Th2 predominance and decreased NK cells in patients with hereditary angioedema
(2025) In Frontiers in Immunology 16.- Abstract
Background: In this study we included patients with hereditary angioedema (HAE) caused by decreased levels of C1 inhibitor (HAE-C1INH). An increased risk of autoimmune disorders, particularly systemic lupus erythematosus (SLE), has been reported in HAE-C1INH. This suggests that complement consumption affects adaptive immunity. Objective: To investigate lymphocyte subpopulations in relation to disease activity and complement activation in HAE-C1INH patients and matched controls. Methods: Flow cytometry of peripheral blood lymphocyte populations, measurements of complement and complement fragments, and collection of clinical data. Results: NK cell counts were lower in HAE-C1INH patients, and their frequencies were related to disease... (More)
Background: In this study we included patients with hereditary angioedema (HAE) caused by decreased levels of C1 inhibitor (HAE-C1INH). An increased risk of autoimmune disorders, particularly systemic lupus erythematosus (SLE), has been reported in HAE-C1INH. This suggests that complement consumption affects adaptive immunity. Objective: To investigate lymphocyte subpopulations in relation to disease activity and complement activation in HAE-C1INH patients and matched controls. Methods: Flow cytometry of peripheral blood lymphocyte populations, measurements of complement and complement fragments, and collection of clinical data. Results: NK cell counts were lower in HAE-C1INH patients, and their frequencies were related to disease activity. The T helper (Th) cell balance was skewed towards more Th2 cells and less Th1 cells in HAE-C1INH patients compared to controls. There were also lower frequencies of class-switched B cells and plasmablasts in patients. Levels of C4 and the complement activation fragment C3d were related to disease activity. Conclusions: Blood lymphocyte populations are altered in HAE-C1INH, a finding which may be of pathophysiological importance considering the increased risks of both autoimmunity and allergy associated with HAE-C1INH.
(Less)
- author
- Sundler Björkman, Linda
LU
; Elmér, Evelina LU
; Egesten, Arne LU and Skattum, Lillemor LU
- organization
- publishing date
- 2025
- type
- Contribution to journal
- publication status
- published
- subject
- keywords
- adaptive immunity, complement activation, hereditary angioedema, NK cells, T helper 2 cells
- in
- Frontiers in Immunology
- volume
- 16
- article number
- 1536128
- publisher
- Frontiers Media S. A.
- external identifiers
-
- scopus:105006803005
- pmid:40438097
- ISSN
- 1664-3224
- DOI
- 10.3389/fimmu.2025.1536128
- language
- English
- LU publication?
- yes
- id
- 0823d2a3-41c4-40b7-ba0d-a74235f6a2bc
- date added to LUP
- 2025-08-19 11:37:44
- date last changed
- 2025-09-30 15:17:37
@article{0823d2a3-41c4-40b7-ba0d-a74235f6a2bc, abstract = {{<p>Background: In this study we included patients with hereditary angioedema (HAE) caused by decreased levels of C1 inhibitor (HAE-C1INH). An increased risk of autoimmune disorders, particularly systemic lupus erythematosus (SLE), has been reported in HAE-C1INH. This suggests that complement consumption affects adaptive immunity. Objective: To investigate lymphocyte subpopulations in relation to disease activity and complement activation in HAE-C1INH patients and matched controls. Methods: Flow cytometry of peripheral blood lymphocyte populations, measurements of complement and complement fragments, and collection of clinical data. Results: NK cell counts were lower in HAE-C1INH patients, and their frequencies were related to disease activity. The T helper (Th) cell balance was skewed towards more Th2 cells and less Th1 cells in HAE-C1INH patients compared to controls. There were also lower frequencies of class-switched B cells and plasmablasts in patients. Levels of C4 and the complement activation fragment C3d were related to disease activity. Conclusions: Blood lymphocyte populations are altered in HAE-C1INH, a finding which may be of pathophysiological importance considering the increased risks of both autoimmunity and allergy associated with HAE-C1INH.</p>}}, author = {{Sundler Björkman, Linda and Elmér, Evelina and Egesten, Arne and Skattum, Lillemor}}, issn = {{1664-3224}}, keywords = {{adaptive immunity; complement activation; hereditary angioedema; NK cells; T helper 2 cells}}, language = {{eng}}, publisher = {{Frontiers Media S. A.}}, series = {{Frontiers in Immunology}}, title = {{Th2 predominance and decreased NK cells in patients with hereditary angioedema}}, url = {{http://dx.doi.org/10.3389/fimmu.2025.1536128}}, doi = {{10.3389/fimmu.2025.1536128}}, volume = {{16}}, year = {{2025}}, }