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PMID: 1834458 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't

Bispecific single chain molecules (Janusins) target cytotoxic lymphocytes on HIV infected cells.

The EMBO journal ·Vol. 10 ·No. 12 ·1991-12-00 ·Pages 3655-9

Traunecker A, Lanzavecchia A, Karjalainen K

Abstract

The human immunodeficiency virus type 1 (HIV-1) uses cell surface CD4 as a receptor to infect susceptible cells. Therefore, different forms of soluble CD4 (sCD4) molecules have been developed recently for potential therapeutic purposes. Here we describe a novel design of sCD4 molecules which exploit cytotoxic T cells as their effector function. The principle of bispecific antibodies was exploited and further developed to create new bispecific reagents which could retarget cytotoxic T cells of any specificity and thus, induce killing of HIV-1 infected cells. The most advanced molecules, Janusins, contain in one polypeptide chain the first two N-terminal CD4 domains and single chain combining site against the human CD3 complex (FvCD3).

MeSH Terms
Amino Acid Sequence Antigens, Differentiation, T-Lymphocyte/immunology Base Sequence CD3 Complex CD4 Antigens/immunology Electrophoresis, Polyacrylamide Gel Genetic Vectors HIV-1/immunology Humans Molecular Sequence Data Oligonucleotides Receptors, Antigen, T-Cell/immunology T-Lymphocytes, Cytotoxic/immunology
Chemicals
Antigens, Differentiation, T-Lymphocyte CD3 Complex CD4 Antigens Oligonucleotides Receptors, Antigen, T-Cell
Authors & Affiliations
3 authors, click to expand affiliations / ORCID
Traunecker A
Basel Institute for Immunology, Switzerland.
Lanzavecchia A
Karjalainen K
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Article Info
Journal
The EMBO journal
Abbr.
EMBO J
ISSN
0261-4189
Published
1991-12-00
Pages
3655-9
Language
English
Region
England
NLM ID
8208664
PMCID
PMC453097
Subset
IM
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