» Articles » PMID: 37587510

CD4 T Lymphocyte Subsets Display Heterogeneous Susceptibility to Apoptosis Induced by Serum from Patients with Systemic Lupus Erythematosus

Overview
Journal Adv Rheumatol
Publisher Biomed Central
Specialty Rheumatology
Date 2023 Aug 16
PMID 37587510
Authors
Affiliations
Soon will be listed here.
Abstract

Background: Serum from systemic lupus erythematosus (SLE) patients has been shown to induce T-lymphocyte (TL) apoptosis. Given that different cells of the immune system display different sensitivity to apoptosis, we set to evaluate the in vitro effect of SLE serum on regulatory T-cells (Treg), Th17, Th1 and Th2 from SLE patients and healthy controls.

Methods: Peripheral blood mononuclear cells from SLE patients or normal controls were exposed to a pool of sera from SLE patients or normal controls. Annexin V was used to label cells in apoptosis or necrosis. Annexin V-labeled Treg, Th17, Th1 and Th2 cells were determined using flow cytometry.

Results: Total CD3 + and CD4 + cells from SLE patients showed higher frequency of spontaneous apoptosis/necrosis, whereas Th1 cells from SLE patients presented reduced spontaneous apoptosis/necrosis rate as compared with cells from controls. Incubation with SLE serum induced increased frequency of apoptotic/necrotic CD3 + , CD4 + and Th2 cells from normal controls or from SLE patients as compared with cultures incubated with normal human serum (NHS) or without human serum at all. Incubation with SLE serum did not increase the apoptosis/necrosis rate in Th1 or Th17 cells. Treg cells from SLE patients were more prone to apoptosis/necrosis induced by SLE serum than Treg cells from normal individuals. Th1, Th2, and Th17 cells presented increased apoptosis rates in cultures without human serum.

Conclusion: Our findings indicate that the serum of patients with active SLE stimulates apoptosis of CD4 + T cells in general and exhibit differentiated effects on CD4 + T-cell subsets.

Citing Articles

Lymphocytes Change Their Phenotype and Function in Systemic Lupus Erythematosus and Lupus Nephritis.

Moysidou E, Christodoulou M, Lioulios G, Stai S, Karamitsos T, Dimitroulas T Int J Mol Sci. 2024; 25(20).

PMID: 39456692 PMC: 11508046. DOI: 10.3390/ijms252010905.


PD-L1- and IL-4-expressing basophils promote pathogenic accumulation of T follicular helper cells in lupus.

Tchen J, Simon Q, Chapart L, Thaminy M, Vibhushan S, Saveanu L Nat Commun. 2024; 15(1):3389.

PMID: 38649353 PMC: 11035650. DOI: 10.1038/s41467-024-47691-w.

References
1.
Perniok A, Wedekind F, Herrmann M, Specker C, Schneider M . High levels of circulating early apoptic peripheral blood mononuclear cells in systemic lupus erythematosus. Lupus. 1998; 7(2):113-8. DOI: 10.1191/096120398678919804. View

2.
Yang F, He Y, Zhai Z, Sun E . Programmed Cell Death Pathways in the Pathogenesis of Systemic Lupus Erythematosus. J Immunol Res. 2019; 2019:3638562. PMC: 6913273. DOI: 10.1155/2019/3638562. View

3.
Lorenz H, Grunke M, Hieronymus T, Herrmann M, Kuhnel A, Manger B . In vitro apoptosis and expression of apoptosis-related molecules in lymphocytes from patients with systemic lupus erythematosus and other autoimmune diseases. Arthritis Rheum. 1997; 40(2):306-17. DOI: 10.1002/art.1780400216. View

4.
Bengtsson A, Sturfelt G, Gullstrand B, Truedsson L . Induction of apoptosis in monocytes and lymphocytes by serum from patients with systemic lupus erythematosus - an additional mechanism to increased autoantigen load?. Clin Exp Immunol. 2004; 135(3):535-43. PMC: 1808958. DOI: 10.1111/j.1365-2249.2003.02386.x. View

5.
Bengtsson A, Gullstrand B, Truedsson L, Sturfelt G . SLE serum induces classical caspase-dependent apoptosis independent of death receptors. Clin Immunol. 2007; 126(1):57-66. DOI: 10.1016/j.clim.2007.10.003. View