Traditional Chinese medicine for long COVID-19: the potential roles of immunity remodeling

Zhao Qianru , Bucchi Annalisa , Duan Xinyu , Yang Zhihua , Molla David , Baruscotti Mirko , Wang Yanyan

Acupuncture and Herbal Medicine ›› 2025, Vol. 5 ›› Issue (4) : 400 -419.

PDF (2427KB)
Acupuncture and Herbal Medicine ›› 2025, Vol. 5 ›› Issue (4) :400 -419. DOI: 10.1097/HM9.0000000000000175
Review Articles
research-article
Traditional Chinese medicine for long COVID-19: the potential roles of immunity remodeling
Author information +
History +
PDF (2427KB)

Abstract

Given that the immunity imbalance in patients with Long COVID-19 (LC) may pose a significant global health and economic post-pandemic burden, there is an emergent need to identify therapeutic targets and treatment options. Traditional Chinese medicine (TCM), as an evidence-based therapeutic approach, can effectively improve the sequelae of LC patients by eliminating pathogenic factors. The purpose of this paper is to discuss how immune remodeling contributes to the pathogenesis of LC, the clinical evidence supporting TCM’s treatment of LC, and the mechanism of TCM modulating immune remodeling and relieving chronic inflammation to develop new ideas for the treatment of LC as well as the development of drugs. Data were retrieved using appropriate keywords from a variety of internet databases, including PubMed and Web of Science. Current evidence shows that LC can affect multiple organ systems, and its prominent manifestations include respiratory complications, neurological symptoms and cardiovascular dysfunction. Immunoassay showed a characteristic increase in interleukin 6 (IL-6), interferon gamma (IFN-γ), and T helper (Th)17/regulatory T (Treg) imbalance. TCM interventions have shown great therapeutic potential, with active compounds such as baicalin reducing lung inflammation and ginsenosides improving heart function. Clinical research reports that Qingfei Paidu decoction (QFPD) can effectively alleviate respiratory symptoms, and Sini powder (SNP) has antidepressant effects. TCM interventions can be tailored based on the specific clinical symptoms of individual patients. This article elucidates the crucial role of inflammation and immune dysfunction in alleviating multiple organ symptoms of LC. TCM used in LC treatment is an important source of new molecules. These new molecules may act synergistically to combat adverse effects such as COVID-19 infection-induced inflammation and oxidative stress.

Keywords

Immunity remodeling / Inflammation / Long COVID-19 / Multi-system complications / SARS-CoV-2 / Traditional Chinese Medicine

Cite this article

Download citation ▾
Zhao Qianru, Bucchi Annalisa, Duan Xinyu, Yang Zhihua, Molla David, Baruscotti Mirko, Wang Yanyan. Traditional Chinese medicine for long COVID-19: the potential roles of immunity remodeling. Acupuncture and Herbal Medicine, 2025, 5(4): 400-419 DOI:10.1097/HM9.0000000000000175

登录浏览全文

4963

注册一个新账户 忘记密码

Conflict of interest statement

Mirko Baruscotti is an editorial board member of this journal. The other authors declare no conflict of interest.

Funding

This research was funded by the National Key R&D Program of China (2021YFE0200300), Science and Technology Program of Tianjin (22JCQNJC00480), Tianjin Education Commission (2022KJ151), and Graduate Research Innovation Project of TUTCM (YJSKC-20240013).

Author contributions

Yanyan Wang and Mirko Baruscotti performed conceptualization, writing—review and editing, supervision. Qianru Zhao, Annalisa Bucchi, and Zhihua Yang performed writing—original draft preparation. Qianru Zhao and David Molla performed visualization. Yanyan Wang performed project administration. All authors have read and agreed to the published version of the manuscript.

Ethical approval of studies and informed consent

Not applicable.

Acknowledgments

All figures were supported by FigDraw.

Data availability

All data generated or analyzed during this study are included in this published article.

References

[1]

Davis HE, Mccorkell L, Vogel JM, et al. Long COVID: major findings, mechanisms and recommendations. Nat Rev Microbiol. 2023; 21(3):133-146.

[2]

Chung YS, Lam CY, Tan PH, et al. Comprehensive review of COVID-19: epidemiology, pathogenesis, advancement in diagnostic and detection techniques, and post-pandemic treatment strategies. Int J Mol Sci. 2024; 25(15):8155.

[3]

Al-Aly Z, Davis H, Mccorkell L, et al. Long COVID science, research and policy. Nat Med. 2024; 30(8):2148-2164.

[4]

Szabo S, Zayachkivska O, Hussain A, et al. What is really “Long COVID?”. Inflammopharmacology. 2023; 31(2):551-557.

[5]

Ashmawy R, Hammouda EA, El-Maradny YA, et al. Interplay between comorbidities and long COVID: challenges and multidisciplinary approaches. Biomolecules. 2024; 14(7):835.

[6]

Peluso MJ, Deeks SG. Mechanisms of long COVID and the path toward therapeutics. Cell. 2024; 187(20):5500-5529.

[7]

Opsteen S, Files JK, Fram T, et al. The role of immune activation and antigen persistence in acute and long COVID. J Investig Med. 2023; 71(5):545-562.

[8]

Umesh A, Pranay K, Pandey RC, et al. Evidence mapping and review of long-COVID and its underlying pathophysiological mechanism. Infection. 2022; 50(5):1053-1066.

[9]

Shah W, Hillman T, Playford ED, et al. Managing the long term effects of COVID-19: summary of NICE, SIGN, and RCGP rapid guideline. BMJ. 2021;372:n136.

[10]

Koc HC, Xiao J, Liu W, et al. Long COVID and its management. Int J Biol Sci. 2022; 18(12):4768-4780.

[11]

Garg M, Maralakunte M, Garg S, et al. The conundrum of ‘Long-COVID-19′: a narrative review. Int J Gen Med. 2021; 14:2491-2506.

