针对间日疟原虫红细胞外期(CelTOS 和 TRAP)和红细胞期(CyRPA)线性 B 细胞表位的 IgM 和 IgG 抗体反应谱的动态变化:后续研究。

IF 3 Q3 IMMUNOLOGY
Antibodies Pub Date : 2024-08-15 DOI:10.3390/antib13030069
Cinthia Magalhães Rodolphi, Isabela Ferreira Soares, Ada da Silva Matos, Rodrigo Nunes Rodrigues-da-Silva, Marcelo Urbano Ferreira, Lilian Rose Pratt-Riccio, Paulo Renato Rivas Totino, Kézia Katiani Gorza Scopel, Josué da Costa Lima-Junior
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引用次数: 0

摘要

疟疾是全世界的一个严重健康问题,主要影响儿童和社会弱势群体。间日疟的生物学特性,如产生休眠肝阶段的能力、配子细胞的快速成熟以及抗药性的出现,给疾病控制带来了困难。在这种情况下,开发有效的疫苗被认为是有效控制和/或消灭间日疟的基本工具。虽然重组蛋白一直是设计疫苗原型的主要策略,但合成免疫原肽已成为这方面的可行替代品。因此,考虑到在巴西疟疾流行人群中,对代表不同 P. vivax 蛋白的合成肽的体液免疫反应概况知之甚少,本研究对其进行了分析。本研究旨在绘制在间日疟急性期(AC)和恢复期(感染后的 Conv30 和 Conv180),代表卵细胞和孢子虫细胞通道蛋白(CelTOS)、凝血酶相关粘附蛋白(TRAP)和富半胱氨酸保护性抗原(CyRPA)线性部分的合成肽的表位特异性抗体图谱。结果显示,研究对象在感染后至少六个月内对所有蛋白都有反应。在疾病的急性期,少数人(3-21%)的 IgM 呈阳性;IgG 的阳性率最高(28-57%)。在亚类方面,IgG2 和 IgG3 在所有肽中最为常见。在随访期间,所有肽中的 IgG 均保持稳定。在 IgM 和暴露时间之间只观察到一个明显的正相关。我们的结论是,对于所有肽,暴露人群都能识别免疫优势表位,其频率和程度相似。但是,如果本研究中检测到的抗体是潜在的保护因子,则需要对此进行调查。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Dynamics of IgM and IgG Antibody Response Profile against Linear B-Cell Epitopes from Exoerythrocytic (CelTOS and TRAP) and Erythrocytic (CyRPA) Phases of Plasmodium vivax: Follow-Up Study.

Malaria is a serious health problem worldwide affecting mainly children and socially vulnerable people. The biological particularities of P. vivax, such as the ability to generate dormant liver stages, the rapid maturation of gametocytes, and the emergence of drug resistance, have contributed to difficulties in disease control. In this context, developing an effective vaccine has been considered a fundamental tool for the efficient control and/or elimination of vivax malaria. Although recombinant proteins have been the main strategy used in designing vaccine prototypes, synthetic immunogenic peptides have emerged as a viable alternative for this purpose. Considering, therefore, that in the Brazilian endemic population, little is known about the profile of the humoral immune response directed to synthetic peptides that represent different P. vivax proteins, the present work aimed to map the epitope-specific antibodies' profiles to synthetic peptides representing the linear portions of the ookinete and sporozoite cell passage protein (CelTOS), thrombospondin-related adhesive protein (TRAP), and cysteine-rich protective antigen (CyRPA) proteins in the acute (AC) and convalescent phases (Conv30 and Conv180 after infection) of vivax malaria. The results showed that the studied subjects responded to all proteins for at least six months following infection. For IgM, a few individuals (3-21%) were positive during the acute phase of the disease; the highest frequencies were observed for IgG (28-57%). Regarding the subclasses, IgG2 and IgG3 stood out as the most prevalent for all peptides. During the follow-up, the stability of IgG was observed for all peptides. Only one significant positive correlation was observed between IgM and exposure time. We conclude that for all the peptides, the immunodominant epitopes are recognized in the exposed population, with similar frequency and magnitude. However, if the antibodies detected in this study are potential protectors, this needs to be investigated.

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来源期刊
Antibodies
Antibodies IMMUNOLOGY-
CiteScore
7.10
自引率
6.40%
发文量
68
审稿时长
11 weeks
期刊介绍: Antibodies (ISSN 2073-4468), an international, peer-reviewed open access journal which provides an advanced forum for studies related to antibodies and antigens. It publishes reviews, research articles, communications and short notes. Our aim is to encourage scientists to publish their experimental and theoretical results in as much detail as possible. There is no restriction on the length of the papers. Full experimental and/or methodical details must be provided. Electronic files or software regarding the full details of the calculation and experimental procedure - if unable to be published in a normal way - can be deposited as supplementary material. This journal covers all topics related to antibodies and antigens, topics of interest include (but are not limited to): antibody-producing cells (including B cells), antibody structure and function, antibody-antigen interactions, Fc receptors, antibody manufacturing antibody engineering, antibody therapy, immunoassays, antibody diagnosis, tissue antigens, exogenous antigens, endogenous antigens, autoantigens, monoclonal antibodies, natural antibodies, humoral immune responses, immunoregulatory molecules.
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