دورية أكاديمية

HCMV-controlling NKG2C+ NK cells originate from novel circulating inflammatory precursors.

التفاصيل البيبلوغرافية
العنوان: HCMV-controlling NKG2C+ NK cells originate from novel circulating inflammatory precursors.
المؤلفون: Bozzano, Federica, Della Chiesa, Mariella, Pelosi, Andrea, Antonini, Francesca, Ascierto, Maria Libera, Del Zotto, Genny, Moretta, Francesca, Muccio, Letizia, Luganini, Anna, Gribaudo, Giorgio, Cenderello, Giovanni, Dentone, Chiara, Nicolini, Laura, Moretta, Alessandro, Moretta, Lorenzo, De Maria, Andrea
المصدر: Journal of Allergy & Clinical Immunology; Jun2021, Vol. 147 Issue 6, p2343-2357, 15p
مستخلص: There is limited knowledge on the origin and development from CD34+ precursors of the ample spectrum of human natural killer (NK) cells, particularly of specialized NK subsets. This study sought to characterize the NK-cell progeny of CD34+DNAM-1brightCXCR4+ and of other precursors circulating in the peripheral blood of patients with chronic viral infections (eg, HIV, hepatitis C virus, cytomegalovirus reactivation). Highly purified precursors were obtained by flow cytometric sorting and cultured in standard NK-cell differentiation media (ie, SCF, FLT3, IL-7, IL-15). Phenotypic and functional analyses on progenies were performed by multiparametric cytofluorimetric assays. Transcriptional signatures of NK-cell progenies were studied by microarray analysis. Inhibition of cytomegalovirus replication was studied by PCR. Unlike conventional CD34+ precursors, LinCD34+DNAM-1brightCXCR4+ precursors from patients with chronic infection, rapidly differentiate into cytotoxic, IFN-γ–secreting CD94/NKG2C+KIR+CD57+ NK-cell progenies. An additional novel subset of common lymphocyte precursors was identified among LinCD34CD56CD16+ cells and characterized by expression of CXCR4 and lack of perforin and CD94. LinCD34CD56CD16+PerfCD94CXCR4+ precursors are also endowed with generation potential toward memory-like NKG2C+NK cells. Maturing NK-cell progenies mediated strong human cytomegalovirus–inhibiting activity. Microarray analysis confirmed a transcriptional signature compatible with NK-cell progenies and with maturing adaptive NK cells. During viral infections, precursors of adaptive NK cells are released and circulate in the peripheral blood. [Display omitted] [ABSTRACT FROM AUTHOR]
Copyright of Journal of Allergy & Clinical Immunology is the property of Elsevier B.V. and its content may not be copied or emailed to multiple sites or posted to a listserv without the copyright holder's express written permission. However, users may print, download, or email articles for individual use. This abstract may be abridged. No warranty is given about the accuracy of the copy. Users should refer to the original published version of the material for the full abstract. (Copyright applies to all Abstracts.)
قاعدة البيانات: Supplemental Index
الوصف
تدمد:00916749
DOI:10.1016/j.jaci.2020.12.648