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PMID: 2531196 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't Research Support, U.S. Gov't, P.H.S.

Lymphokine regulation of CD45R expression on human T cell clones.

The Journal of experimental medicine ·Vol. 170 ·No. 6 ·1989-12-01 ·Pages 2147-52

Brod SA, Rudd CE, Purvee M, Hafler DA

Abstract

Whether the expression of higher molecular weight isoforms of the T-200 complex represents different lineages of T cells and/or a sequential stage of the differential pathway of T cells has been unclear. Understanding T cell expression of higher molecular weight isoforms of the T-200 complex (CD45R) may be important because of their association with regulation of immune responses. By direct single cell cloning, we observed a number of long-term T cell clones that expressed CD45RA (2H4). CD45RA expression could be further regulated by ionomycin or the cytokines IL-1 and IL-6, but not IL-2, IL-4, or IFN-gamma. These results indicate that CD45RA expression may define T cell lineages of activated T cells partially controlled by the cytokines IL-1 and IL-6. Further, these results may associate regulatory actions of IL-1 and IL-6 with their ability to increase CD45RA expression in subpopulations of human T cells.

MeSH Terms
Antigens, Differentiation Clone Cells Humans Interleukin-1/pharmacology Interleukin-6/pharmacology Leukocyte Common Antigens Molecular Weight Receptors, Antigen, T-Cell/genetics T-Lymphocytes/immunology
Chemicals
Antigens, Differentiation Interleukin-1 Interleukin-6 Receptors, Antigen, T-Cell Leukocyte Common Antigens
Authors & Affiliations
4 authors, click to expand affiliations / ORCID
Brod S A
Department of Medicine, Brigham and Women's Hospital, Boston, Massachusetts.
Rudd C E
Purvee M
Hafler D A
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15 references, click to expand
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Article Info
Journal
The Journal of experimental medicine
Abbr.
J Exp Med
ISSN
0022-1007
Published
1989-12-01
Pages
2147-52
Language
English
Region
United States
NLM ID
2985109R
PMCID
PMC2189525
Subset
IM
Grants
NINDS NIH HHS · KO8 NS-00981 · United States
NIAID NIH HHS · R01 AI-12069 · United States
NINDS NIH HHS · R01 NS-24247 · United States
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