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PMID: 9064355 Published · ppublish English Journal Article Research Support, U.S. Gov't, P.H.S.

Identification of a costimulatory molecule rapidly induced by CD40L as CD44H.

The Journal of experimental medicine ·Vol. 184 ·No. 3 ·1996-09-01 ·Pages 955-61

Guo Y, Wu Y, Shinde S, Sy MS, Aruffo A, Liu Y

Abstract

The interaction between CD40 ligand and CD40 is critical for activation of T and B cells in vivo. We have recently demonstrated that this interaction rapidly induces a novel costimulatory activity distinct from B7 and independent of CD28. To study the molecular basis of the costimulatory activity, we have produced a novel monoclonal antibody, TM-1, that binds an 85-kilodalton costimulatory molecule rapidly induced by CD40L. Expression cloning reveals that TM-1 binds CD44H. CD44H expressed on Chinese hamster ovary cells has potent costimulatory activity for clonal expansion of T cells isolated from both wild-type mice and these with a targeted mutation of CD28. Thus, CD44H costimulates T cell proliferation by a CD28-independent mechanism. These results revealed that CD44H is a costimulatory molecule rapidly induced by CD40L.

MeSH Terms
Animals Antibodies, Monoclonal CD40 Antigens/metabolism CD40 Ligand CHO Cells Cloning, Molecular Cricetinae Hyaluronan Receptors/metabolism Membrane Glycoproteins/metabolism Mice Mice, Inbred C57BL Mice, Inbred CBA RNA, Messenger/metabolism Spectrometry, Fluorescence
Chemicals
Antibodies, Monoclonal CD40 Antigens Hyaluronan Receptors Membrane Glycoproteins RNA, Messenger CD40 Ligand
Authors & Affiliations
6 authors, click to expand affiliations / ORCID
Guo Y
Michael Heidelberger Division of Immunology, Department of Pathology, New York University Medical Center, New York 10016, USA.
Wu Y
Shinde S
Sy M S
Aruffo A
Liu Y
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Article Info
Journal
The Journal of experimental medicine
Abbr.
J Exp Med
ISSN
0022-1007
Published
1996-09-01
Pages
955-61
Language
English
Region
United States
NLM ID
2985109R
PMCID
PMC2192764
Subset
IM
Grants
NIAID NIH HHS · AI32981 · United States
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