Salivary IgG to SARS-CoV-2 indicates seroconversion and correlates to serum neutralization in mRNA-vaccinated immunocompromised individuals

  • Katie Healy
  • , Elisa Pin
  • , Puran Chen
  • , Gunnar Söderdahl
  • , Piotr Nowak
  • , Stephan Mielke
  • , Lotta Hansson
  • , Peter Bergman
  • , C. I.Edvard Smith
  • , Per Ljungman
  • , Davide Valentini
  • , Ola Blennow
  • , Anders Österborg
  • , Giorgio Gabarrini
  • , Khaled Al-Manei
  • , Hassan Alkharaan
  • , Michał Jacek Sobkowiak
  • , Jamil Yousef
  • , Sara Mravinacova
  • , Angelica Cuapio
  • Xinling Xu, Mira Akber, Karin Loré, Cecilia Hellström, Sandra Muschiol, Gordana Bogdanovic, Marcus Buggert, Hans Gustaf Ljunggren, Sophia Hober, Peter Nilsson, Soo Aleman, Margaret Sällberg Chen

Research output: Contribution to journalArticlepeer-review

25 Scopus citations

Abstract

Background: Immunocompromised individuals are highly susceptible to severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) infection. Whether vaccine-induced immunity in these individuals involves oral cavity, a primary site of infection, is presently unknown. Methods: Immunocompromised patients (n = 404) and healthy controls (n = 82) participated in a prospective clinical trial (NCT04780659) encompassing two doses of the mRNA BNT162b2 vaccine. Primary immunodeficiency (PID), secondary immunodeficiencies caused by human immunodeficiency virus (HIV) infection, allogeneic hematopoietic stem cell transplantation (HSCT)/chimeric antigen receptor T cell therapy (CAR-T), solid organ transplantation (SOT), and chronic lymphocytic leukemia (CLL) patients were included. Salivary and serum immunoglobulin G (IgG) reactivities to SARS-CoV-2 spike were measured by multiplex bead-based assays and Elecsys anti-SARS-CoV-2 S assay. Findings: IgG responses to SARS-CoV-2 spike antigens in saliva in HIV and HSCT/CAR-T groups were comparable to those of healthy controls after vaccination. The PID, SOT, and CLL patients had weaker responses, influenced mainly by disease parameters or immunosuppressants. Salivary responses correlated remarkably well with specific IgG titers and the neutralizing capacity in serum. Receiver operating characteristic curve analysis for the predictive power of salivary IgG yielded area under the curve (AUC) = 0.95 and positive predictive value (PPV) = 90.7% for the entire cohort after vaccination. Conclusions: Saliva conveys vaccine responses induced by mRNA BNT162b2. The predictive power of salivary spike IgG makes it highly suitable for screening vulnerable groups for revaccination. Funding: Knut and Alice Wallenberg Foundation, Erling Perssons family foundation, Region Stockholm, Swedish Research Council, Karolinska Institutet, Swedish Blood Cancer Foundation, PID patient organization of Sweden, Nordstjernan AB, Center for Medical Innovation (CIMED), Swedish Medical Research Council, and Stockholm County Council (ALF).

Original languageEnglish
Pages (from-to)137-153.e3
JournalMed
Volume3
Issue number2
DOIs
StatePublished - 11 Feb 2022

UN SDGs

This output contributes to the following UN Sustainable Development Goals (SDGs)

  1. SDG 3 - Good Health and Well-being
    SDG 3 Good Health and Well-being

Keywords

  • COVID-19
  • HIV
  • Translation to patients
  • antibody
  • cancer
  • immunodeficiency
  • saliva
  • serum
  • transplantation
  • vaccination

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