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Kinetics of immune responses elicited after three mRNA COVID-19 vaccine doses in predominantly antibody-deficient individuals. | LitMetric

AI Article Synopsis

  • Mass vaccination campaigns have effectively lowered COVID-19 cases and severity, and this study examined the immune responses of patients with primary antibody deficiencies (PAD) after receiving three doses of the mRNA-1273 vaccine.
  • Patients were categorized into groups based on their specific immunodeficiencies, and while unclassified PAD (unPAD) patients and healthy controls showed similar antibody responses after two doses, those with common variable immunodeficiency (CVID) exhibited weaker responses.
  • The third vaccine dose improved antibody levels in most PAD patients but had little effect on enhancing cellular immunity, highlighting the need for individualized monitoring and treatment strategies for PAD individuals.

Article Abstract

Mass vaccination campaigns reduced COVID-19 incidence and severity. Here, we evaluated the immune responses developed in SARS-CoV-2-uninfected patients with predominantly antibody-deficiencies (PAD) after three mRNA-1273 vaccine doses. PAD patients were classified based on their immunodeficiency: unclassified primary antibody-deficiency (unPAD, n = 9), common variable immunodeficiency (CVID, n = 12), combined immunodeficiency (CID, n = 1), and thymoma with immunodeficiency (TID, n = 1). unPAD patients and healthy controls (HCs, n = 10) developed similar vaccine-induced humoral responses after two doses. However, CVID patients showed reduced binding and neutralizing titers compared to HCs. Of interest, these PAD groups showed lower levels of Spike-specific IFN-γ-producing cells. CVID individuals also presented diminished CD8T cells. CID and TID patients developed cellular but not humoral responses. Although the third vaccine dose boosted humoral responses in most PAD patients, it had limited effect on expanding cellular immunity. Vaccine-induced immune responses in PAD individuals are heterogeneous, and should be immunomonitored to define a personalized therapeutic strategies.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC9613776PMC
http://dx.doi.org/10.1016/j.isci.2022.105455DOI Listing

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