Global epidemiology of serogroup B meningococcal disease and opportunities for prevention with novel recombinant protein vaccines

被引:43
作者
Villena, Rodolfo [1 ]
Safadi, Marco Aurelio P. [2 ]
Valenzuela, Maria Teresa [3 ]
Torres, Juan P. [4 ]
Finn, Adam [5 ,6 ]
O'Ryan, Miguel [7 ,8 ]
机构
[1] Univ Chile, Fac Med, Hosp Ninos Exequiel Gonzalez Cortes, Dept Pediat, Santiago, Chile
[2] Santa Casa Sao Paulo Sch Med Sci, Dept Pediat, Sao Paulo, Brazil
[3] Univ Los Andes, Dept Epidemiol & Publ Hlth, Santiago, Chile
[4] Univ Chile, Fac Med, Dept Pediat, Hosp Luis Calvo Mackenna, Santiago, Chile
[5] Univ Bristol, Bristol Childrens Vaccine Ctr, Sch Cellular & Mol Med, Bristol, Avon, England
[6] Univ Bristol, Sch Populat Hlth Sci, Bristol Childrens Vaccine Ctr, Bristol, Avon, England
[7] Univ Chile, Fac Med, Inst Ciencias Biomed, Programa Microbiol & Micol, Santiago, Chile
[8] Univ Chile, Fac Med, Inst Milenio Inmunol & Inmunoterapia, Santiago, Chile
关键词
Neisseria meningitidis; epidemiology; meningococcal serogroup B; meningococcal vaccines; outbreaks; RANDOMIZED CONTROLLED-TRIAL; TO; 10; YEARS; NEISSERIA-MENINGITIDIS; BIVALENT RLP2086; 4CMENB VACCINE; YOUNG-ADULTS; IMMUNIZATION PRACTICES; OBSERVATIONAL COHORT; HEALTHY ADOLESCENTS; ADVISORY-COMMITTEE;
D O I
10.1080/21645515.2018.1458175
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Background: Meningococcal disease (MD) is a major cause of meningitis and sepsis worldwide, with a high case fatality rate and frequent sequelae. Neisseria meningitidis serogroups A, B, C, W, X and Y are responsible for most of these life-threatening infections, and its unpredictable epidemiology can cause outbreaks in communities, with significant health, social and economic impact. Currently, serogroup B is the main cause of MD in Europe and North America and one of the most prevalent serogroups in Latin America. Mass vaccination strategies using polysaccharide vaccines have been deployed since the 1970s and the use of conjugate vaccines has controlled endemic and epidemic disease caused by serogroups A, C, W and Y and more recently serogroup B using geographically-specific outer membrane vesicle based vaccines. Two novel protein-based vaccines are a significant addition to our armamentarium against N. meningitidis as they provide broad coverage against highly diverse strains in serogroup B and other groups. Early safety, effectiveness and impact data of these vaccines are encouraging. These novel serogroup B vaccines should be actively considered for individuals at increased risk of disease and to control serogroup B outbreaks occurring in institutions or specific regions, as they are likely to save lives and prevent severe sequelae. Incorporation into national programs will require thorough country-specific analysis.
引用
收藏
页码:1042 / 1057
页数:16
相关论文
共 122 条
[81]   A Multi-Component Meningococcal Serogroup B Vaccine (4CMenB): The Clinical Development Program [J].
O'Ryan, Miguel ;
Stoddard, Jeffrey ;
Toneatto, Daniela ;
Wassil, James ;
Dull, Peter M. .
DRUGS, 2014, 74 (01) :15-30
[82]   A Bivalent Meningococcal B Vaccine in Adolescents and Young Adults [J].
Ostergaard, Lars ;
Vesikari, Timo ;
Absalon, Judith ;
Beeslaar, Johannes ;
Ward, Brian J. ;
Senders, Shelly ;
Eiden, Joseph J. ;
Jansen, Kathrin U. ;
Anderson, Annaliesa S. ;
York, Laura J. ;
Jones, Thomas R. ;
Harris, Shannon L. ;
O'Neill, Robert ;
Radley, David ;
Maansson, Roger ;
Pregaldien, Jean-Louis ;
Ginis, John ;
Staerke, Nina B. ;
Perez, John L. .
