The Evaluation of Cellular and Humoral Immunity to COVID-19 in Moscow Residents

NCT04898140 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 5340

Last updated 2022-09-14

No results posted yet for this study

Summary

The aim of the research is to estimate the levels of cellular and humoral immunity to the severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) among Moscow residents over 18 years old. During the study, participants will be divided into four groups: healthy volunteers; individuals recovered from coronavirus disease 2019 (COVID-19) with different severity; individuals vaccinated against SARS-CoV-2; individuals who have had COVID-19 concomitantly with comorbidities that characterized by the impact on the immune system (tuberculosis, chronic obstructive pulmonary disease, HIV infection, hematological neoplasia). For all participants included into the study peripheral blood will be collected and the titers of SARS-CoV-2 specific immunoglobulins M (IgM) and immunoglobulins G (IgG), frequencies of the T cells specific to nucleocapsid (N), membrane (M), and spike (S) proteins of SARS-CoV-2 in peripheral blood, as well as the fractions of virus specific T helpers and cytotoxic T cells will be estimated. For smaller cohorts of the participants in all groups the antibody titers and T cell response levels will be examined in dynamics. All participants will be monitored for the incidence of primary or repeated COVID-19 for 1-2 years after inclusion in the study.

Based on the results of the study, the relationship between the formation of humoral and cellular immunity against COVID-19, the duration of these types of immunity, as well as their individual contribution to protection against primary or secondary SARS-CoV-2 infection will be analyzed. Additionally, data concerning patients recovered from COVID-19 and having concomitant diseases will provide a valuable information that may help to understand in more details the mechanisms of the development of the SARS-CoV-2 specific immune response.

Conditions

  • Covid19
  • Respiratory Viral Infection

Interventions

DIAGNOSTIC_TEST

SARS-CoV-2 specific IgM and IgG detection

Detection of IgM and IgG antibodies specific to the SARS-CoV-2 antigens in the blood serum using enzyme-linked immunosorbent assay (ELISA).

DIAGNOSTIC_TEST

ELISpot: detection of the T cells specific to different SARS-CoV-2 proteins

Detection of peripheral blood T lymphocytes which are activated and secrete interferon gamma (IFNgamma) upon stimulation with peptides, covering the immunodominant sequence domains of the nucleocapsid N, membrane M, or spike glycoprotein S proteins of SARS-CoV-2 coronavirus.

DIAGNOSTIC_TEST

Flow cytometry: detection of the SARS-CoV-2 specific T-helpers and cytotoxic T lymphocytes

Detection of peripheral blood T-helpers (CD45+CD3+CD4+)\* and cytotoxic T cells (CD45+CD3+CD8+)\* which are activated and secrete IFNgamma and/or interleukin-2 (IL2) upon stimulation with mixture of peptides, covering the immunodominant sequence domains of the nucleocapsid N, membrane M, and spike glycoprotein S proteins of SARS-CoV-2 coronavirus. \* CD, cluster of differentiation

Sponsors & Collaborators

  • Clinical City Hospital named after I.V. Davydovsky of Moscow Department of Healthcare

    collaborator NETWORK
  • Moscow State University of Medicine and Dentistry

    collaborator OTHER
  • Moscow Institute of Physics and Technology

    collaborator UNKNOWN
  • National Research Center for Hematology, Russia

    collaborator NETWORK
  • State Research Center Institute of Immunology, Russia

    collaborator UNKNOWN
  • Shemyakin-Ovchinnikov Institute of bioorganic chemistry RAS

    collaborator UNKNOWN
  • National Medical Research Center of Phthisiopulmonology and Infectious Diseases

    collaborator OTHER_GOV
  • Moscow Department of Health

    lead OTHER_GOV

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2020-10-20
Primary Completion
2021-12-31
Completion
2021-12-31

Countries

  • Russia

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT04898140 on ClinicalTrials.gov