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Antigen-independent activation of naive and memory resting T cells by a cytokine combination.

Open access
Unutmaz, D, Pileri, P, Abrignani, S·1994·The Journal of experimental medicine

Abstract

We investigated whether human resting T cells could be activated to proliferate and display effector function in the absence of T cell receptor occupancy. We report that combination of interleukin 2 (IL-2), tumor necrosis factor alpha, and IL-6 activated highly purified naive (CD45RA+) and memory (CD45RO+) resting CD4+ T cells to proliferate. Under this condition, memory resting T cells could also display effector function as measured by lymphokine synthesis and help for immunoglobulin production by B cells. This novel Ag-independent pathway of T cell activation may play an important role in vivo in recruiting effector T cells at the site of immune response and in maintaining the clonal size of memory T cells in the absence of antigenic stimulation. Moreover, cytokines can induce proliferation of naive T cells without switch to memory phenotype and this may help the maintenance of the peripheral pool of naive T cells.

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Crossref · 10.1084/jem.180.3.1159

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Metadata

Authors
Unutmaz, D., Pileri, P., & Abrignani, S.
Venue
The Journal of experimental medicine
Published
1994-09-01
Volume
180
Issue
3
Pages
1159-1164
ISSN
  • 0022-1007 (ISSN-L)
  • 1540-9538
OpenAlex
W2137384756
Cited by
524
References
0
FWCI
7.03
Type
journal article
Language
en
Open access
bronze

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Contains information from the Semantic Scholar Academic Graph Datasets, made available under the ODC Attribution License (ODC-BY 1.0).

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