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1
Gut mucosal immunization with reovirus serotype 1/L stimulates virus-specific cytotoxic T cell precursors as well as IgA memory cells in Peyer's patches.用1型呼肠孤病毒/L进行肠道黏膜免疫可刺激派伊尔结中的病毒特异性细胞毒性T细胞前体以及IgA记忆细胞。
J Exp Med. 1987 Mar 1;165(3):830-47. doi: 10.1084/jem.165.3.830.
2
Developmental relationship between cytotoxic alpha/beta T cell receptor-positive intraepithelial lymphocytes and Peyer's patch lymphocytes.细胞毒性α/βT细胞受体阳性上皮内淋巴细胞与派尔集合淋巴结淋巴细胞之间的发育关系。
Eur J Immunol. 1993 Jun;23(6):1333-9. doi: 10.1002/eji.1830230622.
3
CD8 lymphocyte subpopulations in Peyer's patches induced by reovirus serotype 1 infection.呼肠孤病毒1型感染诱导的派尔集合淋巴结中的CD8淋巴细胞亚群
J Immunol. 1990 Apr 15;144(8):3187-94.
4
Reovirus serotype 1/strain Lang-stimulated activation of antigen-specific T lymphocytes in Peyer's patches and distal gut-mucosal sites: activation status and cytotoxic mechanisms.呼肠孤病毒1型/朗株刺激派伊尔结和远端肠道黏膜部位抗原特异性T淋巴细胞的活化:活化状态及细胞毒性机制
J Immunol. 2005 Mar 15;174(6):3580-9. doi: 10.4049/jimmunol.174.6.3580.
5
Murine Peyer's patches are capable of generating a cytotoxic T cell (CTL) response to nominal antigens.小鼠派尔集合淋巴结能够对名义抗原产生细胞毒性T细胞(CTL)应答。
Adv Exp Med Biol. 1987;216A:267-78. doi: 10.1007/978-1-4684-5344-7_31.
6
IgA responses in xid mice: oral antigen primes Peyer's patch cells for in vitro immune responses and secretory antibody production.Xid小鼠中的IgA应答:口服抗原使派尔集合淋巴结细胞致敏以产生体外免疫应答和分泌性抗体。
J Immunol. 1983 Dec;131(6):2616-22.
7
Regulation of mucosal IgA production in vitro by autoreactive immunoregulatory T cells from murine Peyer's patches.来自小鼠派伊尔结的自身反应性免疫调节性T细胞对体外黏膜IgA产生的调节作用。
Cell Immunol. 1988 Jul;114(2):324-35. doi: 10.1016/0008-8749(88)90325-5.
8
Role of maternal antibody in the induction of virus specific and bystander IgA responses in Peyer's patches of suckling mice.母源抗体在诱导乳鼠派尔集合淋巴结中病毒特异性及旁观者IgA应答中的作用
Int Immunol. 1995 Jun;7(6):911-8. doi: 10.1093/intimm/7.6.911.
9
The preference for switching to IgA expression by Peyer's patch germinal center B cells is likely due to the intrinsic influence of their microenvironment.派尔集合淋巴结生发中心B细胞倾向于转换为IgA表达,这可能是由于其微环境的内在影响。
J Immunol. 1991 Dec 15;147(12):4126-35.
10
Intraepithelial lymphocytes contain virus-specific, MHC-restricted cytotoxic cell precursors after gut mucosal immunization with reovirus serotype 1/Lang.在用1型呼肠孤病毒/Lang株进行肠道黏膜免疫后,上皮内淋巴细胞含有病毒特异性、MHC限制的细胞毒性细胞前体。
Reg Immunol. 1989 Mar-Apr;2(2):98-102.

