| Literature DB >> 1834458 |
A Traunecker1, A Lanzavecchia, K Karjalainen.
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).Entities:
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Year: 1991 PMID: 1834458 PMCID: PMC453097 DOI: 10.1002/j.1460-2075.1991.tb04932.x
Source DB: PubMed Journal: EMBO J ISSN: 0261-4189 Impact factor: 11.598