Department of Pediatric of Child Health and Diseases, Istanbul University-Cerrahpasa Cerrahpasa Medical School, Istanbul, Turkey.
Department of Pediatric Allergy and Immunology Istanbul, Istanbul University-Cerrahpasa Cerrahpasa Medical School, Istanbul, Turkey.
Pediatr Int. 2022 Jan;64(1):e15082. doi: 10.1111/ped.15082.
Most patients with organic acidemia suffer from recurrent infections. Although neutropenia has been reported in multiple studies, other components of the immune system have not been evaluated thoroughly. This study was conducted to assess the immune status of patients with organic acidemia (OA).
Thirty-three patients with OA who were followed up in Istanbul University-Cerrahpasa, Cerrahpasa School of Medicine, Nutrition and Metabolism Department and a total of 32 age- and sex-matched healthy controls were enrolled to the study. The demographic and clinical data were recorded retrospectively from patient files. Complete blood counts, immunoglobulins, and lymphocyte immunophenotyping were recorded prospectively in a symptom- (infection-) free period.
Of the 33 patients enrolled to the study, 21 (88%) were diagnosed with methylmalonic acidemia, 10 (33%) with propionic acidemia, and two (6.6%) with isovaleric acidemia. The mean age of the patients with OA and healthy subjects were 5.89 ± 4.11 years and 5.34 ± 4.36, respectively (P = 0.602). Twenty-nine (88%) of the patients had experienced frequent hospital admission, 13 (39%) were admitted to pediatric intensive care unit, and 18 (55%) suffered from sepsis. Naïve helper T cells and recent thymic emigrants were significantly lower in OAs (P < 0.001). Various defects in humoral immunity have also been documented including memory B cells and immunoglobulins.
Patients with OAs may show adaptive immune defects rendering them susceptible to infections. Metabolic reprogramming based on nutritional modifications may be a promising therapeutic option in the future.
大多数有机酸血症患者反复发生感染。尽管多项研究报道了中性粒细胞减少症,但其他免疫系统成分尚未得到充分评估。本研究旨在评估有机酸血症(OA)患者的免疫状态。
本研究纳入了在伊斯坦布尔大学切拉庞大学医学院营养与代谢科随访的 33 名 OA 患者和 32 名年龄和性别匹配的健康对照者。从患者档案中回顾性记录人口统计学和临床数据。在无病症(无感染)期前瞻性记录全血细胞计数、免疫球蛋白和淋巴细胞免疫表型。
本研究共纳入 33 名患者,其中 21 名(88%)诊断为甲基丙二酸血症,10 名(33%)诊断为丙酸血症,2 名(6.6%)诊断为异戊酸血症。OA 患者和健康受试者的平均年龄分别为 5.89±4.11 岁和 5.34±4.36 岁(P=0.602)。29 名(88%)患者经常住院,13 名(39%)入住儿科重症监护病房,18 名(55%)患有败血症。幼稚辅助 T 细胞和近期胸腺移民在 OA 中明显较低(P<0.001)。还记录了各种体液免疫缺陷,包括记忆 B 细胞和免疫球蛋白。
OA 患者可能存在适应性免疫缺陷,使他们容易感染。基于营养修改的代谢重编程可能是未来有前途的治疗选择。