Study of the ex vivo immune response of polytrauma older patients in the ICU on admission: preliminary results

Introduction Immunological status is differentiated with age, influencing treatment and outcome [1] . The aim is to determine the immune response of severely traumatized older patients compared with a group with arterial disease, expressed by proinflammatory cytokine release after ex vivo whole-bloo...

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Veröffentlicht in:Critical care (London, England) England), 2014-03, Vol.18 (S1), p.P236-P236, Article P236
Hauptverfasser: Filippou, L, Venetsanou, K, Voulalas, G, Markopoulou, D, Chroni, D, Maltezos, C, Alamanos, I
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Sprache:eng
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Zusammenfassung:Introduction Immunological status is differentiated with age, influencing treatment and outcome [1] . The aim is to determine the immune response of severely traumatized older patients compared with a group with arterial disease, expressed by proinflammatory cytokine release after ex vivo whole-blood LPS stimulation [2] . Methods The study comprised 16 polytrauma patients admitted to the ICU, aged 78 ± 8 (Group I) and 16 with arterial disease, aged 74 ± 5 (Group II). Ten milliliters of peripheral blood were collected from each patient, divided into two tubes with/without anticoagulant. Diluted 1:10 whole-blood samples were stimulated with 500 pg/ml LPS, at 37°C, for 4 hours. Serum and cell culture supernatants (CCSP) were removed and stored at -70°C. TNF alpha and IL-6 were measured in serum and CCSP by ELISA. Results Serum proinflammatory cytokines were significantly elevated after severe trauma against control group (TNF alpha , P < 0.001 and IL-6, P < 0.001). Ex vivo cytokine release showed the opposite direction. There was a significantly lower TNF alpha and IL-6 release for Group I (TNF alpha , P < 0.05 and IL-6, P < 0.01) compared with Group II. TNF alpha ex vivo release from the samples of Group II was >300 pg/ml. Conclusion Older patients showed adequate immunological response, considering the limit of 300 pg/ml. The incidence of severe trauma was involved in the downregulation of immune activity and should be considered. Group I patients do not have the opportunity to precondition their immune status. Group II patients can better compensate operative therapies.
ISSN:1364-8535
1364-8535
1466-609X
DOI:10.1186/cc13426