Airway Epithelial Innate Immunity.
Airway Epithelial Innate Immunity.
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DOI:
10.3389/fphys.2021.749077
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发表时间:
2021
影响因子:
4
通讯作者:
Dickey BF
中科院分区:
文献类型:
--
作者:
Johnston SL;Goldblatt DL;Evans SE;Tuvim MJ;Dickey BF
Besides providing an essential protective barrier, airway epithelial cells directly sense pathogens and respond defensively. This is a frontline component of the innate immune system with specificity for different pathogen classes. It occurs in the context of numerous interactions with leukocytes, but here we focus on intrinsic epithelial mechanisms. Type 1 immune responses are directed primarily at intracellular pathogens, particularly viruses. Prominent stimuli include microbial nucleic acids and interferons released from neighboring epithelial cells. Epithelial responses revolve around changes in the expression of interferon-sensitive genes (ISGs) that interfere with viral replication, as well as the further induction of interferons that signal in autocrine and paracrine manners. Type 2 immune responses are directed primarily at helminths and fungi. Prominent pathogen stimuli include proteases and chitin, and important responses include mucin hypersecretion and chitinase release. Type 3 immune responses are directed primarily at extracellular microbial pathogens, including bacteria and fungi, as well as viruses during their extracellular phase of infection. Prominent microbial stimuli include bacterial wall components, such as lipopeptides and endotoxin, as well as microbial nucleic acids. Key responses are the release of reactive oxygen species (ROS) and antimicrobial peptides (AMPs). For all three types of response, paracrine signaling to neighboring epithelial cells induces resistance to infection over a wide field. Often, the epithelial effector molecules themselves also have signaling properties, in addition to the release of inflammatory cytokines that boost local innate immunity. Together, these epithelial mechanisms provide a powerful first line of pathogen defense, recruit leukocytes, and instruct adaptive immune responses.
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DOI:
10.1056/nejmra0910061
发表时间:
2010-12-02
期刊:
The New England journal of medicine
影响因子:
--
作者:
Fahy JV;Dickey BF
通讯作者:
Dickey BF
DOI:
10.1016/s2213-2600(20)30566-x
发表时间:
2021-05
期刊:
The Lancet. Respiratory medicine
影响因子:
--
作者:
Feld JJ;Kandel C;Biondi MJ;Kozak RA;Zahoor MA;Lemieux C;Borgia SM;Boggild AK;Powis J;McCready J;Tan DHS;Chan T;Coburn B;Kumar D;Humar A;Chan A;O'Neil B;Noureldin S;Booth J;Hong R;Smookler D;Aleyadeh W;Patel A;Barber B;Casey J;Hiebert R;Mistry H;Choong I;Hislop C;Santer DM;Lorne Tyrrell D;Glenn JS;Gehring AJ;Janssen HLA;Hansen BE
通讯作者:
Hansen BE
影响因子:
15.3
作者:
Campbell, Laura;Hepworth, Matthew R.;Grencis, Richard K.
通讯作者:
Grencis, Richard K.
DOI:
10.1164/rccm.201312-2235oc
发表时间:
2014-07-15
影响因子:
24.7
作者:
Djukanovic, Ratko;Harrison, Tim;Monk, Phillip
通讯作者:
Monk, Phillip
DOI:
10.1126/science.1227091
发表时间:
2012-08-24
期刊:
Science (New York, N.Y.)
影响因子:
--
作者:
Dickey BF
通讯作者:
Dickey BF