Haemorrhage-induced alterations in function and cytokine production of T cells and T cell subpopulations

Abstract

Haemorrhage produces alterations in macrophage, T and B cell function. In order to better define the mechanism for the effects of blood loss on immune response, we examined function of and cytokine production by purified T cells, CD4⁺ and CD8⁺ subpopulations after blood loss. Whereas T and CD4⁺ cells from control, unhaemorrhaged animals produced no alteration in proliferation when added to cultures of mitogen-stimulated splenocytes from normal mice, proliferation was decreased when T or CD4⁺ cells from haemorrhaged mice were included. The addition of CD8⁺ cells from haemorrhaged animals to mitogen-stimulated cultures reduced proliferation by approximately 50% more than that found when CD8⁺ cells from control, unhaemorrhaged animals were included. Supernatants of mitogen-stimulated splenocytes from haemorrhaged mice contained significantly less IL-2 and interferon-gamma (IFN-γ) than did those from control, unhaemorrhaged mice. CD4⁺ populations from haemorrhaged mice produced significantly more IL-10, and significantly less IFN-γ, than did CD4⁺ cells from control, unhaemorrhaged mice. There were no significant differences in IL-2, IL-4, IL-10 or IFN-γ production by CD8⁺ cells from haemorrhaged or control mice. The present experiments demonstrate that haemorrhage affects both CD4⁺ and CD8⁺ T cell subsets. In particular, haemorrhage appeared to activate CD4⁺, Th2 cells, with concomitant suppression of the Thl subpopulation. These results provide a mechanism which may contribute to the alterations in cytokine production previously described to occur following blood loss.