Abstract

CD4+ T cell activation requires inflammatory cytokines to provide a third signal (3SI), such as interleukin-12 (IL-12). We recently reported that bovine neutrophils can enhance the activation of bovine CD4+ T cells. To explore the interactions between neutrophils and third signal cytokines in bovine CD4+ T cell activation, naïve CD4+ T cells were isolated from cattle lymph nodes and stimulated for 3.5 days with anti-bovine CD3 (first signal; 1SI), anti-bovine CD28 (second signal; 2SI), and recombinant human IL-12 (3SI) in the presence or absence of neutrophils harvested from the same animals. Indeed, the strongest activation was achieved in the presence of all three signals, as demonstrated by CD25 upregulation, IFNγ production in CD4+ T cells, and secretion of IFNγ and IL-2 in cell supernatants. More importantly, 1SI plus neutrophils led to enhanced CD25 expression that was further increased by IL-12, suggesting synergistic action by IL-12 and neutrophils. Consistently, neutrophils significantly increased IFNγ production in 1SI plus IL-12-stimulated CD4+ T cells. Our data suggest the synergy of neutrophils and IL-12 as a novel regulator on bovine CD4+ T cell activation in addition to three signals. This knowledge could assist the development of immune interventions for the control of infectious diseases in cattle.

Highlights

  • CD4+ T cells contribute to adaptive immunity against pathogens in animals by helping B cells to produce pathogen-specific antibodies, including neutralizing antibodies [1,2], and enhance the killing capacity of CD8+ T cells against pathogen-infected or malignant cells, and are instrumental in the induction of CD8+ T cell memory after vaccination [3,4,5]

  • CD28 costimulatory pathway has been thoroughly studied [40,41], and its costimulatory function to TCR signaling is reflected in cattle as described in this report

  • CD28 and CTLA-4 are highly homologous, but they deliver opposite effects to T cells during activation [41]. We speculate that this Clone#TE1A may target an antigen epitope shared between CTLA-4 and CD28 in cattle T cells

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Summary

Introduction

CD4+ T cells contribute to adaptive immunity against pathogens in animals by helping B cells to produce pathogen-specific antibodies, including neutralizing antibodies [1,2], and enhance the killing capacity of CD8+ T cells against pathogen-infected or malignant cells, and are instrumental in the induction of CD8+ T cell memory after vaccination [3,4,5]. Full activation of naive CD4+ T cells depends on three signals: antigen (1SI), costimulation (2SI), and third signal cytokines (3SI) [8]. Professional antigenpresenting cells (APCs) provide these signals via expression of MHC II, which presents pathogen-derived peptides to naive CD4+ T cells, and the expression of costimulatory molecules and production of cytokines to determine the type of response required [9,10,11]. It is not clear if bovine naive CD4+ T cells are activated and directed in the same manner

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