[12]

Greenhalgh T, Sivan M, Perlowski A, et al. Long COVID: a clinical update. Lancet. 2024; 404(10453):707-724.

[13]

Dennis A, Wamil M, Alberts J, et al. Multiorgan impairment in low-risk individuals with post-COVID-19 syndrome: a prospective, community-based study. BMJ Open. 2021; 11(3):e048391.

[14]

Townsend L, Dowds J, O’brien K, et al. Persistent poor health after COVID-19 is not associated with respiratory complications or initial disease severity. Ann Am Thorac Soc. 2021; 18(6):997-1003.

[15]

Van Den Borst B, Peters JB, Brink M, et al. Comprehensive health assessment 3 months after recovery from acute coronavirus disease 2019 (COVID-19). Clin Infect Dis. 2021; 73(5):e1089-e1098.

[16]

Lai CC, Hsu CK, Yen MY, et al. Long COVID: an inevitable sequela of SARS-CoV-2 infection. J Microbiol Immunol Infect. 2023; 56(1):1-9.

[17]

Sorensen AIV, Spiliopoulos L, Bager P, et al. A nationwide questionnaire study of post-acute symptoms and health problems after SARS-CoV-2 infection in Denmark. Nat Commun. 2022; 13(1):4213.

[18]

Huang C, Wang Y, Li X, et al. Clinical features of patients infected with 2019 novel coronavirus in Wuhan, China. Lancet. 2020; 395(10223):497-506.

[19]

Yong SJ. Long COVID or post-COVID-19 syndrome: putative pathophysiology, risk factors, and treatments. Infect Dis (Lond). 2021; 53(10):737-754.

[20]

Truffaut L, Demey L, Bruyneel AV, et al. Post-discharge critical COVID-19 lung function related to severity of radiologic lung involvement at admission. Respir Res. 2021; 22(1):29.

[21]

Carod-Artal FJ. Post-COVID-19 syndrome: epidemiology, diagnostic criteria and pathogenic mechanisms involved. Rev Neurol. 2021; 72(11):384-396.

[22]

Natarajan A, Shetty A, Delanerolle G, et al. A systematic review and meta-analysis of long COVID symptoms. Syst Rev. 2023; 12(1):88.

[23]

Yang ZH, Liu YX, Wang L, et al. Traditional Chinese medicine against COVID-19: role of the gut microbiota. Biomed Pharmacother. 2022; 149:112787.

[24]

Luo D, Liu B, Wang P, et al. Traditional Chinese medicine combined with moxibustion in the treatment of “long-COVID”: a protocol for systematic review and meta-analysis. Medicine (Baltim). 2022; 101(43):e31447.

[25]

Astin R, Banerjee A, Baker MR, et al. Long COVID: mechanisms, risk factors and recovery. Exp Physiol. 2023; 108(1):12-27.

[26]

Chun HJ, Coutavas E, Pine A, et al. Immunofibrotic drivers of impaired lung function in postacute sequelae of SARS-CoV-2 infection. Jci Insight. 2021; 6(14):e148476.

[27]

Cares-Marambio K, Montenegro-Jiménez Y, Torres-Castro R, et al. Prevalence of potential respiratory symptoms in survivors of hospital admission after coronavirus disease 2019 (COVID-19): a systematic review and meta-analysis. Chron Resp Dis. 2021; 18:14799731211002240.

[28]

Mancini DM, Brunjes DL, Lala A, et al. Use of cardiopulmonary stress testing for patients with unexplained dyspnea post-coronavirus disease. Jacc-Heart Fail. 2021; 9(12):92737.

[29]

Pedersen SF, Ho YC. SARS-CoV-2: a storm is raging. J Clin Invest. 2020; 130(5):2202-2205.

[30]

Morice A, Dicpinigaitis P, Mcgarvey L, et al. Chronic cough: new insights and future prospects. Eur Respir Rev. 2021; 30(162):210127.

[31]

Zawilska JB, Kuczynska K. Psychiatric and neurological complications of long COVID. J Psychiatr Res. 2022; 156:349-360.

[32]

Stefanou MI, Palaiodimou L, Bakola E, et al. Neurological manifestations of long-COVID syndrome: a narrative review. Ther Adv Chronic Dis. 2022; 13:20406223221076890.

[33]

Slama Schwok A, Henri J. Long neuro-COVID-19: current mechanistic views and therapeutic perspectives. Biomolecules. 2024; 14(9):1081.

[34]

Raman B, Cassar MP, Tunnicliffe EM, et al. Medium-term effects of SARS-CoV-2 infection on multiple vital organs, exercise capacity, cognition, quality of life and mental health, post-hospital discharge. Eclinicalmedicine. 2021; 31:100683.

[35]

Hernández-Fernández F, Valencia HS, Barbella-Aponte RA, et al. Cerebrovascular disease in patients with COVID-19: neuroimaging, histological and clinical description. Brain. 2020; 143:3089-3103.

[36]

Leng AL, Shah MN, Ahmad SA, et al. Pathogenesis underlying neurological manifestations of long COVID syndrome and potential therapeutics. Cells. 2023;12(5):816.

[37]

Etter MM, Martins TA, Kulsvehagen L, et al. Severe Neuro-COVID is associated with peripheral immune signatures, autoimmunity and neurodegeneration: a prospective cross-sectional study. Nat Commun. 2022; 13(1):6777.

[38]

Zuo T, Zhang F, Lui GCY, et al. Alterations in gut microbiota of patients with COVID-19 during time of hospitalization. Gastroenterology. 2020; 159(3):944-94+.

[39]

Raman B, Bluemke DA, Luscher TF, et al. Long COVID: post-acute sequelae of COVID-19 with a cardiovascular focus. Eur Heart J. 2022; 43(11):1157-1172.

