The present report describes different aspects of two populations of peritoneal cells (PC) obtained from rats injected i.p. 2 h or 24 h previously with a suppressor dose of a purified fraction (FI) of rat male accessory glands (RAG) (FI-PC2h and FI-PC24h, respectively). The FI-PC2h, which are mainly I-E (OX17) positive and can suppress the autoimmune response to RAG autoantigens, have an elevated phagocytic activity against Candida albicans and capacity to reduce the dye nitroblue tetrazolium. In contrast, FI-PC24h, which are mainly I-A (OX6) positive and can potentiate the autoimmunity to RAG autoantigens, have a diminished capacity to reduce the dye and a diminished phagocytic activity. Moreover, the Toxoplasma gondii appear to have a different effect on both populations. The parasites can invade FI-PC2h while FI-PC24h offer resistance to T. gondii aggression. FI-PC2h cultured during 22 h (FI-PC2-24h in vitro), or PC obtained from syngeneic recipients injected i.p. 22 h previously with FI-PC2h (FI-PC2-24h in vivo) show, as FI-PC2h, an increase of the I-E+ cells and capacity to induce suppression of the delayed-type hypersensitivity response to RAG autoantigens when they are injected to syngeneic rats 10 and 3 days prior to the immunization with chemically modified (diazotized arsanilic and sulfanilic acid) RAG in complete Freund's adjuvant. The PC obtained 24 h after injection of irradiated rats with N-PC plus FI show an increase of I-E+ cells whereas an enhancement of I-A+ cells can be observed when the PC are obtained 24 h after injection of irradiated and bone marrow-reconstituted rats with N-PC plus FI. These findings appear to indicate that FI-PC2h and FI-PC24h are functionally different and that the population obtained 24 h after injection of FI of RAG could not originate from either the population present 2 h after injection of FI of RAG injection nor from normal PC. They appear to require bone marrow precursors.

A model of autoimmunity to rat male accessory glands (RAG) was recently developed by intraperitoneal administration of three doses of native RAG associated with liposomes. In this work we analysed the effects of gangliosides in the cellular response to RAG when they were intraperitoneally administrated prior to the second dose of liposome-associated RAG. Results show that the ganglioside treatment could modify an established DTH response. Also, gangliosides markedly reduced the number of Ia antigen-positive peritoneal exudated cells (PEC). However, they modified neither the processing of liposomes through PEC nor their viability. Moreover, we obtained cellular response by transferring PEC from immunized donors into naive receptors.

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Adult female rats were immunized with 5 mg or 25 mg of modified rat male accessory glands (MRAG) incorporated to complete Freund's adjuvant (CFA) before, during, and after pregnancy. The mothers and litters were exchanged between the experimental and normal groups. The offspring were brought up to 20 days of age and immunized with 5 mg of MRAG-CFA and 5 mg of human serum albumin (HSA)-CFA. Anti-MRAG antibodies were detected in the offspring brought up by the immunized mothers and the titers were similar to those of the foster mothers whereas in the offspring of the experimental group fostered by normal mothers antibodies to MRAG were not detected. The DTH performed in the offspring 13 days after the immunization was significantly diminished in male and female offspring from the 5 mg and 25 mg experimental group fostered by normal mothers (P less than 0.0005 for all groups). Similar results were found when the offspring from normal mothers were suckled by mothers immunized with MRAG-CFA. To assess whether MRAG or HSA administered to female rats reached the offspring via the placenta or the milk, female rats were immunized with 3 mg of 125I-MRAG-CFA or with 3 mg of 125I-HSA-CFA. When radioactivity was measured in neonates (n = 11) that were suckled by the 125I-MRAG-CFA immunized mothers, the specific activity was 116 in stomach (0.4 micrograms of MRAG) and 940 in the total organs (3.8 micrograms of MRAG).(ABSTRACT TRUNCATED AT 250 WORDS)