Systematic Review of Group A Streptococcal emm Types Associated with Acute Post-Streptococcal Glomerulonephritis

被引:20
作者
Worthing, Kate A. [1 ]
Lacey, Jake A. [2 ]
Price, David J. [3 ,4 ]
McIntyre, Liam [1 ]
Steer, Andrew C. [5 ]
Tong, Steven Y. C. [6 ,7 ]
Davies, Mark R. [1 ]
机构
[1] Univ Melbourne, Peter Doherty Inst Infect & Immun, Dept Microbiol & Immunol, 792 Elizabeth St, Melbourne, Vic 3000, Australia
[2] Univ Melbourne, Peter Doherty Inst Infect & Immun, Doherty Dept, Melbourne, Vic, Australia
[3] Univ Melbourne, Peter Doherty Inst Infect & Immun, Victorian Infect Dis Reference Lab, Epidemiol Unit, Melbourne, Vic, Australia
[4] Univ Melbourne, Melbourne Sch Populat & Global Hlth, Ctr Epidemiol & Biostat, Melbourne, Vic, Australia
[5] Murdoch Childrens Res Inst, Trop Dis Res Grp, Melbourne, Vic, Australia
[6] Univ Melbourne, Peter Doherty Inst Infect & Immun, Royal Melbourne Hosp, Victorian Infect Dis Serv,Doherty Dept, Melbourne, Vic, Australia
[7] Menzies Sch Hlth Res, Darwin, NT, Australia
基金
英国医学研究理事会; 澳大利亚国家健康与医学研究理事会;
关键词
EPIDEMIC ACUTE NEPHRITIS; M-PROTEIN; GLOBAL BURDEN; REAPPEARANCE; SEROTYPES;
D O I
10.4269/ajtmh.18-0827
中图分类号
R1 [预防医学、卫生学];
学科分类号
1004 ; 120402 ;
摘要
Acute post-streptococcal glomerulonephritis (APSGN) is a postinfectious immune-mediated kidney disease associated with group A Streptococcus (GAS). The prevalence of APSGN varies within and between countries and is influenced by socioeconomic, host, and bacterial factors. The disease is more prevalent in developing countries and resource-poor settings of developed countries, such as the Indigenous populations residing in tropical Australia. The M-protein is a universally present GAS surface antigen that is the focus of molecular typing and vaccine research. Early reports suggested that some M-proteins (emm types) are more likely to cause APSGN than others. Here, we present the first systematic review of the global distribution of APSGN-associated GAS emm types. There were 46 emm types among the 676 cases described in 15 reviewed articles. Only 43% APSGN cases would have had theoretical coverage from the experimental M protein-based GAS vaccine. Vaccine coverage was higher in regions such as North America (97%) and the United Kingdom (98%) than Africa (67%) and Australia (38%). Variable vaccine coverage against APSGN-associated emm types highlights the need for further research into this disease, particularly in settings of poverty, where APSGN prevalence is higher. Three GAS emm types (emm49, emm60, and emm55) consistently occur in APSGN cases around the world. Future studies would therefore benefit from examining the genomic epidemiology of these emm types to unravel potential markers of APSGN.
引用
收藏
页码:1066 / 1070
页数:5
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