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Clinical Trials/NCT05072496
NCT05072496
Completed
Not Applicable

A Prospective Cohort Study on Antibody Persistence and Immune Memory After Two Doses of Inactivated COVID-19 Vaccine in 150 People

Centers for Disease Control and Prevention, China1 site in 1 country150 target enrollmentJuly 20, 2020
ConditionsCOVID-19

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
COVID-19
Sponsor
Centers for Disease Control and Prevention, China
Enrollment
150
Locations
1
Primary Endpoint
Durability of humoral and cellular immune responses
Status
Completed
Last Updated
4 years ago

Overview

Brief Summary

The study describe 1 year durability of humoral and cellular immune responses in 150 individuals who received COVID-19 inactivated vaccine. all participants were recruited aged between 18 and 59 years old. Every participant was familiarized with the aim of the study and asked to sign an informed consent agreement, and be required blood sampling at the day 0 of first dose vaccine and 1 month, 3 months, 6 months and 12 months after fully vaccination separately. From every sample, 10 ml, 10 ml, and 5 ml were dispensed in three vacuum blood collection tubes. Peripheral blood lymphocytes cell (PBMC) were isolated with the two 10 ml samples contained heparin to detect immune memory cells and cytokines. RBD-IgG and neutralizing antibody be detected by 5ml sample from separating gel vacuum tubes. every individual conducted a detailed analysis comparing neutralizing antibody, TEM, TCM , and report on the cellular and humoral immunity 1 year after accept COVID-19 vaccine.

Registry
clinicaltrials.gov
Start Date
July 20, 2020
End Date
September 27, 2021
Last Updated
4 years ago
Study Type
Observational
Sex
All

Investigators

Sponsor
Centers for Disease Control and Prevention, China
Responsible Party
Principal Investigator
Principal Investigator

Wu Jiang

Director of Institute for Vaccines and Immunization

Centers for Disease Control and Prevention, China

Eligibility Criteria

Inclusion Criteria

  • Working at the CDC
  • Between the ages of 18 and 59
  • Not vaccinated with COVID-19 vaccine
  • Agreed to take a blood sample

Exclusion Criteria

  • who cannot take the COVID-19 vaccine due to some personal reasons
  • history of SARS-CoV, SARS-CoV-2, or Middle East respiratory syndrome infection
  • high-risk epidemiology history within 14 days before enrolment (eg, travel or residence history in communities with case reports, or contact history with someone infected with SARS-CoV-2)
  • axillary temperature of more than 37·0℃
  • history of allergy to any vaccine component.

Outcomes

Primary Outcomes

Durability of humoral and cellular immune responses

Time Frame: 12 months after fully vaccination

The humoral immunogenicity outcomes include the RBD-specific IgG titers and neutralising antibodies amounts at 1, 3, 6, and 12 months after the second shot. The positive cutoff for RBD-specific IgG antibodies was defined as the sample cutoff (S/CO) value ≥1.0. Seroconversion of neutralising antibodies was defined as a change from seronegative at baseline to seropositive or a four-fold titre increase. The positive cutoff of the titre for neutralising antibodies was 1/4. The cellular immune response outcomes measured by ICS assays across the blood collection time points.the percentage of RBD-specific CD4+ CD8+ memory T cells after vaccination.

Secondary Outcomes

  • The dynamic variation of the level of antibody(1,3,6 , 12 month)
  • Cytokine secretion by peripheral blood mononuclear cells(1,3,6,12 month)
  • TCM and TEM amount varies at different time points(1,3,6,12 month)

Study Sites (1)

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