Published online before print July 20, 2006

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(Journal of Leukocyte Biology. 2006;80:774-786.)
© 2006 by Society for Leukocyte Biology

Critical role for serum opsonins and complement receptors CR3 (CD11b/CD18) and CR4 (CD11c/CD18) in phagocytosis of Francisella tularensis by human dendritic cells (DC): uptake of Francisella leads to activation of immature DC and intracellular survival of the bacteria

Abdelhakim Ben Nasr^*, Judith Haithcoat^*, Joseph E. Masterson^*, John S. Gunn, Tonyia Eaves-Pyles^* and Gary R. Klimpel^*,1

^* Department of Microbiology and Immunology, University of Texas Medical Branch, Galveston, Texas; and
Tzagournis Medical Research Facility, The Ohio State University, Columbus, Ohio

¹ Correspondence: Department of Microbiology and Immunology, Medical Research Building, University of Texas Medical Branch, Galveston, TX 77555-1070. E-mail: gklimpel{at}utmb.edu

ABSTRACT

Francisella tularensis is one of the most infectious human pathogens known. Although much has been learned about the immune response of mice using an attenuated live vaccine strain (LVS) derived from F. tularensis subspecies holarctica (Type B), little is known about the responses of human monocyte-derived immature dendritic cells (DC). Here, we show that optimal phagocytosis of LVS by DC is dependent on serum opsonization. We demonstrate that complement factor C3-derived opsonins and the major complement receptors expressed by DC, the integrins CR3 (CD11b/CD18) and CR4 (CD11c/CD18), play a critical role in this adhesion-mediated phagocytosis. LVS induced proinflammatory cytokine production and up-regulation of costimulatory surface proteins (CD40, CD86, and MHC Class II) on DC but resisted killing. Once taken up, LVS grew intracellularly, resulting in DC death. DC maturation and cytokine production were induced by direct contact/phagocytosis of LVS or interaction with soluble products of the bacteria, and enhanced activation was seen when LVS was pretreated with serum. Sonicated LVS and supernatants from LVS cultures were potent activators of DC, but LVS LPS failed to activate DC maturation or cytokine production. Serum-treated LVS rapidly induced (within 6 h) a number of cytokines including IL-10, a potent suppressor of macrophage functions and down-regulator of Th1-like responses and the Th1 response inducer IL-12. These results suggest that the simultaneous production of an activating (IL-12, IL-1ß, and TNF-) and a suppressing (IL-10) cytokine profile could contribute to the immunopathogenesis of tularemia.

Key Words: bacterial infection • cytokines • lipopolysacchiride • LPS • innate immunity

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