Shao,
Willi K. Born,
Rebecca L. O’Brien,
Henry J. Kaplan,
Deming Sun
Publication year - 2018
Publication title -
plos one
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.99
H-Index - 332
ISSN - 1932-6203
DOI - 10.1371/journal.pone.0197189
Subject(s) - adenosine , foxp3 , microbiology and biotechnology , t cell , purinergic signalling , adenosine receptor , extracellular , adenosine a3 receptor , adenosine a2b receptor , chemistry , biology , receptor , immune system , biochemistry , immunology , agonist
Whether γδ T cells inhibit or enhance the Foxp3 T cell response depends upon their activation status. The critical enhancing effector in the supernatant is adenosine. Activated γδ T cells express adenosine receptors at high levels, which enables them to deprive Foxp3 + T cells of adenosine, and to inhibit their expansion. Meanwhile, cell-free supernatants of γδ T cell cultures enhance Foxp3 T cell expansion. Thus, inhibition and enhancement by γδ T cells of Foxp3 T cell response are a reflection of the balance between adenosine production and absorption by γδ T cells. Non-activated γδ T cells produce adenosine but bind little, and thus enhance the Foxp3 T cell response. Activated γδ T cells express high density of adenosine receptors and have a greatly increased ability to bind adenosine. Extracellular adenosine metabolism and expression of adenosine receptor A2ARs by γδ T cells played a major role in the outcome of γδ and Foxp3 T cell interactions. A better understanding of the functional conversion of γδ T cells could lead to γδ T cell-targeted immunotherapies for related diseases.

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