2020, Number 4
An immunomodulatory peptide CIGB-258 for the treatment of critical and severe COVID-19 patients
Language: Spanish
References: 25
Page:
PDF size: 514.63 Kb.
ABSTRACT
Introduction: CIGB-258 is an immunomodulatory peptide with anti-inflammatory properties.Objectives: To establish the therapeutic schedule with CIGB-258 peptide for COVID-19 critically ill patients. In addition, to define the criteria for use and schedule of this peptide for COVID-19 seriously ill patients.
Methods: 9 critically ill patients and 3 seriously ill patients were included in this study. Clinical, radiological and laboratory evaluations were recorded according to the established protocol. Serum samples were obtained before and after treatment with CIGB-258, for the determination of the inflammation biomarkers.
Results: The therapeutic protocol was established with the CIGB-258 peptide, which consists of intravenous administration of 1 mg of peptide every 12 hours for critically ill patients. The dose should be increased to 2 mg every 12 hours, for patients who do not show clinical and radiological improvement in 24 hours. After extubation, patients should receive 1 mg of CIGB-258 daily, for another three days. Seriously ill patients should receive 1 mg of CIGB-258 every 12 hours, until their clinical condition resolves.
Conclusions: CIGB-258 showed an excellent safety profile. The established therapeutic protocol contributed to all critically ill patients recovering from respiratory distress and being extubated. Seriously ill patients improved considerably. The levels of the biomarkers associated with hyperinflammation and cytokines decreased significantly during treatment.
REFERENCES
Capraa R, DeRossia N, Mattiolib F, Romanelli G, Scarpazza C, Sormani MP, et al. Impact of low dose tocilizumab on mortality rate in patients with COVID-19 related pneumonia. European Journal of Internal Medicine. 2020[acceso: 08/06/2020]; 76: 31-35. Disponible en: https://doi.org/10.1016/j.ejim.2020.05.009
Domínguez MC, Lorenzo N, Barberá A, Darrasse-Jeze G, Hernandez MV, Torres AM, et al. An altered peptide ligand corresponding to a novel epitope from heat-shock protein 60 induces regulatory T cells and suppresses pathogenic response in an animal model of adjuvant induced arthritis. Autoimmunity. 2011[acceso: 21/12/2010]; 44(6):471-82. Disponible en: https://www.tandfonline.com/doi/abs/10.3109/08916934.2010.550590
Barberá A, Lorenzo N, van Kooten P, van Roon, Jager W, Parda D, et al. APL1, an altered peptide ligand derived from human heat-shock protein 60, increases the frequency of Tregs and its suppressive capacity against antigen responding effector CD4+T cells from rheumatoid arthritis patients. Cell Stress and Chaperones. 2016[acceso: 07/10/2013]; 21:735-744. Disponible en: https://doi.org/10.1007/s12192-016-0698-0
Lorenzo N, Altruda F, Silengo L, Dominguez MC. APL-1, an altered peptide ligand derived from heat-shock protein, alone or combined with methotrexate attenuates murine collagen induced arthritis. Clin Exp Med. 2017[acceso: 13/02/2016]; 17:209-216. Disponible en: https://doi.org/10.1007/s10238-016-0412-7
