Anti-Ro/SSA antibodies are the antinuclear antibodies most commonly fo
und in everyday clinical practice and are closely associated with Sjog
ren's syndrome, systemic lupus erythematosus and neonatal lupus. They
play a pathogenic role in a variety of clinical manifestations, includ
ing skin lesions and neonatal lupus heart block. Autoantibodies to Ro(
SS-A) recognize a ribonucleoprotein complex composed of small single-s
tranded RNAs (hYRNAs) and of one or more peptides. Four molecular form
s of this complex have been differentiated based on the nature of the
peptide: a lymphocyte and an erythrocyte Ro with a 60 kDa peptide, a l
ymphocyte Ro with a 52 kDa peptide and an erythrocyte Ro with a 54 kDa
peptide. The Ro complex is found in most tissues and cells (erythrocy
tes, platelets), with differences in structure and quantity across tis
sues, species and embryonic development stages. Although its function
remains unknown, its ability to bind nucleic acids and the fact that i
t shares homologies with gene regulation proteins suggest that it may
participate in RNA transcription processes. A number of environmental
factors (exposure to ultraviolet radiation, viral infections) may caus
e translocation of the Ro complex to nucleocytoplasmic and membrane si
tes where it is not normally found, thereby leading to the development
of autoimmunity. The structure of the Ro(SS-A)-hYRNA complex and the
development of autoimmunity are currently the focus of active research
efforts that can be expected to improve our understanding of the clin
ical manifestations directly related to anti-Ro(SS-A) antibodies.