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Interferon production in sickle cell disease
S C Taylor1, S J Shacks, S M Villicana
1Department of Pediatrics, Charles R. Drew University of Medicine and Science, Los Angeles, CA.
Insights
Sickle cell disease patients show diminished gamma interferon (IFN) production, particularly during infection-associated crisis. This impaired immune response may explain increased infection susceptibility in SCD.
Area of Science:
- Immunology
- Hematology
- Infectious Diseases
Background:
- Cytokine production data in sickle cell disease (SCD) is limited.
- SCD patients experience increased frequency and severity of infections.
Purpose of the Study:
- To compare alpha and gamma interferon (IFN) production in individuals with sickle cell disease (SCD) versus healthy controls.
- To investigate potential correlations between IFN levels and infection susceptibility in SCD.
Main Methods:
- Measured alpha and gamma interferon (IFN) production in 62 steady-state SCD patients and 21 SCD patients in crisis with infection.
- Assessed IFN levels in 30 healthy controls and 14 controls with infections.
- Analyzed individual IFN titers to identify impaired production compared to controls.
Main Results:
- Gamma interferon (IFN) production was significantly diminished in both steady-state and crisis-state SCD patients compared to healthy controls (P < .005).
- A notable percentage of SCD patients (24% steady-state, 52% with infection) exhibited impaired gamma IFN production.
- Alpha interferon (IFN) production levels were comparable across all groups, including those with and without infections.
Conclusions:
- A significant proportion of SCD patients exhibit impaired gamma interferon (IFN) production.
- This gamma IFN deficiency may contribute to the heightened susceptibility and severity of infections observed in sickle cell disease.
- Further research into the immunomodulatory roles of gamma IFN in SCD is warranted.
Abstract:
There is limited data on cytokine production in sickle cell disease (SCD). In this study, both alpha (Poly IC-induced) and gamma (PHA-induced) interferon (IFN) were measured in 62 SCD steady state patients, and 21 in the crisis state associated with infections. Comparable normal controls (30 healthy and 14 with infections) were assessed in a similar manner. Gamma IFN production in both SCD groups, steady state (35 +/- 6 U/ml) and crisis state (24 +/- 11 U/ml) was significantly diminished when compared to the normal healthy controls (65 +/- 14 U/ml) with P less than .005. Both SCD groups were also less than normals with infections (56 +/- 23 U/ml) with P less than .005. On closer analysis of individual titers, 15/62 (24%) in the steady state, 11/21 (52%) of SCD patients with infection and 2/14 (14%) of normals with infection, showed impaired gamma IFN when compared to normals without infection (range 27-2187 U/ml). Alpha IFN production in the SCD groups; steady state (512 +/- 113 U/ml) and SCD crisis with infection (559 +/- 110 U/ml) was virtually equivalent to normals (524 +/- 170 U/ml) and normals with infection (509 +/- 116 U/ml). Analysis of individual titers, in contrast to gamma IFN, also showed no significant differences. These results indicate that a significant percentage of SCD patients in both the steady state and infectious state associated with crisis, have impaired gamma IFN production. In view of the known immunomodulatory functions of gamma IFN, this apparent defect may be another factor to explain the increased frequency and severity of infections in SCD.
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