Anti‐SARS‐CoV‐2 spike immunoglobulin G and immunoglobulin M titers decline as interval from the second inactivated vaccine dose to the onset of illness is prolonged in breakthrough infection patients

Author:

Xu Chuan‐cai1ORCID,He Zhi‐song2,Lei Wei1,Zhu Jin‐zhou3,Zhao Da‐guo4,Kong Jin‐dan4,Wei Yao4,Xu Ying5,Huang Jian‐An1

Affiliation:

1. Department of Pulmonary and Critical Care Medicine the First Affiliated Hospital of Soochow University Suzhou China

2. Department of Cardiology the First Affiliated Hospital of Soochow University Suzhou China

3. Department of Gastroenterology the First Affiliated Hospital of Soochow University Suzhou China

4. Department of Critical Care Medicine the First Affiliated Hospital of Soochow University Suzhou China

5. Department of Infectious Diseases the First Affiliated Hospital of Soochow University Suzhou China

Abstract

AbstractBackgroundUnderstanding of the early immune response in severe acute respiratory syndrome coronavirus 2 (SARS‐CoV‐2) breakthrough infections is limited.MethodsNinety‐eight patients with coronavirus disease 2019 (COVID‐19) breakthrough infections were divided into two groups, with intervals from receiving the second dose of inactivated vaccine to the onset of illness <60 or ≥60 days.ResultsThe median lymphocyte count and the median anti‐SARS‐CoV‐2 spike immunoglobulin G (IgG) and immunoglobulin M (IgM) titers were higher in the <60‐day interval group compared with the corresponding medians in the ≥60‐day interval group (p = 0.005, p = 0.001, and p = 0.001, respectively). The median interleukin‐6 (IL‐6) level in the <60‐day interval group was significantly lower than the median IL‐6 level in the ≥60‐day interval group (p < 0.001).ConclusionsOur results highlight the different anti‐SARS‐CoV‐2 spike IgG and IgM antibody titers among patients with different intervals from receiving the second dose of inactivated vaccine to the onset of illness.

Publisher

Wiley

Subject

Genetics (clinical),Pulmonary and Respiratory Medicine,Immunology and Allergy

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