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PMID: 1836479 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't Research Support, U.S. Gov't, P.H.S.

Clonal anergy blocks the response to IL-4, as well as the production of IL-2, in dual-producing T helper cell clones.

Journal of immunology (Baltimore, Md. : 1950) ·Vol. 147 ·No. 12 ·1991-12-15 ·Pages 4118-25

Mueller DL, Chiodetti L, Bacon PA, Schwartz RH

Abstract

In this report we extend the in vitro clonal anergy model to examine the regulation of proliferation in T cells that secrete both IL-2 and IL-4. Newly cloned Ag-specific murine T cells are shown to depend on both IL-2 and IL-4 synthesis for maximal proliferation. Whereas IL-2 responsiveness is constitutive in these cells, IL-4 responsiveness develops only after Ag and APC stimulation. Remarkably, proliferation of these cells to Ag is sensitive to inhibition by clonal anergy, even though IL-4 synthesis remains inducible. Anergy in these cells is associated with an inability to respond to IL-4, in addition to the development of an IL-2 production defect. The results suggest that anergy induction may be capable of preventing the clonal expansion of autoreactive T cells producing both IL-2 and IL-4 in vivo.

MeSH Terms
Animals Antigen-Presenting Cells/physiology Antigens/immunology Cells, Cultured Clone Cells Interleukin-2/biosynthesis Interleukin-4/biosynthesis Lymphocyte Activation Mice Mice, Inbred C57BL T-Lymphocytes, Helper-Inducer/immunology,metabolism
Chemicals
Antigens Interleukin-2 Interleukin-4
Authors & Affiliations
4 authors, click to expand affiliations / ORCID
Mueller D L
Harold C. Simmons Arthritis Research Center, Dallas, TX.
Chiodetti L
Bacon P A
Schwartz R H
Article Info
Journal
Journal of immunology (Baltimore, Md. : 1950)
Abbr.
J Immunol
ISSN
0022-1767
Published
1991-12-15
Pages
4118-25
Language
English
Region
United States
NLM ID
2985117R
Subset
IM
Grants
NIAMS NIH HHS · 2-T32-AR07055 · United States
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