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PMID: 2960730 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't Research Support, U.S. Gov't, P.H.S.

The influence of valence on the functional activities of monoclonal anti-L3T4 antibodies. Discrimination of signaling from other effects.

Journal of immunology (Baltimore, Md. : 1950) ·Vol. 139 ·No. 10 ·1987-11-15 ·Pages 3207-12

Haque S, Saizawa K, Rojo J, Janeway CA

Abstract

Anti-L3T4 antibodies have different functional effects on different ligands that activate a cloned, L3T4+ helper T cell line. It is reported here that some of these effects involve positive or negative signaling induced by cross-linking L3T4 molecules, because such effects are not observed using the Fab fragment of anti-L3T4. However, the Fab fragment does inhibit responses to antigen:self class II major histocompatibility complex (MHC) and to anti-T cell receptor monoclonal antibodies directed at a particular V region epitope. The finding that the Fab fragment of anti-L3T4, which does not block binding of anti-T cell receptor V region antibodies and does not negative signal can still block activation by such antibodies suggests an intimate association of L3T4 with the T3: alpha: beta T cell receptor complex. This association may normally be induced by interaction of both structures with antigen:self class II MHC complexes. The data also support the hypothesis that cross-linking the L3T4 molecule in the absence of engagement of the T3: alpha: beta complex generates negative or inhibitory signals. Thus, L3T4 plays a central role in the process of class II MHC-restricted T cell antigen recognition and activation.

MeSH Terms
Animals Antibodies/immunology Antibodies, Monoclonal/immunology Antigens, Differentiation, T-Lymphocyte/immunology Cell Line Histocompatibility Antigens Class II/immunology Immunoglobulin Fab Fragments/immunology Lymphocyte Activation Mice Receptors, Antigen, T-Cell/immunology T-Lymphocytes, Helper-Inducer/immunology
Chemicals
Antibodies Antibodies, Monoclonal Antigens, Differentiation, T-Lymphocyte Histocompatibility Antigens Class II Immunoglobulin Fab Fragments Receptors, Antigen, T-Cell
Authors & Affiliations
4 authors, click to expand affiliations / ORCID
Haque S
Section of Immunobiology, Howard Hughes Medical Institute at Yale University School of Medicine, New Haven, CT 06510.
Saizawa K
Rojo J
Janeway C A
Article Info
Journal
Journal of immunology (Baltimore, Md. : 1950)
Abbr.
J Immunol
ISSN
0022-1767
Published
1987-11-15
Pages
3207-12
Language
English
Region
United States
NLM ID
2985117R
Subset
IM
Grants
NIAID NIH HHS · AI-14579 · United States
NCI NIH HHS · CA-29606 · United States
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