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1
Engineering Recombinant Reoviruses To Display gp41 Membrane-Proximal External-Region Epitopes from HIV-1.工程改造重组呼肠孤病毒以展示来自HIV-1的gp41膜近端外部区域表位
mSphere. 2016 May 18;1(3). doi: 10.1128/mSphere.00086-16. eCollection 2016 May-Jun.
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Effects of Mycotoxins on mucosal microbial infection and related pathogenesis.霉菌毒素对黏膜微生物感染及相关发病机制的影响。
Toxins (Basel). 2015 Oct 30;7(11):4484-502. doi: 10.3390/toxins7114484.
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The mucosal immune system: From dentistry to vaccine development.黏膜免疫系统:从牙科学到疫苗研发
Proc Jpn Acad Ser B Phys Biol Sci. 2015;91(8):423-39. doi: 10.2183/pjab.91.423.
4
The role of type I interferons in intestinal infection, homeostasis, and inflammation.I型干扰素在肠道感染、内环境稳定及炎症中的作用。
Immunol Rev. 2014 Jul;260(1):145-67. doi: 10.1111/imr.12195.
5
Engineering recombinant reoviruses with tandem repeats and a tetravirus 2A-like element for exogenous polypeptide expression.利用串联重复序列和四病毒 2A 样元件工程重组呼肠孤病毒用于外源多肽表达。
Proc Natl Acad Sci U S A. 2013 May 14;110(20):E1867-76. doi: 10.1073/pnas.1220107110. Epub 2013 Apr 29.
6
Salivary glands act as mucosal inductive sites via the formation of ectopic germinal centers after site-restricted MCMV infection.唾液腺在局部受限的 MCMV 感染后通过形成异位生发中心作为黏膜诱导部位发挥作用。
FASEB J. 2011 May;25(5):1680-96. doi: 10.1096/fj.10-174656. Epub 2011 Feb 9.
7
Enteric reovirus infection stimulates peanut-specific IgG2a responses in a mouse food allergy model.肠传轮状病毒感染可刺激小鼠食物过敏模型中花生特异性 IgG2a 反应。
Immunobiology. 2010 Dec;215(12):941-8. doi: 10.1016/j.imbio.2010.02.004. Epub 2010 Mar 4.
8
3,3'-Diindolylmethane stimulates murine immune function in vitro and in vivo.3,3'-二吲哚甲烷在体外和体内均能刺激小鼠的免疫功能。
J Nutr Biochem. 2008 May;19(5):336-44. doi: 10.1016/j.jnutbio.2007.05.004. Epub 2007 Aug 17.
9
Type I interferons produced by hematopoietic cells protect mice against lethal infection by mammalian reovirus.造血细胞产生的I型干扰素可保护小鼠免受呼肠孤病毒的致命感染。
J Exp Med. 2007 Jun 11;204(6):1349-58. doi: 10.1084/jem.20061587. Epub 2007 May 14.
10
T-2 toxin impairment of enteric reovirus clearance in the mouse associated with suppressed immunoglobulin and IFN-gamma responses.T-2毒素损害小鼠肠道呼肠孤病毒清除,与免疫球蛋白和γ干扰素反应受抑制有关。
Toxicol Appl Pharmacol. 2006 Aug 1;214(3):318-25. doi: 10.1016/j.taap.2006.01.007. Epub 2006 Feb 28.

本文引用的文献

1
Molecular basis of reovirus virulence. Role of the M2 gene.呼肠孤病毒毒力的分子基础。M2基因的作用。
J Exp Med. 1980 Oct 1;152(4):853-68. doi: 10.1084/jem.152.4.853.
2
Characteristics of natural killer cells in the murine intestinal epithelium and lamina propria.小鼠肠道上皮和固有层中自然杀伤细胞的特征
J Exp Med. 1982 Jun 1;155(6):1785-96. doi: 10.1084/jem.155.6.1785.
3
Patterns of isotype expression by B cell clones responding to thymus-dependent and thymus-independent antigens in vitro.体外对胸腺依赖性和胸腺非依赖性抗原作出反应的B细胞克隆的同种型表达模式。
Eur J Immunol. 1982 Apr;12(4):342-8. doi: 10.1002/eji.1830120416.
4
In vivo immune response to a T-cell-dependent antigen by cultures of disassociated murine Peyer's patch.用分离的小鼠派尔集合淋巴结培养物对T细胞依赖性抗原的体内免疫反应。
Proc Natl Acad Sci U S A. 1982 Jan;79(2):596-600. doi: 10.1073/pnas.79.2.596.
5
Special features of the priming process for a secretory IgA response. B cell priming with cholera toxin.分泌型IgA应答启动过程的特殊特征。用霍乱毒素启动B细胞。
J Exp Med. 1981 Mar 1;153(3):534-44. doi: 10.1084/jem.153.3.534.
6
Type-specific reovirus antiserum blocks the cytotoxic T-cell-target cell interaction: evidence for the association of the viral hemagglutinin of a nonenveloped virus with the cell surface.型特异性呼肠孤病毒抗血清阻断细胞毒性T细胞与靶细胞的相互作用:无包膜病毒的病毒血凝素与细胞表面相关的证据。
Infect Immun. 1981 Feb;31(2):646-9. doi: 10.1128/iai.31.2.646-649.1981.
7
T cells that encounter virus in the complete absence of a particular H-2 antigen are nonresponsive when stimulated again in the context of that H-2 antigen.在完全缺乏特定H - 2抗原的情况下接触病毒的T细胞,当在该H - 2抗原的背景下再次受到刺激时无反应。
J Exp Med. 1980 Jan 1;151(1):166-73. doi: 10.1084/jem.151.1.166.
8
T-cell recirculation in the sheep: migratory properties of cells from lymph nodes.绵羊中的T细胞再循环:来自淋巴结细胞的迁移特性
Immunology. 1982 Nov;47(3):415-21.
9
Role of environmental antigens in the ontogeny of the secretory immune response.环境抗原在分泌性免疫反应个体发育中的作用。
J Reticuloendothel Soc. 1980 Dec;28(Suppl):61s-71s.
10
The response of gut-associated T lymphocytes to intestinal viral immunization.肠道相关T淋巴细胞对肠道病毒免疫的反应。
J Immunol. 1984 Dec;133(6):2955-60.

