Abstract
We generated a new humanized mouse model to study HLA-restricted immune responses. For this purpose, we created unique murine hosts by enforcing the expression of human SIRPα by murine phagocytes in murine MHC-deficient HLA-transgenic alymphoid hosts, an approach that allowed the immune reconstitution of nonpermissive mice following injection of human hematopoietic stem cells. We showed that these mouse/human chimeras were able to generate HLA-restricted responses to immunization. These new humanized mice may offer attractive models to study immune responses to human diseases, such as HIV and EBV infections, as well as to assay new vaccine strategies.
Copyright © 2014 by The American Association of Immunologists, Inc.
Publication types
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Research Support, Non-U.S. Gov't
MeSH terms
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Animals
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Animals, Newborn
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Antigens, Differentiation / administration & dosage
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Antigens, Differentiation / blood
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Antigens, Differentiation / genetics
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Cell Survival / genetics
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Cell Survival / immunology
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Disease Models, Animal
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Female
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HLA Antigens / administration & dosage*
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HLA Antigens / genetics
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HLA Antigens / immunology*
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Hematopoietic Stem Cell Transplantation / methods*
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Humans
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Mice
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Mice, 129 Strain
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Mice, Inbred C57BL
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Mice, Inbred NOD
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Mice, Knockout
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Mice, SCID
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Mice, Transgenic
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Organ Culture Techniques
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Radiation Chimera / genetics
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Radiation Chimera / immunology*
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Receptors, Immunologic / administration & dosage
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Receptors, Immunologic / blood
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Receptors, Immunologic / genetics
Substances
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Antigens, Differentiation
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HLA Antigens
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Receptors, Immunologic
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SIRPA protein, human