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Human T-Cell-Mediated Destruction of Allogeneic Dermal Microvessels in a Severe Combined Immunodeficient Mouse
Allan G. Murray, Peter Petzelbauer, Christopher C. W. Hughes, Jose Costa, Philip Askenase and Jordan S. Pober
Proceedings of the National Academy of Sciences of the United States of America
Vol. 91, No. 19 (Sep. 13, 1994), pp. 9146-9150
Published by: National Academy of Sciences
Stable URL: http://www.jstor.org/stable/2365987
Page Count: 5
You can always find the topics here!Topics: T lymphocytes, Skin, Humans, Microvessels, Skin grafts, Tissue grafting, Lymphocytes, Keratinocytes, Epidermis, Molecules
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We developed a chimeric human-severe combined immunodeficient mouse model to study human allograft rejection. Mice received first partial thickness human skin grafts and then, after anastomosis of the mouse with graft human microvessels, human lymphocytes allogeneic to the skin. By 2 weeks, the skin grafts uniformly developed changes that resemble first-set skin rejection in humans. Vascular cell adhesion molecule 1 and major histocompatibility complex class II molecules were induced on the human vascular endothelium at day 6, prior to significant T-cell infiltration. Perivascular human CD4+ and CD8+ T-cell infiltrates were marked by day 11. Some T cells, adjacent to injured human vessels, expressed the cytolytic granule protein perforin. The human microvessels were destroyed by day 16 without significant damage to human keratinocytes or adjacent mouse microvessels. This small animal model may permit evaluation of potential therapeutic reagents that inhibit human T-cell-mediated injury.
Proceedings of the National Academy of Sciences of the United States of America © 1994 National Academy of Sciences