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Infect. Immun., 04 1995, 1211-1217, Vol 63, No. 4
LM Vila, HM Haftel, HS Park, MS Lin, NC Romzek, SM Hanash and J Holoshitz
Human gamma delta T cells expressing the V gamma 9/V delta 2 T-cell
receptor have been previously found to proliferate in response to certain
microorganisms and to expand throughout life, presumably because of
extrathymic activation by foreign antigens. In vitro expansion of V gamma
9/V delta 2 cells by mycobacteria has been previously shown to be dependent
on accessory cells. In order to gain an insight into the mechanisms
involved in the expansion of these cells, we have undertaken to identify
the peripheral blood subset of cells on which proliferation of V gamma 9/V
delta 2 cells in response to mycobacteria is dependent. Contrary to their
role in antigen presentation to alpha beta T cells, professional
antigen-presenting cells, such as monocytes, B cells, and dendritic cells,
were unable to provide the cellular support for the expansion of V gamma
9/V delta 2 cells. Selective depletion of T-cell subsets, as well as the
use of highly purified T-cell populations, indicated that the only subset
of peripheral blood cells that could expand V gamma 9/V delta 2 cells were
CD4+ CD45RO+ CD7- alpha beta T cells. These cells underwent distinct
intracellular signaling events after stimulation with the mycobacterial
antigen. Expansion of V gamma 9/V delta 2 cells by alpha beta T cells was
dependent on cell-cell contact. This is the first evidence that a small
subset of the memory helper T-cell population is exclusively responsible
for the peripheral expansion of V gamma 9/V delta 2 cells. These data
illustrate a unique aspect of antigen recognition by gamma delta T cells
and provide new means to study their immune defense role.
Copyright © 1995, American Society for Microbiology
Expansion of mycobacterium-reactive gamma delta T cells by a subset of memory helper T cells
University of Michigan Specialized Center of Research in Rheumatoid Arthritis, Department of Internal Medicine, Ann Arbor.
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