Humanized animal models for autoimmune diseases.

The development of transgenic mice expressing human DR and DQ major histocompatibility complex (MHC) class II molecules has been of value in studying the immunopathology of human MHC class II-associated autoimmune diseases such as rheumatoid arthritis, multiple sclerosis, insulin-dependent diabetes...

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Main Authors: Gregersen, J, Holmes, S, Fugger, L
格式: Journal article
語言:English
出版: 2004
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author Gregersen, J
Holmes, S
Fugger, L
author_facet Gregersen, J
Holmes, S
Fugger, L
author_sort Gregersen, J
collection OXFORD
description The development of transgenic mice expressing human DR and DQ major histocompatibility complex (MHC) class II molecules has been of value in studying the immunopathology of human MHC class II-associated autoimmune diseases such as rheumatoid arthritis, multiple sclerosis, insulin-dependent diabetes mellitus and celiac disease. Such mice have been used to identify the target antigens that are involved in the initiation of these diseases. Many of the mice develop aspects of the human diseases, either spontaneously or following immunization with the relevant antigen, thus providing an in vivo disease model, which may be used as a tool for further understanding the disease mechanisms and testing novel immunotherapies.
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spelling oxford-uuid:b48ad0c3-6a06-476c-aa7c-9a8bcdb6298b2022-03-27T04:26:57ZHumanized animal models for autoimmune diseases.Journal articlehttp://purl.org/coar/resource_type/c_dcae04bcuuid:b48ad0c3-6a06-476c-aa7c-9a8bcdb6298bEnglishSymplectic Elements at Oxford2004Gregersen, JHolmes, SFugger, LThe development of transgenic mice expressing human DR and DQ major histocompatibility complex (MHC) class II molecules has been of value in studying the immunopathology of human MHC class II-associated autoimmune diseases such as rheumatoid arthritis, multiple sclerosis, insulin-dependent diabetes mellitus and celiac disease. Such mice have been used to identify the target antigens that are involved in the initiation of these diseases. Many of the mice develop aspects of the human diseases, either spontaneously or following immunization with the relevant antigen, thus providing an in vivo disease model, which may be used as a tool for further understanding the disease mechanisms and testing novel immunotherapies.
spellingShingle Gregersen, J
Holmes, S
Fugger, L
Humanized animal models for autoimmune diseases.
title Humanized animal models for autoimmune diseases.
title_full Humanized animal models for autoimmune diseases.
title_fullStr Humanized animal models for autoimmune diseases.
title_full_unstemmed Humanized animal models for autoimmune diseases.
title_short Humanized animal models for autoimmune diseases.
title_sort humanized animal models for autoimmune diseases
work_keys_str_mv AT gregersenj humanizedanimalmodelsforautoimmunediseases
AT holmess humanizedanimalmodelsforautoimmunediseases
AT fuggerl humanizedanimalmodelsforautoimmunediseases