» Articles » PMID: 38675778

Vaccines Induce Homeostatic Immunity, Generating Several Secondary Benefits

Overview
Date 2024 Apr 27
PMID 38675778
Authors
Affiliations
Soon will be listed here.
Abstract

The optimal immune response eliminates invading pathogens, restoring immune equilibrium without inflicting undue harm to the host. However, when a cascade of immunological reactions is triggered, the immune response can sometimes go into overdrive, potentially leading to harmful long-term effects or even death. The immune system is triggered mostly by infections, allergens, or medical interventions such as vaccination. This review examines how these immune triggers differ and why certain infections may dysregulate immune homeostasis, leading to inflammatory or allergic pathology and exacerbation of pre-existing conditions. However, many vaccines generate an optimal immune response and protect against the consequences of pathogen-induced immunological aggressiveness, and from a small number of unrelated pathogens and autoimmune diseases. Here, we propose an "immuno-wave" model describing a vaccine-induced "Goldilocks immunity", which leaves fine imprints of both pro-inflammatory and anti-inflammatory milieus, derived from both the innate and the adaptive arms of the immune system, in the body. The resulting balanced, 'quiet alert' state of the immune system may provide a jump-start in the defense against pathogens and any associated pathological inflammatory or allergic responses, allowing vaccines to go above and beyond their call of duty. In closing, we recommend formally investigating and reaping many of the secondary benefits of vaccines with appropriate clinical studies.

Citing Articles

WISIT vaccines based on IL-31-derived peptides as a novel therapeutic approach for chronic pruritic dermatoses.

Schmidhuber S, Dickie J, Cserepes M, Tovari J, Schneeberger A, Mandler M PLoS One. 2025; 20(2):e0318293.

PMID: 39932924 PMC: 11813111. DOI: 10.1371/journal.pone.0318293.


Molecular Pathways Linking High-Fat Diet and PM Exposure to Metabolically Abnormal Obesity: A Systematic Review and Meta-Analysis.

Lobato S, Salomon-Soto V, Espinosa-Mendez C, Herrera-Moreno M, Garcia-Solano B, Perez-Gonzalez E Biomolecules. 2025; 14(12.

PMID: 39766314 PMC: 11674716. DOI: 10.3390/biom14121607.


In Silico Identification of Peanut Peptides Suitable for Allergy Immunotherapy in HLA-DRB1*03:01-Restricted Patients.

Doytchinova I, Atanasova M, Sotirov S, Dimitrov I Pharmaceuticals (Basel). 2024; 17(8).

PMID: 39204201 PMC: 11357649. DOI: 10.3390/ph17081097.

References
1.
Santos A, Matos D, Bertho A, Mendonca S, Marcovistz R . Detection of Th1/Th2 cytokine signatures in yellow fever 17DD first-time vaccinees through ELISpot assay. Cytokine. 2008; 42(2):152-155. DOI: 10.1016/j.cyto.2008.02.007. View

2.
Covian C, Rios M, Berrios-Rojas R, Bueno S, Kalergis A . Induction of Trained Immunity by Recombinant Vaccines. Front Immunol. 2021; 11:611946. PMC: 7873984. DOI: 10.3389/fimmu.2020.611946. View

3.
Chang R, Chen T, Wang S, Hung Y, Chen H, Wei C . Risk of autoimmune diseases in patients with COVID-19: A retrospective cohort study. EClinicalMedicine. 2023; 56:101783. PMC: 9830133. DOI: 10.1016/j.eclinm.2022.101783. View

4.
Netea M, Joosten L, Latz E, Mills K, Natoli G, Stunnenberg H . Trained immunity: A program of innate immune memory in health and disease. Science. 2016; 352(6284):aaf1098. PMC: 5087274. DOI: 10.1126/science.aaf1098. View

5.
Netea M, Kullberg B, van der Meer J . Circulating cytokines as mediators of fever. Clin Infect Dis. 2000; 31 Suppl 5:S178-84. DOI: 10.1086/317513. View