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CD318 is a ligand for CD6.
Enyindah-Asonye, Gospel; Li, Yan; Ruth, Jeffrey H; Spassov, Danislav S; Hebron, Katie E; Zijlstra, Andries; Moasser, Mark M; Wang, Benlian; Singer, Nora G; Cui, Huadong; Ohara, Ray A; Rasmussen, Stephanie M; Fox, David A; Lin, Feng.
Affiliation
  • Enyindah-Asonye G; Department of Immunology, Lerner Research Institute, Cleveland Clinic, Cleveland, OH 44195.
  • Li Y; Department of Immunology, Lerner Research Institute, Cleveland Clinic, Cleveland, OH 44195.
  • Ruth JH; Division of Rheumatology and Clinical Autoimmunity Center of Excellence, University of Michigan, Ann Arbor, MI 48109.
  • Spassov DS; Department of Medicine and Helen Diller Family Comprehensive Cancer Center, University of California, San Francisco, CA 94143.
  • Hebron KE; Department of Pathology, Microbiology, and Immunology, Vanderbilt University, Nashville, TN 37240.
  • Zijlstra A; Department of Pathology, Microbiology, and Immunology, Vanderbilt University, Nashville, TN 37240.
  • Moasser MM; Department of Medicine and Helen Diller Family Comprehensive Cancer Center, University of California, San Francisco, CA 94143.
  • Wang B; Center for Proteomics and Bioinformatics, Case Western Reserve University, Cleveland, OH 44106.
  • Singer NG; Division of Rheumatology, MetroHealth Medical Center, Cleveland, OH 44109.
  • Cui H; Division of Rheumatology and Clinical Autoimmunity Center of Excellence, University of Michigan, Ann Arbor, MI 48109.
  • Ohara RA; Division of Rheumatology and Clinical Autoimmunity Center of Excellence, University of Michigan, Ann Arbor, MI 48109.
  • Rasmussen SM; Division of Rheumatology and Clinical Autoimmunity Center of Excellence, University of Michigan, Ann Arbor, MI 48109.
  • Fox DA; Division of Rheumatology and Clinical Autoimmunity Center of Excellence, University of Michigan, Ann Arbor, MI 48109; dfox@umich.edu linf2@ccf.org.
  • Lin F; Department of Immunology, Lerner Research Institute, Cleveland Clinic, Cleveland, OH 44195; dfox@umich.edu linf2@ccf.org.
Proc Natl Acad Sci U S A ; 114(33): E6912-E6921, 2017 08 15.
Article in En | MEDLINE | ID: mdl-28760953
ABSTRACT
It has been proposed that CD6, an important regulator of T cells, functions by interacting with its currently identified ligand, CD166, but studies performed during the treatment of autoimmune conditions suggest that the CD6-CD166 interaction might not account for important functions of CD6 in autoimmune diseases. The antigen recognized by mAb 3A11 has been proposed as a new CD6 ligand distinct from CD166, yet the identity of it is hitherto unknown. We have identified this CD6 ligand as CD318, a cell surface protein previously found to be present on various epithelial cells and many tumor cells. We found that, like CD6 knockout (KO) mice, CD318 KO mice are also protected in experimental autoimmune encephalomyelitis. In humans, we found that CD318 is highly expressed in synovial tissues and participates in CD6-dependent adhesion of T cells to synovial fibroblasts. In addition, soluble CD318 is chemoattractive to T cells and levels of soluble CD318 are selectively and significantly elevated in the synovial fluid from patients with rheumatoid arthritis and juvenile inflammatory arthritis. These results establish CD318 as a ligand of CD6 and a potential target for the diagnosis and treatment of autoimmune diseases such as multiple sclerosis and inflammatory arthritis.
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Membrane Glycoproteins / Antigens, Differentiation, T-Lymphocyte / Antigens, CD / Encephalomyelitis, Autoimmune, Experimental / Antigens, Neoplasm Limits: Animals / Humans Language: En Journal: Proc Natl Acad Sci U S A Year: 2017 Document type: Article

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Membrane Glycoproteins / Antigens, Differentiation, T-Lymphocyte / Antigens, CD / Encephalomyelitis, Autoimmune, Experimental / Antigens, Neoplasm Limits: Animals / Humans Language: En Journal: Proc Natl Acad Sci U S A Year: 2017 Document type: Article