[40]

Gyongyosi M, Alcaide P, Asselbergs FW, et al. Long COVID and the cardiovascular system-elucidating causes and cellular mechanisms in order to develop targeted diagnostic and therapeutic strategies: a joint scientific statement of the ESC working groups on cellular biology of the heart and myocardial and pericardial diseases. Cardiovasc Res. 2023; 119(2):336-356.

[41]

Depace NL, Colombo J. Long-COVID syndrome and the cardiovascular system: a review of neurocardiologic effects on multiple systems. Curr Cardiol Rep. 2022; 24(11):1711-1726.

[42]

Gaebler C, Wang Z, Lorenzi JCC, et al. Evolution of antibody immunity to SARS-CoV-2. Nature. 2021; 591(7851):639-644.

[43]

Clemens DJ, Ye D, Zhou W, et al. SARS-CoV-2 spike protein-mediated cardiomyocyte fusion may contribute to increased arrhythmic risk in COVID-19. PLoS One. 2023; 18(3):e0282151.

[44]

Meng QT, Song WQ, Churilov LP, et al. Psychophysical therapy and underlying neuroendocrine mechanisms for the rehabilitation of long COVID-19. Front Endocrinol. 2023; 14:1120475.

[45]

Ilias I, Diamantopoulos A, Pratikaki M, et al. Glycemia, beta-cell function and sensitivity to insulin in mildly to critically ill COVID-19 patients. Medicina(Lithuania). 2021; 57(1):68.

[46]

Raghavan S, Leo MD. Histamine potentiates SARS-CoV-2 spike protein entry into endothelial cells. Front Pharmacol. 2022; 13:872736.

[47]

Bornstein SR, Cozma D, Kamel M, et al. Long-COVID, metabolic and endocrine disease. Horm Metab Res. 2022; 54(8):562-566.

[48]

Steenblock C, Schwarz PEH, Ludwig B, et al. COVID-19 and metabolic disease: mechanisms and clinical management. Lancet Diabetes Endocrinol. 2021; 9(11):786-798.

[49]

Dworakowska D, Grossman AB. Thyroid disease in the time of COVID-19. Endocrine. 2020; 68(3):471-474.

[50]

Baldelli R, Nicastri E, Petrosillo N, et al. Thyroid dysfunction in COVID-19 patients. J Endocrinol Invest. 2021; 44(12):2735-2739.

[51]

Mcmillan P, Turner AJ, Uhal BD. Mechanisms of gut-related viral persistence in long COVID. Viruses. 2024; 16(8):1266.

[52]

Mohammed I, Podhala S, Zamir F, et al. Gastrointestinal sequelae of COVID-19: investigating post-infection complications-a systematic review. Viruses. 2024; 16(10):1516.

[53]

Qi FR, Qian S, Zhang SY, et al. Single cell RNA sequencing of 13 human tissues identify cell types and receptors of human coronaviruses. Biochem Bioph Res Co. 2020; 526(1):135-140.

[54]

Elbeltagi R, Al-Beltagi M, Saeed NK, et al. COVID-19-induced gastrointestinal autonomic dysfunction: a systematic review. World J Clin Cases. 2023; 11(22):5252-5272.

[55]

Raveendran AV, Jayadevan R, Sashidharan S. Long COVID: an overview. Diabetes Metab Syndr. 2021; 15(3):869-875.

[56]

Ramakrishnan RK, Kashour T, Hamid Q, et al. Unraveling the mystery surrounding post-acute sequelae of COVID-19. Front Immunol. 2021; 12:686029.

[57]

Merad M, Blish CA, Sallusto F, et al. The immunology and immunopathology of COVID-19. Science. 2022; 375(6585):1122-1127.

[58]

Townsend L, Dyer AH, Naughton A, et al. Longitudinal analysis of COVID-19 patients shows age-associated T cell changes independent of ongoing ill-health. Front Immunol. 2021; 12:676932.

[59]

Utrero-Rico A, Ruiz-Ruigomez M, Laguna-Goya R, et al. A short corticosteroid course reduces symptoms and immunological alterations underlying long-COVID. Biomedicines. 2021; 9(11):1540.

[60]

Evcik D. Musculoskeletal involvement: COVID-19 and post COVID 19. Turk J Phys Med Rehabil. 2023; 69(1):1-7.

[61]

Hirschenberger M, Hunszinger V, Sparrer KMJ. Implications of innate immunity in post-acute sequelae of non-persistent viral infections. Cells. 2021; 10(8):2134.

[62]

Nalbandian A, Sehgal K, Gupta A, et al. Post-acute COVID-19 syndrome. Nat Med. 2021; 27(4):601-615.

[63]

Spagnolo P, Balestro E, Aliberti S, et al. Pulmonary fibrosis secondary to COVID-19: a call to arms? Lancet Respir Med. 2020; 8(8):750-752.

[64]

Crook H, Raza S, Nowell J, et al. Long COVID-mechanisms, risk factors, and management. BMJ. 2021;374:n1648.

[65]

Tandon P, Abrams ND, Avula LR, et al. Unraveling links between chronic inflammation and long COVID: workshop report. J Immunol. 2024; 212(4):505-512.

[66]

Queiroz M AF, Neves P, Lima SS, et al. Cytokine profiles associated with acute COVID-19 and long COVID-19 syndrome. Front Cell Infect Microbiol. 2022; 12:922422.

[67]

Valente Coronel PM, Luiz Soares Basilio DC, Teixeira Espinoca I, et al. Involvement of oxidative stress in post-acute sequelae of COVID-19: clinical implications. Redox Rep. 2025; 30(1):2471738.

[68]

Tilikete C, Zamali I, Meddeb Z, et al. Exploring the landscape of symptom-specific inflammatory cytokines in post-COVID syndrome patients. BMC Infect Dis. 2024; 24(1):1337.

[69]

Lorkiewicz P, Waszkiewicz N. Biomarkers of post-COVID depression. J Clin Med. 2021; 10(18):4142.

