دورية أكاديمية

IL-18–induced CD83+ CCR7+ NK helper cells

التفاصيل البيبلوغرافية
العنوان: IL-18–induced CD83+ CCR7+ NK helper cells
المؤلفون: Mailliard, Robbie B., Alber, Sean M., Shen, Hongmei, Watkins, Simon C., Kirkwood, John M., Herberman, Ronald B., Kalinski, Pawel
المصدر: The Journal of Experimental Medicine ; volume 202, issue 7, page 941-953 ; ISSN 1540-9538 0022-1007
بيانات النشر: Rockefeller University Press
سنة النشر: 2005
الوصف: In addition to their cytotoxic activities, natural killer (NK) cells can have immunoregulatory functions. We describe a distinct “helper” differentiation pathway of human CD56+CD3− NK cells into CD56+/CD83+/CCR7+/CD25+ cells that display high migratory responsiveness to lymph node (LN)–associated chemokines, high ability to produce interferon-γ upon exposure to dendritic cell (DC)- or T helper (Th) cell–related signals, and pronounced abilities to promote interleukin (IL)-12p70 production in DCs and the development of Th1 responses. This helper pathway of NK cell differentiation, which is not associated with any enhancement of cytolytic activity, is induced by IL-18, but not other NK cell–activating factors. It is blocked by prostaglandin (PG)E2, a factor that induces a similar CD83+/CCR7+/CD25+ LN-homing phenotype in maturing DCs. The current data demonstrate independent regulation of the “helper” versus “effector” pathways of NK cell differentiation and novel mechanisms of immunoregulation by IL-18 and PGE2.
نوع الوثيقة: article in journal/newspaper
اللغة: English
DOI: 10.1084/jem.20050128
الإتاحة: https://doi.org/10.1084/jem.20050128Test
https://rupress.org/jem/article-pdf/202/7/941/1719058/jem2027941.pdfTest
رقم الانضمام: edsbas.C7F2A97D
قاعدة البيانات: BASE