• N R Ferguson, H F Galley, and N R Webster.
• Academic Unit of Anaesthesia & Intensive Care, Institute of Medical Sciences, Foresterhill, Aberdeen, UK.
• Intensive Care Med. 1999 Jan 1; 25 (1): 106-9.

BackgroundT helper 1 (Thl) lymphocytes produce interferon gamma (IFNgamma), favouring cell mediated immunity; Th2 cells secrete interleukin-4 (IL-4), favouring humoral immunity. Cytokines produced in sepsis may effect Th subset predominance and subsequent immune responses.MethodsWe measured Th subsets in ten patients with severe sepsis, seven APACHE II score-matched non-septic critically ill control patients, and ten healthy subjects. Mononuclear leukocytes were isolated and Th subsets identified by flow cytometry.ResultsThe median (range) Th1/Th2 ratio was 0.46 (0.2-2.5) in patients with sepsis, which was significantly lower than both non-septic controls (median 2.5 (0.2-5.9), p = 0.050) and healthy subjects (median 3.9 (1.2-10.8), p = 0.01).ConclusionsIn patients with sepsis, Th2 antibody mediated (humoral) immune responses predominate. This type of response may lead to fibroblast activation and ultimately immunosuppression. Modulation of Th cell subset predominance may present a novel therapeutic option in the treatment of severe sepsis.

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