Virucidal effect of myeloperoxidase on human immunodeficiency virus type 1-infected T cells

Antimicrob Agents Chemother. 1994 May;38(5):969-72. doi: 10.1128/AAC.38.5.969.

Abstract

Myeloperoxidase is virucidal to human immunodeficiency virus type 1 (HIV-1) in the persistently infected CEM human T-cell line or in acutely infected human peripheral blood mononuclear cells, as judged by viral infectivity and P24 radioimmunoassay. HIV-1 was specifically inactivated by low doses of the human myeloperoxidase (1.4 to 14.3 mU/ml) and the cells were spared. A higher enzyme concentration (143 mU/m) was cytotoxic, but uninfected CEM cells and normal lymphocytes were resistant to > or = 143 mU of myeloperoxidase per ml. The enzyme was virucidal with the Cl- present in medium and did not require exogenous H2O2. Catalase, an antioxidant enzyme, partially inhibited the virucidal effect of myeloperoxidase. Hence, the H2O2 probably came from the HIV-infected cells themselves. These in vitro findings indicate that the myeloperoxidase system is capable of inactivating HIV-1 of infected cells.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Antiviral Agents / pharmacology*
  • Catalase / pharmacology
  • Cell Line
  • Glucose Oxidase / pharmacology
  • HIV Core Protein p24 / immunology
  • HIV Core Protein p24 / metabolism
  • HIV-1 / drug effects*
  • HIV-1 / metabolism
  • Humans
  • Lactoperoxidase / pharmacology
  • Peroxidase / pharmacology*
  • Phytohemagglutinins / pharmacology
  • Radioimmunoassay
  • T-Lymphocytes / drug effects
  • T-Lymphocytes / microbiology*

Substances

  • Antiviral Agents
  • HIV Core Protein p24
  • Phytohemagglutinins
  • Glucose Oxidase
  • Lactoperoxidase
  • Catalase
  • Peroxidase