Spike protein is a key target for stronger and more persistent T-cell responses-a study of mild and asymptomatic SARS-CoV-2 infection

Copyright © 2023 The Authors. Published by Elsevier Ltd.. All rights reserved..

OBJECTIVES: Understanding the immune response in very mild and asymptomatic COVID-19 is crucial for developing effective vaccines and immunotherapies, yet remains poorly characterized. This longitudinal study examined the evolution of interferon (IFN)-γ responses to SARS-CoV-2 peptides in 109 asymptomatic or mildly symptomatic Ugandan COVID-19 patients across 365 days and explored their association with antibody generation.

METHODS: T-cell responses to spike-containing clusters of differentiation (CD4)-S and CD8 nCoV-A (CD8-A) megapools, and the non-spike CD4-R and CD8 nCoV-B (CD8-B) megapools, were assessed and correlated with demographic and temporal variables.

RESULTS: SARS-CoV-2-specific IFN-γ responses were consistently detected in all peptide pools and time points, with the spike-targeted response exhibiting higher potency and durability than the non-spike responses. Throughout the entire 365-day infection timeline, a robust positive correlation was observed between CD4 T-cell responses to the spike-derived peptides and anti-spike immunoglobulin G antibody levels, underscoring their interdependent dynamics in the immune response against SARS-CoV-2; in contrast, CD8 T-cell responses exhibited no such correlation, highlighting their distinctive, autonomous role in defense. No meaningful variations in complete blood count parameters were observed between individuals with COVID-19 infection and those without, indicating clinical insignificance.

CONCLUSIONS: This study highlights the dominant role of spike-directed T-cell responses in mild and asymptomatic disease and provides crucial longitudinal data from Sub-Saharan African settings. The findings provide valuable insights into the dynamics of T-cell responses and their potential significance in developing effective strategies for combating COVID-19.

Medienart:

E-Artikel

Erscheinungsjahr:

2023

Erschienen:

2023

Enthalten in:

Zur Gesamtaufnahme - volume:136

Enthalten in:

International journal of infectious diseases : IJID : official publication of the International Society for Infectious Diseases - 136(2023) vom: 20. Nov., Seite 49-56

Sprache:

Englisch

Beteiligte Personen:

Ssali, Ivan [VerfasserIn]
Mugaba, Susan [VerfasserIn]
Watelo, Arthur Kalyebi [VerfasserIn]
Bemanzi, Juliana [VerfasserIn]
Katende, Joseph Ssebwana [VerfasserIn]
Oluka, Gerald Kevin [VerfasserIn]
Ankunda, Violet [VerfasserIn]
Baine, Claire [VerfasserIn]
Kato, Laban [VerfasserIn]
COVID-19 Immunoprofiling Team [VerfasserIn]
Onyachi, Nathan [VerfasserIn]
Muwanga, Moses [VerfasserIn]
Jjuuko, Mark [VerfasserIn]
Kayiwa, John [VerfasserIn]
Nsereko, Christopher [VerfasserIn]
Auma, Betty Oliver [VerfasserIn]
Weiskopf, Daniela [VerfasserIn]
Sette, Alessandro [VerfasserIn]
Lutalo, Tom [VerfasserIn]
Musenero, Monica [VerfasserIn]
Kaleebu, Pontiano [VerfasserIn]
Serwanga, Jennifer [VerfasserIn]

Links:

Volltext

Themen:

82115-62-6
Antibodies, Viral
Hematological parameters
IFN-γ
Immunodominance
Interferon-gamma
Journal Article
Long-term immunity
Mild and asymptomatic COVID-19
Spike Glycoprotein, Coronavirus
Spike protein
Spike protein, SARS-CoV-2

Anmerkungen:

Date Completed 27.10.2023

Date Revised 14.02.2024

published: Print-Electronic

Citation Status MEDLINE

doi:

10.1016/j.ijid.2023.09.001

funding:

Förderinstitution / Projekttitel:

PPN (Katalog-ID):

NLM361812442