Neutralizing Antibody and T-Cell Spike Targeted Responses Following Receipt of a Monovalent Omicron JN.1-Adapted mRNA COVID-19 Vaccine in Immunosuppressed and Healthy Individuals.

Publication date: Jun 01, 2025

We evaluated homologous neutralizing antibody (NtAb) and T-cell responses after receipt of a JN. 1-adapted mRNA vaccine in a mixed population comprising healthy controls (HC) (n = 15), end-stage chronic kidney disease (CKD) patients (n = 17), and allogeneic hematopoietic stem cell transplant recipients (allo-HCT) (n = 13). Most participants (42/45) were SARS-CoV-2-experienced at the time of immunological testing. JN. 1-spike-binding NtAbs were measured with a vesicular stomatitis virus pseudotype-based neutralization assay, whereas interferon (IFN)-γ-producing spike-directed CD4 or CD8 T-cell frequencies were enumerated using flow cytometry for intracellular staining. All participants had detectable JN. 1 NtAbs at baseline; overall, JN. 1-NtAb levels increased in HC (median, ∼1 log; p 

Concepts Keywords
Cd4 Adult
Healthy Aged
Hematopoietic anti‐RBD antibodies
Kidney Antibodies, Neutralizing
Vaccine Antibodies, Neutralizing
Antibodies, Viral
Antibodies, Viral
CD4-Positive T-Lymphocytes
CD8-Positive T-Lymphocytes
COVID-19
COVID-19 Vaccines
COVID-19 Vaccines
COVID‐19 vaccine
Female
Humans
Immunocompromised Host
Male
Middle Aged
neutralizing antibodies
Omicron JN.1
SARS-CoV-2
SARS‐CoV‐2
Spike Glycoprotein, Coronavirus
Spike Glycoprotein, Coronavirus
spike protein, SARS-CoV-2
Vaccines, Synthetic
Vaccines, Synthetic

Semantics

Type Source Name
disease IDO cell
disease MESH chronic kidney disease
disease IDO assay
disease MESH COVID-19
disease MESH Immunocompromised Host

Original Article

(Visited 4 times, 1 visits today)