用1型呼肠孤病毒/L进行肠道黏膜免疫可刺激派伊尔结中的病毒特异性细胞毒性T细胞前体以及IgA记忆细胞。

Gut mucosal immunization with reovirus serotype 1/L stimulates virus-specific cytotoxic T cell precursors as well as IgA memory cells in Peyer's patches.

作者信息

London S D, Rubin D H, Cebra J J

出版信息

J Exp Med. 1987 Mar 1;165(3):830-47. doi: 10.1084/jem.165.3.830.

DOI:10.1084/jem.165.3.830
PMID:2950199
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC2188298/
Abstract

In this report we have shown that reovirus 1/L is an effective mucosal immunogen capable of generating a cytotoxic T cell (CTL) and associated helper T cell response to the nominal antigens associated with reovirus 1/L. The effectors that mediate reovirus-specific cytotoxicity are Thy-1+, Lyt-2+, and major histocompatibility complex (MHC)-restricted in their recognition of reovirus antigens, and can therefore be classified as CTLs. Frequency analysis of precursor CTLs occurring in Peyer's patches (PP) and peripheral lymph nodes (PLN) 6 d and 6 mo after intraduodenal stimulation have demonstrated that a persistent gradient of precursors is established, with higher frequencies present in PP. The generation of a CTL response in PP may be important in preferentially repopulating mucosal tissues with effector CTLs that could result in the local containment of infections in the gut. We also found that reovirus 1/L generates a virus-specific B cell response that is dominated by IgA memory cells after intraduodenal immunization. We hypothesize that the efficacy of reovirus 1/L at stimulating T and B cells in the gut mucosa is related to its ability to selectively enter PP via microfold (M) cells after enteric application. In this study we have also demonstrated that PP cells, upon in vitro culture and unrelated to prior reovirus priming, can generate natural killer-like (NK) cytotoxic activity. This may be an in vitro correlate of the in vivo generation of effectors that may populate mucosal tissues (i.e., the intestinal epithelium) with NK-like effector cells.

摘要

在本报告中,我们已表明呼肠孤病毒1/L是一种有效的粘膜免疫原,能够产生细胞毒性T细胞(CTL)以及针对与呼肠孤病毒1/L相关的名义抗原的相关辅助性T细胞应答。介导呼肠孤病毒特异性细胞毒性的效应细胞为Thy-1⁺、Lyt-2⁺,且在识别呼肠孤病毒抗原时受主要组织相容性复合体(MHC)限制,因此可归类为CTL。对十二指肠内刺激后6天和6个月在派尔集合淋巴结(PP)和外周淋巴结(PLN)中出现的前体CTL进行频率分析表明,建立了持续的前体梯度,PP中的频率更高。PP中CTL应答的产生可能在优先用效应CTL重新填充粘膜组织方面很重要,这可能导致肠道感染的局部控制。我们还发现,呼肠孤病毒1/L在十二指肠内免疫后产生以IgA记忆细胞为主的病毒特异性B细胞应答。我们推测呼肠孤病毒1/L在肠道粘膜中刺激T和B细胞的功效与其在肠道应用后通过微褶(M)细胞选择性进入PP的能力有关。在本研究中,我们还证明,PP细胞在体外培养时,与先前的呼肠孤病毒引发无关,可产生自然杀伤样(NK)细胞毒性活性。这可能是体内产生效应细胞的体外相关因素,这些效应细胞可能会使粘膜组织(即肠上皮)充满NK样效应细胞。