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一种新的犬内脏利什曼病重组抗原的免疫预防潜力:一项发现。

Immunoprophylactic Potential of a New Recombinant Antigen for Canine Visceral Leishmaniasis: An Finding.

机构信息

Department of Microbiology, Aggeu Magalhães Institute, Recife, Brazil.

Tabosa de Almeida University Center, Caruaru, Brazil.

出版信息

Front Immunol. 2021 Jan 8;11:605044. doi: 10.3389/fimmu.2020.605044. eCollection 2020.

Abstract

The development and application of safe and effective immunoprophylactic/immunotherapeutic agents against canine visceral leishmaniasis (CanL) have been pointed out as the only means for the real control of the disease. Thus, this study aimed to evaluate the cellular immune response of dogs, elicited by the new recombinant proteins of , Lci10 and Lci13, in order to investigate their potential for vaccinology. Twenty-four dogs were submitted to clinical, parasitological, serological and molecular tests, and then separated into two study groups: 12 infected (InD) and 12 non-infected dogs (NInD), and six of each group were directed for Lci10 and Lci13 evaluation. Peripheral blood mononuclear cells (PBMC) were cultured and stimulated with Lci10 (10 μg/ml) or Lci13 (5 μg/ml), and with soluble antigen (LSA) (25 μg/ml) or no stimulus (NS) as controls. Afterwards, the mRNA levels of different cytokines were quantified through qPCR, and Nitric Oxide (NO) production was assessed in the culture supernatants. Significant differences were considered when p ≤ 0.05. The comparative analysis revealed that, in the NInD group, Lci13 promoted a significant increase in the expression of IFN-γ in relation to LSA ( = 0.0362), and the expression of this cytokine in NInD was significantly higher than that presented in the InD ( = 0.0028). A negative expression for TGF-β was obtained in both groups. Lci13 also induced a greater production of NO in relation to the NS sample in the NInD group. No significant differences were observed after stimulation with Lci10. In conclusion, the results suggest a protective role of Lci13 for uninfected animals, thus with a potential for immunoprophylaxis. The results will help to direct the antigen Lci13 for further studies (pre-clinical trials), in order to determine its immunogenicity and reactogenicity effects, as a way to consolidate its real applicability for vaccinology against CanL.

摘要

犬内脏利什曼病(CanL)的安全有效免疫预防/免疫治疗制剂的开发和应用已被指出是该病真正控制的唯一手段。因此,本研究旨在评估新的重组蛋白 、Lci10 和 Lci13 诱导的犬细胞免疫应答,以研究其在疫苗学中的潜力。24 只狗接受了临床、寄生虫学、血清学和分子检测,然后分为两组:12 只感染(InD)和 12 只非感染狗(NInD),每组 6 只用于 Lci10 和 Lci13 评估。外周血单核细胞(PBMC)经培养并分别用 Lci10(10 μg/ml)或 Lci13(5 μg/ml)、可溶性抗原(LSA)(25 μg/ml)或无刺激物(NS)作为对照物进行刺激。随后,通过 qPCR 定量测定不同细胞因子的 mRNA 水平,并评估培养上清液中的一氧化氮(NO)产生。当 p ≤ 0.05 时认为存在显著差异。比较分析表明,在 NInD 组中,Lci13 与 LSA 相比显著增加 IFN-γ 的表达( = 0.0362),并且 NInD 中该细胞因子的表达明显高于 InD( = 0.0028)。两组均未检测到 TGF-β的表达。Lci13 还诱导 NInD 组中 NS 样本相比产生更多的 NO。用 Lci10 刺激后未观察到显著差异。结论表明,Lci13 对未感染动物具有保护作用,因此具有免疫预防的潜力。这些结果将有助于指导抗原 Lci13 进行进一步研究(临床前试验),以确定其免疫原性和反应原性作用,从而巩固其在犬内脏利什曼病疫苗学中的实际应用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/85d1/7819978/43e24a1a8de7/fimmu-11-605044-g001.jpg

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