Autor: |
Gallina MC; Department of Immunology, Research Institute of Scripps Clinic, La Jolla, California 92037., Steele JK |
Jazyk: |
angličtina |
Zdroj: |
Journal of autoimmunity [J Autoimmun] 1991 Oct; Vol. 4 (5), pp. 755-68. |
DOI: |
10.1016/0896-8411(91)90171-8 |
Abstrakt: |
The MRL-lpr murine model of systemic lupus erythematosus (SLE) has provided many insights into the pathology of human lupus. The model is characterized by an age-dependent expansion of a Thy-1+ alpha beta/CD3+ CD4-, CD8- T-cell subset in the nodes and spleen. In this study, a lpr T-cell specific monoclonal antibody, Ye19.1, was found to bind to a 200 kDa cell surface molecule (termed LTA) which has a phosphotyrosine phosphatase (PTPase) enzymatic function. The significance of this marker in the development of autoimmune pathology in MRL/lpr mice was also demonstrated; treatment of MRL-lpr mice with the Ye19.1 Ab was shown to retard the development of the autoimmune syndrome and to restore the T cell-dependent immune response to ovalbumin. |
Databáze: |
MEDLINE |
Externí odkaz: |
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