Pathophysiology of ANCA vasculitides (notice n° 192102)
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| fixed length control field | 02272cam a2200169 4500500 |
| 005 - DATE AND TIME OF LATEST TRANSACTION | |
| control field | 20250112044756.0 |
| 041 ## - LANGUAGE CODE | |
| Language code of text/sound track or separate title | fre |
| 042 ## - AUTHENTICATION CODE | |
| Authentication code | dc |
| 100 10 - MAIN ENTRY--PERSONAL NAME | |
| Personal name | Augusto, Jean-François |
| Relator term | author |
| 245 00 - TITLE STATEMENT | |
| Title | Pathophysiology of ANCA vasculitides |
| 260 ## - PUBLICATION, DISTRIBUTION, ETC. | |
| Date of publication, distribution, etc. | 2023.<br/> |
| 500 ## - GENERAL NOTE | |
| General note | 56 |
| 520 ## - SUMMARY, ETC. | |
| Summary, etc. | ANCA vasculitides (AAV) are autoimmune diseases responsible for damage to small-size vessels. Three entities are distinguished from clinical, histological, and biological criteria: microscopic polyangiitis (MPA), granulomatosis with polyangiitis (GPA), and eosinophilic granulomatosis with polyangiitis (EGPA). The neutrophil–ANCA couple is central to the pathophysiology of AAV. However, the mechanisms that lead to the breakdown of tolerance to myeloperoxidase or proteinase-3 remain hypothetical. They are probably multifactorial, occurring in patients with a predisposing genetic background. The understanding of the injury mechanisms involved in AAV has made great progress thanks to the study of a murine model of immunization against myeloperoxidase. This work has made it possible to show the central role of PNNs in vivo, which are activated under sterile conditions, under the effect of the ANCAs, which recognize the self-antigen expressed on their surface. Understanding the role of the alternative complement pathway and in particular that of C5a, a powerful anaphylatoxin, has been a major advance. C5a acts as an amplifying factor for PNN activation, and blocking its receptor (C5aR) prevents the occurrence of vasculitis lesions in the murine model. These discoveries have led to therapeutic trials in humans, highlighting the interest of blocking C5aR and validating this therapeutic strategy. It should be emphasized that the AAV study model is, above all, an anti-MPO model and that the mechanisms involved in anti-PR3 ANCA or ANCA-negative vasculitis remain very hypothetical. Finally, the mechanisms that account for the heterogeneity of the presentation or severity of AAV remain poorly understood. |
| 700 10 - ADDED ENTRY--PERSONAL NAME | |
| Personal name | Brilland, Benoit |
| Relator term | author |
| 786 0# - DATA SOURCE ENTRY | |
| Note | Néphrologie & Thérapeutique | Volume 19 | Suppl. Issue 1 | 2023-09-26 | p. 30-38 | 1769-7255 |
| 856 41 - ELECTRONIC LOCATION AND ACCESS | |
| Uniform Resource Identifier | <a href="https://shs.cairn.info/journal-nephrologie-et-therapeutique-2024-HS1-page-30?lang=en">https://shs.cairn.info/journal-nephrologie-et-therapeutique-2024-HS1-page-30?lang=en</a> |
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