Polymorphism of human haptoglobin and its clinical importance
Haptoglobin (Hp) is a plasma glycoprotein, the main biological function of which is to bind free hemoglobin (Hb) and prevent the loss of iron and subsequent kidney damage following intravascular hemolysis. Haptoglobin is also a positive acute-phase protein with immunomodulatory properties. In humans, the HP locus is polymorphic, with two codominant alleles (HP1 and HP2) that yield three distinct genotypes/phenotypes (Hp1-1, Hp2-1 and Hp2-2). The corresponding proteins have structural and functional differences that may influence the susceptibility and/or outcome in several diseases. This article summarizes the available data on the structure and functions of Hp and the possible effects of Hp polymorphism in a number of important human disorders.
| Autores principales: | , , |
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| Formato: | Digital revista |
| Idioma: | English |
| Publicado: |
Sociedade Brasileira de Genética
2008
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| Acceso en línea: | http://old.scielo.br/scielo.php?script=sci_arttext&pid=S1415-47572008000400002 |
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