• 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

HLA 限制性细胞毒性 T 淋巴细胞是巨细胞病毒感染中的一种早期免疫反应和重要防御机制。

HLA-restricted cytotoxic T lymphocytes are an early immune response and important defense mechanism in cytomegalovirus infections.

作者信息

Quinnan G V, Burns W H, Kirmani N, Rook A H, Manischewitz J, Jackson L, Santos G W, Saral R

出版信息

Rev Infect Dis. 1984 Mar-Apr;6(2):156-63. doi: 10.1093/clinids/6.2.156.

DOI:10.1093/clinids/6.2.156
PMID:6328614
Abstract

Eighty-eight bone marrow transplant recipients were studied for development of cytomegalovirus (CMV) infections and associated cytotoxic lymphocyte responses. Sixty-one patients developed CMV infection that was diagnosed by virus isolation (18 patients), fourfold rises in serum antibodies (13), or both (30). Interstitial pneumonitis developed in 27 patients. Among patients tested during infection, HLA-restricted, CMV-specific cytotoxic T cell responses occurred in 25 patients, and non-restricted, non-T cell cytotoxic responses, or responses of undetermined cell type, occurred in 10 patients. Levels of CMV-specific cytotoxicity in infected and uninfected patients were compared in two ways. Eighty-nine percent of patients (32 of 36) with cytotoxicity greater than or equal to 15% lysis (50:1 effector-to-target-cell ratio) and 100% of patients (21 of 21) with sequential increases in cytotoxicity of greater than or equal to 15% lysis were infected. The median time of occurrence of CMV-specific cytotoxic responses preceded the median onset of viral shedding by 1.4 weeks, or rises in titers of serum antibody by 1.7 weeks, and of interstitial pneumonitis by 2.5 weeks. Immune competence, as demonstrated by survival from infection, was always associated with a CMV-specific cytotoxic response. The HLA-restricted cytotoxic T cell response appears to be important as an early host-defense mechanism and an early diagnostic evidence of infection.

摘要

对88名骨髓移植受者进行了研究,以观察巨细胞病毒(CMV)感染的发生情况及相关的细胞毒性淋巴细胞反应。61名患者发生了CMV感染,通过病毒分离确诊的有18例,血清抗体呈四倍升高的有13例,两者均符合的有30例。27名患者发生了间质性肺炎。在感染期间接受检测的患者中,25名患者出现了HLA限制的、CMV特异性细胞毒性T细胞反应,10名患者出现了非限制的、非T细胞细胞毒性反应或细胞类型未确定的反应。以两种方式比较了感染患者和未感染患者的CMV特异性细胞毒性水平。细胞毒性大于或等于15%裂解(效应细胞与靶细胞比例为50:1)患者中的89%(36例中的32例)以及细胞毒性连续升高大于或等于15%裂解患者中的100%(21例中的21例)被感染。CMV特异性细胞毒性反应出现的中位时间比病毒排出的中位时间提前1.4周,比血清抗体滴度升高提前1.7周,比间质性肺炎提前2.5周。从感染中存活所证明的免疫能力始终与CMV特异性细胞毒性反应相关。HLA限制的细胞毒性T细胞反应作为一种早期宿主防御机制和感染的早期诊断证据似乎很重要。

相似文献

1
HLA-restricted cytotoxic T lymphocytes are an early immune response and important defense mechanism in cytomegalovirus infections.HLA 限制性细胞毒性 T 淋巴细胞是巨细胞病毒感染中的一种早期免疫反应和重要防御机制。
Rev Infect Dis. 1984 Mar-Apr;6(2):156-63. doi: 10.1093/clinids/6.2.156.
2
Cytotoxic t cells in cytomegalovirus infection: HLA-restricted T-lymphocyte and non-T-lymphocyte cytotoxic responses correlate with recovery from cytomegalovirus infection in bone-marrow-transplant recipients.巨细胞病毒感染中的细胞毒性T细胞:骨髓移植受者中HLA限制性T淋巴细胞和非T淋巴细胞的细胞毒性反应与巨细胞病毒感染的恢复相关。
N Engl J Med. 1982 Jul 1;307(1):7-13. doi: 10.1056/NEJM198207013070102.
3
Cytomegalovirus (CMV)-specific lysis of CMV-infected target cells can be mediated by both NK-like and virus-specific cytotoxic T lymphocytes.巨细胞病毒(CMV)感染的靶细胞的巨细胞病毒特异性裂解可由自然杀伤样细胞和病毒特异性细胞毒性T淋巴细胞介导。
Clin Exp Immunol. 1985 Jul;61(1):80-9.
4
Cytotoxic T-lymphocyte response to cytomegalovirus after human allogeneic bone marrow transplantation: pattern of recovery and correlation with cytomegalovirus infection and disease.人类同种异体骨髓移植后细胞毒性T淋巴细胞对巨细胞病毒的反应:恢复模式及其与巨细胞病毒感染和疾病的相关性
Blood. 1991 Sep 1;78(5):1373-80.
5
Natural cytotoxic activity against cytomegalovirus-infected target cells following marrow transplantation.
Transplantation. 1987 Oct;44(4):504-8. doi: 10.1097/00007890-198710000-00009.
6
Definition of human cytomegalovirus-specific target antigens recognized by cytotoxic T cells generated in vitro by using an autologous lymphocyte system.利用自体淋巴细胞系统体外产生的细胞毒性T细胞所识别的人巨细胞病毒特异性靶抗原的定义。
J Immunol. 1986 Jul 1;137(1):330-6.
7
HLA-DR-restricted cytotoxicity of cytomegalovirus-infected monocytes mediated by Leu-3-positive T cells.由Leu-3阳性T细胞介导的巨细胞病毒感染单核细胞的HLA-DR限制性细胞毒性。
J Immunol. 1986 Apr 15;136(8):3045-51.
8
Early detection of cytomegalovirus-specific cytotoxic T lymphocytes against cytomegalovirus antigenemia in human leukocyte antigen haploidentical hematopoietic stem cell transplantation.在人类白细胞抗原半相合造血干细胞移植中,针对巨细胞病毒血症的巨细胞病毒特异性细胞毒性T淋巴细胞的早期检测。
Ann Hematol. 2015 Oct;94(10):1707-15. doi: 10.1007/s00277-015-2446-4. Epub 2015 Jul 22.
9
[Anti-cytomegalovirus T-cell immunity and HLA restriction in the transplanted kidney patient].[移植肾患者的抗巨细胞病毒T细胞免疫及HLA限制]
Ann Med Interne (Paris). 1987;138(5):334-7.
10
Virus-specific cytotoxic lymphocyte responses are predictive of the outcome of cytomegalovirus infection of renal transplant recipients.
Transplant Proc. 1984 Dec;16(6):1466-9.

