Group A Streptococcal Carriage and Seroepidemiology in Children up to 10 Years of Age in Australia

被引:13
|
作者
Marshall, Helen S. [1 ,2 ,3 ]
Richmond, Peter [4 ,5 ]
Nissen, Michael [6 ,7 ]
Lambert, Stephen [6 ,7 ]
Booy, Robert [8 ,9 ]
Reynolds, Graham [10 ]
Sebastian, Shite [11 ]
Pride, Michael [11 ]
Jansen, Kathrin U. [11 ]
Anderson, Annaliesa S. [11 ]
Scully, Ingrid L. [11 ]
机构
[1] Womens & Childrens Hosp, Vaccinol & Immunol Res Trials Unit, Adelaide, SA 5006, Australia
[2] Univ Adelaide, Sch Paediat & Reprod Hlth, Adelaide, SA, Australia
[3] Univ Adelaide, Robinson Res Inst, Adelaide, SA, Australia
[4] Univ Western Australia, Sch Paediat & Child Hlth, Subiaco, WA, Australia
[5] Telethon Kids Inst, Wesfarmers Ctr Vaccines & Infect Dis, Vaccine Trials Grp, Subiaco, WA, Australia
[6] Queensland Childrens Med Res Inst, Queensland Paediat Infect Dis Lab, Brisbane, Qld, Australia
[7] Univ Queensland, Royal Childrens Hosp, Brisbane, Qld, Australia
[8] Childrens Hosp Westmead, Natl Ctr Immunisat Res & Surveillance Vaccine Pre, Westmead, NSW, Australia
[9] Univ Sydney, Marie Bashir Inst, Sydney, NSW 2006, Australia
[10] ANU Med Sch, Canberra Hosp, Dept Paediat & Child Hlth, Canberra, ACT, Australia
[11] Pfizer Vaccine Res, Pearl River, NY USA
关键词
Group A streptococcus; carriage; anti-streptococcal C5a peptidase gene; GAS vaccines; acute rheumatic fever; children; BETA-HEMOLYTIC STREPTOCOCCI; ACUTE POSTSTREPTOCOCCAL GLOMERULONEPHRITIS; IMMUNE-RESPONSE; C5A PEPTIDASE; NORTHERN-TERRITORY; UNITED-STATES; M-PROTEIN; VACCINE; EPIDEMIOLOGY; DISEASE;
D O I
10.1097/INF.0000000000000745
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Background: Group A streptococci (GAS) and other -hemolytic streptococci (BHS) cause pharyngitis, severe invasive disease and serious nonsuppurative sequelae including rheumatic heart disease and post streptococcal glomerulonephritis. The aim of this study was to assess carriage rates and anti-streptococcal C5a peptidase (anti-SCP) IgG levels and identify epidemiologic factors related to carriage or seropositivity in Australian children. Methods: A throat swab and blood sample were collected for microbiological and serological analysis (anti-SCP IgG) in 542 healthy children aged 0-10 years. Sequence analysis of the SCP gene was performed. Serological analysis used a competitive Luminex Immunoassay designed to preferentially detect functional antibody. Results: GAS-positive culture prevalence in throat swabs was 5.0% (range 0-10%), with the highest rate in 5 and 9 years old children. The rate of non-GAS BHS carriage was low (<1%). The scp gene was present in all 22 isolates evaluated. As age of child increased, the rate of carriage increased; odds ratio, 1.14 (1.00, 1.29); P = 0.50. Geometric mean anti-SCP titers increased with each age-band from 2 to 7 years, then plateaued. Age, geographic location and number of children within the household were significantly associated with the presence of anti-SCP antibodies. Conclusions: Children are exposed to GAS and other BHS at a young age, which is important for determining the target age for vaccination to protect before the period of risk.
引用
收藏
页码:831 / 838
页数:8
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