NEW ENGLAND JOURNAL OF MEDICINE, 2017, 377 (24) :2349-2362
[83]   A phase 3, randomized, active-controlled study to assess the safety and tolerability of meningococcal serogroup B vaccine bivalent rLP2086 in healthy adolescents and young adults [J].
Ostergaard, Lars ;
Lucksinger, Gregg H. ;
Absalon, Judith ;
Beeslaar, Johannes ;
Eiden, Joseph ;
Jansen, Kathrin U. ;
York, Laura J. ;
Quinn, Angela ;
Graversen, Mette E. ;
Perez, John L. .
VACCINE, 2016, 34 (12) :1465-1471
[84]  
Parikh SR, 2017, LANCET INFECT DIS, V3099, P1
[85]   Effectiveness and impact of a reduced infant schedule of 4CMenB vaccine against group B meningococcal disease in England: a national observational cohort study [J].
Parikh, Sydel R. ;
Andrews, Nick J. ;
Beebeejaun, Kazim ;
Campbell, Helen ;
Ribeiro, Sonia ;
Ward, Charlotte ;
White, Joanne M. ;
Borrow, Ray ;
Ramsay, Mary E. ;
Ladhani, Shamez N. .
LANCET, 2016, 388 (10061) :2775-2782
[86]   Updated Recommendations for Use of MenB-FHbp Serogroup B Meningococcal Vaccine - Advisory Committee on Immunization Practices, 2016 [J].
Patton, Monica E. ;
Stephens, David ;
Moore, Kelly ;
MacNeil, Jessica R. .
MMWR-MORBIDITY AND MORTALITY WEEKLY REPORT, 2017, 66 (19) :509-513
[87]   A phase 2 randomized controlled trial of a multicomponent meningococcal serogroup B vaccine (I) Effects of prophylactic paracetamol on immunogenicity and reactogenicity of routine infant vaccines and 4CMenB [J].
Prymula, Roman ;
Esposito, Susanna ;
Zuccotti, Gian Vincenzo ;
Xie, Fang ;
Toneatto, Daniela ;
Kohl, Igor ;
Dull, Peter M. .
HUMAN VACCINES & IMMUNOTHERAPEUTICS, 2014, 10 (07) :1993-2004
[88]   Reverse vaccinology 2.0: Human immunology instructs vaccine antigen design [J].
Rappuoli, Rino ;
Bottomley, Matthew J. ;
D'Oro, Ugo ;
Finco, Oretta ;
De Gregorio, Ennio .
JOURNAL OF EXPERIMENTAL MEDICINE, 2016, 213 (04) :469-481
[89]   Effect of a quadrivalent meningococcal ACWY glycoconjugate or a serogroup B meningococcal vaccine on meningococcal carriage: an observer-blind, phase 3 randomised clinical trial [J].
Read, Robert C. ;
Baxter, David ;
Chadwick, David R. ;
Faust, Saul N. ;
Finn, Adam ;
Gordon, Stephen B. ;
Heath, Paul T. ;
Lewis, David J. M. ;
Pollard, Andrew J. ;
Turner, David P. J. ;
Bazaz, Rohit ;
Ganguli, Amitava ;
Havelock, Tom ;
Neal, Keith R. ;
Okike, Ifeanyichukwu O. ;
Morales-Aza, Begonia ;
Patel, Kamlesh ;
Snape, Matthew D. ;
Williams, John ;
Gilchrist, Stefanie ;
Gray, Steve J. ;
Maiden, Martin C. J. ;
Toneatto, Daniela ;
Wang, Huajun ;
McCarthy, Maggie ;
Dull, Peter M. ;
Borrow, Ray .
LANCET, 2014, 384 (9960) :2123-2131
[90]  
Richmond PC, 2012, LANCET, V3099, P1