1. Academic Validation
  2. The anti-caspase inhibitor Q-VD-OPH prevents AIDS disease progression in SIV-infected rhesus macaques

The anti-caspase inhibitor Q-VD-OPH prevents AIDS disease progression in SIV-infected rhesus macaques

  • J Clin Invest. 2018 Apr 2;128(4):1627-1640. doi: 10.1172/JCI95127.
Mireille Laforge 1 Ricardo Silvestre 1 2 3 Vasco Rodrigues 1 4 5 Julie Garibal 1 Laure Campillo-Gimenez 1 Shahul Mouhamad 1 Valérie Monceaux 6 Marie-Christine Cumont 6 Henintsoa Rabezanahary 7 Alain Pruvost 8 Anabela Cordeiro-da-Silva 4 5 Bruno Hurtrel 6 Guido Silvestri 9 Anna Senik 1 Jérôme Estaquier 1 7
Affiliations

Affiliations

  • 1 CNRS FR 3636, Université Paris Descartes, Paris, France.
  • 2 Microbiology and Infection Research Domain, Life and Health Sciences Research Institute (ICVS), School of Medicine, University of Minho, Braga, Portugal.
  • 3 ICVS/3B's - PT Government Associate Laboratory, Braga/Guimarães, Portugal.
  • 4 i3S - Instituto de Investigação e Inovação em Saúde and.
  • 5 Instituto de Biologia Molecular e Celular, Universidade do Porto, Porto, Portugal.
  • 6 Unité de Physiopathologie des Infections Lentivirales, Institut Pasteur, Paris, France.
  • 7 Université Laval, Centre de Recherche du CHU de Québec, Quebec City, Quebec, Canada.
  • 8 CEA, iBiTecS, SPI, Laboratoire d'Etude du Métabolisme des Médicaments, Gif-sur-Yvette, France.
  • 9 Yerkes National Primate Research Center, Emory University, Atlanta, Georgia, USA.
Abstract

Apoptosis has been proposed as a key mechanism responsible for CD4+ T cell depletion and immune dysfunction during HIV Infection. We demonstrated that Q-VD-OPH, a Caspase Inhibitor, inhibits spontaneous and activation-induced death of T cells from SIV-infected rhesus macaques (RMs). When administered during the acute phase of Infection, Q-VD-OPH was associated with (a) reduced levels of T cell death, (b) preservation of CD4+/CD8+ T cell ratio in lymphoid organs and in the gut, (c) maintenance of memory CD4+ T cells, and (d) increased specific CD4+ T cell response associated with the expression of cytotoxic molecules. Although therapy was limited to the acute phase of Infection, Q-VD-OPH-treated RMs showed lower levels of both viral load and cell-associated SIV DNA as compared with control SIV-infected RMs throughout the chronic phase of Infection, and prevented the development of AIDS. Overall, our data demonstrate that Q-VD-OPH injection in SIV-infected RMs may represent an adjunctive therapeutic agent to control HIV Infection and delaying disease progression to AIDS.

Keywords

AIDS/HIV; Apoptosis; Apoptosis inhibitors; Immunology; T cells.

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