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The Journal of Immunology, 2003, 170: 788-794.
Copyright © 2003 by The American Association of Immunologists

Complement Component 3 Is Required for Optimal Expansion of CD8 T Cells During a Systemic Viral Infection1

M. Suresh2,*, Hector Molina{ddagger}, Maria S. Salvato§, Dimitrios Mastellos, John D. Lambris and Matyas Sandor{dagger}

Departments of * Pathobiological Sciences and {dagger} Laboratory Medicine and Pathology, University of Wisconsin, Madison, WI 53706; {ddagger} Department of Internal Medicine, Washington University, St. Louis, MO 63110; § Institute of Human Virology, University of Maryland Biotechnology Institute, Baltimore, MD 21201; and Department of Pathology and Laboratory Medicine, University of Pennsylvania, Philadelphia, PA 19104

In addition to its established role in innate immune mechanisms, complement component C3 is also of critical importance in B cell activation and T cell-dependent Ab responses. In this study, we have examined the requirement for C3 in the generation of primary CD8 T cell responses to an acute systemic viral infection. We compared Ag-specific CD8 T cell responses to lymphocytic choriomeningitis virus (LCMV) between wild-type (+/+) and C3-deficient (C3-/-) mice on both 129/B6 and B6 backgrounds. These studies revealed that C3 activity is required for optimal expansion of LCMV-specific effector CD8 T cells in an epitope-dependent fashion, which is influenced by the genetic background of the mice. Studies in complement receptor 1/2 (CR1/CR2)-deficient mice showed that regulation of LCMV-specific CD8 T cell responses by C3 is not dependent upon CR1/CR2. These findings may have implications in vaccine development, therapy of autoimmune diseases, and prevention of graft rejection.




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