Therapeutic uses of recombinant complement protein inhibitors |
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Authors: | Kimberly R. Kalli Peihong Hsu Douglas T. Fearon |
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Affiliation: | (1) The Graduate Program in Immunology, The Johns Hopkins University School of Medicine, 21205 Baltimore, MD, USA;(2) Division of Molecular and Clinical Rheumatology and Department of Medicine, The Johns Hopkins University School of Medicine, 21205 Baltimore, MD, USA;(3) Present address: Department of Medicine, University of Cambridge School of Clinical Medicine, Addenbrooke's Hospital, Hills Road, CB2 2SP Cambridge, UK |
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Abstract: | Conclusion In conclusion, it is apparent that researchers are poised at the threshold of developing inhibitors of complement activation from the molecules in the RCA family. By creating soluble forms of these protective proteins for in vivo administration, or by making transgenic animals expressing these proteins or their derivatives, it may be possible to inhibit complement-mediated pathology stemming from autoimmune disease, reperfusion injuries, and physical trauma. This technology combined with current attempts to protect allografts from cellular rejection with monoclonal antibodies against members of the integrin family of adhesion molecules [52] makes it possible that the excessive mortality due to the severe shortage of human donor organs could be overcome by the use of xenografts. |
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