[70]

Patterson BK, Guevara-Coto J, Yogendra R, et al. Immune-based prediction of COVID-19 severity and chronicity decoded using machine learning. Front Immunol. 2021; 12:700782.

[71]

Kim EY, Moudgil KD. Immunomodulation of autoimmune arthritis by pro-inflammatory cytokines. Cytokine. 2017; 98:87-96.

[72]

Zamora C, Canto E, Vidal S. The dual role of platelets in the cardiovascular risk of chronic inflammation. Front Immunol. 2021; 12:625181.

[73]

Research Accessibility Team (RAT). The microvascular hypothesis underlying neurologic manifestations of long COVID-19 and possible therapeutic strategies. Cardiovasc Endocrinol Metab. 2021; 10(4):193-203.

[74]

Lee CCE, Ali K, Connell D, et al. COVID-19-associated cardiovascular complications. Diseases. 2021; 9(3):47.

[75]

Giannitrapani L, Mirarchi L, Amodeo S, et al. Can baseline IL-6 levels predict long COVID in subjects hospitalized for SARS-CoV-2 disease? Int J Mol Sci. 2023; 24(2):1731.

[76]

Elbadawy HM, Khattab A, El-Agamy DS, et al. IL-6 at the center of cytokine storm: circulating inflammation mediators as biomarkers in hospitalized COVID-19 patients. J Clin Lab Anal. 2023; 37(7):e24881.

[77]

Siripanthong B, Nazarian S, Muser D, et al. Recognizing COVID-19-related myocarditis: the possible pathophysiology and proposed guideline for diagnosis and management. Heart Rhythm. 2020; 17(9):1463-1471.

[78]

Lazzerini PE, Boutjdir M, Capecchi PL. COVID-19, arrhythmic risk, and inflammation: mind the gap! Circulation. 2020; 142(1):7-9.

[79]

Goertz YMJ, Van Herck M, Delbressine JM, et al. Persistent symptoms 3 months after a SARS-CoV-2 infection: the post-COVID-19 syndrome? ERJ Open Res. 2020; 6(4):542-2020.

[80]

Islam MF, Cotler J, Jason LA. Post-viral fatigue and COVID-19: lessons from past epidemics. Fatigue Biomed Health Behav. 2020; 8(2):61-69.

[81]

Kappelmann N, Dantzer R, Khandaker GM. Interleukin-6 as potential mediator of long-term neuropsychiatric symptoms of COVID-19. Psychoneuroendocrino. 2021; 131:105295.

[82]

Higgins V, Sohaei D, Diamandis EP, et al. COVID-19: from an acute to chronic disease? Potential long-term health consequences. Crit Rev Clin Lab Sci. 2021; 58(5):297-310.

[83]

Duong-Quy S, Vo-Pham-Minh T, Tran-Xuan Q, et al. Post-COVID-19 pulmonary fibrosis: facts-challenges and futures: a narrative review. Pulm Ther. 2023; 9(3):295-307.

[84]

Li X, Li J, Zhang Y, et al. The role of IL-8 in the chronic airway inflammation and its research progress. Lin Chuang Er Bi Yan Hou Tou Jing Wai Ke Za Zhi. 2021; 35(12):1144-1148.

[85]

D’rozario R, Raychaudhuri D, Bandopadhyay P, et al. Circulating interleukin-8 dynamics parallels disease course and is linked to clinical outcomes in severe COVID-19. Viruses. 2023; 15(2):549.

[86]

Udwadia ZF, Koul PA, Richeldi L. Post-COVID lung fibrosis: the tsunami that will follow the earthquake. Lung India. 2021;38(Supplement):S41-S47.

[87]

Zhang Z, Zhao L, Zhou X, et al. Role of inflammation, immunity, and oxidative stress in hypertension: new insights and potential therapeutic targets. Front Immunol. 2022; 13:1098725.

[88]

Perumal R, Shunmugam L, Naidoo K, et al. Biological mechanisms underpinning the development of long COVID. iScience. 2023; 26(6):106935.

[89]

Cunningham L, Kimber I, Basketter D, et al. Perforin, COVID-19 and a possible pathogenic auto-inflammatory feedback loop. Scand J Immunol. 2021; 94(5):e13102.

[90]

Yin K, Peluso MJ, Thomas R, et al. Long COVID manifests with T cell dysregulation, inflammation, and an uncoordinated adaptive immune response to SARS-CoV-2. bioRxiv. 2023; 25(2):218-225.

[91]

Roe K. A role for T-cell exhaustion in long COVID-19 and severe outcomes for several categories of COVID-19 patients. J Neurosci Res. 2021; 99(10):2367-2376.

[92]

Zhang HP, Sun YL, Wang YF, et al. Recent developments in the immunopathology of COVID-19. Allergy. 2023; 78(2):369-388.

[93]

Sette A, Crotty S. Adaptive immunity to SARS-CoV-2 and COVID-19. Cell. 2021; 184(4):861-880.

[94]

Klein J, Wood J, Jaycox J, et al. Distinguishing features of long COVID identified through immune profiling. medRxiv. 2022; 623(7985):139-148.

[95]

Titov A, Kaminskiy Y, Ganeeva I, et al. Knowns and unknowns about CAR-T cell dysfunction. Cancers (Basel). 2022; 14(4):1078.

[96]

Glynne P, Tahmasebi N, Gant V, et al. Long COVID following mild SARS-CoV-2 infection: characteristic T cell alterations and response to antihistamines. J Investig Med. 2022; 70(1):61-67.

[97]

Crawford A, Angelosanto JM, Kao C, et al. Molecular and transcriptional basis of CD4(+) T cell dysfunction during chronic infection. Immunity. 2014; 40(2):289-302.

