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A Chlamydia trachomatis-specific Th2 clone does not provide protection against a genital infection and displays reduced trafficking to the infected genital mucosa.一株沙眼衣原体特异性Th2克隆不能预防生殖器感染,且向受感染的生殖器黏膜的迁移能力降低。
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2
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3
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4
Initial route of antigen administration alters the T-cell cytokine profile produced in response to the mouse pneumonitis biovar of Chlamydia trachomatis following genital infection.抗原的初始给药途径会改变生殖器感染后针对沙眼衣原体小鼠肺炎生物变种产生的T细胞细胞因子谱。
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Monoclonal immunoglobulin A antibody to the major outer membrane protein of the Chlamydia trachomatis mouse pneumonitis biovar protects mice against a chlamydial genital challenge.针对沙眼衣原体小鼠肺炎生物变种主要外膜蛋白的单克隆免疫球蛋白A抗体可保护小鼠免受衣原体生殖道感染的挑战。
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Resolution of murine chlamydial genital infection by the adoptive transfer of a biovar-specific, Th1 lymphocyte clone.通过生物变种特异性Th1淋巴细胞克隆的过继转移来解决小鼠衣原体性生殖器感染。
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Genital tract infection with Chlamydia trachomatis fails to induce protective immunity in gamma interferon receptor-deficient mice despite a strong local immunoglobulin A response.尽管存在强烈的局部免疫球蛋白A反应,但沙眼衣原体生殖道感染在γ干扰素受体缺陷小鼠中未能诱导保护性免疫。
Infect Immun. 1997 Mar;65(3):1032-44. doi: 10.1128/IAI.65.3.1032-1044.1997.

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本文引用的文献

1
Resolution of secondary Chlamydia trachomatis genital tract infection in immune mice with depletion of both CD4+ and CD8+ T cells.在CD4+和CD8+ T细胞均耗竭的免疫小鼠中,沙眼衣原体生殖道继发感染的消退情况。
Infect Immun. 2001 Apr;69(4):2643-9. doi: 10.1128/IAI.69.4.2643-2649.2001.
2
P-Selectin glycoprotein ligand 1 (PSGL-1) is a physiological ligand for E-selectin in mediating T helper 1 lymphocyte migration.P-选择素糖蛋白配体1(PSGL-1)是介导辅助性T1淋巴细胞迁移过程中E-选择素的生理配体。
J Exp Med. 2000 Dec 4;192(11):1669-76. doi: 10.1084/jem.192.11.1669.
3
Immunity to murine Chlamydia trachomatis genital tract reinfection involves B cells and CD4(+) T cells but not CD8(+) T cells.对小鼠沙眼衣原体生殖道再感染的免疫涉及B细胞和CD4(+) T细胞,但不涉及CD8(+) T细胞。
Infect Immun. 2000 Dec;68(12):6979-87. doi: 10.1128/IAI.68.12.6979-6987.2000.
4
Expression of mucosal homing receptor alpha4beta7 is associated with enhanced migration to the Chlamydia-infected murine genital mucosa in vivo.黏膜归巢受体α4β7的表达与体内向衣原体感染的小鼠生殖黏膜的迁移增强相关。
Infect Immun. 2000 Oct;68(10):5587-94. doi: 10.1128/IAI.68.10.5587-5594.2000.
5
Suppression of endogenous IL-10 gene expression in dendritic cells enhances antigen presentation for specific Th1 induction: potential for cellular vaccine development.抑制树突状细胞内源性白细胞介素-10基因表达可增强抗原呈递以特异性诱导Th1细胞:细胞疫苗开发潜力
J Immunol. 2000 Apr 15;164(8):4212-9. doi: 10.4049/jimmunol.164.8.4212.
6
Differential regulation of CD4 lymphocyte recruitment between the upper and lower regions of the genital tract during Chlamydia trachomatis infection.沙眼衣原体感染期间生殖道上下区域CD4淋巴细胞募集的差异调节
Infect Immun. 2000 Mar;68(3):1519-28. doi: 10.1128/IAI.68.3.1519-1528.2000.
7
Prior genital tract infection with a murine or human biovar of Chlamydia trachomatis protects mice against heterotypic challenge infection.先前感染沙眼衣原体鼠生物变种或人生物变种的生殖道可保护小鼠免受异型攻击感染。
Infect Immun. 1999 Jun;67(6):3019-25. doi: 10.1128/IAI.67.6.3019-3025.1999.
8
Chlamydia trachomatis infections: progress and problems.沙眼衣原体感染:进展与问题
J Infect Dis. 1999 Mar;179 Suppl 2:S380-3. doi: 10.1086/513844.
9
IL-10 gene knockout mice show enhanced Th1-like protective immunity and absent granuloma formation following Chlamydia trachomatis lung infection.白细胞介素-10基因敲除小鼠在沙眼衣原体肺部感染后表现出增强的Th1样保护性免疫且无肉芽肿形成。
J Immunol. 1999 Jan 15;162(2):1010-7.
10
Gene knockout B cell-deficient mice demonstrate that B cells play an important role in the initiation of T cell responses to Chlamydia trachomatis (mouse pneumonitis) lung infection.基因敲除的B细胞缺陷小鼠表明,B细胞在T细胞对沙眼衣原体(小鼠肺炎)肺部感染的反应启动中发挥重要作用。
J Immunol. 1998 Aug 1;161(3):1439-46.

