Hematology Research Center, Shiraz University of Medical Sciences, Shiraz, Iran.
Neshat Laboratory Research Center, Shiraz University of Medical Sciences, Shiraz, Iran.
BMC Pediatr. 2022 Mar 21;22(1):149. doi: 10.1186/s12887-022-03216-2.
Acute lymphoblastic leukemia (ALL) is the most common type of cancer in the age range of under 15 years old and accounts for 25-30% of all childhood cancers. Although conventional chemotherapy regimens are used to improve the overall survival rate, it has been associated with some complications, amongst which allergic manifestations with unknown mechanisms are more common.
Our study compared serum IgE and IL-4 concentration, as a hallmark of allergic responses in pediatric ALL patients before and after 6 months of intensive (high-dose) chemotherapy, to show whether changes in the level of these markers may be associated with atopy. Serum level of IL-4 and IgE was measured using enzyme-linked immunosorbent assay (ELISA) method.
The results showed that the level of IgE and IL-4 increased following chemotherapy in both ALL patients with and without atopy. In addition, post-chemotherapy treatment IgE and IL-4 levels were significantly elevated in patients with atopy compared to those without it. The difference between baseline and post-chemotherapy level of IgE and IL-4 was significantly higher in patients with atopy compared to those without it.
To the best of our knowledge, this is the first study that showed a connection between post-chemotherapy allergic manifestations in pediatric ALL patients and IL-4 and IgE level. Flow cytometry analysis of the T-helper 2 (Th2) lymphocytes and other allergy-related T cell subsets like Tc2 and Th9 as well as the study of the genetic variations in atopy-related genes like IL-4/IL-4R, IL-5, IL-9, IL-13, and high affinity FcεRI IgE receptor and also HLA genes is necessary to clearly define the underlying mechanism responsible for post-chemotherapy hypersensitivity reaction in pediatric ALL patients.
急性淋巴细胞白血病(ALL)是 15 岁以下年龄段最常见的癌症类型,占所有儿童癌症的 25-30%。虽然常规化疗方案可用于提高总体生存率,但它与一些并发症有关,其中过敏表现的机制尚不清楚。
我们的研究比较了儿科 ALL 患者在强化(高剂量)化疗前和化疗后 6 个月时血清 IgE 和 IL-4 浓度,作为过敏反应的标志,以显示这些标志物水平的变化是否与过敏有关。使用酶联免疫吸附试验(ELISA)法测量血清中 IL-4 和 IgE 的水平。
结果表明,ALL 患者无论是否过敏,化疗后 IgE 和 IL-4 水平均升高。此外,与无过敏患者相比,过敏患者在化疗后的 IgE 和 IL-4 水平显著升高。与无过敏患者相比,过敏患者的 IgE 和 IL-4 的基线和化疗后水平之间的差异显著更高。
据我们所知,这是第一项表明儿科 ALL 患者化疗后过敏表现与 IL-4 和 IgE 水平之间存在联系的研究。通过对 T 辅助 2(Th2)淋巴细胞进行流式细胞术分析,以及对与过敏相关的 T 细胞亚群,如 Tc2 和 Th9 以及与过敏相关的基因如 IL-4/IL-4R、IL-5、IL-9、IL-13 和高亲和力 FcεRI IgE 受体和 HLA 基因的遗传变异进行研究,有助于明确导致儿科 ALL 患者化疗后过敏反应的潜在机制。