• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

印度和美国婴儿的多个免疫参数差异。

Differences in multiple immune parameters between Indian and U.S. infants.

机构信息

Pediatric Biology Center, Translational Health Science & Technology Institute, NCR Biotech Science Cluster, 3rd Milestone, Faridabad-Gurgaon Expressway, Faridabad, Haryana, India.

Institute for Immunity, Transplantation, and Infection, Stanford University School of Medicine, Stanford, United States of America.

出版信息

PLoS One. 2018 Nov 16;13(11):e0207297. doi: 10.1371/journal.pone.0207297. eCollection 2018.

DOI:10.1371/journal.pone.0207297
PMID:30444901
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6239317/
Abstract

To compare immune phenotypes across two geographic and ethnic communities, we examined umbilical cord blood by flow cytometry and Luminex in parallel cohorts of 53 newborns from New Delhi, India, and 46 newborns from Stanford, California. We found that frequencies of a B cell subset suggested to be B-1-like, and serum IgM concentration were both significantly higher in the Stanford cohort, independent of differences in maternal age. While serum IgA levels were also significantly higher in the Stanford cohort, IgG1, IgG2, and IgG4 were significantly higher in the New Delhi samples. We found that neutrophils, plasmacytoid dendritic cells, CD8+ T cells, and total T cells were higher in the U.S. cohort, while dendritic cells, patrolling monocytes (CD14dimCD16+), natural killer cells, CD4+ T cells, and naïve B cells were higher in the India cohort. Within the India cohort, we also identified cell types whose frequency was positively or negatively predictive of occurrence of infection(s) in the first six months of life. Monocytes, total T cells, and memory CD4+ T cells were most prominent in having an inverse relationship with infection. We suggest that these data provide impetus for follow-up studies linking phenotypic differences to environmental versus genetic factors, and to infection outcomes.

摘要

为了比较两个地理和种族社区的免疫表型,我们通过流式细胞术和 Luminex 平行检测了来自印度新德里的 53 名新生儿和来自加利福尼亚斯坦福的 46 名新生儿的脐带血。我们发现,斯坦福队列中的 B 细胞亚群频率(提示为 B-1 样)和血清 IgM 浓度均显著更高,这与母体年龄差异无关。虽然斯坦福队列中的血清 IgA 水平也显著更高,但新德里样本中的 IgG1、IgG2 和 IgG4 水平显著更高。我们发现美国队列中的中性粒细胞、浆细胞样树突状细胞、CD8+T 细胞和总 T 细胞更高,而印度队列中的树突状细胞、巡逻单核细胞(CD14dimCD16+)、自然杀伤细胞、CD4+T 细胞和幼稚 B 细胞更高。在印度队列中,我们还确定了一些细胞类型,其频率与生命前 6 个月发生感染的情况呈正相关或负相关。单核细胞、总 T 细胞和记忆 CD4+T 细胞与感染的关系最为密切。我们认为这些数据为后续研究提供了动力,这些研究将表型差异与环境与遗传因素以及感染结果联系起来。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/13ea/6239317/a28ebf77129e/pone.0207297.g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/13ea/6239317/d752e0943d43/pone.0207297.g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/13ea/6239317/9ecd60c578b5/pone.0207297.g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/13ea/6239317/f3480caf662f/pone.0207297.g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/13ea/6239317/e1887b5d5420/pone.0207297.g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/13ea/6239317/a28ebf77129e/pone.0207297.g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/13ea/6239317/d752e0943d43/pone.0207297.g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/13ea/6239317/9ecd60c578b5/pone.0207297.g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/13ea/6239317/f3480caf662f/pone.0207297.g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/13ea/6239317/e1887b5d5420/pone.0207297.g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/13ea/6239317/a28ebf77129e/pone.0207297.g005.jpg

