Jernelle C Miller, Alan S Cross, Sharon M Tennant, Scott M Baliban
{"title":"肺炎克雷伯氏菌脂多糖作为疫苗靶点以及抗体在预防疾病中的作用。","authors":"Jernelle C Miller, Alan S Cross, Sharon M Tennant, Scott M Baliban","doi":"10.3390/vaccines12101177","DOIUrl":null,"url":null,"abstract":"<p><p><i>Klebsiella pneumoniae</i> is well recognized as a serious cause of infection in healthcare-associated settings and immunocompromised individuals; however, accumulating evidence from resource-limited nations documents an alarming rise in community-acquired <i>K</i>. <i>pneumoniae</i> infections, manifesting as bacteremia and pneumonia as well as neonatal sepsis. The emergence of hypervirulent and antibiotic-resistant <i>K</i>. <i>pneumoniae</i> strains threatens treatment options for clinicians. Effective vaccination strategies could represent a viable alternative that would both preempt the need for antibiotics to treat <i>K</i>. <i>pneumoniae</i> infections and reduce the burden of <i>K</i>. <i>pneumoniae</i> disease globally. There are currently no approved <i>K. pneumoniae</i> vaccines. We review the evidence for <i>K</i>. <i>pneumoniae</i> lipopolysaccharide (LPS) as a vaccine and immunotherapeutic target and discuss the role of antibodies specific for the core or O-antigen determinants within LPS in protection against <i>Klebsiella</i> spp. disease. We expand on the known role of the <i>Klebsiella</i> spp. capsule and O-antigen modifications in antibody surface accessibility to LPS as well as the in vitro and in vivo effector functions reported for LPS-specific antibodies. We summarize key hypotheses stemming from these studies, review the role of humoral immunity against <i>K</i>. <i>pneumoniae</i> O-antigen for protection, and identify areas requiring further research.</p>","PeriodicalId":23634,"journal":{"name":"Vaccines","volume":"12 10","pages":""},"PeriodicalIF":5.2000,"publicationDate":"2024-10-17","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11512408/pdf/","citationCount":"0","resultStr":"{\"title\":\"<i>Klebsiella pneumoniae</i> Lipopolysaccharide as a Vaccine Target and the Role of Antibodies in Protection from Disease.\",\"authors\":\"Jernelle C Miller, Alan S Cross, Sharon M Tennant, Scott M Baliban\",\"doi\":\"10.3390/vaccines12101177\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><p><i>Klebsiella pneumoniae</i> is well recognized as a serious cause of infection in healthcare-associated settings and immunocompromised individuals; however, accumulating evidence from resource-limited nations documents an alarming rise in community-acquired <i>K</i>. <i>pneumoniae</i> infections, manifesting as bacteremia and pneumonia as well as neonatal sepsis. The emergence of hypervirulent and antibiotic-resistant <i>K</i>. <i>pneumoniae</i> strains threatens treatment options for clinicians. Effective vaccination strategies could represent a viable alternative that would both preempt the need for antibiotics to treat <i>K</i>. <i>pneumoniae</i> infections and reduce the burden of <i>K</i>. <i>pneumoniae</i> disease globally. There are currently no approved <i>K. pneumoniae</i> vaccines. We review the evidence for <i>K</i>. <i>pneumoniae</i> lipopolysaccharide (LPS) as a vaccine and immunotherapeutic target and discuss the role of antibodies specific for the core or O-antigen determinants within LPS in protection against <i>Klebsiella</i> spp. disease. We expand on the known role of the <i>Klebsiella</i> spp. capsule and O-antigen modifications in antibody surface accessibility to LPS as well as the in vitro and in vivo effector functions reported for LPS-specific antibodies. We summarize key hypotheses stemming from these studies, review the role of humoral immunity against <i>K</i>. <i>pneumoniae</i> O-antigen for protection, and identify areas requiring further research.</p>\",\"PeriodicalId\":23634,\"journal\":{\"name\":\"Vaccines\",\"volume\":\"12 10\",\"pages\":\"\"},\"PeriodicalIF\":5.2000,\"publicationDate\":\"2024-10-17\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11512408/pdf/\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Vaccines\",\"FirstCategoryId\":\"3\",\"ListUrlMain\":\"https://doi.org/10.3390/vaccines12101177\",\"RegionNum\":3,\"RegionCategory\":\"医学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q1\",\"JCRName\":\"IMMUNOLOGY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Vaccines","FirstCategoryId":"3","ListUrlMain":"https://doi.org/10.3390/vaccines12101177","RegionNum":3,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"IMMUNOLOGY","Score":null,"Total":0}
引用次数: 0
摘要
众所周知,肺炎克雷伯菌是导致医疗相关环境和免疫力低下人群感染的严重病因;然而,来自资源有限国家的大量证据表明,社区获得性肺炎克雷伯菌感染呈惊人上升趋势,表现为菌血症、肺炎和新生儿败血症。高病毒性和抗生素耐药肺炎克氏菌菌株的出现威胁着临床医生的治疗方案。有效的疫苗接种策略是一种可行的替代方案,既能避免使用抗生素治疗肺炎克氏菌感染,又能减轻全球肺炎克氏菌疾病的负担。目前还没有获得批准的肺炎克氏杆菌疫苗。我们回顾了肺炎克雷伯菌脂多糖(LPS)作为疫苗和免疫治疗靶点的证据,并讨论了针对 LPS 核心抗原或 O 抗原决定簇的特异性抗体在预防克雷伯菌属疾病中的作用。我们阐述了已知的克雷伯氏菌菌囊和 O 抗原修饰在抗体表面对 LPS 的可及性中的作用,以及已报道的 LPS 特异性抗体的体外和体内效应功能。我们总结了这些研究提出的关键假设,回顾了体液免疫对肺炎克雷伯菌 O 抗原的保护作用,并确定了需要进一步研究的领域。
Klebsiella pneumoniae Lipopolysaccharide as a Vaccine Target and the Role of Antibodies in Protection from Disease.
Klebsiella pneumoniae is well recognized as a serious cause of infection in healthcare-associated settings and immunocompromised individuals; however, accumulating evidence from resource-limited nations documents an alarming rise in community-acquired K. pneumoniae infections, manifesting as bacteremia and pneumonia as well as neonatal sepsis. The emergence of hypervirulent and antibiotic-resistant K. pneumoniae strains threatens treatment options for clinicians. Effective vaccination strategies could represent a viable alternative that would both preempt the need for antibiotics to treat K. pneumoniae infections and reduce the burden of K. pneumoniae disease globally. There are currently no approved K. pneumoniae vaccines. We review the evidence for K. pneumoniae lipopolysaccharide (LPS) as a vaccine and immunotherapeutic target and discuss the role of antibodies specific for the core or O-antigen determinants within LPS in protection against Klebsiella spp. disease. We expand on the known role of the Klebsiella spp. capsule and O-antigen modifications in antibody surface accessibility to LPS as well as the in vitro and in vivo effector functions reported for LPS-specific antibodies. We summarize key hypotheses stemming from these studies, review the role of humoral immunity against K. pneumoniae O-antigen for protection, and identify areas requiring further research.
VaccinesPharmacology, Toxicology and Pharmaceutics-Pharmacology
CiteScore
8.90
自引率
16.70%
发文量
1853
审稿时长
18.06 days
期刊介绍:
Vaccines (ISSN 2076-393X) is an international, peer-reviewed open access journal focused on laboratory and clinical vaccine research, utilization and immunization. Vaccines publishes high quality reviews, regular research papers, communications and case reports.