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PMID: 8605923 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't

Interleukin-13 is produced by activated human CD45RA+ and CD45RO+ T cells: modulation by interleukin-4 and interleukin-12.

European journal of immunology ·Vol. 26 ·No. 3 ·1996-03-00 ·Pages 571-7

Jung T, Wijdenes J, Neumann C, de Vries JE, Yssel H

Abstract

Interleukin (IL)-13 is a cytokine originally identified as a product of activated T cells. Little is known however, about IL-13 production by human T cells and its modulation by other cytokines. Here, we show that IL-13 is produced by activated human CD4+ and CD8+ CD45RO+ memory T cells and CD4+ and CD8+ CD45RA+ naive T cells. In contrast, IL-4, which shares many biological activities with IL-13, is only produced by CD45RO+ T cells following activation. Analysis of intracellular cytokine production by single CD45RA+ and CD45RO+ T cells indicated that IL-13 continued to be produced for more than 24 h after stimulation, whereas IL-4 could not be detected after 24 h. These data were confirmed by measurement of specific mRNA and suggest that IL-13, unlike IL-4, but like interferon-gamma (IFN-gamma), is a cytokine with long-lasting kinetics. The majority of human CD45RO+ T cells produced IL-4 and IL-13 simultaneously. In contrast, IFN-gamma protein was generally not co-expressed with IL-4 or IL-13. IL-4 added to primary cultures of highly purified peripheral blood T cells activated by the combination of anti-CD3+anti-CD28 mAb enhanced IL-13 production by CD45RA+ and to a lesser extent by CD45RO+ T cells. Under these conditions, however, IL-12 inhibited IL-13 production by CD45RA+ T cells and to a lesser extent by CD45RO+ T cells in a dose-dependent fashion. These inhibiting effects were not related to enhanced IFN-gamma production induced by IL-12, since IFN-gamma by itself did not affect IL-13 production. Collectively, our data indicate that IL-13 is produced by peripheral blood T cells which also produce IL-4, but not IFN-gamma, and by naive CD45RA+ T cells which, in contrast, fail to produce IL-4. These observations, together with the long-lasting production of IL-13, suggest that IL-13 may have IL-4 like functions in situations where T cell-derived IL-4 is still absent or where its production has already been down-regulated.

MeSH Terms
Adjuvants, Immunologic/pharmacology Base Sequence Humans Immunophenotyping Interferon-gamma/biosynthesis Interleukin-12/biosynthesis,pharmacology Interleukin-13/biosynthesis,metabolism Interleukin-4/biosynthesis,pharmacology Leukocyte Common Antigens/immunology Lymphocyte Activation/drug effects Molecular Sequence Data T-Lymphocytes/drug effects,immunology,metabolism
Chemicals
Adjuvants, Immunologic Interleukin-13 Interleukin-12 Interleukin-4 Interferon-gamma Leukocyte Common Antigens
Authors & Affiliations
5 authors, click to expand affiliations / ORCID
Jung T
Department of Dermatology, University of Göttingen, Germany.
Wijdenes J
Neumann C
de Vries J E
Yssel H
Article Info
Journal
European journal of immunology
Abbr.
Eur J Immunol
ISSN
0014-2980
Published
1996-03-00
Pages
571-7
Language
English
Region
Germany
NLM ID
1273201
Subset
IM
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