An antigen related to mammalian type-C RNA viral p30 proteins was shown by the use of anti-p30 sera and the indirect immunofluorescence method to be present in the kidneys and spleen in a fulminant fatal case of human systemic lupus erythematosus and to be located in the glomeruli, the site of active lupus diffuse glomerulonephritis.Systemic lupus erythematosus is widely held to be a prototype of human systemic autoimmune disease. The possibility of viral etiology is raised by the study of the autoimmune New Zealand mouse model of systemic lupus (1), since it has been shown that the development of the lupus-like immunecomplex glomerulonephritis of these mice is related to the expression of an endogenous murine type-C RNA virus (2, 3). Type-C RNA virus genes are widely distributed in the vertebrate animal kingdom, are transmitted vertically, apparently as cellular genes, and, although usually covert, are expressed by malignant cells and normal cells of several animal species (4, 5). The structural proteins of different type-C viruses are known to have several kinds of antigenic determinants, termed group-or intraspecies-specific (6, 7), interspecies-specific, and type-specific determinants. Interspecies-specific determinants (8) coexisting with intraspecies determinants (9) are present in the two major structural proteins of mammalian type-C viruses, the p27 to p30 (10) major internal protein of approximately 30,000 daltons (9, 11-13) and the gp69/71 major envelope glycopeptides (13-15), as well as the viral reverse transcriptase (16-18). The study of the interspecies determinants of purified p30 proteins shows immunological cross-reaction between all species of mammalian type-C viruses tested (11,15,19,20), including murine, feline, endogenous feline (RD-114), and woolly monkey viruses (21), and also distinguishable sets of interspecies determinants that are shared by closely related viruses, murine and feline (21-23), and baboon (endogenous primate) (23, 24), woolly monkey and gibbon ape (infectious primate) (23,25,26), and murine, feline, and infectious primate viruses (21, 23). A high degree of aminoacid sequence homology is found in the p,30 proteins of closely related mammalian type-C viruses (27). The development of assays for type-C viral nucleic acids and proteins advances the search for putative human type-C viruses; recent reports indicate that type-C virus genetic information is expressed in human tissues. Type-C virus-like particles are seen in normal human placentas by careful electron microscopic study (28) (31, 32); infectious primate virus-related reverse transcriptase (33), p30 protein antigen (34), and nucleic-acid sequences (35) are identifiable in cultured human leukemia cells; and both endogenous and infectious primate, as well as murine, virus-related p30 protein antigens are present in relatively high concentration in extracts of tissues obtained from patients with systemic lupus erythematosus (36). It has been reported also that an interspecies antigen recognized by antisera aga...