Small CD4 Mimetics Prevent HIV-1 Uninfected Bystander CD4 + T Cell Killing Mediated by Antibody-dependent Cell-mediated Cytotoxicity

نویسندگان

  • Jonathan Richard
  • Maxime Veillette
  • Shilei Ding
  • Daria Zoubchenok
  • Nirmin Alsahafi
  • Mathieu Coutu
  • Nathalie Brassard
  • Jongwoo Park
  • Joel R. Courter
  • Bruno Melillo
  • Amos B. Smith
  • George M. Shaw
  • Beatrice H. Hahn
  • Joseph Sodroski
  • Daniel E. Kaufmann
  • Andrés Finzi
چکیده

Human immunodeficiency virus type 1 (HIV-1) infection causes a progressive depletion of CD4 + T cells. Despite its importance for HIV-1 pathogenesis, the precise mechanisms underlying CD4 + T-cell depletion remain incompletely understood. Here we make the surprising observation that antibody-dependent cell-mediated cytotoxicity (ADCC) mediates the death of uninfected bystander CD4 + T cells in cultures of HIV-1-infected cells. While HIV-1-infected cells are protected from ADCC by the action of the viral Vpu and Nef proteins, uninfected bystander CD4 + T cells bind gp120 shed from productively infected cells and are efficiently recognized by ADCC-mediating antibodies. Thus, gp120 shedding represents a viral mechanism to divert ADCC responses towards uninfected bystander CD4 + T cells. Importantly, CD4-mimetic molecules redirect ADCC responses from uninfected bystander cells to HIV-1-infected cells; therefore, CD4-mimetic compounds might have therapeutic utility in new strategies aimed at specifically eliminating HIV-1-infected cells.

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عنوان ژورنال:

دوره 3  شماره 

صفحات  -

تاریخ انتشار 2016