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   <subfield code="a">Enhanced survival from CLP-induced sepsis following late administration of low doses of anti-IFNγ F(ab′)2 antibody fragments</subfield>
   <subfield code="h">[Elektronische Daten]</subfield>
   <subfield code="c">[R. Márquez-Velasco, A. Martínez-Velázquez, L. Amezcua-Guerra, F. Flores-Guzmán, A. Díaz-Quiñonez, F. Massó, J. Paniagua-Solís, R. Bojalil]</subfield>
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   <subfield code="a">Objective: To assess the impact of different doses of anti-interferon gamma (anti-IFNγ) F(ab′)2 fragments, administered prophylactically, on survival and on serum concentration of cytokines in a murine model of sepsis induced by cecal ligation and puncture (CLP). We further explore the impact of therapeutic administration of the most protective dose on survival. Subjects and treatment: Balb/c mice were prophylactically treated by the intraperitoneal route with anti-IFNγ initiated 2h before CLP and every 24h for a total of five times in each of the following doses: 0.01, 0.1, or 1mg/kg. Sham and control groups received sterile saline solution in a similar scheme. Methods: Serum tumor necrosis factor (TNF), interleukin (IL)-1β, IL-6, IL-10 and IFNγ were measured at 3, 24 and 48h after CLP by ELISA. Survival curves were compared using a Mantel-Haenzel method. Results: Significant prophylactic protection was found only with 0.01mg/kg, in association with regulation of IL-1β and IL-10 concentrations. As therapy, anti-IFNγ fragments were protective only when initiated 24h after CLP. Conclusions: Delicate modulation of IFNγ at the correct timing, even when the septic process has begun, is an exciting alternative to explore in the treatment of sepsis.</subfield>
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   <subfield code="a">Sepsis</subfield>
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