The significance of T-follicular helper and T-follicular regulatory cells in autoimmune hemolytic anemia

Background Autoimmune hemolytic anemia (AIHA) is an acquired autoimmune disease resulting in the production of antibodies directed against the patient’s red blood cells, causing destruction of red blood cells. T-follicular helpers (Tfh) and T-follicular regulatory cells (Tfr) perform opposing actions in regulating germinal center responses. The dysregulation of their actions may ultimately advance the development of autoimmune diseases. There is evidence that patients with autoimmune diseases, such as rheumatoid arthritis, systemic lupus erythematosus, and systemic sclerosis, exhibit an imbalance of Tfh and Tfr cells. Aim To study the characteristics of Tfh and Tfr cells and analyze the Tfh/Tfr cells ratio in AIHA. Patients and methods The study was carried out on 50 patients with AIHA (primary not on treatment) who presented to Assiut University Hospital and 25 healthy age-matched and sex-matched controls. We determined Tfh and Tfr cell expression by flow cytometry using monoclonal antibodies CD3, CD4, CD185, PD1, and Foxp3. Results Within the CD3 + CD4 + lymphocytes we gated on C-X-C motif chemokine receptor type 5 (CXCR5 + ) T cells (CD185) and we determined the fraction of PD1 + FOXP3 - and PD1 + FOXP3 + from peripheral blood in patients with AIHA to analyze Tfh (CD4 + CXCR5 + PD1 + Foxp3 - ) and Tfr (CD4 + CXCR5 + PD1 + Foxp3 + ) cells. There was a statistically significantly higher median expression level of Tfh (CD4 + CXCR5 + PD1 + Foxp3 - ) (26.70 vs. 1.80%), P value less than 0.001, and lower median expression level of Tfr (CD4 + CXCR5 + PD1 + Foxp3 + ) cells among cases compared to controls (1.87 vs. 33.30%), P value less than 0.001. There was a statistically significant higher Tfh/Tfr cells ratio among cases compared to controls (15.19 vs. 0.09), P value less than 0.001. Conclusion Our results suggested that the increased Tfh cells and decreased Tfr cells may be involved in the immunopathogenesis of AIHA. Tfh/Tfr cells ratio has the most important role in the pathogenesis of AIHA. Our results may provide new insight into the role of Tfh cells as a new cellular target in AIHA treatment.

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Publication Details

Journal
The Egyptian Journal of Haematology
Published
2025-04-01
DOI
https://doi.org/10.4103/ejh.ejh_3_25
Primary Topic
Blood groups and transfusion
Type
article
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article

The significance of T-follicular helper and T-follicular regulatory cells in autoimmune hemolytic anemia

Hesham Abdelraheem, Suzanne Elgammal, Zeinab Albadry M. Zahran, Randa Amin Osman et al.
The Egyptian Journal of Haematology
Blood groups and transfusion
article

The significance of T-follicular helper and T-follicular regulatory cells in autoimmune hemolytic anemia

Hesham Abdelraheem, Suzanne Elgammal, Zeinab Albadry M. Zahran, Randa Amin Osman, Eman NasrEldin, Mohamed S. Sayed
article en

Abstract

Background Autoimmune hemolytic anemia (AIHA) is an acquired autoimmune disease resulting in the production of antibodies directed against the patient’s red blood cells, causing destruction of red blood cells. T-follicular helpers (Tfh) and T-follicular regulatory cells (Tfr) perform opposing actions in regulating germinal center responses. The dysregulation of their actions may ultimately advance the development of autoimmune diseases. There is evidence that patients with autoimmune diseases, such as rheumatoid arthritis, systemic lupus erythematosus, and systemic sclerosis, exhibit an imbalance of Tfh and Tfr cells. Aim To study the characteristics of Tfh and Tfr cells and analyze the Tfh/Tfr cells ratio in AIHA. Patients and methods The study was carried out on 50 patients with AIHA (primary not on treatment) who presented to Assiut University Hospital and 25 healthy age-matched and sex-matched controls. We determined Tfh and Tfr cell expression by flow cytometry using monoclonal antibodies CD3, CD4, CD185, PD1, and Foxp3. Results Within the CD3 + CD4 + lymphocytes we gated on C-X-C motif chemokine receptor type 5 (CXCR5 + ) T cells (CD185) and we determined the fraction of PD1 + FOXP3 - and PD1 + FOXP3 + from peripheral blood in patients with AIHA to analyze Tfh (CD4 + CXCR5 + PD1 + Foxp3 - ) and Tfr (CD4 + CXCR5 + PD1 + Foxp3 + ) cells. There was a statistically significantly higher median expression level of Tfh (CD4 + CXCR5 + PD1 + Foxp3 - ) (26.70 vs. 1.80%), P value less than 0.001, and lower median expression level of Tfr (CD4 + CXCR5 + PD1 + Foxp3 + ) cells among cases compared to controls (1.87 vs. 33.30%), P value less than 0.001. There was a statistically significant higher Tfh/Tfr cells ratio among cases compared to controls (15.19 vs. 0.09), P value less than 0.001. Conclusion Our results suggested that the increased Tfh cells and decreased Tfr cells may be involved in the immunopathogenesis of AIHA. Tfh/Tfr cells ratio has the most important role in the pathogenesis of AIHA. Our results may provide new insight into the role of Tfh cells as a new cellular target in AIHA treatment.

The Egyptian Journal of HaematologyVol. 50(2)
Children Cancer Hospital (EG), Assiut University (EG)
Openalex Percentile: Top 74%
Blood groups and transfusion
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