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The Role of Serotype-Specific Immunological Memory in Pneumococcal Vaccination: Current Knowledge and Future Prospects

机译:血清型特异性免疫记忆在肺炎球菌疫苗接种中的作用:当前的知识和未来的前景。

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摘要

Streptococcus pneumoniae ( S. pneumoniae , pneumococcus) is a major cause of morbidity and mortality worldwide. Achieving long-term immunity against S. pneumoniae through immunization is an important public health priority. Long-term protection after immunization is thought to rely both on protective serum antibody levels and immunological memory in the form of antigen-specific memory B cells (MBCs). Although the ability to achieve protective antibody levels shortly after pneumococcal vaccination has been well documented for the various infant immunization schedules currently in use worldwide, the examination of immunological memory in the form of antigen-specific MBCs has been much more limited. Such responses are critical for long-term protection against pneumococcal colonization and disease. This review summarizes the published literature on the MBC response to primary or booster immunization with either pneumococcal polysaccharide vaccine (PPV23) or pneumococcal conjugate vaccines (PCVs), aiming to elucidate the immunological mechanisms that determine the magnitude and longevity of vaccine protection against pneumococcus. There is evidence that PCVs induce the production of antigen-specific MBCs, whereas immunization with PPV23 does not result in the formation of MBCs. Increased understanding of the immunological factors that facilitate the induction, maintenance and recall of MBCs in response to pneumococcal vaccination could enable the use of MBC enumeration as novel correlates of protection against S. pneumoniae . Ongoing studies that examine MBC response to pneumococcal vaccination in high burden settings will be extremely important in our understanding of long-term protection induced by pneumococcal conjugate vaccines.
机译:肺炎链球菌(肺炎链球菌,肺炎球菌)是全世界发病率和死亡率的主要原因。通过免疫获得针对肺炎链球菌的长期免疫是重要的公共卫生重点。免疫后的长期保护被认为既依赖于血清保护性抗体水平,又依赖于抗原特异性记忆B细胞(MBC)形式的免疫记忆。尽管肺炎球菌疫苗接种后不久即可达到保护性抗体水平的能力已在全球目前使用的各种婴儿免疫方案中得到了很好的证明,但以抗原特异性MBC形式进行的免疫记忆的检查受到了更大的限制。这种反应对于长期预防肺炎球菌定植和疾病至关重要。这篇综述总结了关于MBC对肺炎球菌多糖疫苗(PPV23)或肺炎球菌结合疫苗(PCV)初次或加强免疫的反应的文献,旨在阐明确定针对肺炎球菌的疫苗保护程度和寿命的免疫学机制。有证据表明PCV诱导了抗原特异性MBC的产生,而用PPV23免疫不会导致MBC的形成。对有助于肺炎球菌疫苗接种诱导,维持和召回MBC的免疫学因素的更多了解可以使MBC枚举成为抵抗肺炎链球菌的新型相关手段。正在进行的研究在高负荷情况下检查MBC对肺炎球菌疫苗接种的反应,对于我们理解由肺炎球菌结合疫苗诱导的长期保护非常重要。

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