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Structural, Genetic, and Serological Elucidation of Streptococcus pneumoniae Serogroup 24 Serotypes: Discovery of a New Serotype, 24C, with a Variable Capsule Structure.结构、遗传和血清学阐明肺炎链球菌 24 血清型:发现一种新的血清型 24C,其荚膜结构具有可变性。
J Clin Microbiol. 2021 Jun 18;59(7):e0054021. doi: 10.1128/JCM.00540-21.
2
Pneumococcal Choline-Binding Proteins Involved in Virulence as Vaccine Candidates.参与毒力的肺炎球菌胆碱结合蛋白作为疫苗候选物
Vaccines (Basel). 2021 Feb 20;9(2):181. doi: 10.3390/vaccines9020181.
3
The Role of Streptococcus pneumoniae in Community-Acquired Pneumonia.肺炎链球菌在社区获得性肺炎中的作用。
Semin Respir Crit Care Med. 2020 Aug;41(4):455-469. doi: 10.1055/s-0040-1702193. Epub 2020 Jun 13.
4
Designing ecologically optimized pneumococcal vaccines using population genomics.利用群体基因组学设计生态优化的肺炎球菌疫苗。
Nat Microbiol. 2020 Mar;5(3):473-485. doi: 10.1038/s41564-019-0651-y. Epub 2020 Feb 3.
5
Selective pressure: Rise of the nonencapsulated pneumococcus.选择压力:非包膜肺炎球菌的兴起
PLoS Pathog. 2019 Aug 29;15(8):e1007911. doi: 10.1371/journal.ppat.1007911. eCollection 2019 Aug.
6
Should Pneumococcal Vaccines Eliminate Nasopharyngeal Colonization?肺炎球菌疫苗能否消除鼻咽部定植?
mBio. 2016 May 24;7(3):e00545-16. doi: 10.1128/mBio.00545-16.
7
Immune Responses to pneumococcal vaccines in children and adults: Rationale for age-specific vaccination.儿童和成人对肺炎球菌疫苗的免疫应答:针对特定年龄接种疫苗的理由。
Aging Dis. 2012 Feb;3(1):51-67. Epub 2011 Jul 20.
8
CHEMO-IMMUNOLOGICAL STUDIES ON CONJUGATED CARBOHYDRATE-PROTEINS : II. IMMUNOLOGICAL SPECIFICITY OF SYNTHETIC SUGAR-PROTEIN ANTIGENS.糖蛋白-结合物的化学免疫研究:II. 合成糖蛋白抗原的免疫学特异性。
J Exp Med. 1929 Sep 30;50(4):533-50. doi: 10.1084/jem.50.4.533.
9
Incidence of pneumococcal disease due to non-pneumococcal conjugate vaccine (PCV7) serotypes in the United States during the era of widespread PCV7 vaccination, 1998-2004.1998 - 2004年广泛接种7价肺炎球菌结合疫苗(PCV7)时代美国非PCV7血清型肺炎球菌疾病的发病率
J Infect Dis. 2007 Nov 1;196(9):1346-54. doi: 10.1086/521626. Epub 2007 Oct 4.

如果不是现在,那是何时?非血清型肺炎球菌蛋白疫苗。

If Not Now, When? Nonserotype Pneumococcal Protein Vaccines.

作者信息

McDaniel Larry S, Swiatlo Edwin

机构信息

Department of Microbiology and Immunology, University of Mississippi Medical Center, Jackson, Mississippi, USA.

Southeast Louisiana Veterans Health Care Network, New Orleans, Louisiana, USA.

出版信息

Open Forum Infect Dis. 2021 Dec 18;8(12):ofab576. doi: 10.1093/ofid/ofab576. eCollection 2021 Dec.

DOI:10.1093/ofid/ofab576
PMID:34934775
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8684483/
Abstract

The sudden emergence and global spread of severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) have greatly accelerated the adoption of novel vaccine strategies, which otherwise would have likely languished for years. In this light, vaccines for certain other pathogens could certainly benefit from reconsideration. One such pathogen is (pneumococcus), an encapsulated bacterium that can express >100 antigenically distinct serotypes. Current pneumococcal vaccines are based exclusively on capsular polysaccharide-either purified alone or conjugated to protein. Since the introduction of conjugate vaccines, the valence of pneumococcal vaccines has steadily increased, as has the associated complexity and cost of production. There are many pneumococcal proteins invariantly expressed across all serotypes, which have been shown to induce robust immune responses in animal models. These proteins could be readily produced using recombinant DNA technology or by mRNA technology currently used in SARS-CoV-2 vaccines. A door may be opening to new opportunities in affordable and broadly protective vaccines.

摘要

严重急性呼吸综合征冠状病毒2(SARS-CoV-2)的突然出现和全球传播极大地加速了新型疫苗策略的采用,否则这些策略可能会停滞数年。有鉴于此,某些其他病原体的疫苗肯定会受益于重新审视。这样一种病原体就是肺炎链球菌,一种可表达100多种抗原性不同血清型的包膜细菌。目前的肺炎球菌疫苗完全基于荚膜多糖——单独纯化或与蛋白质结合。自结合疫苗推出以来,肺炎球菌疫苗的价数稳步增加,生产的相关复杂性和成本也随之增加。在所有血清型中都有许多恒定表达的肺炎球菌蛋白,这些蛋白已被证明能在动物模型中诱导强烈的免疫反应。这些蛋白可以很容易地通过重组DNA技术或目前用于SARS-CoV-2疫苗的mRNA技术来生产。一扇通往价格合理且具有广泛保护作用疫苗的新机遇之门可能正在打开。