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PMID: 6980570 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't Research Support, U.S. Gov't, P.H.S.

The molecular basis for cytolytic T lymphocyte function: analysis with blocking monoclonal antibodies.

Advances in experimental medicine and biology ·Vol. 146 ·1982-00-00 ·Pages 447-68

Martz E, Davignon D, Kürzinger K, Springer TA

Abstract

During the past decade the mechanism of CTL-mediated killing has been resolved into 3 steps, and its cation requirements, and general nature have been well defined. However, biochemical understanding of the CTL-target interaction has made little progress. Recently, we have developed a monoclonal antibody (MAb) which blocks killing by binding to a previously undescribed molecule on the CTL membrane, a molecule which we therefore have termed lymphocyte function-associated antigen one (LFA-1). LFA-1 and Lyt-2,3 are the only presently identified sites for such blocking; antibodies to over a dozen other molecules expressed on the CTL do not block killing. Present evidence suggests that LFA-1 is crucial in the adhesive interaction of T cells with other cells (e.g., targets, macrophages, perhaps B cells) The continuing search for blocking MAbs provides a systematic way to link specific molecules with CTL function.

MeSH Terms
Animals Antibodies, Monoclonal Antigen-Antibody Complex Antigens, Surface/immunology Cell Membrane/immunology Cytotoxicity, Immunologic Humans Isoantibodies/immunology Leukemia, Experimental/immunology Mice Rats T-Lymphocytes/immunology
Chemicals
Antibodies, Monoclonal Antigen-Antibody Complex Antigens, Surface Isoantibodies Lyt antibodies
Authors & Affiliations
4 authors, click to expand affiliations / ORCID
Martz E
Davignon D
Kürzinger K
Springer T A
Article Info
Journal
Advances in experimental medicine and biology
Abbr.
Adv Exp Med Biol
ISSN
0065-2598
Published
1982-00-00
Pages
447-68
Language
English
Region
United States
NLM ID
0121103
Subset
IM
Grants
NCI NIH HHS · CA-14723 · United States
NCI NIH HHS · CA-31798 · United States
NCI NIH HHS · CA-31799 · United States
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