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How Times Have Changed! A Cornucopia of Antigens for Membranous Nephropathy.
Caza, Tiffany N; Al-Rabadi, Laith F; Beck, Laurence H.
Afiliação
  • Caza TN; Arkana Laboratories, Little Rock, AR, United States.
  • Al-Rabadi LF; Department of Internal Medicine (Nephrology & Hypertension), University of Utah, Salt Lake City, UT, United States.
  • Beck LH; Department of Medicine (Nephrology), Boston University School of Medicine and Boston Medical Center, Boston, MA, United States.
Front Immunol ; 12: 800242, 2021.
Article em En | MEDLINE | ID: mdl-34899763
ABSTRACT
The identification of the major target antigen phospholipase A2 receptor (PLA2R) in the majority of primary (idiopathic) cases of membranous nephropathy (MN) has been followed by the rapid identification of numerous minor antigens that appear to define phenotypically distinct forms of disease. This article serves to review all the known antigens that have been shown to localize to subepithelial deposits in MN, as well as the distinctive characteristics associated with each subtype of MN. We will also shed light on the novel proteomic approaches that have allowed identification of the most recent antigens. The paradigm of an antigen normally expressed on the podocyte cell surface leading to in-situ immune complex formation, complement activation, and subsequent podocyte injury will be discussed and challenged in light of the current repertoire of multiple MN antigens. Since disease phenotypes associated with each individual target antigens can often blur the distinction between primary and secondary disease, we encourage the use of antigen-based classification of membranous nephropathy.
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Texto completo: 1 Bases de dados: MEDLINE Assunto principal: Autoantígenos / Glomerulonefrite Membranosa Tipo de estudo: Prognostic_studies Limite: Humans Idioma: En Revista: Front Immunol Ano de publicação: 2021 Tipo de documento: Article País de afiliação: Estados Unidos

Texto completo: 1 Bases de dados: MEDLINE Assunto principal: Autoantígenos / Glomerulonefrite Membranosa Tipo de estudo: Prognostic_studies Limite: Humans Idioma: En Revista: Front Immunol Ano de publicação: 2021 Tipo de documento: Article País de afiliação: Estados Unidos