[98]

Mcgonagle D, Sharif K, O’regan A, et al. The role of cytokines including interleukin-6 in COVID-19 induced pneumonia and macrophage activation syndrome-like disease. Autoimmun Rev. 2020; 19(6):102537.

[99]

Phetsouphanh C, Darley DR, Wilson DB, et al. Immunological dysfunction persists for 8 months following initial mild-to-moderate SARS-CoV-2 infection. Nat Immunol. 2022; 23(2):210-216.

[100]

Rha MS, Shin EC. Activation or exhaustion of CD8(+) T cells in patients with COVID-19. Cell Mol Immunol. 2021; 18(10):2325-2333.

[101]

Zheng YY, Ma YT, Zhang JY, et al. COVID-19 and the cardiovascular system. Nat Rev Cardiol. 2020; 17(5):259-260.

[102]

Sadeghi A, Tahmasebi S, Mahmood A, et al. Th17 and treg cells function in SARS-CoV2 patients compared with healthy controls. J Cell Physiol. 2021; 236(4):2829-2839.

[103]

Meckiff BJ, Ramirez-Suastegui C, Fajardo V, et al. Imbalance of regulatory and cytotoxic SARS-CoV-2-reactive CD4(+) T cells in COVID-19. Cell. 2020; 183(5):1340-1360.

[104]

Dhawan M, Rabaan AA, Alwarthan S, et al. Regulatory T Cells (Tregs) and COVID-19: unveiling the mechanisms, and therapeutic potentialities with a special focus on long COVID. Vaccines (Basel). 2023; 11(3):699.

[105]

Jin D, An XD, Zhang YQ, et al. Potential mechanism prediction of herbal medicine for pulmonary fibrosis associated with SARS-CoV-2 infection based on network analysis and molecular docking. Front Pharmacol. 2021; 12:602218.

[106]

Bian YQ, Ma J, Ren Y, et al. Discovery of intervention effect of Chinese herbal formulas on COVID-19 pulmonary fibrosis treated by VEGFR and FGFR inhibitors. Zhongguo Zhong Yao Za Zhi. 2020; 45(7):1481-1487.

[107]

Jiang LL, An XD, Duan YY, et al. The pathological mechanism of the COVID-19 convalescence and its treatment with traditional Chinese medicine. Front Pharmacol. 2023; 13:1054312.

[108]

Chen YQ, Liu CL, Wang TP, et al. Efficacy and safety of Bufei Huoxue capsules in the management of convalescent patients with COVID-19 infection: a multicentre, double-blind, and randomised controlled trial. J Ethnopharmacol. 2022; 284:114830.

[109]

Zhao P, Liu XF, Dong HR, et al. Bufei yishen formula restores Th17/Treg balance and attenuates chronic obstructive pulmonary disease activation of the adenosine 2a receptor. Front Pharmacol. 2020; 11:1212.

[110]

Hongjiao G, Yanming X. Discussion on the mechanism of immune function regulation of traditional Chinese medicine in convalescent and discharged patients with new coronavirus pneumonia. Mod Tradit Chin Med Materia Med World Sci Technol. 2021; 23(2):482-487.

[111]

Bai RB, Zhang YJ, Fan JM, et al. Immune-enhancement effects of oligosaccharides from Codonopsis pilosula on cyclophosphamide induced immunosuppression in mice. Food Funct. 2020; 11(4):3306-3315.

[112]

Saeed M, Naveed M, Arain MA, et al. Quercetin: nutritional and beneficial effects in poultry. Worlds Poult Sci J. 2017; 73(2):355-364.

[113]

Bohan W, Suofang S, Xiaona Z. Exploration on mechanism of futu shengjin rehabilitation formula in regulating immune function during COVID-19 convalescence based on the network pharmacology. Nanjing Univ Tradit Chin Med. 2021; 37(1):91-95.

[114]

Ma CH, Ma ZQ, Fu Q, et al. Anti-asthmatic effects of baicalin in a mouse model of allergic asthma. Phytother Res. 2014; 28(2):231-237.

[115]

Xu L, Li JX, Zhang Y, et al. Regulatory effect of baicalin on the imbalance of Th17/Treg responses in mice with allergic asthma. J Ethnopharmacol. 2017; 208:199-206.

[116]

Sun J, Li LL, Wu JF, et al. Effects of baicalin on airway remodeling in asthmatic mice. Planta Med. 2013; 79(3-4):199-206.

[117]

Xiong GH, Liu SY, Gao JL, et al. Naringin protects ovalbumin-induced airway inflammation in a mouse model of asthma. Inflammation. 2016; 39(2):891-899.

[118]

Huang WC, Liu CY, Shen SC, et al. Protective effects of licochalcone a improve airway hyper-responsiveness and oxidative stress in a mouse model of asthma. Cells. 2019; 8(6):617.

[119]

Andre DM, Calixto MC, Sollon C, et al. Therapy with resveratrol attenuates obesity-associated allergic airway inflammation in mice. Int Immunopharmacol. 2016; 38:298-305.

[120]

Huang X, Tang L, Wang F, et al. Astragaloside IV attenuates allergic inflammation by regulation Th1/Th2 cytokine and enhancement CD4(+)CD25(+)Foxp3 T cells in ovalbumin-induced asthma. Immunobiology. 2014; 219(7):565-571.

[121]

Shen ZQ, Yu M, Dong ZF. Research progress on the pharmacodynamic mechanisms of sini powder against depression from the perspective of the central nervous system. Med Lith. 2023; 59(4):741.

[122]

Yan X, Zhang Z, Xu F, et al. Effect of Sini San freeze-dried powder on sleep-waking cycle in insomnia rats. J Tradit Chin Med. 2014; 34(5):572-575.

[123]

Wei SS, Yang HJ, Huang JW, et al. Traditional herbal formula Sini Powder extract produces antidepressant-like effects through stress-related mechanisms in rats. Chin J Nat Med. 2016; 14(8):590-598.

