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ILDR2 Is a novel B7-like protein that negatively regulates T cell responses

Abstract:
The B7-like protein family members play critical immunomodulatory roles and constitute attractive targets for the development of novel therapies for human diseases. We identified Ig-like domain–containing receptor (ILDR)2 as a novel B7-like protein with robust T cell inhibitory activity, expressed in immune cells and in immune-privileged and inflamed tissues. A fusion protein, consisting of ILDR2 extracellular domain with an Fc fragment, that binds to a putative counterpart on activated T cells showed a beneficial effect in the collagen-induced arthritis model and abrogated the production of proinflammatory cytokines and chemokines in autologous synovial-like cocultures of macrophages and cytokine-stimulated T cells. Collectively, these findings point to ILDR2 as a novel negative regulator for T cells, with potential roles in the development of immune-related diseases, including autoimmunity and cancer.
Publication status:
Published
Peer review status:
Peer reviewed

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Publisher copy:
10.4049/jimmunol.1700325

Authors


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Role:
Author
ORCID:
0000-0002-5818-8515


Publisher:
American Association of Immunologists
Journal:
Journal of Immunology More from this journal
Volume:
200
Issue:
6
Pages:
2025-2037
Publication date:
2018-03-15
Acceptance date:
2018-01-03
DOI:
EISSN:
1550-6606
ISSN:
0022-1767
Pmid:
29431694


Language:
English
Pubs id:
pubs:826445
UUID:
uuid:4094a2d4-5aee-4643-b279-ae4d17065289
Local pid:
pubs:826445
Source identifiers:
826445
Deposit date:
2018-05-15

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