Abstract

Paraquat (PQ) is a toxic non-selective herbicide. To date, the effect of PQ on memory immune response is still unknown. We investigated the impact of PQ on memory immune response. Adult C57BL/6 mice were subcutaneously injected with 2 mg/kg PQ, 20 mg/kg PQ or vehicle control every three days for two weeks. A single injection of keyhole limpet hemocyanin (KLH) at day four after the initial PQ treatment was used to induce a primary immune response; a second KLH challenge was performed at three months post the first KLH immunization to induce a secondary immune response. In steady state, treatment with 20 mg/kg PQ reduced the level of serum total IgG, but not that of IgM; treatment with 20 mg/kg PQ decreased the number of effector and memory lymphocytes, but not naïve or inactivated lymphocytes. During the primary immune response to KLH, treatment with 20 mg/kg PQ did not influence the proliferation of lymphocytes or expression of co-stimulatory molecules. Instead, treatment with 20 mg/kg PQ increased the apoptosis of lymphocytes at late stage, but not early stage of the primary immune response. During the secondary immune response to KLH, treatment with 20 mg/kg PQ reduced the serum anti-KLH IgG and KLH-responsive CD4 T cells and B cells. Moreover, effector or activated lymphocytes were more sensitive to PQ-induced apoptosis in vitro. Treatment with 2 mg/kg PQ did not impact memory immune response to KLH. Thus, treatment with 20 mg/kg PQ increased apoptosis of late stage effector cells to yield less memory cells and thereafter impair memory immune response, providing a novel understanding of the immunotoxicity of PQ.

Highlights

  • Paraquat (PQ) is a highly toxic non-selective herbicide that is widely used throughout the world.PQ is known to causes damage to numerous organs including the lung, brain, kidney, heart, liver, and immune system [1,2,3]

  • PQ toxicities to the lung and kidney included an increased level of pro-inflammatory cytokines such as interleukin 1β (IL-1β), IL-6 and tumor necrosis factor α (TNFα) [5,6,7,8,9], indicating that innate immune cells such as macrophages and neutrophils were activated by PQ exposure

  • We found that PQ impaired memory immune response to keyhole limpet hemocyanin (KLH) likely due to increased apoptosis of effector CD4 T cells and activated B cells at the end of the primary immune response, which is a previously unknown toxicity of PQ to the immune system

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Summary

Introduction

PQ is known to causes damage to numerous organs including the lung, brain, kidney, heart, liver, and immune system [1,2,3]. The immunotoxicities of PQ are complex, PQ is a confirmed toxicant to both innate and adaptive immune system [3]. Cells via induction of metallothionein in mice [4]. PQ toxicities to the lung and kidney included an increased level of pro-inflammatory cytokines such as interleukin 1β (IL-1β), IL-6 and tumor necrosis factor α (TNFα) [5,6,7,8,9], indicating that innate immune cells such as macrophages and neutrophils were activated by PQ exposure. PQ was reported to cause oxidative stress both in vivo and in vitro in that reactive oxygen species (ROS) and malondialdehyde (MDA), a product of lipid

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