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抗体亲和分离的疟原虫抗原的实验免疫。

Experimental Immunization Based on Plasmodium Antigens Isolated by Antibody Affinity.

机构信息

Department of Biochemistry and Molecular Biology IV, Universidad Complutense de Madrid, Facultad de Veterinaria, Ciudad Universitaria, 28040 Madrid, Spain ; Department of Biology, Faculty of Basic Sciences, Islamic Azad University, Central Tehran Branch, Tehran 14676-86831, Iran.

Department of Biochemistry and Molecular Biology IV, Universidad Complutense de Madrid, Facultad de Veterinaria, Ciudad Universitaria, 28040 Madrid, Spain ; Department of Medicine and Surgery, Psychology, Preventive Medicine and Public Health and Medical Immunology and Microbiology, Faculty of Health Sciences, Universidad Rey Juan Carlos, Alcorcón, 28922 Madrid, Spain.

出版信息

J Immunol Res. 2015;2015:723946. doi: 10.1155/2015/723946. Epub 2015 Oct 11.

DOI:10.1155/2015/723946
PMID:26539558
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC4619943/
Abstract

Vaccines blocking malaria parasites in the blood-stage diminish mortality and morbidity caused by the disease. Here, we isolated antigens from total parasite proteins by antibody affinity chromatography to test an immunization against lethal malaria infection in a murine model. We used the sera of malaria self-resistant ICR mice to lethal Plasmodium yoelii yoelii 17XL for purification of their IgGs which were subsequently employed to isolate blood-stage parasite antigens that were inoculated to immunize BALB/c mice. The presence of specific antibodies in vaccinated mice serum was studied by immunoblot analysis at different days after vaccination and showed an intensive immune response to a wide range of antigens with molecular weight ranging between 22 and 250 kDa. The humoral response allowed delay of the infection after the inoculation to high lethal doses of P. yoelii yoelii 17XL resulting in a partial protection against malaria disease, although final survival was managed in a low proportion of challenged mice. This approach shows the potential to prevent malaria disease with a set of antigens isolated from blood-stage parasites.

摘要

阻断血液阶段疟原虫的疫苗可降低疾病导致的死亡率和发病率。在这里,我们通过抗体亲和层析从全寄生虫蛋白中分离抗原,以在小鼠模型中测试针对致死性疟疾感染的免疫接种。我们使用抗致死性疟原虫自我抵抗的 ICR 小鼠血清来纯化其 IgG,随后用于分离血阶段寄生虫抗原,然后将其接种到 BALB/c 小鼠中进行免疫接种。在接种后不同天数通过免疫印迹分析研究了接种小鼠血清中特异性抗体的存在情况,结果显示对分子量在 22 至 250 kDa 之间的广泛抗原存在强烈的免疫反应。体液反应允许在接种后感染高致死剂量的 P. yoelii yoelii 17XL 后延迟,从而对疟疾疾病产生部分保护作用,尽管在受挑战的小鼠中,最终的存活率较低。这种方法显示了用从血阶段寄生虫中分离的一组抗原预防疟疾疾病的潜力。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5b91/4619943/a0792bb983b0/JIR2015-723946.006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5b91/4619943/8d7085fb6947/JIR2015-723946.001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5b91/4619943/9438a447064a/JIR2015-723946.002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5b91/4619943/1c0fea7ce823/JIR2015-723946.003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5b91/4619943/f177ffcfd1ed/JIR2015-723946.004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5b91/4619943/aebd60281972/JIR2015-723946.005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5b91/4619943/a0792bb983b0/JIR2015-723946.006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5b91/4619943/8d7085fb6947/JIR2015-723946.001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5b91/4619943/9438a447064a/JIR2015-723946.002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5b91/4619943/1c0fea7ce823/JIR2015-723946.003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5b91/4619943/f177ffcfd1ed/JIR2015-723946.004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5b91/4619943/aebd60281972/JIR2015-723946.005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5b91/4619943/a0792bb983b0/JIR2015-723946.006.jpg

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Differential immune response associated to malaria outcome is detectable in peripheral blood following Plasmodium yoelii infection in mice.在小鼠感染约氏疟原虫后,外周血中可检测到与疟疾转归相关的差异性免疫反应。
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