Prada D, Gómez J, Lorenzo N, Corrales O, Lopez A, Gonzalez E, et al. Phase I Clinical Trial with a Novel Altered Peptide Ligand Derived from Human Heat-Shock Protein 60 for Treatment of Rheumatoid Arthritis: Safety, Pharmacokinetics and Preliminary Therapeutic Effects. Journal of Clinical Trials. 2018[acceso: 08/02/2018]; 8(1):2167-0870. Disponible en: https://www.researchgate.net/profile/Maria_Dominguez_Horta/publication/323265216_Phase_I_Clinical_Trial_with_a_Novel_Altered_Peptide_Ligand_Derived_from_Human_Heat-Shock_Protein_60_for_Treatment_of_Rheumatoid_Arthritis_Safety_Pharmacokinetics_and_Preliminary_Therapeutic_Effects/links/5a8adef8aca272017e62ae6e/Phase-I-Clinical-Trial-with-a-Novel-Altered-Peptide-Ligand-Derived-from-Human-Heat-Shock-Protein-60-for-Treatment-of-Rheumatoid-Arthritis-Safety-Pharmacokinetics-and-Preliminary-Therapeutic-Effects.pdf
Corrales O, Hernández L, Prada D, Gómez J, Reyes Y, López AM, et al. CIGB-814, an altered peptide ligand derived from human heat-shock protein 60, decreases anti-cyclic citrullinated peptides antibodies in patients with rheumatoid arthritis. Clinical Rheumatology. 2019 acceso: 05/11/2018;38(3):955-960. Disponible en: https://pubmed.ncbi.nlm.nih.gov/30415439/
Ministerio de Salud Pública. Protocolo de actuación nacional para la covid-19: versión 1.4. La Habana: Minsap; 2020. [acceso: 24/08/2020]. Disponible en: Disponible en: https://files.sld.cu/editorhome/files/2020/05/MINSAP_Protocolo-de-Actuaci%c3%b3n-Nacional-para-la-COVID-19_versi%c3%b3n-1.4_mayo-2020.pdf
Ministerio de Salud Pública. Regulación No. 45-2007: Requerimientos para la notificación y el reporte de eventos adversos graves e inesperados en los ensayos clínicos. La Habana: CECMED; 2007. [acceso: 24/08/2020]. Disponible en: Disponible en: https://www.cecmed.cu/sites/default/files/adjuntos/Reglamentacion/reg_45-07_requerimientos_para_la_notificacion_y_el_reporte_de_eventos_adversos_graves_e_inesperados_en_los_ensayos_clinicos.pdf
Domínguez MC, Cabrales A, Lorenzo N, Padrón G and Gonzalez LJ. Biodistribution and pharmacokinetic profiles of an Altered Peptide Ligand derived from Heat-shock proteins 60 in Lewis rats. Cell Stress and Chaperones. 2020 acceso: 20/11/2020;25(1):133-140. Disponible en: https://pubmed.ncbi.nlm.nih.gov/31802366/
16 . Cabrales-Rico A, Ramos Y, Besada V,Dominguez M C, Lorenzo N, Garcia O, et al. Development and validation of a bioanalytical method based on LC-MS/MS analysis for the quantitation of CIGB-814 peptide in plasma from Rheumatoid Arthritis patients. J Pharm.Biomed Anal. 2017[acceso: 05/09/2017];143: 130-140. Disponible en: https://doi.org/10.1016/j.jpba.2017.05.030
Capraa R, DeRossia N, Mattiolib F, Romanelli G, Scarpazza C, Sormani M, et al. Impact of low dose tocilizumab on mortality rate in patients with COVID-19 related pneumonia. European Journal of Internal Medicine. 2020 acceso: 06/08/2020; 76: 31-35. Disponible en: https://doi.org/10.1016/j.ejim.2020.05.009
González M, González R, Hernández M, Bequet M, Rosario L, Grecesqui I, et al.CIGB-258, An Immunomodulatory Peptide for the Treatment of a COVID-19-associated Hepatic Encephalopathy: A Case Report. Preprint from Preprints. 2020[enviado: 09/09/2020; acceso: 09/09/2020]: [aprox. 10 pant.]. Disponible en: https://www.preprints.org/manuscript/202009.0240/v1
Gong J, Dong H, Xia Q, Huang Z, Wang D, Zhao Y, et al. Correlation analysis between disease severity and inflammation-related parameters in patients with COVID-19 pneumonia. Preprint from Med Rxiv. 2020[enviado: 27/02/2020; acceso: 27/02/2020]:[aprox. 17 pant.]. Disponible en: https://doi.org/10.1101/2020.02.25.20025643
Qin C, Zhou L, Hu Z, Zhang S, Yang S, Tao Y, et al. Dysregulation of immune response in patients with COVID-19 in Wuhan, China. Clin Infect Dis. 2020 [acceso: 23/05/2020]; 71(15): 762-768. Disponible en: https://search.bvsalud.org/global-literature-on-novel-coronavirus-2019-ncov/resource/es/covidwho-7937