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Pathogens. 2025 Jan 19;14(1):97. doi: 10.3390/pathogens14010097.
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mBio. 2024 Apr 10;15(4):e0030324. doi: 10.1128/mbio.00303-24. Epub 2024 Mar 19.
2
Distribution of A genotypes in patients attending a sexually transmitted disease outpatient clinic in New Delhi, India.在印度新德里的一家性传播疾病门诊病人中 A 基因型的分布。
Indian J Med Res. 2019 May;149(5):662-670. doi: 10.4103/ijmr.IJMR_1171_17.
3
Safety and immunogenicity of the chlamydia vaccine candidate CTH522 adjuvanted with CAF01 liposomes or aluminium hydroxide: a first-in-human, randomised, double-blind, placebo-controlled, phase 1 trial.CTH522 佐剂用 CAF01 脂质体或氢氧化铝的衣原体疫苗候选物的安全性和免疫原性:首次人体、随机、双盲、安慰剂对照、1 期试验。
Lancet Infect Dis. 2019 Oct;19(10):1091-1100. doi: 10.1016/S1473-3099(19)30279-8. Epub 2019 Aug 12.
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The Potential Role for Host Genetic Profiling in Screening for Chlamydia-Associated Tubal Factor Infertility (TFI)-New Perspectives.宿主遗传分析在衣原体相关输卵管因素不孕(TFI)筛查中的潜在作用——新视角。
Genes (Basel). 2019 May 28;10(6):410. doi: 10.3390/genes10060410.
5
Cervical Cytokines Associated With Chlamydia trachomatis Susceptibility and Protection.与沙眼衣原体易感性和保护相关的宫颈细胞因子。
J Infect Dis. 2019 Jun 19;220(2):330-339. doi: 10.1093/infdis/jiz087.
6
Molecular epidemiology and genotyping of infection in a cohort of young asymptomatic sexually active women (18-25 years) in Milan, Italy.意大利米兰一组年轻无症状性活跃女性(18至25岁)感染的分子流行病学与基因分型研究
J Prev Med Hyg. 2016 Sep;57(3):E128-E134.
7
Intravaginal Chlamydia trachomatis Challenge Infection Elicits TH1 and TH17 Immune Responses in Mice That Promote Pathogen Clearance and Genital Tract Damage.阴道内沙眼衣原体激发感染在小鼠中引发促进病原体清除和生殖道损伤的TH1和TH17免疫反应。
PLoS One. 2016 Sep 8;11(9):e0162445. doi: 10.1371/journal.pone.0162445. eCollection 2016.
8
The global roadmap for advancing development of vaccines against sexually transmitted infections: Update and next steps.推进性传播感染疫苗研发的全球路线图:更新与后续步骤
Vaccine. 2016 Jun 3;34(26):2939-2947. doi: 10.1016/j.vaccine.2016.03.111. Epub 2016 Apr 19.
9
The natural history of Chlamydia trachomatis infection in women: a multi-parameter evidence synthesis.女性沙眼衣原体感染的自然史:多参数证据综合分析
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10
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在C3H/HeN小鼠中,C复合体以及B和C相关复合体中的血清型比B复合体中的血清型致病性更强,但在BALB/c小鼠中并非如此。

Serovars from the C-Complex and the B- and C-Related Complexes Are Significantly More Pathogenic than Those from the B-Complex in C3H/HeN but Not in BALB/c Mice.

作者信息

Pal Sukumar, Carmichael Jennifer R, Tifrea Delia F, Tatarenkova Olga, de la Maza Luis M

机构信息

Department of Pathology and Laboratory Medicine, Medical Sciences I, Room D440, University of California, Irvine, Irvine, CA 92697-4800, USA.

出版信息

Pathogens. 2025 Jan 19;14(1):97. doi: 10.3390/pathogens14010097.

DOI:10.3390/pathogens14010097
PMID:39861058
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11768385/
Abstract

Studies in humans indicate that certain serovars are more pathogenic than others. Specifically, several studies concluded that serovars from the C-complex are more pathogenic than those from the B-complex, although there are reports that do not support this finding. To investigate these results in an animal model, the eight genitourinary serovars were tested in two strains of mice: C3H/HeN and BALB/c. These two strains of mice were investigated because C3H/HeN is more susceptible to infections than BALB/c, indicative of differences in their immunogenetic background. Mice were infected transcervically with 10 inclusion forming units of each of the serovars, and vaginal cultures were collected. To determine the pathogenicity and its impact on fertility, at week seven post-infection, female mice were caged with male mice. In the C3H/HeN mice, significant differences in vaginal shedding and fertility were observed between serovars from the B-complex (D and E) and those from the C-complex (H, I, J) and B- and C-related complexes (G, F, and K). The animals infected with serovars F, G, H, I, J, and K shed less but had significantly more infertility than the mice infected with serovars D or E. The experiments in the BALB/c mice, however, did not show major differences in pathogenicity between the eight serovars. These results support the findings in humans and emphasize the critical importance of the immunogenetic background of the host on the outcome of infections. The data imply that management of -infected patients may require a more personalized approach.

摘要

对人类的研究表明,某些血清型比其他血清型更具致病性。具体而言,多项研究得出结论,C 复合体的血清型比 B 复合体的血清型更具致病性,尽管有一些报告并不支持这一发现。为了在动物模型中研究这些结果,对八种泌尿生殖系统血清型在两种小鼠品系中进行了测试:C3H/HeN 和 BALB/c。选择这两种小鼠品系进行研究是因为 C3H/HeN 比 BALB/c 更容易受到感染,这表明它们的免疫遗传背景存在差异。小鼠经宫颈接种每种血清型的 10 个包涵体形成单位,并收集阴道培养物。为了确定致病性及其对生育能力的影响,在感染后第七周,将雌性小鼠与雄性小鼠关在一个笼子里。在 C3H/HeN 小鼠中,观察到 B 复合体(D 和 E)的血清型与 C 复合体(H、I、J)以及 B 和 C 相关复合体(G、F 和 K)的血清型在阴道排菌和生育能力方面存在显著差异。感染血清型 F、G、H、I、J 和 K 的动物排菌较少,但不育率明显高于感染血清型 D 或 E 的小鼠。然而,BALB/c 小鼠的实验并未显示出这八种血清型在致病性上有重大差异。这些结果支持了在人类中的发现,并强调了宿主免疫遗传背景对感染结果的至关重要性。数据表明,对感染患者的管理可能需要更个性化的方法。