[124]

Qu S, Liu M, Cao C, et al. Chinese medicine formula Kai-Xin-San ameliorates neuronal inflammation of CUMS-induced depression-like mice and reduces the expressions of inflammatory factors via inhibiting TLR4/IKK/NF-kappaB pathways on BV2 cells. Front Pharmacol. 2021; 12:626949.

[125]

Li X, Qin XM, Tian JS, et al. Integrated network pharmacology and metabolomics to dissect the combination mechanisms of DC-Pall herb pair for treating depression. J Ethnopharmacol. 2021; 264:113281.

[126]

Chen JJ, Li T, Qin XM, et al. Integration of non-targeted metabolomics and targeted quantitative analysis to elucidate the synergistic antidepressant effect of bupleurum Chinense DC Paeonia Lactiflora Pall Herb Pair by regulating purine metabolism. Front Pharmacol. 2022; 13:900459.

[127]

Yan Y, Han R, Ma Y, et al. Plant adaptive agents: promising therapeutic molecules in the treatment of post-viral fatigue. Acupunct Herb Med. 2023; 3(1):20-27.

[128]

Liu HB, Lu XY, Hu Y, et al. Chemical constituents of Panax ginseng and Panax notoginseng explain why they differ in therapeutic efficacy. Pharmacol Res. 2020; 161:105263.

[129]

Yi LT, Zhu JX, Dong SQ, et al. Berberine exerts antidepressant-like effects via regulating miR-34a-synaptotagmin1/Bcl-2 axis. Chin Herb Med. 2021; 13(1):116-123.

[130]

Wang Y, Tong Q, Ma SR, et al. Oral berberine improves brain DOPA/dopamine levels to ameliorate Parkinson’s disease by regulating gut microbiota. Signal Transduct Target Ther. 2021; 6(1):77.

[131]

Pingali S, Donahue JP, Payton-Stewart F. Tetrahydroberberine, a pharmacologically active naturally occurring alkaloid. Acta Crystallogr C Struct Chem. 2015; 71:262-265.

[132]

Bai X, Fu RJ, Zhang S, et al. Potential medicinal value of celastrol and its synthesized analogues for central nervous system diseases. Biomed Pharmacother. 2021; 139:111551.

[133]

Zhang XM, Zhao WP, Liu XF, et al. Celastrol ameliorates inflammatory pain and modulates HMGB1/NF-κB signaling pathway in dorsal root ganglion. Neurosci Lett. 2019; 692:83-89.

[134]

Yan LL, Zhang WY, Wei XH, et al. Gualou Xiebai decoction, a traditional Chinese medicine, prevents cardiac reperfusion injury of hyperlipidemia rat via energy modulation. Front Physiol. 2018; 9:296.

[135]

Zhong Y, Chen L, Li M, et al. Dangshen erling decoction ameliorates myocardial hypertrophy via inhibiting myocardial inflammation. Front Pharmacol. 2021; 12:725186.

[136]

Chen J, Liu Z, Deng F, et al. Mechanisms of Lian-Gui-Ning-Xin-Tang in the treatment of arrhythmia: integrated pharmacology and in vivo pharmacological assessment. Phytomedicine. 2022; 99:153989.

[137]

Kim JH. Pharmacological and medical applications of and ginsenosides: a review for use in cardiovascular diseases. J Ginseng Res. 2018; 42(3):264-269.

[138]

Lee CH, Kim JH. A review on the medicinal potentials of ginseng and ginsenosides on cardiovascular diseases. J Ginseng Res. 2014; 38(3):161-166.

[139]

Furukawa T, Bai CX, Kaihara A, et al. Ginsenoside Re, a main phytosterol of Panax ginseng, activates cardiac potassium channels via a nongenomic pathway of sex hormones. Mol Pharmacol. 2006; 70(6):1916-1924.

[140]

Deng J, Lv XT, Wu Q, et al. Ginsenoside Rg(1) inhibits rat left ventricular hypertrophy induced by abdominal aorta coarctation: involvement of calcineurin and mitogen-activated protein kinase signalings. Eur J Pharmacol. 2009; 608(1-3):42-47.

[141]

Tang F, Lu M, Yu L, et al. Inhibition of TNF-alpha-mediated NF-kappaB activation by Ginsenoside Rg1 contributes the attenuation of cardiac hypertrophy induced by abdominal aorta coarctation. J Cardiovasc Pharmacol. 2016; 68(4):257-264.

[142]

Wang Z, Li M, Wu WK, et al. Ginsenoside Rb1 preconditioning protects against myocardial infarction after regional ischemia and reperfusion by activation of phosphatidylinositol-3-kinase signal transduction. Cardiovasc Drugs Ther. 2008; 22(6):443-452.

[143]

Hao DC, Ge GB, Xiao PG. Anticancer drug targets of salvia phytometabolites: chemistry, biology and omics. Curr Drug Targets. 2018; 19(1):1-20.

[144]

Guo R, Li L, Su J, et al. Pharmacological activity and mechanism of tanshinone IIA in related diseases. Drug Des Devel Ther. 2020; 14:4735-4748.

[145]

Tang B, Zhang JG, Tan HY, et al. Astragaloside IV inhibits ventricular remodeling and improves fatty acid utilization in rats with chronic heart failure. Biosci Rep. 2018; 38(3):BSR20171036.

[146]

Nie P, Meng FJ, Zhang JG, et al. Astragaloside IV exerts a myocardial protective effect against cardiac hypertrophy in rats, partially via activating the Nrf2/HO-1 signaling pathway. Oxid Med Cell Longevity. 2019; 2019:4625912.

[147]

Tan YQ, Chen HW, Li J. Astragaloside IV: an effective drug for the treatment of cardiovascular diseases. Drug Des Devel Ther. 2020; 14:3731-3746.

[148]

Lontchi-Yimagou E, Sobngwi E, Matsha TE, et al. Diabetes mellitus and inflammation. Curr Diab Rep. 2013; 13(3):435-444.

