HIV-infected cells are killed by rCD4-ricin A chain

Mark A. Till, Victor Ghetie, Timothy Gregory, Eric J. Patzer, James P. Porter, Jonathan W. Uhr, Daniel J. Capon, Ellen S. Vitetta

Research output: Contribution to journalArticlepeer-review

129 Scopus citations


The gpl20 envelope glycoprotein of the human immunodeficiency virs (HIV), which is expressed on the surface of many HIV-infected cells, binds to the cell surface molecule CD4. Soluble derivatives of recombinant CD4 (rCD4) that bind gpl20 with high affinity are attractive vehicles for targeting a cytotoxic reagent to HIV-infected cells. Soluble rCD4 was conjugated to the active subunit of the toxin ricin. This conjugate killed HIV-infected H9 cells but was 1/1000 as toxic to uninfected H9 cells (which do not express gp120) and was not toxic to Daudi cells (which express major histocompatibility class II antigens, the putative natural ligand for cell surface CD4). Specific killing of infected cells can be blocked by rgpl2O, rCD4, or a monoclonal antibody to the gpl20 binding site on CD4.

Original languageEnglish (US)
Pages (from-to)1166-1168
Number of pages3
Issue number4882
StatePublished - 1988

ASJC Scopus subject areas

  • General


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