相似文献

1
Differences in multiple immune parameters between Indian and U.S. infants.印度和美国婴儿的多个免疫参数差异。
PLoS One. 2018 Nov 16;13(11):e0207297. doi: 10.1371/journal.pone.0207297. eCollection 2018.
2
Extended immunophenotyping reference values in a healthy pediatric population.健康儿童人群的扩展免疫表型参考值。
Cytometry B Clin Cytom. 2019 May;96(3):223-233. doi: 10.1002/cyto.b.21728. Epub 2018 Oct 17.
3
Flow cytometric characterization of human umbilical cord blood lymphocytes: immunophenotypic features.人脐带血淋巴细胞的流式细胞术特征:免疫表型特征
Haematologica. 1998 Mar;83(3):197-203.
4
Comparative Proliferation Capacity of Gag-C-Specific Naive and Memory CD4+ and CD8+ T Lymphocytes in Rapid, Viremic Slow, and Slow Progressors During Human Immunodeficiency Virus Infection.人类免疫缺陷病毒感染期间,快速进展者、病毒血症缓慢进展者和缓慢进展者中,Gag-C特异性初始及记忆CD4+和CD8+ T淋巴细胞的增殖能力比较
Viral Immunol. 2018 Sep;31(7):513-524. doi: 10.1089/vim.2018.0012. Epub 2018 Aug 29.
5
Long-term immune reconstitution and infection burden after mismatched hematopoietic stem cell transplantation.异基因造血干细胞移植后长期免疫重建和感染负担。
Biol Blood Marrow Transplant. 2014 Apr;20(4):507-17. doi: 10.1016/j.bbmt.2014.01.001. Epub 2014 Jan 7.
6
Disturbances in B- and T-cell homeostasis in rheumatoid arthritis: suggested relationships with antigen-driven immune responses.类风湿关节炎中B细胞和T细胞稳态的紊乱:与抗原驱动的免疫反应的潜在关系。
J Autoimmun. 2007 Sep-Nov;29(2-3):154-63. doi: 10.1016/j.jaut.2007.07.002.
7
Analysis of the clinical profile, autoimmune phenomena and T cell subsets (CD4 and CD8) in Takayasu's arteritis: a hospital-based study.高安动脉炎的临床特征、自身免疫现象及T细胞亚群(CD4和CD8)分析:一项基于医院的研究
Clin Exp Rheumatol. 2003 Nov-Dec;21(6 Suppl 32):S112-6.
8
Decreased memory B cells and increased CD8 memory T cells in blood of breastfed children: the generation R study.母乳喂养儿童血液中记忆B细胞减少而CD8记忆T细胞增加:Generation R研究
PLoS One. 2015 May 18;10(5):e0126019. doi: 10.1371/journal.pone.0126019. eCollection 2015.
9
Significantly skewed memory CD8+ T cell subsets in HIV-1 infected infants during the first year of life.在生命的第一年,HIV-1感染婴儿的记忆性CD8+ T细胞亚群显著失衡。
Clin Immunol. 2009 Mar;130(3):280-9. doi: 10.1016/j.clim.2008.09.006. Epub 2008 Nov 8.
10
Alternative G1m, G2m and G3m allotypes of IGHG genes correlate with atopic and nonatopic pathways of immune regulation in children with bronchial asthma.IGHG基因的替代G1m、G2m和G3m同种异型与支气管哮喘儿童免疫调节的特应性和非特应性途径相关。
Int Arch Allergy Immunol. 1998 Mar;115(3):215-9. doi: 10.1159/000023903.

