A new mutation,aly, that induces a generalized lack of lymph nodes accompanied by immunodeficiency in mice |
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Authors: | Shigeki Miyawaki Yutaka Nakamura Hirotsugu Suzuka Masahiro Koba Yoshihisa Shibata Ryoji Yasumizu Susumu Ikehara |
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Abstract: | We have found a new spontaneous autosomal recessive mutation in mice that causes a systemic absence of lymph nodes and Peyer's patches. The name “alymphoplasia”, with the gene symbol “uly”, is proposed for this mutant. The spleen of alylay mice is devoid of well-defined lymphoid follicles, and the thymus does not show a clear cortical-medullary distinction. The mutant homozygotes are deficient in both humoral and cell-mediated immune functions, and are highly susceptible to infections. They have a reduced level of IgM and severely depressed levels of IgG and IgA in their sera, and do not reject allogeneic skin grafts. However, they have mature T and B cells as determined from their cell surface antigens. The results of bone marrow transplantation experiments suggest a mesenchymal disorder as a possible cause of the lack of lymph nodes and of immunodeficiency in the aly mouse. The aly mutant mouse may be a useful animal model of primary immunodeficiency, as are the nu (nude) and scid (severe combined immunodeficiency) mice. |
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Keywords: | Immunodeficiency Alymphoplasia Animal model Autosomal recessive mutation Mouse |
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