Cargando…
Antiphospholipid Antibodies: Their Origin and Development
Antiphospholipid antibodies (aPL) are a hallmark of the antiphospholipid syndrome (APS), which is the most commonly acquired thrombophilia. To date there is consensus that aPL cause the clinical manifestations of this potentially devastating disorder. However, there is good evidence that not all aPL...
Autores principales: | , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2016
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6698834/ https://www.ncbi.nlm.nih.gov/pubmed/31557996 http://dx.doi.org/10.3390/antib5020015 |
_version_ | 1783444624095838208 |
---|---|
author | Lackner, Karl J. Müller-Calleja, Nadine |
author_facet | Lackner, Karl J. Müller-Calleja, Nadine |
author_sort | Lackner, Karl J. |
collection | PubMed |
description | Antiphospholipid antibodies (aPL) are a hallmark of the antiphospholipid syndrome (APS), which is the most commonly acquired thrombophilia. To date there is consensus that aPL cause the clinical manifestations of this potentially devastating disorder. However, there is good evidence that not all aPL are pathogenic. For instance, aPL associated with syphilis show no association with the manifestations of APS. While there has been intensive research on the pathogenetic role of aPL, comparably little is known about the origin and development of aPL. This review will summarize the current knowledge and understanding of the origin and development of aPL derived from animal and human studies. |
format | Online Article Text |
id | pubmed-6698834 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-66988342019-09-05 Antiphospholipid Antibodies: Their Origin and Development Lackner, Karl J. Müller-Calleja, Nadine Antibodies (Basel) Review Antiphospholipid antibodies (aPL) are a hallmark of the antiphospholipid syndrome (APS), which is the most commonly acquired thrombophilia. To date there is consensus that aPL cause the clinical manifestations of this potentially devastating disorder. However, there is good evidence that not all aPL are pathogenic. For instance, aPL associated with syphilis show no association with the manifestations of APS. While there has been intensive research on the pathogenetic role of aPL, comparably little is known about the origin and development of aPL. This review will summarize the current knowledge and understanding of the origin and development of aPL derived from animal and human studies. MDPI 2016-06-02 /pmc/articles/PMC6698834/ /pubmed/31557996 http://dx.doi.org/10.3390/antib5020015 Text en © 2016 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC-BY) license (http://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Review Lackner, Karl J. Müller-Calleja, Nadine Antiphospholipid Antibodies: Their Origin and Development |
title | Antiphospholipid Antibodies: Their Origin and Development |
title_full | Antiphospholipid Antibodies: Their Origin and Development |
title_fullStr | Antiphospholipid Antibodies: Their Origin and Development |
title_full_unstemmed | Antiphospholipid Antibodies: Their Origin and Development |
title_short | Antiphospholipid Antibodies: Their Origin and Development |
title_sort | antiphospholipid antibodies: their origin and development |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6698834/ https://www.ncbi.nlm.nih.gov/pubmed/31557996 http://dx.doi.org/10.3390/antib5020015 |
work_keys_str_mv | AT lacknerkarlj antiphospholipidantibodiestheiroriginanddevelopment AT mullercallejanadine antiphospholipidantibodiestheiroriginanddevelopment |