# Concomitant immunity in persistent Leishmania infections: could it represent an evolutionary balance and a vaccine target?

**Authors:** Francesca Divenuto, Simona Gigliotti, Grazia Pavia, Fabrizio Vitale, Sofia Cortes, Carla Maia, Nadia Marascio, Angela Quirino, Giovanni Matera

PMC · DOI: 10.1186/s13071-025-07188-x · Parasites & Vectors · 2025-12-08

## TL;DR

The paper explores concomitant immunity in Leishmania infections, suggesting it could be a balance between host and parasite that may inform vaccine development.

## Contribution

The paper proposes that concomitant immunity in Leishmania could represent an evolutionary balance and a potential vaccine target.

## Key findings

- Concomitant immunity allows Leishmania to persist at low levels while protecting the host from reinfection.
- CD4+ T cell populations are likely involved in the immune response during concomitant immunity.
- CI mechanisms in Leishmania and similar pathogens remain poorly understood and warrant further study.

## Abstract

Concomitant immunity (CI) can be viewed as an example of coevolution between the microorganisms and their long-lived hosts. Such an ecological trade-off may be advantageous to both the microbe and the host, as it allows protozoa and helminths to maintain their genetic features while providing the host, particularly mammals, with long-standing protection against reinfection by the same microbe. In Leishmania infection, CI is the mechanism whereby parasites remain at low-level infection in the host, which develops a strong immune reaction that protects against reinfection. Mechanistically, several CD4+ T cell populations seem to be involved in such fine immune responses. While immunity against Leishmania, Plasmodium, Taenia, Schistosoma, and Echinococcus is well known, the mechanisms of CI involving these pathogens have been poorly studied. Finally, the phenomenon of CI should be carefully assessed in the design of novel vaccine preparations.

## Full-text entities

- **Genes:** CD4 (CD4 molecule) [NCBI Gene 920] {aka CD4mut, IMD79, Leu-3, OKT4D, T4}
- **Diseases:** infection (MESH:D007239), Leishmania infection (MESH:D007896)
- **Species:** Leishmania (subgenus) [taxon 38568], Plasmodium (subgenus) [taxon 418103], Echinococcus (genus) [taxon 6209], Taenia (genus) [taxon 6202], Schistosoma (genus) [taxon 6181]

## Full text

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## Figures

5 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12801518/full.md

## References

1 references — full list in the complete paper: https://tomesphere.com/paper/PMC12801518/full.md

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Source: https://tomesphere.com/paper/PMC12801518