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盘尾丝虫病发病机制中的交叉反应性抗原

Cross-reactive antigens in the pathogenesis of onchocerciasis.

作者信息

McKechnie N M, Braun G, Kläger S, Connor V, Kasp E, Wallace G, Whiston R

机构信息

Department of Pathology, University of Cambridge, U.K.

出版信息

Ann Trop Med Parasitol. 1993 Dec;87(6):649-52. doi: 10.1080/00034983.1993.11812824.

DOI:10.1080/00034983.1993.11812824
PMID:8122928
Abstract

The ocular disease associated with infection with Onchocerca volvulus is unique in that there is a wealth of epidemiological evidence to support the casual nature of the association but there is little known about the pathogenic mechanisms involved. We have identified a 44,000 M(r) component of ocular tissues that shows immunological cross-reactivity with an O. volvulus antigen. This immunological cross-reactivity between parasite and a component of host tissues may underlie the development of ocular disease in onchocerciasis. Preliminary experiments indicate that it is possible to initiate ocular disease in susceptible rats using the recombinant parasite antigen. This should allow the development of a laboratory model of ocular onchocerciasis and further our understanding of the mechanisms by which an infective organism can produce an auto-immune-like disease in the host.

摘要

与盘尾丝虫感染相关的眼部疾病具有独特性,即有大量流行病学证据支持这种关联的因果性质,但对于其中涉及的致病机制却知之甚少。我们已鉴定出眼部组织中一种分子量为44,000的成分,它与盘尾丝虫抗原呈现免疫交叉反应。寄生虫与宿主组织成分之间的这种免疫交叉反应可能是盘尾丝虫病中眼部疾病发生的基础。初步实验表明,使用重组寄生虫抗原在易感大鼠中引发眼部疾病是可能的。这将有助于建立眼部盘尾丝虫病的实验室模型,并加深我们对感染性生物体如何在宿主体内产生类似自身免疫性疾病机制的理解。

相似文献

1
Cross-reactive antigens in the pathogenesis of onchocerciasis.盘尾丝虫病发病机制中的交叉反应性抗原
Ann Trop Med Parasitol. 1993 Dec;87(6):649-52. doi: 10.1080/00034983.1993.11812824.
2
Immunologic cross-reactivity in the pathogenesis of ocular onchocerciasis.眼部盘尾丝虫病发病机制中的免疫交叉反应性。
Invest Ophthalmol Vis Sci. 1993 Sep;34(10):2888-902.
3
Antigenic mimicry: Onchocerca volvulus antigen-specific T cells and ocular inflammation.抗原模拟:盘尾丝虫抗原特异性T细胞与眼部炎症。
Invest Ophthalmol Vis Sci. 2002 Feb;43(2):411-8.
4
Characterization of native pathogenic antigens of Onchocerca volvulus: identification of high molecular mass protein antigens eliciting interstitial keratitis in a guinea pig model.盘尾丝虫天然致病抗原的特性:在豚鼠模型中鉴定引发间质性角膜炎的高分子量蛋白质抗原。
Exp Eye Res. 1995 Apr;60(4):347-58. doi: 10.1016/s0014-4835(05)80092-2.
5
Absence of cellular responses to a putative autoantigen in onchocercal chorioretinopathy: cellular autoimmunity in onchocercal chorioretinopathy.盘尾丝虫性脉络膜视网膜炎中对假定自身抗原的细胞反应缺失:盘尾丝虫性脉络膜视网膜炎中的细胞自身免疫
Invest Ophthalmol Vis Sci. 1996 Aug;37(9):1717-9.
6
Immune mechanisms in Onchocerca volvulus-mediated corneal disease (river blindness).盘尾丝虫介导的角膜疾病(河盲症)中的免疫机制。
Parasite Immunol. 2000 Dec;22(12):625-31. doi: 10.1046/j.1365-3024.2000.00345.x.
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Patterns of Onchocerca volvulus recombinant antigen recognition in a bovine model of onchocerciasis.
Parasitology. 1999 Dec;119 ( Pt 6):603-12. doi: 10.1017/s0031182099005065.
8
Immune recognition of Onchocerca volvulus proteins in the human host and animal models of onchocerciasis.在人类宿主和盘尾丝虫病动物模型中对盘尾丝虫蛋白的免疫识别。
J Helminthol. 2015 May;89(3):375-86. doi: 10.1017/S0022149X14000224. Epub 2014 Apr 10.
9
Humoral autoimmune response against S-antigen and IRBP in ocular onchocerciasis.
Invest Ophthalmol Vis Sci. 1990 Jul;31(7):1374-80.
10
Immunization with the cross-reactive antigens Ov39 from Onchocerca volvulus and hr44 from human retinal tissue induces ocular pathology and activates retinal microglia.用来自旋盘尾丝虫的交叉反应抗原Ov39和来自人类视网膜组织的hr44进行免疫接种会诱发眼部病变并激活视网膜小胶质细胞。
J Infect Dis. 1997 Nov;176(5):1334-43. doi: 10.1086/514130.

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Res Rep Trop Med. 2024 Dec 24;15:111-121. doi: 10.2147/RRTM.S481554. eCollection 2024.
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High Prevalence of Glaucoma among Patients in an Onchocerciasis Endemic Area (Mahenge, Tanzania).盘尾丝虫病流行地区(坦桑尼亚马亨格)患者中青光眼的高患病率
Pathogens. 2022 Sep 14;11(9):1046. doi: 10.3390/pathogens11091046.
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Ocular onchocerciasis: current management and future prospects.盘尾丝虫性眼病:当前治疗方法与未来展望
Clin Ophthalmol. 2011;5:1479-91. doi: 10.2147/OPTH.S8372. Epub 2011 Oct 13.
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Retinopathies associated with antiretinal antibodies.与抗视网膜抗体相关的视网膜病变。
Clin Diagn Lab Immunol. 2001 Sep;8(5):853-8. doi: 10.1128/CDLI.8.5.853-858.2001.