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Lymphoid tissue fibrosis is associated with impaired vaccine responses.淋巴组织纤维化与疫苗应答受损有关。
J Clin Invest. 2018 Jul 2;128(7):2763-2773. doi: 10.1172/JCI97377. Epub 2018 May 21.
2
Telmisartan Therapy Does Not Improve Lymph Node or Adipose Tissue Fibrosis More Than Continued Antiretroviral Therapy Alone.替米沙坦治疗并不能比继续单独抗逆转录病毒治疗更有效地改善淋巴结或脂肪组织纤维化。
J Infect Dis. 2018 May 5;217(11):1770-1781. doi: 10.1093/infdis/jiy064.
3
The Equity Impact Vaccines May Have On Averting Deaths And Medical Impoverishment In Developing Countries.疫苗对避免发展中国家死亡和医疗贫困的公平影响。
Health Aff (Millwood). 2018 Feb;37(2):316-324. doi: 10.1377/hlthaff.2017.0861.
4
Sex and Gender Differences in the Outcomes of Vaccination over the Life Course.疫苗接种在整个生命历程中的效果的性别差异。
Annu Rev Cell Dev Biol. 2017 Oct 6;33:577-599. doi: 10.1146/annurev-cellbio-100616-060718.
5
The potential of the microbiota to influence vaccine responses.微生物组影响疫苗反应的潜力。
J Leukoc Biol. 2018 Feb;103(2):225-231. doi: 10.1189/jlb.5MR0617-216R. Epub 2017 Dec 28.
6
Schistosoma mansoni Infection Can Jeopardize the Duration of Protective Levels of Antibody Responses to Immunizations against Hepatitis B and Tetanus Toxoid.曼氏血吸虫感染可能会危及针对乙肝和破伤风类毒素免疫接种产生的抗体反应的保护水平持续时间。
PLoS Negl Trop Dis. 2016 Dec 7;10(12):e0005180. doi: 10.1371/journal.pntd.0005180. eCollection 2016 Dec.
7
Significant Correlation Between the Infant Gut Microbiome and Rotavirus Vaccine Response in Rural Ghana.加纳农村地区婴儿肠道微生物群与轮状病毒疫苗反应之间的显著相关性。
J Infect Dis. 2017 Jan 1;215(1):34-41. doi: 10.1093/infdis/jiw518. Epub 2016 Oct 31.
8
Searching for the human genetic factors standing in the way of universally effective vaccines.寻找阻碍通用有效疫苗研发的人类遗传因素。
Philos Trans R Soc Lond B Biol Sci. 2015 Jun 19;370(1671). doi: 10.1098/rstb.2014.0341.
9
Stool microbiota and vaccine responses of infants.婴儿的粪便微生物群与疫苗反应
Pediatrics. 2014 Aug;134(2):e362-72. doi: 10.1542/peds.2013-3937. Epub 2014 Jul 7.
10
Immune activation alters cellular and humoral responses to yellow fever 17D vaccine.免疫激活会改变对黄热病17D疫苗的细胞和体液反应。
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淋巴结纤维化:释放有效疫苗免疫的结构性障碍。

Lymph node fibrosis: a structural barrier to unleashing effective vaccine immunity.

出版信息

J Clin Invest. 2018 Jul 2;128(7):2743-2745. doi: 10.1172/JCI121053. Epub 2018 May 21.

DOI:10.1172/JCI121053
PMID:29781815
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6026002/
Abstract

There is marked variability in vaccine efficacy among global populations. In particular, individuals in low- to middle-income countries have been shown to be less responsive to vaccines than those from developed nations. Several factors, including endemic infections, nutrition, genetics, and gut microbiome composition, have been proposed to underlie discrepancies in vaccine response. In this issue of the JCI, Kityo et al. evaluated response to yellow fever virus vaccine, inflammation, and lymphatic tissue architecture and fibrosis in three cohorts: two from the U.S. and one from Uganda. Compared with the U.S. subjects, the Ugandan cohort exhibited enhanced cytokine responses, increased lymph node fibrosis, reduced CD4+ T cell levels, and reduced vaccine response. Together, these results provide a link among chronic inflammation, damaged lymphoid architecture, and poor vaccine outcome, and set the stage for future studies to identify strategies to overcome these barriers.

摘要

在全球人群中,疫苗的效果存在明显的差异。特别是,来自中低收入国家的个体对疫苗的反应不如来自发达国家的个体敏感。一些因素,包括地方性感染、营养、遗传和肠道微生物组组成,被认为是疫苗反应差异的基础。在本期 JCI 中,Kityo 等人评估了三个队列(两个来自美国,一个来自乌干达)对黄热病病毒疫苗、炎症、淋巴组织结构和纤维化的反应。与美国受试者相比,乌干达队列表现出更强的细胞因子反应、增加的淋巴结纤维化、降低的 CD4+T 细胞水平和降低的疫苗反应。这些结果共同提供了慢性炎症、受损的淋巴组织结构和不良疫苗结果之间的联系,并为未来的研究确定克服这些障碍的策略奠定了基础。