Kageyama Yasunari, Nishizaki Yasuhiro, Aida Koichi, Yayama Katsuyuki, Ebisui Tomoka, Akiyama Tetsu, Nakamura Tsutomu
Takanawa Clinic, Tokyo 108-0074, Japan.
Tokai University Hospital, Isehara-shi, Kanagawa 259-1193, Japan.
Exp Ther Med. 2022 Jan;23(1):20. doi: 10.3892/etm.2021.10942. Epub 2021 Nov 2.
Intestinal microbiota can indirectly modulate airway physiology and immunity through the gut-lung axis. Recent microbiome studies indicate that patients with coronavirus disease 2019 (COVID-19) exhibit a specific intestinal dysbiosis that is closely associated with the disease pathophysiology. Therefore, rebalancing the intestinal microbiome using probiotics may be effective for controlling COVID-19. However, the rationale for using probiotics in COVID-19 remains unclear. In the present study, an cytokine response assay was conducted, followed by a single-arm, double-blind, prospective trial to evaluate the immunological efficacy of probiotic lactic acid bacteria against COVID-19. The present study focused on (), and ssp. , which exhibit robust protective effects against infection with respiratory RNA viruses. Considering the feasibility of long-term daily intake for prophylactic purposes, healthy uninfected individuals were enrolled as subjects. Our previous pilot trial demonstrated that oral Qingfei Paidu decoction (QFPD), a Chinese herbal medicine formulated specifically against COVID-19, upregulates plasma TNF-α, IL-1β, IL-18 and IL-8. Therefore, the present study utilized the cytokine changes induced by QFPD to define the innate cytokine index QICI [=(TNF-α) x (IL-1β) x (IL-18) x (IL-8)/(IL-6)] as an indicator of the anti-COVID-19 immunomodulatory potential of the lactic acid bacteria. A total of 20 eligible volunteers were enrolled, 18 of whom completed the intervention. demonstrated a strikingly high innate cytokine index in all subjects in the cytokine response assay. In the subsequent trial, oral intake of significantly increased the innate cytokine index (mean fold change, 17-fold; P=0.0138) and decreased the plasma level of IL-6 (P=0.0128), a key driver of complex immune dysregulation in COVID-19, as compared with the baseline. The cytokine index increased in 16 of 18 subjects (88.9%) with considerable individual differences in the fold change (1- to 128-fold). In line with these innate cytokine changes, ingestion significantly enhanced the activity of natural killer cells. By contrast, oral failed to induce a significant increase in the innate cytokine index (mean fold change, 2-fold; P=0.474) as compared with the baseline. In conclusion, demonstrated superior QFPD-like immunomodulatory ability and mimicked the blood cytokine environment produced by early immune responses to viral infection. Daily consumption of as an anti-COVID-19 probiotic may be a possible option for preventing COVID-19 during the pandemic. The present study was prospectively registered in the University Hospital Medical Information Network-Clinical Trials Registry under the trial number UMIN000040479 on 22 May 2020 (https://upload.umin.ac.jp/cgi-open-bin/ctr_e/ctr_view.cgi?recptno=R000046202).
肠道微生物群可通过肠-肺轴间接调节气道生理和免疫。最近的微生物组研究表明,2019冠状病毒病(COVID-19)患者表现出特定的肠道生态失调,这与疾病病理生理学密切相关。因此,使用益生菌恢复肠道微生物群平衡可能对控制COVID-19有效。然而,在COVID-19中使用益生菌的基本原理仍不清楚。在本研究中,进行了细胞因子反应测定,随后进行了一项单臂、双盲、前瞻性试验,以评估益生菌乳酸菌对COVID-19的免疫疗效。本研究重点关注了对呼吸道RNA病毒感染具有强大保护作用的嗜酸乳杆菌、约氏乳杆菌和副干酪乳杆菌亚种。考虑到长期每日摄入用于预防目的的可行性,招募健康未感染个体作为受试者。我们之前的初步试验表明,专门针对COVID-19配制的中药清肺排毒汤(QFPD)可上调血浆TNF-α、IL-1β、IL-18和IL-8。因此,本研究利用QFPD诱导的细胞因子变化,将先天细胞因子指数QICI[=(TNF-α)×(IL-1β)×(IL-18)×(IL-8)/(IL-6)]定义为乳酸菌抗COVID-19免疫调节潜力的指标。共招募了20名符合条件的志愿者,其中18人完成了干预。细胞因子反应测定显示所有受试者的先天细胞因子指数都非常高。在随后的试验中,与基线相比,口服嗜酸乳杆菌显著提高了先天细胞因子指数(平均变化倍数为17倍;P=0.0138),并降低了IL-6的血浆水平(P=0.0128),IL-6是COVID-19中复杂免疫失调的关键驱动因素。18名受试者中有16名(88.9%)的细胞因子指数增加,变化倍数存在相当大的个体差异(1至128倍)。与这些先天细胞因子变化一致,嗜酸乳杆菌摄入显著增强了自然杀伤细胞的活性。相比之下,口服约氏乳杆菌与基线相比未能显著提高先天细胞因子指数(平均变化倍数为2倍;P=0.474)。总之,嗜酸乳杆菌表现出优于QFPD的免疫调节能力,并模拟了病毒感染早期免疫反应产生的血液细胞因子环境。在大流行期间,每日食用嗜酸乳杆菌作为抗COVID-19益生菌可能是预防COVID-19的一种可能选择。本研究于2020年5月22日在大学医院医学信息网络-临床试验注册中心进行前瞻性注册,试验编号为UMIN000040479(https://upload.umin.ac.jp/cgi-open-bin/ctr_e/ctr_view.cgi?recptno=R000046202)。