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一种新型免疫调节肽,具有在疫苗接种策略中补充寡脱氧核苷酸介导的佐剂活性的潜力。

A novel immunomodulating peptide with potential to complement oligodeoxynucleotide-mediated adjuvanticity in vaccination strategies.

机构信息

InterK Peptide Therapeutics Limited, Lane Cove West, NSW, Australia.

Australian Institute for Bioengineering and Nanotechnology and the ARC Training Centre for Innovation in Biomedical Imaging Technologies, University of Queensland, Brisbane, Australia.

出版信息

Sci Rep. 2024 Nov 5;14(1):26737. doi: 10.1038/s41598-024-78150-7.

Abstract

The identification of adjuvants to improve vaccination efficacy is a major unmet need. One approach is to augment the functionality of dendritic cells (DCs) by using Toll-like receptor-9 (TLR9) agonists such as cytosine-phosphate-guanine oligodeoxynucleotides (CpG ODNs) as adjuvants. Another approach is adjuvant selection based on production of bioactive interleukin-12 (IL-12). We report a D-peptide isomer, designated D-15800, that induces monocyte differentiation to the DC phenotype in vitro and more effectively stimulates IL-12p70 production upon T cell receptor (TCR) activation than the L-isomer. In the absence of TCR activation and either IL-12p70 or interleukin-2 production, only D-15800 activates CD4 T and natural killer cells. In the presence of CpG ODN, D-15800 synergistically enhances production of interferon-alpha (IFN-α). Taken together with its biostability in human serum and depot retention upon injection, co-delivery of D-15800 with TLR9 agonists could serve to improve vaccine efficacy.

摘要

鉴定佐剂以提高疫苗效力是一个主要的未满足的需求。一种方法是通过使用 Toll 样受体 9(TLR9)激动剂(如胞嘧啶-磷酸-鸟嘌呤寡脱氧核苷酸(CpG ODN))来增强树突状细胞(DC)的功能。另一种方法是根据产生生物活性白细胞介素 12(IL-12)来选择佐剂。我们报告了一种 D- 肽异构体,命名为 D-15800,它在体外诱导单核细胞向 DC 表型分化,并在 T 细胞受体(TCR)激活时比 L-异构体更有效地刺激 IL-12p70 的产生。在没有 TCR 激活和 IL-12p70 或白细胞介素 2 产生的情况下,只有 D-15800 能激活 CD4 T 细胞和自然杀伤细胞。在 CpG ODN 的存在下,D-15800 协同增强干扰素-α(IFN-α)的产生。考虑到其在人血清中的生物稳定性和注射后的储存能力,与 TLR9 激动剂共同递送 D-15800 可能有助于提高疫苗效力。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2850/11538426/e5ba0ffcf90d/41598_2024_78150_Fig1_HTML.jpg

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