Abstract
gamma delta T cells respond to a variety of microbial pathogens and transformed cells. Their limited receptor repertoire and activation by mycobacterial antigens resistant to proteases suggest that they may recognize nonpeptide antigens. We have tested a variety of nonpeptide molecules for stimulation of human gamma delta T cells. Synthetic alkyl phosphates, particularly monoethyl phosphate (MEP), selectively activated gamma delta T cells and stimulated their proliferation in vitro. All gamma delta T cells stimulated by MEP expressed V gamma 2/V delta 2 receptors. The purified natural ligand of mycobacteria is chemically similar to, though distinct from, MEP and contains a phosphate residue that is critical for biological activity. Recognition and expansion of a specific T-cell receptor-bearing population to non-peptide ligands is unprecedented among T cells. We suggest that MEP mimics small natural ligands capable of expanding one subset of gamma delta T cells and that this recognition of nonpeptide antigens may play an important role in human immunity to pathogens.
MeSH Terms
Antibodies/pharmacology
Antigens, Bacterial/pharmacology
Arthritis, Rheumatoid/immunology
Clone Cells
Cytotoxicity, Immunologic
Flow Cytometry
Humans
Ligands
Lymphocyte Activation
Mycobacterium tuberculosis/immunology
Organophosphates/metabolism,pharmacology
Receptors, Antigen, T-Cell, gamma-delta/drug effects,immunology,physiology
Synovial Fluid/immunology
T-Lymphocytes/drug effects,immunology
Chemicals
Antibodies
Antigens, Bacterial
Ligands
Organophosphates
Receptors, Antigen, T-Cell, gamma-delta
monoethyl phosphate
Authors & Affiliations
9 authors, click to expand affiliations / ORCID
Tanaka Y
Howard Hughes Medical Institute, Albert Einstein College of Medicine, Bronx, NY 10461.
Sano S
Nieves E
De Libero G
Rosa D
Modlin R L
Brenner M B
Bloom B R
Morita C T
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