SARS-CoV-2-specific T cell responses and immune regulation in infected pregnant women.
SARS-CoV-2-specific T cell responses and immune regulation in infected pregnant women.
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DOI:
10.1016/j.jri.2021.103464
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发表时间:
2022-03
影响因子:
3.4
通讯作者:
Franco A
中科院分区:
文献类型:
--
作者:
Hsieh LE;Grifoni A;Dave H;Wang J;Johnson D;Zellner J;Sidney J;Chambers C;Franco A
We studied the T cell response to SARS-CoV-2 spike and non-spike peptide epitopes in eight convalescent pregnant women together with the immune monitoring that included innate tolerogenic dendritic cell populations important to maintain the immunological mother/fetus interface to address a potential risk for the antiviral cellular response in the outcome of pregnancy. Four subjects had pre-existing chronic inflammatory conditions that could have potentially affected the SARS-CoV-2-specific T cell response. Seven of eight subjects responded to SARS-CoV-2 peptides with differences within CD4+ T helper (Th) and CD8+ cytotoxic T cells (CTL). SARS-CoV-2-specific inducible regulatory T cells (iTreg) were numerous in circulation. CD4+ T cell memory included central memory T cells (TCM) and effector memory (TEM). As far as the CD8+ memory repertoire, TCM and TEM were very low or absent in eight of eight subjects and only effector cells that revert to CD45RA+, defined as TEMRA were measurable in circulation. T cells were in the normal range in all subjects regardless of pre-existing inflammatory conditions. The immune phenotype indicated the expansion and activation of tolerogenic myeloid dendritic cells including CD14+ cDC2 and CD4+ ILT-4+ tmDC. In summary, SARS-CoV-2 infection induced a physiological anti-viral T cell response in pregnant women that included SARS-CoV-2-specific iTreg with no negative effects on the tolerogenic innate dendritic cell repertoire relevant to the immune homeostasis of the maternal-fetal interface. All eight subjects studied delivered full-term, healthy infants.
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影响因子:
10.1
作者:
Amodio, Giada;Comi, Michela;Gregori, Silvia
通讯作者:
Gregori, Silvia
影响因子:
7.3
作者:
Gregori S;Amodio G;Quattrone F;Panina-Bordignon P
通讯作者:
Panina-Bordignon P
影响因子:
3.7
作者:
Chambers, Christina D.;Johnson, Diana L.;Jones, Kenneth Lyons
通讯作者:
Jones, Kenneth Lyons
DOI:
10.15585/mmwr.mm6938e1
发表时间:
2020-09-25
期刊:
MMWR. Morbidity and mortality weekly report
影响因子:
--
作者:
Delahoy MJ;Whitaker M;O'Halloran A;Chai SJ;Kirley PD;Alden N;Kawasaki B;Meek J;Yousey-Hindes K;Anderson EJ;Openo KP;Monroe ML;Ryan PA;Fox K;Kim S;Lynfield R;Siebman S;Davis SS;Sosin DM;Barney G;Muse A;Bennett NM;Felsen CB;Billing LM;Shiltz J;Sutton M;West N;Schaffner W;Talbot HK;George A;Spencer M;Ellington S;Galang RR;Gilboa SM;Tong VT;Piasecki A;Brammer L;Fry AM;Hall AJ;Wortham JM;Kim L;Garg S;COVID-NET Surveillance Team
通讯作者:
COVID-NET Surveillance Team
DOI:
10.1038/s41577-020-00460-4
发表时间:
2020-11
期刊:
Nature reviews. Immunology
影响因子:
--
作者:
Lipsitch M;Grad YH;Sette A;Crotty S
通讯作者:
Crotty S