دورية أكاديمية

IL-12 induces monocyte IL-18 binding protein expression via IFN-gamma.

التفاصيل البيبلوغرافية
العنوان: IL-12 induces monocyte IL-18 binding protein expression via IFN-gamma.
المؤلفون: Veenstra KG; Department of Medicine, Division of Hematology/Oncology, Beth Israel Deaconess Medical Center, Harvard Medical School, 330 Brookline Avenue, Boston, MA 02215, USA., Jonak ZL, Trulli S, Gollob JA
المصدر: Journal of immunology (Baltimore, Md. : 1950) [J Immunol] 2002 Mar 01; Vol. 168 (5), pp. 2282-7.
نوع المنشور: Journal Article; Research Support, Non-U.S. Gov't; Research Support, U.S. Gov't, P.H.S.
اللغة: English
بيانات الدورية: Publisher: American Association of Immunologists Country of Publication: United States NLM ID: 2985117R Publication Model: Print Cited Medium: Print ISSN: 0022-1767 (Print) Linking ISSN: 00221767 NLM ISO Abbreviation: J Immunol Subsets: MEDLINE
أسماء مطبوعة: Publication: Bethesda, MD : American Association of Immunologists
Original Publication: Baltimore : Williams & Wilkins, c1950-
مواضيع طبية MeSH: Transcriptional Activation*, Glycoproteins/*biosynthesis , Interferon-gamma/*physiology , Interleukin-12/*pharmacology , Monocytes/*immunology, Antibodies/pharmacology ; Cells, Cultured ; Cytokines/pharmacology ; Glycoproteins/genetics ; Humans ; Intercellular Signaling Peptides and Proteins ; Interferon-gamma/antagonists & inhibitors ; Interferon-gamma/immunology ; Interleukin-12/therapeutic use ; Killer Cells, Natural/immunology ; Kinetics ; Monocytes/drug effects ; Neoplasms/drug therapy ; Neoplasms/immunology ; RNA, Messenger/biosynthesis ; Th1 Cells/immunology
مستخلص: IL-18 is a Th1 cytokine that synergizes with IL-12 and IL-2 in the stimulation of lymphocyte IFN-gamma production. IL-18 binding protein (IL-18BP) is a recently discovered inhibitor of IL-18 that is distinct from the IL-1 and IL-18 receptor families. In this report we show that IL-18BPa, the IL-18BP isoform with the highest affinity for IL-18, was strongly induced by IL-12 in human PBMC. Other Th1 cytokines, including IFN-gamma, IL-2, IL-15, and IL-18, were also capable of augmenting IL-18BPa expression. In contrast, IL-1alpha, IL-1beta, TNF-alpha, IFN-gamma-inducible protein-10, and Th2 cytokines such as IL-4 and IL-10 did not induce IL-18BPa. Although monocytes were found to be the primary source of IL-18BPa, the induction of IL-18BPa by IL-12 was mediated through IFN-gamma derived predominantly from NK cells. IL-18BPa production was observed in cancer patients receiving recombinant human IL-12 and correlated with the magnitude of IFN-gamma production. The IFN-gamma/IL-18BPa negative feedback loop identified in this study may be capable of broadly controlling immune activation by cytokines that synergize with IL-18 to induce IFN-gamma and probably plays a key role in the modulation of both innate and adaptive immunity.
معلومات مُعتمدة: K23 RR 15541-02 United States RR NCRR NIH HHS
المشرفين على المادة: 0 (Antibodies)
0 (Cytokines)
0 (Glycoproteins)
0 (Intercellular Signaling Peptides and Proteins)
0 (RNA, Messenger)
0 (interleukin-18 binding protein)
187348-17-0 (Interleukin-12)
82115-62-6 (Interferon-gamma)
تواريخ الأحداث: Date Created: 20020223 Date Completed: 20020315 Latest Revision: 20190515
رمز التحديث: 20231215
DOI: 10.4049/jimmunol.168.5.2282
PMID: 11859116
قاعدة البيانات: MEDLINE
الوصف
تدمد:0022-1767
DOI:10.4049/jimmunol.168.5.2282