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化学合成具有血清型 6C 和 6D 的截短荚膜寡糖及其免疫研究。

Chemical Synthesis of Truncated Capsular Oligosaccharide of Serotypes 6C and 6D of with Their Immunological Studies.

机构信息

Genomics Research Center, Academia Sinica, 128 Academia Road, Section 2, Nankang, Taipei 11529, Taiwan.

Institute of Biochemistry and Molecular Biology, National Yang Ming Chiao Tung University, No. 155, Section 2, Linong Street, Taipei 112304, Taiwan.

出版信息

ACS Infect Dis. 2024 Jun 14;10(6):2161-2171. doi: 10.1021/acsinfecdis.4c00147. Epub 2024 May 21.

DOI:10.1021/acsinfecdis.4c00147
PMID:38770797
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11184553/
Abstract

Serotypes 6C and 6D of are two major variants that cause invasive pneumococcal disease (IPD) in serogroup 6 alongside serotypes 6A and 6B. Since the introduction of the pneumococcal conjugate vaccines PCV7 and PCV13, the number of cases of IPD caused by pneumococcus in children and the elderly population has greatly decreased. However, with the widespread use of vaccines, a replacement effect has recently been observed among different serotypes and lowered the effectiveness of the vaccines. To investigate protection against the original serotypes and to explore protection against variants and replacement serotypes, we created a library of oligosaccharide fragments derived from the repeating units of the capsular polysaccharides of serotypes 6A, 6B, 6C, and 6D through chemical synthesis. The library includes nine pseudosaccharides with or without exposed terminal phosphate groups and four pseudotetrasaccharides bridged by phosphate groups. Six carbohydrate antigens related to 6C and 6D were prepared as glycoprotein vaccines for immunogenicity studies. Two 6A and two 6B glycoconjugate vaccines from previous studies were included in immunogenicity studies. We found that the conjugates containing four phosphate-bridged pseudotetrasaccharides were able to induce good immune antibodies and cross-immunogenicity by showing superior activity and broad cross-protective activity in OPKA bactericidal experiments.

摘要

6C 和 6D 血清型是导致 6 群侵袭性肺炎球菌病(IPD)的两个主要变异株,与血清型 6A 和 6B 一起。自从肺炎球菌结合疫苗 PCV7 和 PCV13 问世以来,儿童和老年人群中由肺炎球菌引起的 IPD 病例数量大大减少。然而,随着疫苗的广泛使用,最近不同血清型之间出现了替代效应,降低了疫苗的有效性。为了研究对原始血清型的保护作用,并探讨对变异株和替代血清型的保护作用,我们通过化学合成方法从血清型 6A、6B、6C 和 6D 的荚膜多糖重复单元中创建了一个寡糖片段文库。该文库包括九个带有或不带有暴露的末端磷酸基团的假糖和四个通过磷酸基团桥接的假四糖。制备了与 6C 和 6D 相关的六种糖抗原作为糖蛋白疫苗进行免疫原性研究。我们将之前研究中的两种 6A 和两种 6B 糖缀合物疫苗纳入免疫原性研究。我们发现,含有四个磷酸桥接假四糖的缀合物能够通过在 OPKA 杀菌实验中表现出更好的活性和广泛的交叉保护活性来诱导良好的免疫抗体和交叉免疫原性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/20df/11184553/47104b679658/id4c00147_0005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/20df/11184553/cc884cd64522/id4c00147_0001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/20df/11184553/5192bb7fc030/id4c00147_0002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/20df/11184553/dc966da5da96/id4c00147_0006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/20df/11184553/58bbc97ee1ee/id4c00147_0007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/20df/11184553/fc87041cefb3/id4c00147_0008.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/20df/11184553/766a1720c9b2/id4c00147_0009.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/20df/11184553/878d6b444512/id4c00147_0003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/20df/11184553/4d7f6dc6d0f8/id4c00147_0004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/20df/11184553/47104b679658/id4c00147_0005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/20df/11184553/cc884cd64522/id4c00147_0001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/20df/11184553/5192bb7fc030/id4c00147_0002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/20df/11184553/dc966da5da96/id4c00147_0006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/20df/11184553/58bbc97ee1ee/id4c00147_0007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/20df/11184553/fc87041cefb3/id4c00147_0008.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/20df/11184553/766a1720c9b2/id4c00147_0009.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/20df/11184553/878d6b444512/id4c00147_0003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/20df/11184553/4d7f6dc6d0f8/id4c00147_0004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/20df/11184553/47104b679658/id4c00147_0005.jpg

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