Cytokine pattern during asymptomatic Anaplasma spp. infections and effect of co-infections by malaria and helminths in schoolchildren of Franceville, southeastern Gabon.

IF 3.5 2区 医学 Q1 PARASITOLOGY Parasites & Vectors Pub Date : 2025-03-27 DOI:10.1186/s13071-025-06714-1
Chérone Nancy Mbani Mpega Ntigui, Sandrine Lydie Oyegue-Liabagui, Jenny Mouloungui-Mavoungou, Nal Kennedy Ndjangangoye, Desly Luide Madoungou Idoumi, Lady Charlene Kouna, Roland Fabrice Kassa Kassa, Nancy Diamella Moukodoum, Steede Seinnat Ontoua, Roméo Karl Imboumy Limoukou, Jean-Claude Biteghe Bi Essone, Alain Prince Okouga, Félicien Bagueboussa, Jean-Bernard Lekana-Douki
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Abstract

Background: Asymptomatic infections by Anaplasma spp. and the basis of the immune response during these infections have not yet been established. This study investigated the inflammatory cytokine responses during Anaplasma spp. infection in school children and the effect of co-infection with Plasmodium spp. and helminths.

Methods: Blood and stool samples were taken from children aged 5 to 17 years. Parasitological diagnosis was carried out by RDT and microscopy, while microscopy and PCR were used to diagnose infection by Anaplasma spp. Plasma was used for cytokine assays using the ELISA technique.

Results: A total of 219 children were included in the present study, of whom 205 were infected with Anaplasma spp. and 14 were uninfected. Levels of IL-6, IL-22 and TGF-β were lower not only in children mono-infected with Anaplasma spp. but also in those co-infected with Anaplasma spp. and Plasmodium spp., Anaplasma spp. and helminths, and Anaplasma spp., Plasmodium spp. and helminths compared to controls. However, higher levels of IL-6 and IL-22 were observed in children mono-infected with Anaplasma spp. compared to those co-infected with Anaplasma spp. and helminths. The latter group also had lower levels of IL-6, IL-22, TGF-β and IL-10 than children co-infected with Anaplasma spp. and Plasmodium spp. In addition, children co-infected with Anaplasma spp. and helminths had also lower TGF-β and IL-10 levels than children co-infected with Anaplasma spp., Plasmodium spp. and helminths. An increase of IFN-γ and IL-10 were observed in children co-infected with Anaplasma spp. and Plasmodium spp. compared to those mono-infected with Anaplasma spp. Finally, the results showed that febrile children infected with Anaplasma spp. had higher levels of IFN-γ and lower levels of TGF-β than afebrile children.

Conclusions: These results suggest that infection with Anaplasma spp. downregulates cytokines including IL-6, IL-22 and TGF-β and that co-infection with Plasmodium spp. might have a protective effect on the host, while co-infection with helminths might have a negative effect.

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加蓬东南部弗朗斯维尔学童无症状无形体感染期间的细胞因子模式及疟疾和寄生虫合并感染的影响
背景:无症状的解脲脲原体感染以及感染期间免疫反应的基础尚未确定。本研究调查了学龄儿童感染解脲脲原体期间的炎症细胞因子反应,以及疟原虫和蠕虫共感染的影响:方法:采集 5 至 17 岁儿童的血液和粪便样本。寄生虫学诊断采用 RDT 和显微镜检查法,阿纳疟原虫感染诊断采用显微镜检查法和 PCR 法,血浆采用 ELISA 技术进行细胞因子检测:本研究共纳入 219 名儿童,其中 205 人感染了阿纳疟原虫,14 人未感染。与对照组相比,不仅单感染阿纳疟原虫的儿童 IL-6、IL-22 和 TGF-β 的水平较低,而且同时感染阿纳疟原虫和疟原虫、阿纳疟原虫和蠕虫以及阿纳疟原虫、疟原虫和蠕虫的儿童 IL-6 和 TGF-β 的水平也较低。然而,与同时感染阿纳疟原虫和蠕虫的儿童相比,单感染阿纳疟原虫的儿童 IL-6 和 IL-22 水平较高。此外,与同时感染阿纳疟原虫属、疟原虫属和蠕虫的儿童相比,同时感染阿纳疟原虫属和蠕虫的儿童的 TGF-β 和 IL-10 水平也较低。最后,研究结果表明,与发热儿童相比,感染了阿纳疟原虫的发热儿童的IFN-γ水平较高,而TGF-β水平较低:这些结果表明,感染解脲脲原体会下调细胞因子,包括 IL-6、IL-22 和 TGF-β,同时感染疟原虫可能会对宿主产生保护作用,而同时感染蠕虫可能会产生负面影响。
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来源期刊
Parasites & Vectors
Parasites & Vectors 医学-寄生虫学
CiteScore
6.30
自引率
9.40%
发文量
433
审稿时长
1.4 months
期刊介绍: Parasites & Vectors is an open access, peer-reviewed online journal dealing with the biology of parasites, parasitic diseases, intermediate hosts, vectors and vector-borne pathogens. Manuscripts published in this journal will be available to all worldwide, with no barriers to access, immediately following acceptance. However, authors retain the copyright of their material and may use it, or distribute it, as they wish. Manuscripts on all aspects of the basic and applied biology of parasites, intermediate hosts, vectors and vector-borne pathogens will be considered. In addition to the traditional and well-established areas of science in these fields, we also aim to provide a vehicle for publication of the rapidly developing resources and technology in parasite, intermediate host and vector genomics and their impacts on biological research. We are able to publish large datasets and extensive results, frequently associated with genomic and post-genomic technologies, which are not readily accommodated in traditional journals. Manuscripts addressing broader issues, for example economics, social sciences and global climate change in relation to parasites, vectors and disease control, are also welcomed.
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