design and evaluation of meningococcal vaccines through structure-based modification of host and pathogen molecules脑膜炎球菌疫苗的设计和评价通过基于结构修改宿主和病原体分子.pdfVIP

design and evaluation of meningococcal vaccines through structure-based modification of host and pathogen molecules脑膜炎球菌疫苗的设计和评价通过基于结构修改宿主和病原体分子.pdf

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design and evaluation of meningococcal vaccines through structure-based modification of host and pathogen molecules脑膜炎球菌疫苗的设计和评价通过基于结构修改宿主和病原体分子

Design and Evaluation of Meningococcal Vaccines through Structure-Based Modification of Host and Pathogen Molecules Steven Johnson1., Lionel Tan2., Stijn van der Veen1., Joseph Caesar1., Elena Goicoechea De Jorge3., 1. 4 1 1 2 2 Rachel J. Harding , Xilian Bai , Rachel M. Exley , Philip N. Ward , Nicola Ruivo , Kaushali Trivedi , 1 1 1 5 6 4 Elspeth Cumber , Rhian Jones , Luke Newham , David Staunton , Rafael Ufret-Vincenty , Ray Borrow , 3 1 1,2 Matthew C. Pickering *, Susan M. Lea *, Christoph M. Tang * 1 Sir William Dunn School of Pathology, University of Oxford, Oxford, United Kingdom, 2 Centre for Molecular Microbiology and Infection, Imperial College, London, United Kingdom, 3 Centre for Complement and Inflammation Research (CCIR), Department of Medicine, Imperial College, London, United Kingdom, 4 Vaccine Evaluation Unit, Public Health Laboratory, Manchester Medical Microbiology Partnership, Manchester, United Kingdom, 5 Department of Biochemistry, University of Oxford, Oxford, United Kingdom, 6 Department of Ophthalmology, UT Southwestern Medical Center, Dallas, Texas, United States of America Abstract Neisseria meningitis remains a leading cause of sepsis and meningitis, and vaccines are required to prevent infections by this important human pathogen. Factor H binding protein (fHbp) is a key antigen that elicits protective immunity against the meningococcus and recruits the host complement regulator, fH. As the high affinity interaction between fHbp and fH could

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