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Periapical cytokine expression in sickle cell disease
Shirlene Barbosa Pimentel Ferreira1, Luciana Carla Neves de Brito2, Michelle Pimenta Oliveira3
1Departamento de Odontologia Restauradora, Faculdade de Odontologia, Universidade Federal de Minas Gerais (UFMG), Belo Horizonte.
Sickle cell anemia patients show a heightened inflammatory response, with elevated levels of certain cytokines in periapical fluid compared to healthy individuals. However, no significant differences in these inflammatory markers were found between sickle cell anemia and non-SCA patients.
Area of Science:
- Immunology
- Genetics
- Oral Medicine
Background:
- Sickle cell anemia (SCA) is a prevalent global genetic disorder.
- SCA patients have a persistently activated immune system with increased proinflammatory mediators.
Purpose of the Study:
- To compare mRNA expression of key cytokines and chemokines in periapical interstitial fluid between SCA patients and healthy controls.
- To investigate potential differences in periapical immune responses in SCA individuals.
Main Methods:
- Real-time polymerase chain reaction (PCR) was used to quantify mRNA levels.
- Samples were collected from periapical fluid of SCA patients, non-SCA patients with apical periodontitis, and healthy controls with vital pulp.
- Analyzed mRNA expression of interferon (IFN-γ), tumor necrosis factor, interleukins (IL-1β, IL-17A, IL-10), and chemokines (CCL2, CCL5).
Main Results:
- SCA patients exhibited significantly higher mRNA expression of Th1-associated cytokines IFN-γ, tumor necrosis factor-α, and IL-1β compared to controls.
- Interleukin-17A and IL-10 mRNA levels were also significantly elevated in SCA patients relative to controls.
- No significant differences in the expression of these inflammatory markers were observed between SCA and non-SCA individuals.
Conclusions:
- SCA patients demonstrate a predisposition towards a proinflammatory state.
- Despite elevated general inflammation in SCA, specific periapical immune responses did not significantly differ between SCA and non-SCA patients with apical periodontitis.
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