Effect of biannual azithromycin distribution on antibody responses to malaria, bacterial, and protozoan pathogens in Niger.
Effect of biannual azithromycin distribution on antibody responses to malaria, bacterial, and protozoan pathogens in Niger.
复制标题
DOI:
10.1038/s41467-022-28565-5
复制
发表时间:
2022-02-21
影响因子:
16.6
通讯作者:
MORDOR-Niger Study Group
中科院分区:
文献类型:
--
作者:
Arzika AM;Maliki R;Goodhew EB;Rogier E;Priest JW;Lebas E;O'Brien KS;Le V;Oldenburg CE;Doan T;Porco TC;Keenan JD;Lietman TM;Martin DL;Arnold BF;MORDOR-Niger Study Group
The MORDOR trial in Niger, Malawi, and Tanzania found that biannual mass distribution of azithromycin to children younger than 5 years led to a 13.5% reduction in all-cause mortality (NCT02048007). To help elucidate the mechanism for mortality reduction, we report IgG responses to 11 malaria, bacterial, and protozoan pathogens using a multiplex bead assay in pre-specified substudy of 30 communities in the rural Niger placebo-controlled trial over a three-year period (n = 5642 blood specimens, n = 3814 children ages 1–59 months). Mass azithromycin reduces Campylobacter spp. force of infection by 29% (hazard ratio = 0.71, 95% CI: 0.56, 0.89; P = 0.004) but serological measures show no significant differences between groups for other pathogens against a backdrop of high transmission. Results align with a recent microbiome study in the communities. Given significant sequelae of Campylobacter infection among preschool aged children, our results support an important mechanism through which biannual mass distribution of azithromycin likely reduces mortality in Niger. In a randomized placebo-controlled trial in rural Niger, biannual azithromycin distribution to children 1-59 months reduced all-cause mortality. Based on serology, Arzika et al. here report a reduction of Campylobacter infection, supporting one mechanism for the intervention’s impact on mortality.
登录
查看更多内容
DOI:
10.1016/s0140-6736(17)31758-0
发表时间:
2017-11-11
期刊:
Lancet (London, England)
影响因子:
--
作者:
Golding N;Burstein R;Longbottom J;Browne AJ;Fullman N;Osgood-Zimmerman A;Earl L;Bhatt S;Cameron E;Casey DC;Dwyer-Lindgren L;Farag TH;Flaxman AD;Fraser MS;Gething PW;Gibson HS;Graetz N;Krause LK;Kulikoff XR;Lim SS;Mappin B;Morozoff C;Reiner RC Jr;Sligar A;Smith DL;Wang H;Weiss DJ;Murray CJL;Moyes CL;Hay SI
通讯作者:
Hay SI
DOI:
10.1093/cid/ciw542
发表时间:
2016-11-01
期刊:
Clinical infectious diseases : an official publication of the Infectious Diseases Society of America
影响因子:
--
作者:
Amour C;Gratz J;Mduma E;Svensen E;Rogawski ET;McGrath M;Seidman JC;McCormick BJ;Shrestha S;Samie A;Mahfuz M;Qureshi S;Hotwani A;Babji S;Trigoso DR;Lima AA;Bodhidatta L;Bessong P;Ahmed T;Shakoor S;Kang G;Kosek M;Guerrant RL;Lang D;Gottlieb M;Houpt ER;Platts-Mills JA;Etiology, Risk Factors, and Interactions of Enteric Infections and Malnutrition and the Consequences for Child Health and Development Project (MAL-ED) Network Investigators
通讯作者:
Etiology, Risk Factors, and Interactions of Enteric Infections and Malnutrition and the Consequences for Child Health and Development Project (MAL-ED) Network Investigators
影响因子:
7.7
作者:
Knee J;Sumner T;Adriano Z;Anderson C;Bush F;Capone D;Casmo V;Holcomb D;Kolsky P;MacDougall A;Molotkova E;Braga JM;Russo C;Schmidt WP;Stewart J;Zambrana W;Zuin V;Nalá R;Cumming O;Brown J
通讯作者:
Brown J
DOI:
10.1111/j.2517-6161.1995.tb02031.x
发表时间:
1995-01-01
影响因子:
5.8
作者:
BENJAMINI, Y;HOCHBERG, Y
通讯作者:
HOCHBERG, Y
影响因子:
34.3
作者:
Kotloff, Karen L.;Nasrin, Dilruba;Levine, Myron M.
通讯作者:
Levine, Myron M.