Cargando…

Triggering T cells by otherwise inert hybrid anti-CD3/antitumor antibodies requires encounter with the specific target cell

We used a purified bispecific antibody (Ab) against CD3 and an ovarian carcinoma (OVCA) antigen to ask whether the binding of a monovalent ligand to CD3 can induce triggering of T cells. In the presence of OVCA cells, this Ab bridges the CD3 complex to the target cell and triggers proliferation and...

Descripción completa

Detalles Bibliográficos
Formato: Texto
Lenguaje:English
Publicado: The Rockefeller University Press 1989
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2189365/
https://www.ncbi.nlm.nih.gov/pubmed/2526194
_version_ 1782146625226932224
collection PubMed
description We used a purified bispecific antibody (Ab) against CD3 and an ovarian carcinoma (OVCA) antigen to ask whether the binding of a monovalent ligand to CD3 can induce triggering of T cells. In the presence of OVCA cells, this Ab bridges the CD3 complex to the target cell and triggers proliferation and cytotoxicity in T cells. In the absence of target cells, however, this monovalent Ab, even when bound to T cells at high levels, fails to induce any increase in cytosolic Ca2+, nor does it induce responsiveness to IL-2 or modulation of the CD3 complex. Because it is inert when bound monovalently, this hybrid Ab can be used to arm in vitro CTL clones, which then retain the capacity to kill the specific tumor for up to 2 d.
format Text
id pubmed-2189365
institution National Center for Biotechnology Information
language English
publishDate 1989
publisher The Rockefeller University Press
record_format MEDLINE/PubMed
spelling pubmed-21893652008-04-17 Triggering T cells by otherwise inert hybrid anti-CD3/antitumor antibodies requires encounter with the specific target cell J Exp Med Articles We used a purified bispecific antibody (Ab) against CD3 and an ovarian carcinoma (OVCA) antigen to ask whether the binding of a monovalent ligand to CD3 can induce triggering of T cells. In the presence of OVCA cells, this Ab bridges the CD3 complex to the target cell and triggers proliferation and cytotoxicity in T cells. In the absence of target cells, however, this monovalent Ab, even when bound to T cells at high levels, fails to induce any increase in cytosolic Ca2+, nor does it induce responsiveness to IL-2 or modulation of the CD3 complex. Because it is inert when bound monovalently, this hybrid Ab can be used to arm in vitro CTL clones, which then retain the capacity to kill the specific tumor for up to 2 d. The Rockefeller University Press 1989-07-01 /pmc/articles/PMC2189365/ /pubmed/2526194 Text en This article is distributed under the terms of an Attribution–Noncommercial–Share Alike–No Mirror Sites license for the first six months after the publication date (see http://www.rupress.org/terms). After six months it is available under a Creative Commons License (Attribution–Noncommercial–Share Alike 4.0 Unported license, as described at http://creativecommons.org/licenses/by-nc-sa/4.0/).
spellingShingle Articles
Triggering T cells by otherwise inert hybrid anti-CD3/antitumor antibodies requires encounter with the specific target cell
title Triggering T cells by otherwise inert hybrid anti-CD3/antitumor antibodies requires encounter with the specific target cell
title_full Triggering T cells by otherwise inert hybrid anti-CD3/antitumor antibodies requires encounter with the specific target cell
title_fullStr Triggering T cells by otherwise inert hybrid anti-CD3/antitumor antibodies requires encounter with the specific target cell
title_full_unstemmed Triggering T cells by otherwise inert hybrid anti-CD3/antitumor antibodies requires encounter with the specific target cell
title_short Triggering T cells by otherwise inert hybrid anti-CD3/antitumor antibodies requires encounter with the specific target cell
title_sort triggering t cells by otherwise inert hybrid anti-cd3/antitumor antibodies requires encounter with the specific target cell
topic Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2189365/
https://www.ncbi.nlm.nih.gov/pubmed/2526194