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CD4+ Foxp3+调节性T细胞在减毒活复制型I型弓形虫疫苗株诱导的保护作用中的角色

Role of CD4+ Foxp3+ Regulatory T Cells in Protection Induced by a Live Attenuated, Replicating Type I Vaccine Strain of Toxoplasma gondii.

作者信息

Akbar Haroon, Dimier-Poisson Isabelle, Moiré Nathalie

机构信息

Université de Tours, UMR1282 Infectiologie et Santé Publique, Tours, France, and INRA, UMR1282 Infectiologie et Santé Publique, Nouzilly, France.

Université de Tours, UMR1282 Infectiologie et Santé Publique, Tours, France, and INRA, UMR1282 Infectiologie et Santé Publique, Nouzilly, France

出版信息

Infect Immun. 2015 Sep;83(9):3601-11. doi: 10.1128/IAI.00217-15. Epub 2015 Jun 29.

Abstract

Vaccination with the live attenuated Toxoplasma gondii Mic1.3KO strain induced long-lasting immunity against challenge with Toxoplasma gondii type I and type II strains. The involvement of regulatory T cells (Tregs) in the protection mechanism was investigated. Intraperitoneal injection of Mic1.3KO induced a weak and transient influx of CD4(+) Foxp3(+) T regulatory cells followed by recruitment/expansion of CD4(+) Foxp3(-) CD25(+) effector cells and control of the parasite at the site of infection. The local and systemic cytokine responses associated with this recruitment of Tregs were of the TH1/Treg-like type. In contrast, injection of RH, the wild-type strain from which the vaccinal strain is derived, induced a low CD4(+) Foxp3(+) cell influx and uncontrolled multiplication of the parasites at this local site, followed by death of the mice. The associated local and systemic cytokine responses were of the TH1/TH17-like type. In addition, in vivo Treg induction in RH-infected mice with interleukin-2 (IL-2)/anti-IL-2 complexes induced control of the parasite and a TH1/Treg cytokine response similar to the response after Mic1.3KO vaccination. These results suggest that Tregs may contribute to the protective response after vaccination with Mic1.3KO.

摘要

用减毒活弓形虫Mic1.3KO株进行疫苗接种可诱导针对I型和II型弓形虫攻击的持久免疫力。研究了调节性T细胞(Tregs)在保护机制中的作用。腹腔注射Mic1.3KO诱导了CD4(+) Foxp3(+) T调节细胞的微弱且短暂的流入,随后是CD4(+) Foxp3(-) CD25(+)效应细胞的募集/扩增以及在感染部位对寄生虫的控制。与这种Tregs募集相关的局部和全身细胞因子反应属于TH1/Treg样类型。相比之下,注射RH(疫苗株所源自的野生型菌株)诱导了低水平的CD4(+) Foxp3(+)细胞流入以及寄生虫在该局部部位的不受控制的增殖,随后小鼠死亡。相关的局部和全身细胞因子反应属于TH1/TH17样类型。此外,用白细胞介素-2(IL-2)/抗IL-2复合物在感染RH的小鼠中进行体内Treg诱导可诱导对寄生虫的控制以及类似于Mic1.3KO疫苗接种后反应的TH1/Treg细胞因子反应。这些结果表明,Tregs可能有助于Mic1.3KO疫苗接种后的保护性反应。

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