Immune cellular networks underlying recovery from influenza virus infection in acute hospitalized patients.
Immune cellular networks underlying recovery from influenza virus infection in acute hospitalized patients.
复制标题
DOI:
10.1038/s41467-021-23018-x
复制
发表时间:
2021-05-11
影响因子:
16.6
通讯作者:
Kedzierska K
中科院分区:
文献类型:
--
作者:
Nguyen THO;Koutsakos M;van de Sandt CE;Crawford JC;Loh L;Sant S;Grzelak L;Allen EK;Brahm T;Clemens EB;Auladell M;Hensen L;Wang Z;Nüssing S;Jia X;Günther P;Wheatley AK;Kent SJ;Aban M;Deng YM;Laurie KL;Hurt AC;Gras S;Rossjohn J;Crowe J;Xu J;Jackson D;Brown LE;La Gruta N;Chen W;Doherty PC;Turner SJ;Kotsimbos TC;Thomas PG;Cheng AC;Kedzierska K
How innate and adaptive immune responses work in concert to resolve influenza disease is yet to be fully investigated in one single study. Here, we utilize longitudinal samples from patients hospitalized with acute influenza to understand these immune responses. We report the dynamics of 18 important immune parameters, related to clinical, genetic and virological factors, in influenza patients across different severity levels. Influenza disease correlates with increases in IL-6/IL-8/MIP-1α/β cytokines and lower antibody responses. Robust activation of circulating T follicular helper cells correlates with peak antibody-secreting cells and influenza heamaglutinin-specific memory B-cell numbers, which phenotypically differs from vaccination-induced B-cell responses. Numbers of influenza-specific CD8+ or CD4+ T cells increase early in disease and retain an activated phenotype during patient recovery. We report the characterisation of immune cellular networks underlying recovery from influenza infection which are highly relevant to other infectious diseases. The immunological parameters that define severe influenza disease are not clear within human real time infections. Here the authors compare a severe influenza infection cohort with an influenza vaccinated cohort to understand correlates of severe influenza disease.
登录
查看更多内容
影响因子:
8.8
作者:
Hall MW;Geyer SM;Guo CY;Panoskaltsis-Mortari A;Jouvet P;Ferdinands J;Shay DK;Nateri J;Greathouse K;Sullivan R;Tran T;Keisling S;Randolph AG;Pediatric Acute Lung Injury and Sepsis Investigators (PALISI) Network PICFlu Study Investigators
通讯作者:
Pediatric Acute Lung Injury and Sepsis Investigators (PALISI) Network PICFlu Study Investigators
影响因子:
4.1
作者:
Falfán-Valencia R;Narayanankutty A;Reséndiz-Hernández JM;Pérez-Rubio G;Ramírez-Venegas A;Nava-Quiroz KJ;Bautista-Félix NE;Vargas-Alarcón G;Castillejos-López MDJ;Hernández A
通讯作者:
Hernández A
影响因子:
3.7
作者:
Diao H;Cui G;Wei Y;Chen J;Zuo J;Cao H;Chen Y;Yao H;Tian Z;Li L
通讯作者:
Li L
DOI:
10.1126/science.1256427
发表时间:
2014-11-21
期刊:
Science (New York, N.Y.)
影响因子:
--
作者:
Fonville JM;Wilks SH;James SL;Fox A;Ventresca M;Aban M;Xue L;Jones TC;Le NMH;Pham QT;Tran ND;Wong Y;Mosterin A;Katzelnick LC;Labonte D;Le TT;van der Net G;Skepner E;Russell CA;Kaplan TD;Rimmelzwaan GF;Masurel N;de Jong JC;Palache A;Beyer WEP;Le QM;Nguyen TH;Wertheim HFL;Hurt AC;Osterhaus ADME;Barr IG;Fouchier RAM;Horby PW;Smith DJ
通讯作者:
Smith DJ
DOI:
10.1038/s41572-018-0002-y
发表时间:
2018-06-28
期刊:
Nature reviews. Disease primers
影响因子:
--
作者:
Krammer F;Smith GJD;Fouchier RAM;Peiris M;Kedzierska K;Doherty PC;Palese P;Shaw ML;Treanor J;Webster RG;García-Sastre A
通讯作者:
García-Sastre A