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本文引用的文献

1
Tolerogenic microenvironment in neonatal period induced by maternal immunization with ovalbumin.卵清蛋白母体免疫诱导新生儿期的免疫耐受微环境。
Immunobiology. 2014 May;219(5):377-84. doi: 10.1016/j.imbio.2014.01.002. Epub 2014 Jan 10.
2
Targeting gamma delta T cells for cancer immunotherapy: bench to bedside.靶向γδ T细胞用于癌症免疫治疗:从 bench 到 bedside(此处 bench 和 bedside 保留英文,因为在医学研究领域常这样表述,有特定含义,bench 指基础研究阶段,bedside 指临床应用阶段)
Indian J Med Res. 2013 Nov;138(5):755-61.
3
Epithelial and dendritic cells in the thymic medulla promote CD4+Foxp3+ regulatory T cell development via the CD27-CD70 pathway.胸腺髓质中的上皮细胞和树突状细胞通过 CD27-CD70 途径促进 CD4+Foxp3+调节性 T 细胞的发育。
J Exp Med. 2013 Apr 8;210(4):715-28. doi: 10.1084/jem.20112061. Epub 2013 Apr 1.
4
Antigen-specific regulation of IgE antibodies by non-antigen-specific γδ T cells.非抗原特异性 γδ T 细胞对 IgE 抗体的抗原特异性调节。
J Immunol. 2013 Feb 1;190(3):913-21. doi: 10.4049/jimmunol.1202230. Epub 2012 Dec 28.
5
Invariant NKT cells suppress CD8(+) T-cell-mediated allergic contact dermatitis independently of regulatory CD4(+) T cells.不变自然杀伤 T 细胞独立于调节性 CD4(+) T 细胞抑制 CD8(+) T 细胞介导的变应性接触性皮炎。
J Invest Dermatol. 2013 Apr;133(4):980-7. doi: 10.1038/jid.2012.404. Epub 2012 Nov 29.
6
Lipids are required for the development of Brazil nut allergy: the role of mouse and human iNKT cells.脂质是发展巴西坚果过敏所必需的:小鼠和人类 iNKT 细胞的作用。
Allergy. 2013 Jan;68(1):74-83. doi: 10.1111/all.12057. Epub 2012 Nov 9.
7
Understanding the complexity of γδ T-cell subsets in mouse and human.理解鼠类和人类 γδ T 细胞亚群的复杂性。
Immunology. 2012 Jul;136(3):283-90. doi: 10.1111/j.1365-2567.2012.03582.x.
8
The intraepithelial T cell response to NKG2D-ligands links lymphoid stress surveillance to atopy.上皮内 T 细胞对 NKG2D 配体的反应将淋巴细胞应激监测与特应性联系起来。
Science. 2011 Dec 2;334(6060):1293-7. doi: 10.1126/science.1211250.
9
Changes in thymic regulatory T-cell maturation from birth to puberty: differences in atopic children.胸腺调节性 T 细胞成熟从出生到青春期的变化:特应性儿童的差异。
J Allergy Clin Immunol. 2012 Jan;129(1):199-206.e1-4. doi: 10.1016/j.jaci.2011.10.016. Epub 2011 Nov 21.
10
Airborne lipid antigens mobilize resident intravascular NKT cells to induce allergic airway inflammation.空气中的脂质抗原动员血管内固有 NKT 细胞诱导过敏性气道炎症。
J Exp Med. 2011 Sep 26;208(10):2113-24. doi: 10.1084/jem.20110522. Epub 2011 Sep 19.

变应原母体免疫对具有调节潜能的淋巴细胞胸腺成熟的影响:广阔的探索领域。

Influence of maternal immunization with allergens on the thymic maturation of lymphocytes with regulatory potential in children: a broad field for further exploration.

机构信息

Laboratory of Dermatology and Immunodeficiencies, LIM-56, Medical School, University of Sao Paulo, Avenida Dr. Eneas de Carvalho Aguiar 500, Third Floor, 05403-000 Sao Paulo, SP, Brazil.

出版信息

J Immunol Res. 2014;2014:780386. doi: 10.1155/2014/780386. Epub 2014 Jun 9.

DOI:10.1155/2014/780386
PMID:25009823
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC4070472/
Abstract

A variety of mechanisms are involved in the regulation of offspring allergy development through maternal immunization with allergens. The passive transfer of antigens, antibodies, and cytokines, the induction of phenotypic alterations in offspring lymphocytes, and the induction of regulatory populations in offspring have been proposed, but these mechanisms remain incompletely understood. It is likely that maternal immunization could affect the intrathymic maturation of offspring TCD4+, TCD8+, γδT, nTreg, iNKT, and B lymphocytes, although there are currently no human maternal immunization protocols for the regulation of allergic responses in children. Some studies have suggested a direct interaction between the maternal immune status and the offspring intrathymic microenvironment; this interaction could influence the maturation of offspring regulatory cells and must be explored for the development of therapies to control allergy development in children.

摘要

通过过敏原母体免疫,多种机制参与了子代过敏发展的调控。抗原、抗体和细胞因子的被动转移、子代淋巴细胞表型改变的诱导,以及子代调节群体的诱导等机制已被提出,但这些机制仍不完全清楚。尽管目前尚无用于调节儿童过敏反应的人类母体免疫接种方案,但母体免疫接种可能影响子代 TCD4+、TCD8+、γδT、nTreg、iNKT 和 B 淋巴细胞的胸腺内成熟。一些研究表明,母体免疫状态与子代胸腺内微环境之间存在直接相互作用;这种相互作用可能影响子代调节细胞的成熟,必须加以探索,以开发控制儿童过敏发展的治疗方法。