Involvement of an IgE/Mast cell/B cell amplification loop in abdominal aortic aneurysm progression.

Loste, Alexia; Clément, Marc; Delbosc, Sandrine; Guedj, Kevin; Sénémaud, Jean; Gaston, Anh-Thu; Morvan, Marion; Even, Guillaume; Gautier, Grégory; Eggel, Alexander; Arock, Michel; Procopio, Emanuele; Deschildre, Catherine; Louedec, Liliane; Michel, Jean-Baptiste; Deschamps, Lydia; Castier, Yves; Coscas, Raphaël; Alsac, Jean-Marc; Launay, Pierre; ... (2023). Involvement of an IgE/Mast cell/B cell amplification loop in abdominal aortic aneurysm progression. PLoS ONE, 18(12), e0295408. Public Library of Science 10.1371/journal.pone.0295408

Preview

Text journal.pone.0295408.pdf - Published Version Available under License Creative Commons: Attribution (CC-BY). Download (2MB) | Preview

AIMS

IgE type immunoglobulins and their specific effector cells, mast cells (MCs), are associated with abdominal aortic aneurysm (AAA) progression. In parallel, immunoglobulin-producing B cells, organised in tertiary lymphoid organs (TLOs) within the aortic wall, have also been linked to aneurysmal progression. We aimed at investigating the potential role and mechanism linking local MCs, TLO B cells, and IgE production in aneurysmal progression.

METHODS AND RESULTS

Through histological assays conducted on human surgical samples from AAA patients, we uncovered that activated MCs were enriched at sites of unhealed haematomas, due to subclinical aortic wall fissuring, in close proximity to adventitial IgE+ TLO B cells. Remarkably, in vitro the IgEs deriving from these samples enhanced MC production of IL-4, a cytokine which favors IgE class-switching and production by B cells. Finally, the role of MCs in aneurysmal progression was further analysed in vivo in ApoE-/- mice subjected to angiotensin II infusion aneurysm model, through MC-specific depletion after the establishment of dissecting aneurysms. MC-specific depletion improved intramural haematoma healing and reduced aneurysmal progression.

CONCLUSIONS

Our data suggest that MC located close to aortic wall fissures are activated by adventitial TLO B cell-produced IgEs and participate to their own activation by providing support for further IgE synthesis through IL-4 production. By preventing prompt repair of aortic subclinical fissures, such a runaway MC activation loop could precipitate aneurysmal progression, suggesting that MC-targeting treatments may represent an interesting adjunctive therapy for reducing AAA progression.

Interest & Impact

Downloads

13 since deposited on 08 Dec 2023
13 in the past 12 months

Citations

5 Citations in Web of Science ®
6 Citations in Scopus

Search

in Google Scholar™

Services

Actions (login required)

Edit item

Actions (login required)

Edit item