Phenotypical characterization of regulatory T cells in acute Zika infection.
Phenotypical characterization of regulatory T cells in acute Zika infection.
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DOI:
10.1016/j.cyto.2021.155651
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发表时间:
2021-10
期刊:
影响因子:
3.8
通讯作者:
Keesen TSL
中科院分区:
文献类型:
--
作者:
Guerra-Gomes IC;Gois BM;Peixoto RF;Palmeira PHS;Dias CNS;Csordas BG;Araújo JMG;Veras RC;de Medeiros IA;de Azevedo FLAA;Boyton RJ;Altmann DM;Keesen TSL
Zika virus (ZIKV), alongside Dengue virus (DENV), Chikungunya virus (CHIKV), and Yellow Fever Virus (YFV) are prevalent arboviruses in the Americas. Each of these infections is associated with the development of associated disease immunopathology. Immunopathological processes are an outcome of counter-balancing impacts between effector and regulatory immune mechanisms. In this context, regulatory T cells (Tregs) are key in modulating the immune response and, therefore, in tissue damage control. However, to date, Treg phenotypes and mechanisms during acute infection of the ZIKV in humans have not been fully investigated. The main aim of this work was to characterize Tregs and their immunological profile related to cytokine production and molecules that are capable of controlling the exacerbated inflammatory profile in acute Zika infected patients. Using whole blood analyses of infected patients, an ex vivo phenotypical characterization of Tregs, circulating during acute Zika virus infection, was conducted by flow cytometry. We found that though there are no differences in absolute Treg frequency between infected and healthy control groups. However, pro-inflammatory cytokine up-regulation such as IFN-γ and LAP was observed in the acute disease. Furthermore, acute ZIKV patients expressed increased levels of CD39/CD73, perforin/granzyme B, PD-1, and CTLA-4, all markers involved in mechanisms used by Tregs to attempt to control strong inflammatory responses. Thus, the data indicates a potential contribution of Tregs during the inflammatory ZIKV infection response.
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影响因子:
6.7
作者:
Manangeeswaran M;Ireland DD;Verthelyi D
通讯作者:
Verthelyi D
DOI:
10.1093/cid/cix732
发表时间:
2018-01-06
期刊:
Clinical infectious diseases : an official publication of the Infectious Diseases Society of America
影响因子:
--
作者:
Lai L;Rouphael N;Xu Y;Natrajan MS;Beck A;Hart M;Feldhammer M;Feldpausch A;Hill C;Wu H;Fairley JK;Lankford-Turner P;Kasher N;Rago P;Hu YJ;Edupuganti S;Patel SM;Murray KO;Mulligan MJ;Emory Zika Patient Study Team
通讯作者:
Emory Zika Patient Study Team
影响因子:
5.4
作者:
Tappe D;Pérez-Girón JV;Zammarchi L;Rissland J;Ferreira DF;Jaenisch T;Gómez-Medina S;Günther S;Bartoloni A;Muñoz-Fontela C;Schmidt-Chanasit J
通讯作者:
Schmidt-Chanasit J
DOI:
10.1093/infdis/jiy225
发表时间:
2018-07-24
期刊:
The Journal of infectious diseases
影响因子:
--
作者:
Lum FM;Lye DCB;Tan JJL;Lee B;Chia PY;Chua TK;Amrun SN;Kam YW;Yee WX;Ling WP;Lim VWX;Pang VJX;Lee LK;Mok EWH;Chong CY;Leo YS;Ng LFP
通讯作者:
Ng LFP
影响因子:
4.6
作者:
Cimini, Eleonora;Castilletti, Concetta;Agrati, Chiara
通讯作者:
Agrati, Chiara