[149]

Liu Y, Wang AT, Wen LN, et al. A Chinese medicine formula (Jinqi Jiangtang Tablet): a review on its chemical constituents, quality control, pharmacokinetics studies, pharmacological properties and clinical applications. J Ethnopharmacol. 2019; 236:1-8.

[150]

Liu CM, Chen J, Yang S, et al. The Chinese herbal formula Zhibai Dihuang Granule treat Yin-deficiency-heat syndrome rats by regulating the immune responses. J Ethnopharmacol. 2018; 225:271-278.

[151]

Liu YX, Song A, Zang SS, et al. Jinlida reduces insulin resistance and ameliorates liver oxidative stress in high-fat fed rats. J Ethnopharmacol. 2015; 162:244-252.

[152]

Shi YL, Liu WJ, Zhang XF, et al. Effect of Chinese herbal medicine Jinlida Granule in treatment of patients with impaired glucose tolerance. Chin Med J (Engl). 2016; 129(19):2281-2286.

[153]

Zang SS, Song A, Liu YX, et al. Chinese medicine Jinlida (JLD) ameliorates high-fat-diet induced insulin resistance in rats by reducing lipid accumulation in skeletal muscle. Int J Clin Exp Med. 2015; 8(3):4620-4634.

[154]

Wang CQ, Dai XL, Zhang DF, et al. Jinlida granules improve dysfunction of hypothalamic-pituitary-thyroid axis in diabetic rats induced by STZ. Biomed Res Int-Uk. 2018; 2018:4764030.

[155]

Hong YJ, Kim N, Lee K, et al. Korean red ginseng (Panax ginseng) ameliorates type 1 diabetes and restores immune cell compartments. J Ethnopharmacol. 2012; 144(2):225-233.

[156]

Gao Y, Li J, Chu S, et al. Ginsenoside Rg1 protects mice against streptozotocin-induced type 1 diabetic by modulating the NLRP3 and Keap1/Nrf2/HO-1 pathways. Eur J Pharmacol. 2020; 866:172801.

[157]

Gao XY, Liu GC, Zhang JX, et al. Pharmacological properties of Ginsenoside Re. Front Pharmacol. 2022; 13:754191.

[158]

Chen Q, Zhu L, Tang Y, et al. Preparation-related structural diversity and medical potential in the treatment of diabetes mellitus with ginseng pectins. Ann N Y Acad Sci. 2017; 1401(1):75-89.

[159]

Li J, Casteels T, Frogne T, et al. Artemisinins target GABA(A) receptor signaling and impair alpha cell identity. Cell. 2017; 168(1-2):86-100.e15.

[160]

Guo Y, Fu W, Xin YK, et al. Antidiabetic and antiobesity effects of artemether in db/db Mice. Biomed Res Int-Uk. 2018; 2018:8639523.

[161]

Lee J, Knu MH, Lee JH, et al. Artemisinic acid is a regulator of adipocyte differentiation and C/EBP δ expression. J Cell Biochem. 2012; 113(7):2488-2499.

[162]

Yuan FY, Zhang M, Xu P, et al. Tanshinone IIA improves diabetes mellitus via the NF-κB-induced AMPK signal pathway. Exp Ther Med. 2018; 16(5):4225-4231.

[163]

Zhu YH, Han QQ, Wang L, et al. Jinhua Qinggan granules attenuates acute lung injury by promotion of neutrophil apoptosis and inhibition of TLR4/MyD88/NF-ΚB pathway. J Ethnopharmacol. 2023; 301:115763.

[164]

Li Q, Ran QS, Sun LD, et al. Lian Hua Qing Wen capsules, a potent epithelial protector in acute lung injury model, block proapoptotic communication between macrophages, and alveolar epithelial cells. Front Pharmacol. 2020; 11:522729.

[165]

Lem FF, Opook F, Lee DJH, et al. Molecular mechanism of action of repurposed drugs and traditional Chinese medicine used for the treatment of patients infected with COVID-19: a systematic scoping review. Front Pharmacol. 2021; 11:585331.

[166]

Zhang FB, Guo FF, Zhang Y, et al. Huashibaidu formula attenuates sepsis-induced acute lung injury suppressing cytokine storm: implications for treatment of COVID-19. Phytomedicine. 2023; 109:154549.

[167]

Li T, Zhao M, Zhu M, et al. Xuanfei Baidu decoction, a Chinese herbal medicine for coronavirus disease 2019 (COVID-19): a randomized clinical trial. Acupunct Herb Med. 2023; 3(3):207-212.

[168]

Zhang S, Yang Z, Chen ZL, et al. Efficacy and safety of “Three Chinese patent medicines and three TCM prescriptions” for COVID-19: a systematic review and network meta-analysis. Evid Based Compl Alt. 2022; 2022:4654793.

[169]

Xiao G, Wang S, Wang R, et al. “Three medicines and three formulas” in COVID-19: from bench to bedside. Acupunct Herb Med. 2023; 3(4):309-322.

[170]

Ma L, Zhao X, Liu T, et al. Xuanfei Baidu decoction attenuates intestinal disorders by modulating NF-κB pathway, regulating T cell immunity and improving intestinal flora. Phytomedicine. 2022; 101:154100.

[171]

Li ZH, Pan HT, Yang JH, et al. Xuanfei Baidu formula alleviates impaired mitochondrial dynamics and activated NLRP 3 inflammasome by repressing NF-κB and MAPK pathways in LPS-induced ALI and inflammation models. Phytomedicine. 2023; 108:114701.

[172]

Wang YY, Wang X, Li YX, et al. Xuanfei Baidu decoction reduces acute lung injury by regulating infiltration of neutrophils and macrophages PD-1/IL17A pathway. Pharmacol Res. 2022; 176:106083.

