Genetic aspects of the pathogenesis of systemic lupus erythematosus in children

Abstract

The paper presents data on the pathogenesis of systemic lupus erythematosus (SLE), and depicts various molecular mechanisms for the development of SLE and lupus-like syndromes. It describes groups of diseases, such as apoptotic defects; NETosis; interferonopathies; complement deficiency; autotolerance disorders associated with mutations in the RAG1/RAG2 genes; hereditary metabolic diseases (prolidase deficiency, deficiency of adenosine deaminase 2; lysinuric protein intolerance; and α-mannosidase deficiency). The table summarizes clinical data on most of the known lupus-like syndromes and their molecular mechanisms.The pathogenesis of many forms of monogenic lupus-like diseases is being studied. The main sign suggesting in favor of the possible monogenic disease in a patient with SLE is its onset in infancy, especially in males. Attention should be also paid to a compromised family history, including to the marriage between close relatives, the resistance of disease to standard therapy, as well as atypical symptoms.

Untitled

“…Involvement of such genes as interferon-regulating factor 5 (T-receptors' signals), gene encoding protein 1, rich in H-leucine, which is repeated (gene for N-leucine-rich-repeat protein -NALP1), interferoninduced helicase C domain 1 gene -1990760 (interferoninduced helicase 1 rs1990760 -IFIH1 rs1990760), N-acetyltransferase 2 gene (N-acetyltransferase 2 -NAT2) was also confirmed. Interferon is thought to be important in the pathogenesis of SLE as well [73,76,79,80,121,126].…”