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加热灭活痤疮丙酸杆菌增强 28kDa 谷胱甘肽 S-转移酶抗原对曼氏血吸虫感染的保护作用。

Heat-killed Propionibacterium acnes augment the protective effect of 28-kDa glutathione S-transferases antigen against Schistosoma mansoni infection.

机构信息

Department of Biochemistry, School of Medicine, Tzu Chi University, Hualien 97004, Taiwan; Institute of Medical Sciences, Tzu Chi University, Hualien 97004, Taiwan.

Department of Laboratory Medicine and Biotechnology, College of Medicine, Tzu Chi University, Hualien 97004, Taiwan.

出版信息

Acta Trop. 2021 Oct;222:106033. doi: 10.1016/j.actatropica.2021.106033. Epub 2021 Jul 3.

DOI:10.1016/j.actatropica.2021.106033
PMID:34224719
Abstract

Sm28GST is one of the candidate antigens for Schistosoma mansoni vaccine. Already Sm28GST vaccine formulations have shown to be protective against S. mansoni infection. Currently, efforts have been put into finding an adjuvant to enhance the immunity induced by Sm28GST. In the present work, we investigated whether heat-killed Propionibacterium acnes can be served as a potential adjuvant for recombinant Sm28GST (rSm28GST) antigen. As the results showed, P. acnes successfully modulated the Th1 humoral immune response induced by rSm28GST. Stronger Th1 cytokines responses were also observed in mice immunized with P. acnes-adjuvanted rSm28GST. Immunization of mice with P. acnes-adjuvanted rSm28GST was able to reduce worm burden and hepatic egg burden by 54.20 and 73.61%. Reduced granuloma size and count, as well as improved liver histology, were seen in P. acnes-adjuvanted rSm28GST immunized mice. These data suggest that P. acnes may evoke a stronger rSm28GST-induced immune response, higher resistance to S. mansoni infection, and more profound protection against S. mansoni-induced liver damages.

摘要

Sm28GST 是曼氏血吸虫疫苗的候选抗原之一。Sm28GST 疫苗配方已被证明能有效预防曼氏血吸虫感染。目前,人们正在努力寻找佐剂来增强 Sm28GST 诱导的免疫应答。在本研究中,我们研究了是否可以使用热灭活痤疮丙酸杆菌作为重组 Sm28GST(rSm28GST)抗原的潜在佐剂。结果表明,痤疮丙酸杆菌成功地调节了 rSm28GST 诱导的 Th1 体液免疫应答。在接受痤疮丙酸杆菌佐剂 rSm28GST 免疫的小鼠中,观察到更强的 Th1 细胞因子反应。用痤疮丙酸杆菌佐剂 rSm28GST 免疫的小鼠能够将虫体负荷和肝内虫卵负荷分别减少 54.20%和 73.61%。在接受痤疮丙酸杆菌佐剂 rSm28GST 免疫的小鼠中,肉芽肿的大小和数量减少,肝组织学得到改善。这些数据表明,痤疮丙酸杆菌可能引发更强的 rSm28GST 诱导的免疫应答,对曼氏血吸虫感染具有更高的抵抗力,并对曼氏血吸虫感染引起的肝损伤提供更深刻的保护。

相似文献

1
Heat-killed Propionibacterium acnes augment the protective effect of 28-kDa glutathione S-transferases antigen against Schistosoma mansoni infection.加热灭活痤疮丙酸杆菌增强 28kDa 谷胱甘肽 S-转移酶抗原对曼氏血吸虫感染的保护作用。
Acta Trop. 2021 Oct;222:106033. doi: 10.1016/j.actatropica.2021.106033. Epub 2021 Jul 3.
2
Increased immunogenicity and protection of recombinant Sm14 antigens by heat-killed Cutibacterium acnes in BALB/c mice infected with Schistosoma mansoni.经加热杀死的痤疮丙酸杆菌增强重组 Sm14 抗原对感染曼氏血吸虫的 BALB/c 小鼠的免疫原性和保护作用。
Parasitol Int. 2022 Feb;86:102446. doi: 10.1016/j.parint.2021.102446. Epub 2021 Sep 2.
3
Induction of cytotoxic T-cell activity by the protective antigen of Schistosoma mansoni Sm28GST or its derived C-terminal lipopeptide.曼氏血吸虫Sm28GST的保护性抗原或其衍生的C末端脂肽诱导细胞毒性T细胞活性。
Scand J Immunol. 1996 Nov;44(5):485-92. doi: 10.1046/j.1365-3083.1996.d01-340.x.
4
Intranasal administration of a Schistosoma mansoni glutathione S-transferase-cholera toxoid conjugate vaccine evokes antiparasitic and antipathological immunity in mice.经鼻给予曼氏血吸虫谷胱甘肽S-转移酶-霍乱类毒素结合疫苗可在小鼠体内引发抗寄生虫和抗病理免疫反应。
J Immunol. 1999 Jul 15;163(2):1045-52.
5
Overproduction of SM28GST in a baculovirus expression vector and its use to evaluate the in vivo immune responses of mice vaccinated against Schistosoma mansoni with naked DNA encoding the SM28GST gene.杆状病毒表达载体中SM28GST的过量表达及其用于评估用编码SM28GST基因的裸DNA免疫的小鼠对曼氏血吸虫的体内免疫反应。
J Parasitol. 1998 Aug;84(4):764-70.
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Intradermal immunization of rats with plasmid DNA encoding Schistosoma mansoni 28 kDa glutathione S-transferase.用编码曼氏血吸虫28 kDa谷胱甘肽S-转移酶的质粒DNA对大鼠进行皮内免疫接种。
Parasite Immunol. 1997 Nov;19(11):505-13. doi: 10.1046/j.1365-3024.1997.d01-163.x.
7
Expression of a 28-kilodalton glutathione S-transferase antigen of Schistosoma mansoni on the surface of filamentous phages and evaluation of its vaccine potential.曼氏血吸虫28千道尔顿谷胱甘肽S-转移酶抗原在丝状噬菌体表面的表达及其疫苗潜力评估。
Clin Diagn Lab Immunol. 2003 Jul;10(4):536-41. doi: 10.1128/cdli.10.4.536-541.2003.
8
KI-1 or Its C-Terminal Fragment Induces Partial Protection Against Infection in Mice.KI-1 或其 C 末端片段可诱导小鼠部分抗感染。
Front Immunol. 2018 Jul 30;9:1762. doi: 10.3389/fimmu.2018.01762. eCollection 2018.
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Combination of the two schistosomal antigens Sm14 and Sm29 elicits significant protection against experimental Schistosoma mansoni infection.两种血吸虫抗原 Sm14 和 Sm29 的联合使用可显著预防实验性曼氏血吸虫感染。
Exp Parasitol. 2014 Oct;145:51-60. doi: 10.1016/j.exppara.2014.07.010. Epub 2014 Aug 1.
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Immunization of mice and baboons with the recombinant Sm28GST affects both worm viability and fecundity after experimental infection with Schistosoma mansoni.用重组Sm28GST对小鼠和狒狒进行免疫接种,会影响曼氏血吸虫实验感染后的虫体活力和繁殖力。
Parasite Immunol. 1991 Sep;13(5):473-90. doi: 10.1111/j.1365-3024.1991.tb00545.x.

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3
A low dose adenovirus vectored vaccine expressing Schistosoma mansoni Cathepsin B protects from intestinal schistosomiasis in mice.
一种低剂量腺病毒载体疫苗,表达曼氏血吸虫组织蛋白酶 B,可预防小鼠的肠道血吸虫病。
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