
To analyze the immune reconstitution after BTKi treatment in patients with chronic lymphocytic leukemia (CLL).The clinical and laboratorial data of 59 CLL patients admitted from January 2017 to March 2022 in Fujian Medical University Union Hospital were collected and analyzed retrospectively.The median age of 59 CLL patients was 60.5(36-78). After one year of BTKi treatment, the CLL clones (CD5 +/CD19 +) of 51 cases (86.4%) were significantly reduced, in which the number of cloned-B cells decreased significantly from (46±6.1)×109/L to (2.3±0.4)×109/L (P =0.0013). But there was no significant change in the number of non-cloned B cells (CD19 + minus CD5 +/CD19 +). After BTKi treatment, IgA increased significantly from (0.75±0.09)g/L to (1.31±0.1)g/L (P 0.05), respectively. Shannon index of BCR in patients with CR was 0.19±0.003 and 0.33±0.15 (P <0.001), while in patients with PR was 0.15±0.009 and 0.23±0.18 (P <0.05), respectively.BTKi treatment can shrink the clone size in CLL patients, promote the expression of IgA, increase the number of functional T cells, and regulate the secretion of cytokines such as IL-2, IL-4, and IFN-γ. BTKi also promote the recovery of diversity of TCR and BCR. BTKi treatment contributes to the reconstitution of immune function in CLL patients.
Immune Reconstitution, Tumor Necrosis Factor-alpha, Receptors, Antigen, T-Cell, Humans, Interleukin-4, Leukemia, Lymphocytic, Chronic, B-Cell, Retrospective Studies, Immunoglobulin A
Immune Reconstitution, Tumor Necrosis Factor-alpha, Receptors, Antigen, T-Cell, Humans, Interleukin-4, Leukemia, Lymphocytic, Chronic, B-Cell, Retrospective Studies, Immunoglobulin A
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