引用本文的文献

1
Immune profiling reveals umbilical cord blood mononuclear cells from South India display an IL-8 dominant, CXCL-10 deficient polyfunctional monocyte response to pathogen-associated molecular patterns that is distinct from adult blood cells.免疫分析显示,来自印度南部的脐带血单核细胞对外源相关分子模式产生的多效性单核细胞反应表现为 IL-8 优势、CXCL-10 缺乏的特征,与成人血细胞不同。
Clin Exp Immunol. 2024 Aug 9;217(3):263-278. doi: 10.1093/cei/uxae034.
2
Footprint of the COVID-19 Pandemic in India: A Study of Immune Landscape and Other Factors Shielding Mortality.印度 COVID-19 大流行的影响:免疫景观及其他降低死亡率因素的研究。
Anal Cell Pathol (Amst). 2020 Dec 24;2020:6692739. doi: 10.1155/2020/6692739. eCollection 2020.
3

本文引用的文献

1
Age-related reference intervals for immunoglobulin levels and lymphocyte subsets in Indian children.印度儿童免疫球蛋白水平和淋巴细胞亚群的年龄相关参考区间。
Indian J Pathol Microbiol. 2017 Jul-Sep;60(3):360-364. doi: 10.4103/IJPM.IJPM_542_16.
2
Cord blood T cell subpopulations and associations with maternal cadmium and arsenic exposures.脐血T细胞亚群及其与母体镉和砷暴露的关联。
PLoS One. 2017 Jun 29;12(6):e0179606. doi: 10.1371/journal.pone.0179606. eCollection 2017.
3
Human immune system variation.人类免疫系统变异。
The Enigma of Low COVID-19 Fatality Rate in India.
印度新冠病毒低死亡率之谜
Front Genet. 2020 Jul 28;11:854. doi: 10.3389/fgene.2020.00854. eCollection 2020.
4
Correction: Differences in multiple immune parameters between Indian and U.S. infants.更正:印度和美国婴儿之间多种免疫参数的差异。
PLoS One. 2019 Mar 28;14(3):e0214749. doi: 10.1371/journal.pone.0214749. eCollection 2019.
Nat Rev Immunol. 2017 Jan;17(1):21-29. doi: 10.1038/nri.2016.125. Epub 2016 Dec 5.
4
Human B-1 and B-2 B Cells Develop from Lin-CD34+CD38lo Stem Cells.人类B-1和B-2 B细胞由Lin-CD34+CD38lo干细胞发育而来。
J Immunol. 2016 Nov 15;197(10):3950-3958. doi: 10.4049/jimmunol.1600630. Epub 2016 Oct 7.
5
A Functional Genomics Approach to Understand Variation in Cytokine Production in Humans.一种功能基因组学方法,用于了解人类细胞因子产生的变异。
Cell. 2016 Nov 3;167(4):1099-1110.e14. doi: 10.1016/j.cell.2016.10.017.
6
Shaping Variation in the Human Immune System.塑造人类免疫系统的多样性。
Trends Immunol. 2016 Oct;37(10):637-646. doi: 10.1016/j.it.2016.08.002.
7
Distinctions among Circulating Antibody-Secreting Cell Populations, Including B-1 Cells, in Human Adult Peripheral Blood.成人外周血中循环抗体分泌细胞群体(包括B-1细胞)之间的差异
J Immunol. 2016 Feb 1;196(3):1060-9. doi: 10.4049/jimmunol.1501843. Epub 2016 Jan 6.
8
Variation in the human immune system is largely driven by non-heritable influences.人类免疫系统的变异很大程度上是由非遗传因素驱动的。
Cell. 2015 Jan 15;160(1-2):37-47. doi: 10.1016/j.cell.2014.12.020.
9
In utero arsenic exposure and fetal immune repertoire in a US pregnancy cohort.美国一个妊娠队列中的子宫内砷暴露与胎儿免疫库
Clin Immunol. 2014 Dec;155(2):188-97. doi: 10.1016/j.clim.2014.09.004. Epub 2014 Sep 16.
10
Control lymphocyte subsets: can one country's values serve for another's?对照淋巴细胞亚群:一个国家的数值能适用于另一个国家吗?
J Allergy Clin Immunol. 2014 Sep;134(3):759-761.e8. doi: 10.1016/j.jaci.2014.06.030.