# Immune Response to COVID-19 Vaccines: Updates in a Fast-Moving Scenario

**Authors:** Federico De Marco

PMC · DOI: 10.3390/vaccines14020168 · Vaccines · 2026-02-12

## TL;DR

This paper summarizes a special issue on recent findings about immune responses to and challenges with using COVID-19 vaccines.

## Contribution

The paper compiles 15 new studies addressing immunity, vaccine safety, and social attitudes related to COVID-19 vaccines.

## Key findings

- Six studies explore the level and durability of protective immunity from vaccines.
- Five studies examine vaccine use, efficacy, and safety in people with immune issues.
- One study reviews cellular mechanisms behind vaccine-dependent myocarditis.

## Abstract

The prompt and extensive use of COVID-19 vaccines has dramatically reduced both cases and casualties, but it has also underscored a number of critical issues that need to be addressed for their full exploitation at global level. This Special Issue was launched to gather fresh data to improve the way we use vaccines that are currently available to contribute to the design and the development of new ones and to elucidate social, ethical and psychological concerns that might hamper vaccine acceptance and use. It includes 15 articles six of which address, under various aspects, the level and durability of protective immunity; five deal with the highly debated field of vaccine use, efficacy and safety, in persons with an impaired/dysregulated immune system; one paper reports on adjuvants’ role in immune stimulation; one on the interference of natural adenovirus immunity with DNA vaccine response; one is a review on the cellular mechanisms of vaccine-dependent myocarditis; and one explores social attitudes to vaccines in different ethnic groups during early phases of the pandemic. Far from being complete and exhaustive, this Special Issue provides the reader with fresh insights into several critical questions raised by or connected to the advent of COVID-19 vaccines. This introductory article provides an overview of their contribution, while offering a quick glance at the current state of the art.

## Linked entities

- **Diseases:** COVID-19 (MONDO:0100096), myocarditis (MONDO:0004496)

## Full-text entities

- **Genes:** CD8A (CD8 subunit alpha) [NCBI Gene 925] {aka CD8, CD8alpha, IMD116, Leu2, p32}, ACE2 (angiotensin converting enzyme 2) [NCBI Gene 59272] {aka ACEH}, S (surface glycoprotein) [NCBI Gene 43740568] {aka spike glycoprotein}, CD4 (CD4 molecule) [NCBI Gene 920] {aka CD4mut, IMD79, Leu-3, OKT4D, T4}
- **Diseases:** GVHD (MESH:D006086), congenital heart defect (MESH:D006330), ARDs (MESH:D012216), Toxicity (MESH:D064420), cancer (MESH:D009369), COVID-19 (MESH:D000086382), infection (MESH:D007239), viral infections (MESH:D014777), inflammation (MESH:D007249), injury to (MESH:D014947), infectious complications (MESH:D003141), HIV (MESH:D015658), cardiac damage (MESH:D006331), myocarditis (MESH:D009205)
- **Chemicals:** selenium (MESH:D012643), S (MESH:D013455), AZD122 (-), steroids (MESH:D013256)
- **Species:** Homo sapiens (human, species) [taxon 9606], Adenoviridae (family) [taxon 10508], Mus musculus (house mouse, species) [taxon 10090], Severe acute respiratory syndrome coronavirus 2 (no rank) [taxon 2697049]

## Full text

_Full body text omitted from this summary view._ Fetch the complete paper as Markdown: https://tomesphere.com/paper/PMC12945231/full.md

## References

15 references — full list in the complete paper: https://tomesphere.com/paper/PMC12945231/full.md

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Source: https://tomesphere.com/paper/PMC12945231