Immune response and severity of Omicron BA.5 reinfection among individuals previously infected with different SARS-CoV-2 variants

Front Cell Infect Microbiol. 2023 Dec 22:13:1277880. doi: 10.3389/fcimb.2023.1277880. eCollection 2023.

Abstract

Introduction: COVID-19 continues to spread worldwide, with an increasing number of individuals experiencing reinfection after recovering from their primary infection. However, the nature and progression of this infection remain poorly understood. We aimed to investigate the immune response, severity and outcomes of Omicron BA.5 reinfection among individuals previously infected with different SARS-CoV-2 variants.

Methods: We enrolled 432 COVID-19 cases who had experienced prior infection with the ancestral SARS-CoV-2 virus, Delta variant or Omicron BA.2 variant between January 2020 and May 2022 in Guangzhou, China. All cases underwent follow-up from March to April, 2023 through telephone questionnaires and clinical visits. Nasal lavage fluid and peripheral blood were collected to assess anti-RBD IgA, anti-RBD IgG and virus-specific IFN-γ secreting T cells.

Results: Our study shows that 73.1%, 56.7% and 12.5% of individuals with a prior infection of the ancestral virus, Delta or Omicron BA.2 variant experienced reinfection with the BA.5 variant, respectively. Fever, cough and sore throat were the most common symptoms of BA.5 reinfection, with most improving within one week and none progressing to a critical condition. Compared with individuals without reinfection, reinfected patients with a prior Delta infection exhibited elevated levels of nasal anti-RBD IgA, serum anti-RBD IgG and IFN-γ secreting T cells, whereas there was no noticeable change in reinfected individuals with a prior BA.2 infection.

Conclusion: These results suggest that BA.5 reinfection is common but severe outcomes are relatively rare. Reinfection with a novel SARS-CoV-2 variant different from the prior infection may induce a more robust immune protection, which should be taken into account during vaccine development.

Keywords: Omicron BA.5; SARS-COV-2 variants; disease severity; immune response; reinfection.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • COVID-19*
  • Humans
  • Immunity
  • Immunoglobulin A
  • Immunoglobulin G
  • Reinfection
  • SARS-CoV-2* / genetics

Substances

  • Immunoglobulin A
  • Immunoglobulin G

Supplementary concepts

  • SARS-CoV-2 variants

Grants and funding

The author(s) declare financial support was received for the research, authorship, and/or publication of this article. This work was supported by the National Key Research and Development Program of China [2022YFC2304803 to XT, 2022YFC0869400 to NY and 2023YFC3041500 to FL]; National Natural Science Foundation of China (92269108 to FL), Emergency Key Program of Guangzhou Laboratory (EKPG21-29 to XT and EKPG21-31 to FL), Key-Area Research and Development Program of Guangdong Province (2022B1111020002 to XT), Guangzhou Science and Technology Plan Project [202201020527 to XD and 202201020338 to QG].