Affiliations 

  • 1 Faculty of Medicine and Health Sciences, Universiti Malaysia Sarawak, 94300, Kota Samarahan, Sarawak, Malaysia. cstan@unimas.my
  • 2 Faculty of Medicine and Health Sciences, Universiti Malaysia Sarawak, 94300, Kota Samarahan, Sarawak, Malaysia
  • 3 Abbott Laboratories, 3 Frase Street #23-28 DUO Tower, Singapore, 189352, Singapore
  • 4 Advanced Pathology (M) Sdn Bhd, Kuching, 93400, Kuching, Sarawak, Malaysia
  • 5 Klinik Morni, Uni Garden, 94300, Kota Samarahan, Sarawak, Malaysia
  • 6 Borneo Medical Centre, 93350, Kuching, Sarawak, Malaysia
  • 7 Normah Specialist Medical Centre, 93050, Petra Jaya, Kuching, Sarawak, Malaysia
Sci Rep, 2022 09 19;12(1):15665.
PMID: 36123431 DOI: 10.1038/s41598-022-19776-3

Abstract

Several vaccines have been fast-tracked through clinical trials to mitigate the progression of the SARS‑CoV‑2 pandemic. We analyzed sequential blood samples from 314 recipients of Comirnaty and CoronaVac in East Malaysia for the spike-binding IgG (IgG-S), nucleocapsid-binding IgG (IgG-N), spike-binding IgM (IgM-S) and serum vitamin D (VitD). A subset of samples was analyzed for the neutralizing antibodies (Ig-RBD). Results showed that IgG-S due to Comirnaty was significantly higher than CoronaVac. IgM-S was detected in 80.0% Comirnaty and 69.5% CoronaVac recipients, while IgG-N was detected in 58.1% CoronaVac but not in Comirnaty recipients. All IgG-S-positive vaccines possessed detectable Ig-RBD after the second dose but with a weak to moderate correlation. The serum VitD levels did not influence the antibody magnitude in both vaccines. In essence, SARS-CoV-2 vaccination is an IgG-S-dominant event, Comirnaty was more effective than CoronaVac in mounting IgG-S and Ig-RBD responses, independent of the patient's VitD level.

* Title and MeSH Headings from MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine.