先天性寨卡病毒综合征小头畸形儿童的免疫失调。

IF 5.5 3区 医学 Q1 IMMUNOLOGY
Medical Microbiology and Immunology Pub Date : 2022-12-01 Epub Date: 2022-07-20 DOI:10.1007/s00430-022-00746-5
Amanda Costa Ayres Salmeron, Wallace Pitanga Bezerra, Rafaela Lúcia Lopes de Souza, Luanderson Cardoso Pereira, Lícia Maria do Nascimento, Anna Cláudia Calvielli Castelo Branco, Luiza Emilia Cavalcanti Simas, Valéria Azevedo de Almeida, Pedro Henrique de Souza Palmeira, Christiane Medeiros Bezerra, Paulo Marcos Matta Guedes, Maria Notomi Sato, Valéria Soraya de Farias Sales, Reginaldo Antônio de Oliveira Freitas Júnior, Tatjana de Souza Lima Keesen, Manuela Sales Lima Nascimento
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引用次数: 1

摘要

先天性寨卡病毒综合征(CZS)引起的小头症儿童表现出已经得到很好描述的神经系统症状。然而,也可以观察到其他一些变化。在这里,我们旨在评估小头畸形CZS儿童的免疫系统。我们发现这些患者胸腺、脾脏和颈部淋巴结肿大,通过超声分析并与健康儿童的参考值进行比较。在外周,即使没有尿路感染、寄生虫感染或其他当前有症状的感染,它们也有嗜酸性粒细胞计数增加和形态改变,如超节段性中性粒细胞和非典型淋巴细胞。与健康对照相比,CZS引起的小头症儿童也有高水平的IFN-γ、IL-2、IL-4、IL-5和I型IFN。此外,该人群表现出细胞免疫记忆缺陷,对结核菌素皮肤试验的低反应性证明了这一点,即使他们在PPD挑战前不到2年接种过卡介苗。总之,我们的数据首次表明,cz可引起原发性和继发性淋巴器官的改变,并改变免疫系统细胞的形态和功能,这扩大了cz症状的范围。这一知识可能有助于为这一患者群体制定特定的治疗性和更有效的疫苗接种方案。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Immunological imbalance in microcephalic children with congenital Zika virus syndrome.

Immunological imbalance in microcephalic children with congenital Zika virus syndrome.

Microcephalic children due congenital Zika virus syndrome (CZS) present neurological symptoms already well described. However, several other alterations can also be observed. Here, we aimed to evaluate the immune system of microcephaly CZS children. We showed that these patients have enlarged thymus, spleen and cervical lymph nodes, analysed by ultrasound and compared to the reference values for healthy children. In the periphery, they have an increase in eosinophil count and morphological alterations as hypersegmented neutrophils and atypical lymphocytes, even in the absence of urinary tract infections, parasitological infections or other current symptomatic infections. Microcephalic children due CZS also have high levels of IFN-γ, IL-2, IL-4, IL-5 and type I IFNs, compared to healthy controls. In addition, this population showed a deficient cellular immune memory as demonstrated by the low reactivity to the tuberculin skin test even though they had been vaccinated with BCG less than 2 years before the challenge with the PPD. Together, our data demonstrate for the first time that CZS can cause alterations in primary and secondary lymphoid organs and also alters the morphology and functionality of the immune system cells, which broadens the spectrum of CZS symptoms. This knowledge may assist the development of specific therapeutic and more efficient vaccination schemes for this population of patients.

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来源期刊
CiteScore
10.60
自引率
0.00%
发文量
29
审稿时长
1 months
期刊介绍: Medical Microbiology and Immunology (MMIM) publishes key findings on all aspects of the interrelationship between infectious agents and the immune system of their hosts. The journal´s main focus is original research work on intrinsic, innate or adaptive immune responses to viral, bacterial, fungal and parasitic (protozoan and helminthic) infections and on the virulence of the respective infectious pathogens. MMIM covers basic, translational as well as clinical research in infectious diseases and infectious disease immunology. Basic research using cell cultures, organoid, and animal models are welcome, provided that the models have a clinical correlate and address a relevant medical question. The journal also considers manuscripts on the epidemiology of infectious diseases, including the emergence and epidemic spreading of pathogens and the development of resistance to anti-infective therapies, and on novel vaccines and other innovative measurements of prevention. The following categories of manuscripts will not be considered for publication in MMIM: submissions of preliminary work, of merely descriptive data sets without investigation of mechanisms or of limited global interest, manuscripts on existing or novel anti-infective compounds, which focus on pharmaceutical or pharmacological aspects of the drugs, manuscripts on existing or modified vaccines, unless they report on experimental or clinical efficacy studies or provide new immunological information on their mode of action, manuscripts on the diagnostics of infectious diseases, unless they offer a novel concept to solve a pending diagnostic problem, case reports or case series, unless they are embedded in a study that focuses on the anti-infectious immune response and/or on the virulence of a pathogen.
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