一株沙眼衣原体特异性Th2克隆不能预防生殖器感染,且向受感染的生殖器黏膜的迁移能力降低。

A Chlamydia trachomatis-specific Th2 clone does not provide protection against a genital infection and displays reduced trafficking to the infected genital mucosa.

作者信息

Hawkins Raymond A, Rank Roger G, Kelly Kathleen A

机构信息

Department of Microbiology and Immunology, University of Arkansas for Medical Sciences, Little Rock, Arkansas, USA.

出版信息

Infect Immun. 2002 Sep;70(9):5132-9. doi: 10.1128/IAI.70.9.5132-5139.2002.

DOI:10.1128/IAI.70.9.5132-5139.2002
PMID:12183563
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC128225/
Abstract

A T helper type 1 (Th1) response is essential for resolving genital infections with the mouse pneumonitis biovar of Chlamydia trachomatis (MoPn). However, T-cell-dependent anti-chlamydial antibody is produced and may also contribute to protective immunity. We produced a MoPn-specific CD4 Th2 clone (Th2-MoPn) to study the role of a Th2 response during infection. We found that Th2-MoPn was unable to eradicate chlamydiae from the genital tract (GT) when it was transferred into MoPn-infected nude mice. Mice that received Th2-MoPn produced greater titers of MoPn-specific serum immunoglobulin G (IgG) antibody than mice that received a MoPn-specific Th1 clone (Th1-MoPn) (log(10) titers, 1.89 +/- 0.84 and 0.58 +/- 0.76 [mean +/- standard deviation], respectively [P < 0.01]). Also, the IgG isotypes were different for the two groups; whereas IgG1 was associated with Th2-MoPn, IgG2a was associated with Th1-MoPn. Also, infected nude mice that received Th2-MoPn produced higher levels of IgA in vaginal secretions. Although clone Th2-MoPn was detected in the GT, it was less efficient at migrating (112 +/- 35.6 labeled Th2 clone cells/10(5) GT cells) than Th1-MoPn (505 +/- 51.6 Th1 clone cells/10(5) GT cells) (P < 0.001, as determined by a t test). This may have been due to reduced expression of alpha4beta7 and P-selectin ligand 1 on Th2-MoPn. However, Th2-MoPn cells were retained in the GT during chronic infection and comprised 10 to 15% of the total GT cells 80 days after transfer. The data show that the MoPn-specific Th2 cells are important for serum and vaginal antibody production and may accumulate in the GT during chronic infection.

摘要

1型辅助性T细胞(Th1)反应对于清除沙眼衣原体小鼠肺炎生物变种(MoPn)引起的生殖道感染至关重要。然而,也会产生T细胞依赖性抗衣原体抗体,其可能也有助于保护性免疫。我们制备了一株MoPn特异性CD4 Th2克隆(Th2-MoPn),以研究Th2反应在感染过程中的作用。我们发现,当将Th2-MoPn转入感染MoPn的裸鼠体内时,它无法从生殖道(GT)清除衣原体。接受Th2-MoPn的小鼠产生的MoPn特异性血清免疫球蛋白G(IgG)抗体滴度高于接受MoPn特异性Th1克隆(Th1-MoPn)的小鼠(对数(10)滴度分别为1.89±0.84和0.58±0.76 [平均值±标准差] [P<0.01])。此外,两组的IgG亚型不同;与Th2-MoPn相关的是IgG1,与Th1-MoPn相关的是IgG2a。而且,接受Th2-MoPn的感染裸鼠在阴道分泌物中产生的IgA水平更高。虽然在生殖道中检测到了克隆Th2-MoPn,但它的迁移效率(112±35.6个标记的Th2克隆细胞/10⁵个生殖道细胞)低于Th1-MoPn(505±51.6个Th1克隆细胞/10⁵个生殖道细胞)(通过t检验确定,P<0.001)。这可能是由于Th2-MoPn上α4β7和P-选择素配体1的表达降低所致。然而,在慢性感染期间,Th2-MoPn细胞保留在生殖道中,转移后80天占生殖道总细胞的10%至15%。数据表明,MoPn特异性Th2细胞对于血清和阴道抗体的产生很重要,并且在慢性感染期间可能在生殖道中积累。