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在夜猴中诱导针对单克隆抗体定义的恶性疟原虫抗原的保护性免疫需要强效佐剂。

Induction of protective immunity to monoclonal-antibody-defined Plasmodium falciparum antigens requires strong adjuvant in Aotus monkeys.

作者信息

Siddiqui W A, Tam L Q, Kan S C, Kramer K J, Case S E, Palmer K L, Yamaga K M, Hui G S

出版信息

Infect Immun. 1986 Apr;52(1):314-8. doi: 10.1128/iai.52.1.314-318.1986.

DOI:10.1128/iai.52.1.314-318.1986
PMID:3514459
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC262236/
Abstract

Monoclonal antibodies to the major Plasmodium falciparum merozoite surface coat and rhoptry antigens were produced. A combination of the affinity-purified polypeptides with Freund complete adjuvant which was given three times completely protected an Aotus lemurinus azure (karotype VI) monkey against homologous challenge; however, immunization with the same polypeptides with a muramyl dipeptide derivative [MDP-Lys(L18)] did not protect a second Aotus monkey, even though comparable high antibody titers were induced.

摘要

制备了针对恶性疟原虫裂殖子主要表面被膜和棒状体抗原的单克隆抗体。将亲和纯化的多肽与弗氏完全佐剂联合使用,对一只青猴(核型VI)进行三次注射后,该猴对同源攻击具有完全的保护作用;然而,用相同的多肽与一种胞壁酰二肽衍生物[MDP-Lys(L18)]进行免疫,尽管诱导了相当高的抗体滴度,但并未保护第二只青猴。

相似文献

1
Induction of protective immunity to monoclonal-antibody-defined Plasmodium falciparum antigens requires strong adjuvant in Aotus monkeys.在夜猴中诱导针对单克隆抗体定义的恶性疟原虫抗原的保护性免疫需要强效佐剂。
Infect Immun. 1986 Apr;52(1):314-8. doi: 10.1128/iai.52.1.314-318.1986.
2
Synthetic low-toxicity muramyl dipeptide and monophosphoryl lipid A replace Freund complete adjuvant in inducing growth-inhibitory antibodies to the Plasmodium falciparum major merozoite surface protein, gp195.合成的低毒性胞壁酰二肽和单磷酰脂质A在诱导针对恶性疟原虫主要裂殖子表面蛋白gp195的生长抑制性抗体方面可替代弗氏完全佐剂。
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3
Merozoite surface coat precursor protein completely protects Aotus monkeys against Plasmodium falciparum malaria.裂殖子表面被膜前体蛋白可使夜猴完全抵御恶性疟原虫疟疾。
Proc Natl Acad Sci U S A. 1987 May;84(9):3014-8. doi: 10.1073/pnas.84.9.3014.
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本文引用的文献

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Use of a synthetic adjuvant in an effective vaccination of monkeys against malaria.在猴子有效接种疟疾疫苗中使用合成佐剂。
Nature. 1981 Jan 1;289(5793):64-6. doi: 10.1038/289064a0.
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A one-step purification of membrane proteins using a high efficiency immunomatrix.使用高效免疫基质一步纯化膜蛋白。
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A large-scale in vitro production system for Plasmodium falciparum.
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针对一种新型恶性疟原虫裂殖子表面蛋白疫苗的抗体反应与对夜猴实验性疟疾感染的保护作用相关。
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Why functional pre-erythrocytic and bloodstage malaria vaccines fail: a meta-analysis of fully protective immunizations and novel immunological model.为什么功能性原虫前期和红内期疟疾疫苗会失败:完全保护免疫接种和新型免疫模型的荟萃分析。
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Adjuvant formulations possess differing efficacy in the potentiation of antibody and cell mediated responses to a human malaria vaccine under selective immune genes knockout environment.在选择性免疫基因敲除环境下,佐剂配方在增强对人类疟疾疫苗的抗体和细胞介导反应方面具有不同的功效。
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Effect of GPI anchor moiety on the immunogenicity of DNA plasmids encoding the 19-kDa C-terminal portion of Plasmodium falciparum MSP-1.糖基磷脂酰肌醇(GPI)锚定部分对编码恶性疟原虫裂殖子表面蛋白1(MSP-1)19-kDa C末端部分的DNA质粒免疫原性的影响。
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7
Evaluation of three Pichia pastoris-expressed Plasmodium falciparum merozoite proteins as a combination vaccine against infection with blood-stage parasites.评估三种毕赤酵母表达的恶性疟原虫裂殖子蛋白作为抗血液期寄生虫感染联合疫苗的效果。
Infect Immun. 2005 Oct;73(10):6530-6. doi: 10.1128/IAI.73.10.6530-6536.2005.
8
In vivo expression and immunological studies of the 42-kilodalton carboxyl-terminal processing fragment of Plasmodium falciparum merozoite surface protein 1 in the baculovirus-silkworm system.恶性疟原虫裂殖子表面蛋白1 42千道尔顿羧基末端加工片段在杆状病毒-家蚕系统中的体内表达及免疫学研究
Infect Immun. 2002 Jun;70(6):2772-9. doi: 10.1128/IAI.70.6.2772-2779.2002.
9
Codon optimization of gene fragments encoding Plasmodium falciparum merzoite proteins enhances DNA vaccine protein expression and immunogenicity in mice.恶性疟原虫裂殖子蛋白编码基因片段的密码子优化可增强DNA疫苗在小鼠体内的蛋白表达及免疫原性。
Infect Immun. 2001 Dec;69(12):7250-3. doi: 10.1128/IAI.69.12.7250-7253.2001.
10
Rhoptry-associated protein 1-binding monoclonal antibody raised against a heterologous peptide sequence inhibits Plasmodium falciparum growth in vitro.针对异源肽序列产生的与棒状体相关蛋白1结合的单克隆抗体可在体外抑制恶性疟原虫的生长。
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Biosynthesis and processing of a Plasmodium falciparum schizont antigen recognized by immune serum and a monoclonal antibody.一种被免疫血清和单克隆抗体识别的恶性疟原虫裂殖体抗原的生物合成与加工
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Human antibodies to a Mr 155,000 Plasmodium falciparum antigen efficiently inhibit merozoite invasion.针对疟原虫恶性疟原虫155,000道尔顿抗原的人源抗体可有效抑制裂殖子入侵。
Proc Natl Acad Sci U S A. 1984 Dec;81(24):7912-6. doi: 10.1073/pnas.81.24.7912.
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Monoclonal antibody characterization of Plasmodium falciparum antigens.恶性疟原虫抗原的单克隆抗体特性分析
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Plasmodium falciparum: comparative analysis of antigens from continuous in vitro cultured and in vivo derived malarial parasites.
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The three major antigens on the surface of Plasmodium falciparum merozoites are derived from a single high molecular weight precursor.恶性疟原虫裂殖子表面的三种主要抗原源自单一的高分子量前体。
J Exp Med. 1984 Aug 1;160(2):624-9. doi: 10.1084/jem.160.2.624.
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Antimalarial immunity in Saimiri monkeys. Immunization with surface components of asexual blood stages.松鼠猴的抗疟免疫。无性血液阶段表面成分免疫接种。
J Exp Med. 1984 Aug 1;160(2):441-51. doi: 10.1084/jem.160.2.441.
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Localization of the major Plasmodium falciparum glycoprotein on the surface of mature intraerythrocytic trophozoites and schizonts.
Mol Biochem Parasitol. 1984 Apr;11:349-62. doi: 10.1016/0166-6851(84)90078-1.