Suppr超能文献

针对疟原虫红外期(CelTOS和TRAP)及红细胞期(CyRPA)线性B细胞表位的IgM和IgG抗体反应谱动态:随访研究

Dynamics of IgM and IgG Antibody Response Profile against Linear B-Cell Epitopes from Exoerythrocytic (CelTOS and TRAP) and Erythrocytic (CyRPA) Phases of : Follow-Up Study.

作者信息

Rodolphi Cinthia Magalhães, Soares Isabela Ferreira, Matos Ada da Silva, Rodrigues-da-Silva Rodrigo Nunes, Ferreira Marcelo Urbano, Pratt-Riccio Lilian Rose, Totino Paulo Renato Rivas, Scopel Kézia Katiani Gorza, Lima-Junior Josué da Costa

机构信息

Research Centre of Parasitology, Department of Parasitology, Microbiology and Immunology and Post-Graduation Program in Biological Science, Federal University of Juiz de Fora, Juiz de Fora 36036-900, Brazil.

Laboratory of Immunoparasitology, Oswaldo Cruz Institute, Fiocruz, Rio de Janeiro 21040-900, Brazil.

出版信息

Antibodies (Basel). 2024 Aug 15;13(3):69. doi: 10.3390/antib13030069.

Abstract

Malaria is a serious health problem worldwide affecting mainly children and socially vulnerable people. The biological particularities of , 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 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.

摘要

疟疾是一个全球性的严重健康问题,主要影响儿童和社会弱势群体。疟原虫的生物学特性,如产生潜伏性肝期的能力、配子体的快速成熟以及耐药性的出现,给疾病控制带来了困难。在这种背景下,开发一种有效的疫苗被认为是有效控制和/或消除间日疟的基本工具。尽管重组蛋白一直是设计疫苗原型的主要策略,但合成免疫原性肽已成为实现这一目的的可行替代方案。因此,考虑到在巴西流行地区人群中,对于针对代表不同疟原虫蛋白质的合成肽的体液免疫反应情况知之甚少,本研究旨在绘制间日疟急性(AC)期和恢复期(感染后Conv30和Conv180)针对代表动合子和子孢子细胞穿越蛋白(CelTOS)、血小板反应蛋白相关黏附蛋白(TRAP)以及富含半胱氨酸的保护性抗原(CyRPA)蛋白线性部分的合成肽的表位特异性抗体谱。结果显示,研究对象在感染后至少六个月内对所有蛋白质都有反应。对于IgM,在疾病急性期少数个体(3 - 21%)呈阳性;IgG的阳性频率最高(28 - 57%)。关于亚类,IgG2和IgG3在所有肽中最为普遍。在随访期间,观察到所有肽的IgG稳定性。仅观察到IgM与暴露时间之间存在一个显著的正相关。我们得出结论,对于所有肽,在暴露人群中可识别出免疫显性表位,其频率和强度相似。然而,本研究中检测到的抗体是否为潜在的保护因子,这需要进一步研究。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c635/11348034/a70df0e87f6a/antibodies-13-00069-g0A1.jpg

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验