دورية أكاديمية

Severe injury triggers antigen-specific T-helper cell dysfunction.

التفاصيل البيبلوغرافية
العنوان: Severe injury triggers antigen-specific T-helper cell dysfunction.
المؤلفون: Kelly JL; Department of Surgery (Immunology), Harvard Medical School/Brigham and Women's Hospital, Boston, MA 02115, USA., O'Suilleabhain CB, Soberg CC, Mannick JA, Lederer JA
المصدر: Shock (Augusta, Ga.) [Shock] 1999 Jul; Vol. 12 (1), pp. 39-45.
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: Lippincott Williams & Wilkins Country of Publication: United States NLM ID: 9421564 Publication Model: Print Cited Medium: Print ISSN: 1073-2322 (Print) Linking ISSN: 10732322 NLM ISO Abbreviation: Shock Subsets: MEDLINE
أسماء مطبوعة: Publication: 2002- : Philadelphia : Lippincott Williams & Wilkins
Original Publication: Augusta, GA : BioMedical Press, [1994-
مواضيع طبية MeSH: Immunity*, Burns/*immunology , Th1 Cells/*immunology , Th2 Cells/*immunology, Animals ; Antibody Formation ; Antigen Presentation ; Immunization ; Interferon-gamma/biosynthesis ; Interferon-gamma/immunology ; Interleukin-10/biosynthesis ; Interleukin-10/immunology ; Interleukin-2/biosynthesis ; Interleukin-2/immunology ; Male ; Mice
مستخلص: Although it is established that post-injury immune dysfunction involves alterations in T-cell function, the effects of injury on T-cell function in vivo are poorly understood. This study uses a mouse injury model and an antigen immunization approach to investigate the influence of injury on antigen-specific T-helper cell function. We report here that injury triggered a significant reduction in antigen-specific T-helper-1 (Th1)-dependent IgG2a antibody formation, while IgM, IgG1, and IgE production was unchanged. In addition, injury caused a reduction in cytokine production (IL-2, IFNgamma and IL-10) by antigen-stimulated T-cells. We also demonstrate that interleukin 12 (IL-12), a cytokine that promotes Th1 cell differentiation, restored IgG2a antibody formation and corrected the injury-induced reduction in antigen-stimulated cytokine production. Taken together, these findings indicate that severe injury induces a dramatic reduction in Th1 cell function in vivo and suggest that therapies designed to restore Th1 cell function may be beneficial to the injured host.
معلومات مُعتمدة: GM 35633 United States GM NIGMS NIH HHS
المشرفين على المادة: 0 (Interleukin-2)
130068-27-8 (Interleukin-10)
82115-62-6 (Interferon-gamma)
تواريخ الأحداث: Date Created: 19990901 Date Completed: 19990921 Latest Revision: 20190915
رمز التحديث: 20221213
DOI: 10.1097/00024382-199907000-00006
PMID: 10468050
قاعدة البيانات: MEDLINE
الوصف
تدمد:1073-2322
DOI:10.1097/00024382-199907000-00006