The in vivo expression of actin/salt-resistant hyperactive DNase I inhibits the development of anti-ssDNA and anti-histone autoantibodies in a murine model of systemic lupus erythematosus
2006

Effects of DNase I on Autoantibodies in Lupus Mice

Sample size: 20 publication 10 minutes Evidence: moderate

Author Information

Author(s): Manderson Anthony P, Carlucci Francesco, Lachmann Peter J, Lazarus Robert A, Festenstein Richard J, Cook H Terence, Walport Mark J, Botto Marina

Primary Institution: Imperial College, London

Hypothesis

Can the over-expression of DNase I in mice reduce the development of autoantibodies associated with systemic lupus erythematosus?

Conclusion

The study found that the mutant DNase I provided some protection against the development of certain autoantibodies but did not prevent renal disease.

Supporting Evidence

  • The ash.DNase I mutant provided significant protection from the development of anti-ssDNA and anti-histone antibodies.
  • Transgenic mice showed lower levels of circulating DNA after LPS treatment.
  • Autoantibody levels were significantly lower in ash.DNase I.Apcs-/- mice compared to controls.

Takeaway

Scientists tested a special protein in mice to see if it could help stop a disease that makes the body attack itself, and it worked a little bit but not enough to stop kidney problems.

Methodology

Transgenic mice expressing wild-type or mutant DNase I were evaluated for autoantibody levels and kidney disease.

Limitations

The study did not observe significant protection against renal disease despite reduced autoantibody levels.

Participant Demographics

Female mice of C57BL/6 and Apcs-/- strains were used.

Statistical Information

P-Value

0.03

Statistical Significance

p<0.05

Digital Object Identifier (DOI)

10.1186/ar1936

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