Immunity, Inflammation and Disease (Jun 2022)

Persistence of immune responses to the Sinopharm/BBIBP‐CorV vaccine

  • Chandima Jeewandara,
  • Inoka Sepali Aberathna,
  • Pradeep Darshana Pushpakumara,
  • Achala Kamaladasa,
  • Dinuka Guruge,
  • Ayesha Wijesinghe,
  • Banuri Gunasekera,
  • Shyrar Tanussiya Ramu,
  • Heshan Kuruppu,
  • Thushali Ranasinghe,
  • Shashika Dayarathna,
  • Osanda Dissanayake,
  • Nayanathara Gamalath,
  • Dinithi Ekanayake,
  • Jeewantha Jayamali,
  • Deshni Jayathilaka,
  • Madushika Dissanayake,
  • Tibutius Thanesh Jayadas,
  • Anushika Mudunkotuwa,
  • Gayasha Somathilake,
  • Michael Harvie,
  • Thashmi Nimasha,
  • Saubhagya Danasekara,
  • Ruwan Wijayamuni,
  • Lisa Schimanski,
  • Pramila Rijal,
  • Tiong K. Tan,
  • Tao Dong,
  • Alain Townsend,
  • Graham S. Ogg,
  • Gathsaurie Neelika Malavige

DOI
https://doi.org/10.1002/iid3.621
Journal volume & issue
Vol. 10, no. 6
pp. n/a – n/a

Abstract

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Abstract Background To determine the kinetics and persistence of immune responses following the Sinopharm/BBIBP‐CorV, we investigated immune responses in a cohort of Sri Lankan individuals. Methods SARS‐CoV‐2 specific total antibodies were measured in 20–39 years (n = 61), 40–59 years (n = 120) and those >60 years of age (n = 22) by enzyme‐linked immunosorbent assay, 12 weeks after the second dose of the vaccine. Angiotensin‐converting enzyme 2 (ACE2) receptor blocking antibodies (ACE2R‐Ab), antibodies to the receptor‐binding domain (RBD) of the ancestral virus (WT) and variants of concern, were measured in a sub cohort. T cell responses and memory B cell responses were assessed by ELISpot assays. Results A total of 193/203 (95.07%) of individuals had detectable SARS‐CoV‐2 specific total antibodies, while 67/110 (60.9%) had ACE2R‐Ab. A total of 14.3%–16.7% individuals in the 20–39 age groups had detectable antibodies to the RBD of the WT and variants of concern, while the positivity rates of those ≥60 years of age was <10%. A total of 14/49 (28.6%) had Interferon gamma ELISpot responses to overlapping peptides of the spike protein, while memory B cell responses were detected in 9/20 to the S1 recombinant protein. The total antibody levels and ACE2R‐Ab declined from 2 to 12 weeks from the second dose, while ex vivo T cell responses remained unchanged. The decline in ACE2R‐Ab levels was significant among the 40–59 (p = .0007) and ≥60 (p = .005) age groups. Conclusions Antibody responses declined in all age groups, especially in those ≥60 years, while T cell responses persisted. The effect of waning of immunity on hospitalization and severe disease should be assessed by long term efficacy studies.

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