引用本文的文献

1
Prospects of Cytomegalovirus-Specific T-Cell Receptors in Clinical Diagnosis and Therapy.巨细胞病毒特异性 T 细胞受体在临床诊断和治疗中的前景。
Viruses. 2023 Jun 7;15(6):1334. doi: 10.3390/v15061334.
2
The Donor Major Histocompatibility Complex Class I Chain-Related Molecule A Allele rs2596538 G Predicts Cytomegalovirus Viremia in Kidney Transplant Recipients.供者主要组织相容性复合体 I 类链相关分子 A 等位基因 rs2596538G 预测肾移植受者巨细胞病毒血症。
Front Immunol. 2018 May 8;9:917. doi: 10.3389/fimmu.2018.00917. eCollection 2018.
3
Characterization and clinical enrichment of HLA-C*07:02-restricted Cytomegalovirus-specific CD8+ T cells.
HLA-C*07:02 限制性巨细胞病毒特异性 CD8+ T 细胞的鉴定和临床富集。
PLoS One. 2018 Feb 28;13(2):e0193554. doi: 10.1371/journal.pone.0193554. eCollection 2018.
4
Comprehensive Analysis of Cytomegalovirus pp65 Antigen-Specific CD8 T Cell Responses According to Human Leukocyte Antigen Class I Allotypes and Intraindividual Dominance.根据人类白细胞抗原I类别型及个体内优势对巨细胞病毒pp65抗原特异性CD8 T细胞反应的综合分析
Front Immunol. 2017 Nov 21;8:1591. doi: 10.3389/fimmu.2017.01591. eCollection 2017.
5
Structural Basis for Clonal Diversity of the Public T Cell Response to a Dominant Human Cytomegalovirus Epitope.针对主要人类巨细胞病毒表位的公共T细胞反应克隆多样性的结构基础
J Biol Chem. 2015 Nov 27;290(48):29106-19. doi: 10.1074/jbc.M115.691311. Epub 2015 Oct 1.
6
Cell-mediated immunity to human CMV infection: a brief overview.针对人巨细胞病毒感染的细胞介导免疫:简要概述。
F1000Prime Rep. 2014 May 6;6:28. doi: 10.12703/P6-28. eCollection 2014.
7
Role of human cytomegalovirus genotype polymorphisms in AIDS patients with cytomegalovirus retinitis.人巨细胞病毒基因型多态性在 AIDS 合并巨细胞病毒性视网膜炎患者中的作用。
Med Microbiol Immunol. 2013 Feb;202(1):37-47. doi: 10.1007/s00430-012-0244-3. Epub 2012 Jun 6.
8
Crystallization and preliminary X-ray crystallographic characterization of a public CMV-specific TCR in complex with its cognate antigen.一种公共巨细胞病毒特异性T细胞受体与其同源抗原复合物的结晶及初步X射线晶体学表征
Acta Crystallogr Sect F Struct Biol Cryst Commun. 2009 Nov 1;65(Pt 11):1157-61. doi: 10.1107/S1744309109037890. Epub 2009 Oct 30.
9
Immune evasion proteins of murine cytomegalovirus preferentially affect cell surface display of recently generated peptide presentation complexes.鼠巨细胞病毒的免疫逃逸蛋白优先影响近期产生的肽呈递复合物在细胞表面的显示。
J Virol. 2010 Feb;84(3):1221-36. doi: 10.1128/JVI.02087-09. Epub 2009 Nov 11.
10
Immune evasion proteins enhance cytomegalovirus latency in the lungs.免疫逃逸蛋白增强巨细胞病毒在肺部的潜伏。
J Virol. 2009 Oct;83(19):10293-8. doi: 10.1128/JVI.01143-09. Epub 2009 Jul 15.