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孕前免疫可调节子代细胞内Th2细胞因子谱:白细胞介素10及B/T细胞协作的影响

Preconception immunization can modulate intracellular Th2 cytokine profile in offspring: influence of interleukin 10 and B/T cell collaboration.

作者信息

de Oliveira Marília Garcia, Lira Aline Aparecida de Lima, Sgnotto Fábio da Ressureição, Inoue Amanda Harumi Sabô, Duarte Alberto José da Silva, Victor Jefferson Russo

机构信息

Laboratory of Medical Investigation LIM 56, Division of Clinical Dermatology, Medical School, University of Sao Paulo, Sao Paulo, Brazil.

Division of Pathology, Medical School, University of Sao Paulo, Sao Paulo, Brazil.

出版信息

Cent Eur J Immunol. 2018;43(4):378-388. doi: 10.5114/ceji.2018.81345. Epub 2018 Dec 31.

Abstract

INTRODUCTION

In the last few years our group has been studying the mechanisms involved in the inhibition of allergy in offspring mediated by preconception maternal immunization, but these mechanisms are not fully understood. Such mechanisms that we have studied aimed at the passive transfer of maternal antibodies and its influence on offspring immune status.

AIM OF THE STUDY

To evaluate whether maternal immunization could modulate intracellular Th1/Th2 profiles in offspring.

MATERIAL AND METHODS

C57BL/6 female wild type mice (WT), interleukin (IL)-10 or CD28 mice were immunized or not with ovalbumin (OVA) and were mated with respective lineage males and offspring were evaluated at 3 days old (d.o.), 20 d.o., or 20 d.o. after neonatal immunization.

RESULTS

Preconception OVA immunization induced a marked reduction in IL-4 secretion by TCD4+ cells of WT offspring when compared with offspring from non-immunized mothers. The maternal immunization of IL-10 mice induced an increase in the TCD4+IL-4+ percentage in offspring and a reduction in TCD4+IFN-γ+ cells. The maternal immunization in CD28 mice induced augment IL-4 intensity in 3 and 20 d.o. offspring TCD4+ cells.

CONCLUSIONS

Our results reveal that maternal immunization with OVA can down-regulate the Th2 pattern in offspring and this regulation is dependent on IL-10 and B/T cell collaboration.

摘要

引言

在过去几年中,我们的研究小组一直在研究孕前母体免疫介导的子代过敏抑制机制,但这些机制尚未完全明确。我们所研究的此类机制旨在探讨母体抗体的被动转移及其对后代免疫状态的影响。

研究目的

评估母体免疫是否能够调节子代细胞内的Th1/Th2细胞谱。

材料与方法

将C57BL/6雌性野生型小鼠(WT)、白细胞介素(IL)-10或CD28小鼠用卵清蛋白(OVA)免疫或不免疫,然后与相应品系的雄性小鼠交配,并在子代3日龄(d.o.)、20日龄或新生期免疫后20日龄时进行评估。

结果

与未免疫母亲的子代相比,孕前OVA免疫显著降低了WT子代TCD4+细胞分泌IL-4的水平。IL-10小鼠的母体免疫导致子代中TCD4+IL-4+百分比增加,TCD4+IFN-γ+细胞减少。CD28小鼠的母体免疫在3日龄和20日龄子代的TCD4+细胞中诱导IL-4强度增加。

结论

我们的结果表明,OVA母体免疫可下调子代的Th2模式,且这种调节依赖于IL-10和B/T细胞协作。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8396/6384423/e96f728173b5/CEJI-43-81345-g001.jpg

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