Role of Hemin in the Immune Response of T Follicular Helper Lymphocytes Expressing T-Cell Immunoreceptor with Immunoglobulin and Immunoreceptor Tyrosine-Based Inhibitory Domains, Programmed Cell Death-1, and Interleukin-21 in Allo-Auto Positive and Negative Thalassemia

• Published in: Journal of blood medicine 2023-01, Vol.14, p.7-17
• Main Authors: Tambunan, Betty Agustina, Ugrasena, I Dewa Gede, Aryati
• Format: Article
• Language: English
• Subjects: Antibodies; Apoptosis; Biochemistry; Blood diseases; Blood groups; Cell culture; Cell death; Cytokines; Flow cytometry; Immune response; Immunoglobulins; interleukin-21; Interleukins; Lymphocytes; Original Research; Patients; pd-1; Phenols; Sample size; T cells; t follicular helper; Thalassemia; thalassemia disease; tigit; Tyrosine
• ISSN: 1179-2736; 1179-2736
• DOI: 10.2147/JBM.S393134

Repeated transfusions in thalassemia patients can cause several complications, including alloimmunization and autoimmunization. This study compares the immune response of T follicular helper (Tfh) lymphocytes expressing T-cell immunoreceptor with immunoglobulin and immunoreceptor tyrosine-based inhibitory domains (TIGIT), programmed cell death-1 (PD-1), and interleukin-21 (IL-21) between patients with allo-auto positive and negative thalassemia before and after hemin administration. This study used a quasi-experimental pre- and post-test design and was performed between April and November 2021 at the Dr. Soetomo General Academic Hospital in Surabaya, Indonesia. It enrolled 29 patients with allo-auto positive thalassemia and 28 with allo-auto negative, and 9 mL of whole blood (WB) was drawn from each patient. Hemin solution (20 µM) was added to 5 mL of WB, incubated for two hours, processed into peripheral blood mononuclear cells (PBMCs) in RPMI media, and cultured with 5% CO for three days. The 4 mL WB sample was also processed into PBMCs. PBMC cells cultured and without cultured were examined by flow cytometry using a BD FACSCalibur after surface and intracellular staining. Differences in Tfh cells expressing TIGIT, PD-1, and IL-21 between thalassemia groups before and after hemin administration were compared using independent -tests or Mann-Whitney -tests (p < 0.05). Tfh cell expression did not differ between groups before hemin administration and increased after hemin administration. The increase in Tfh cell expression was higher in the allo-auto positive group. TIGIT and PD-1 expression in Tfh cells did not differ between groups, but TIGIT decreased after hemin administration in contrast to PD-1 result. IL-21 expression in Tfh cells did not differ between groups and did not change after hemin administration. Hemin affected the expression of Tfh cells in both group thalassemia, but there was no difference of Tfh cell expression between the groups.