[173]

Wang YY, Sang XQ, Shao R, et al. Xuanfei Baidu decoction protects against macrophages induced inflammation and pulmonary fibrosis via inhibiting IL-6/STAT3 signaling pathway. J Ethnopharmacol. 2022; 283:114701.

[174]

Hu T, Li L, Ma Q. Research progress of immunomodulation on Anti-COVID-19 and the effective components from traditional Chinese medicine. Am J Chin Med. 2023; 51(6):1337-1360.

[175]

Huang YF, Bai C, He F, et al. Review on the potential action mechanisms of Chinese medicines in treating coronavirus disease 2019 (COVID-19). Pharmacol Res. 2020; 158:104939.

[176]

Bastaminejad S, Bakhtiyari S. Quercetin and its relative therapeutic potential against COVID-19: a retrospective review and prospective overview. Curr Mol Med. 2021; 21(5):385-391.

[177]

Di Pierro F, Khan A, Bertuccioli A, et al. Quercetin Phytosome® as a potential candidate for managing COVID-19. Minerva Gastroenterol. 2021; 67(2):190-195.

[178]

Liu WH, Zhi AM. The potential of Quercetin to protect against loperamide-induced constipation in rats. Food Sci Nutr. 2021; 9(6):3297-3307.

[179]

Wang LF, Wu F, Hong YL, et al. Research progress in the treatment of slow transit constipation by traditional Chinese medicine. J Ethnopharmacol. 2022; 290:115075.

[180]

Chen GX, Yang ZY, Wen D, et al. Polydatin has anti-inflammatory and antioxidant effects in LPS-induced macrophages and improves DSS-induced mice colitis. Immun Inflammation Dis. 2021; 9(3):959-970.

[181]

Niu YT, Zhang J, Shi DH, et al. Glycosides as potential medicinal components for ulcerative colitis: a review. Molecules. 2023; 28(13):5210.

[182]

Ng CYJ, Bun HH, Zhao Y, et al. TCM “medicine and food homology” in the management of post-COVID disorders. Front Immunol. 2023; 14:1234307.

[183]

Yuan X, Sun S, Wang S, et al. Effects of astragaloside IV on IFN-gamma level and prolonged airway dysfunction in a murine model of chronic asthma. Planta Med. 2011; 77(4):328-333.

[184]

Dong SJ, Zhong YQ, Lu WT, et al. Baicalin inhibits lipopolysaccharide-induced inflammation through signaling NF-κB pathway in HBE 16 airway epithelial cells. Inflammation. 2015; 38(4):1493-1501.

[185]

Lee M, Kim S, Kwon OK, et al. Anti-inflammatory and anti-asthmatic effects of resveratrol, a polyphenolic stilbene, in a mouse model of allergic asthma. Int Immunopharmacol. 2009; 9(4):418-424.

[186]

Li L, Gou CY, Li XM, et al. Effects of Chinese medicine on symptoms, syndrome evolution, and lung inflammation absorption in COVID-19 convalescent patients during 84-day follow-up after hospital discharge: a prospective cohort and nested case-control study. Chin J Integr Med. 2021; 27(4):245-251.

[187]

Li JS, Xie Y, Zhao P, et al. A Chinese herbal formula ameliorates COPD by inhibiting the inflammatory response via downregulation of p65, JNK, and p38. Phytomedicine. 2021; 83:153475.

[188]

Chen XH, Zhang B, Li JY, et al. Celastrol attenuates incision-induced inflammation and pain associated with inhibition of the NF-κB signalling pathway via SARM. Life Sci. 2018; 205:136-144.

[189]

Yang HB, Liu C, Jiang J, et al. Celastrol attenuates multiple sclerosis and optic neuritis in an experimental autoimmune encephalomyelitis model. Front Pharmacol. 2017; 8:44.

[190]

Yang L, Xu HH, Hong Q, et al. Crocus sativus L. produces anti-inflammatory effects and regulates NLRP3-NF-κB pathway. Acupuncture and Herbal Medicine. 2024; 4(3):375-385.

[191]

Mu J, Cheng FF, Wang QG, et al. Sini powder ameliorates the inflammatory response in rats with stress-induced non-alcoholic fatty liver disease by inhibiting the nuclear factor kappa-B/pyrin domain-containing protein 3 pathway. J Tradit Chin Med. 2020; 40(2):253-266.

[192]

Wang Q, Zhang YL, Li YH, et al. The memory enhancement effect of Kai Xin San on cognitive deficit induced by simulated weightlessness in rats. J Ethnopharmacol. 2016; 187:9-16.

[193]

Mei M, Tang FT, Lu ML, et al. Astragaloside IV attenuates apoptosis of hypertrophic cardiomyocyte through inhibiting oxidative stress and calpain-1 activation. Environ Toxicol Phar. 2015; 40(3):764-773.

[194]

Liu Q, Liu SN, Gao LH, et al. Anti-diabetic effects and mechanisms of action of a Chinese herbal medicine preparation JQ-R and in diabetic KK mice. Acta Pharm Sin B. 2017; 7(4):461-469.

[195]

Hsu YH, Chen TH, Wu MY, et al. Protective effects of Zhibai Dihuang Wan on renal tubular cells affected with gentamicin-induced apoptosis. J Ethnopharmacol. 2014; 151(1):635-642.

[196]

Liu ZY, Song N, Li MS, et al. Based on mRNA sequencing techniques to explore the molecular mechanism of Buzhong Yiqi decoction for autoimmune thyroiditis. Comb Chem High T Scr. 2024; 27(3):408-419.

[197]

Huang K, Zhang P, Zhang ZH, et al. Traditional Chinese medicine (TCM) in the treatment of COVID-19 and other viral infections: efficacies and mechanisms. Pharmacol Therapeut. 2021; 225:107843.

PDF (2427KB)

22

Accesses

0

Citation

Detail

Sections
Recommended

/