Mejia-Chew Carlos, Spec Andrej, Walton Andrew H, Ulezko Antonova Alina, Dram Alexandra, Bhalla Sanjeev, Colonna Marco, Morre Michel, Hotchkiss Richard
Infectious Diseases, Washington University School of Medicine, 4523 Clayton Ave., Campus Box 8051, St. Louis, MO 63110-0193, USA.
Division of Infectious Diseases, Department of Medicine, Washington University School of Medicine, St. Louis, MO, USA.
Ther Adv Infect Dis. 2025 May 10;12:20499361251339300. doi: 10.1177/20499361251339300. eCollection 2025 Jan-Dec.
Nontuberculous mycobacteria disease is an emerging opportunistic infection that is often refractory to therapy. Interleukin 7 (IL-7) is a pleiotropic cytokine with broad-ranging effects that enhance immunity and augment monocyte/macrophage anti- killing in vitro.
This study evaluated IL-7 in patients with refractory complex lung disease (MAC-LD).
Prospective, single-center, randomized, study of IL-7 in patients with refractory MAC-LD.
Randomization (two sets of 4 weekly IL-7 injections) was stratified based on the presence of pulmonary cavities. The primary outcome was sputum culture conversion to negative within 6 months. Exploratory outcomes included investigation of potential molecular mechanisms of immunosuppression via single-cell RNA sequencing (scRNA-seq).
Of the eight participants enrolled, six completed the IL-7 regimen, one completed one 4-week therapy, and one received a single dose of IL-7. All six participants who completed the regimen showed an increased absolute lymphocyte count (ALC), yet none converted their sputum culture to negative at 6 months. Similarly, there were no differences in secondary outcomes compared to baseline. IL-7 was well tolerated, and two participants showed an increase in time-positivity for MAC in their sputum culture. scRNA-seq revealed increased expression of genes involved in immunosuppressive pathways.
In adults with refractory MAC-LD, IL-7 did not result in sputum culture conversion. IL-7 reversed the underlying lymphopenia associated with MAC-LD and led to a sustained increase in ALC. The study was limited by a small sample size, and although a longer course of IL-7 combined with newer antimicrobials for may warrant further investigation, structural lung disease may be a stronger predictor of cure than immune dysfunction in MAC-LD.
The trial was registered in clinicaltrials.gov (NCT04154826).
非结核分枝杆菌病是一种新出现的机会性感染,通常对治疗具有难治性。白细胞介素7(IL-7)是一种多效性细胞因子,具有广泛的作用,可增强免疫力并在体外增强单核细胞/巨噬细胞的抗杀伤能力。
本研究评估难治性复杂性肺病(MAC-LD)患者体内的IL-7。
一项针对难治性MAC-LD患者的IL-7前瞻性、单中心、随机研究。
基于肺空洞的存在进行随机分组(两组,每周注射4次IL-7)。主要结局是6个月内痰培养转为阴性。探索性结局包括通过单细胞RNA测序(scRNA-seq)研究免疫抑制的潜在分子机制。
入组的8名参与者中,6人完成了IL-7治疗方案,1人完成了1个为期4周的治疗疗程,1人接受了单剂量IL-7。完成治疗方案的所有6名参与者的绝对淋巴细胞计数(ALC)均增加,但6个月时痰培养均未转为阴性。同样,与基线相比,次要结局没有差异。IL-7耐受性良好,2名参与者的痰培养中MAC的阳性时间增加。scRNA-seq显示免疫抑制途径相关基因的表达增加。
在难治性MAC-LD成人患者中,IL-7未能使痰培养转阴。IL-7逆转了与MAC-LD相关的潜在淋巴细胞减少,并导致ALC持续增加。该研究受样本量小的限制,尽管更长疗程的IL-7联合新型抗菌药物可能值得进一步研究,但在MAC-LD中,结构性肺病可能比免疫功能障碍更能预测治愈情况。
该试验已在clinicaltrials.gov(NCT04154826)注册。