Many pathogens have evolved capabilities for maintaining chronic infections by entering one or more stages of latency to avoid immune system detection and attack. Several latent pathogens are capable of periodic reactivations decades after their initial infections. However, other pathogens have not evolved intrinsic capabilities for latency to maintain chronic infections, but several of these pathogens can maintain chronic infections by what herein will be called “quasi‐latency” in response to suppressions or nutrient deprivation. When later events reduce such suppressions, the quasi‐latent pathogens can achieve “resurgent” infections. These quasi‐latent pathogens can quickly achieve resurgent infections, which are severe and frequently lethal. This raises the question of how some pathogens can be suppressed into quasi‐latency, and how they can become resurgent. Besides innate and adaptive immune cell actions that kill pathogens or pathogen‐infected cells, pathogens can be suppressed by nutritional deprivation. Iron deprivation is frequently effective, since iron is essential for pathogens. For instance, hemolytic protozoan parasite infections can provide heme and iron for the resurgence of quasi‐latent, iron‐deprived pathogens. This could explain the pathogenesis of two puzzling, sometimes lethal pregnancy disorders, pre‐eclampsia and eclampsia, which have caused the deaths of millions of women for centuries.
Latent Pathogens and Quasi‐Latent Pathogens—The Differences and Similarities
Published 2026 in Acta Pathologica, Microbiologica et Immunologica Scandinavica (APMIS)
ABSTRACT
PUBLICATION RECORD
- Publication year
2026
- Venue
Acta Pathologica, Microbiologica et Immunologica Scandinavica (APMIS)
- Publication date
2026-02-01
- Fields of study
Biology, Medicine
- Identifiers
- External record
- Source metadata
Semantic Scholar
CITATION MAP
EXTRACTION MAP
CLAIMS
- No claims are published for this paper.
CONCEPTS
- No concepts are published for this paper.
REFERENCES
Showing 1-69 of 69 references · Page 1 of 1
CITED BY
- No citing papers are available for this paper.
Showing 0-0 of 0 citing papers · Page 1 of 1