The effect of graft-versus-host reaction on the course of concomminant
retrovirus-induced lymphoproliferative disease was investigated. The
graft-versus-host reaction was elicited by a single i.v. injection of
1.2x10(8) parental spleen cells into adult F1 mice. Lymphoproliferativ
e disease was induced by a single transfusion of 0.2 ml of whole blood
from donors with fully developed disease, induced by infection with r
etrovirus LP-BM5 MuLV. Graft-versus-host reaction and the lymphoprolif
erative disease each separately produced similar syndrome consisting o
f splenomegaly, lymphadenopathy, leukopenia, neutrophilia, reduced in
vitro proliferation of spleen cells and suppression of in vivo immune
responsiveness. The above symptoms were usually less pronounced during
graft-versus-host reaction. Ongoing graft-versus-host reaction neithe
r aggravated nor accelerated the course of the virus-induced lymphopro
liferative disease in genetically susceptible F1 hybrids. Likewise, an
ongoing graft-versus-host reaction in genetically resistant F1 hybrid
s did not alter their susceptibility to the retrovirus infection. The
apparent lack of the effect of graft-versus-host reaction -dependent i
mmunosuppression on the severity and the course of the concommitant re
trovirus-induced lymphoproliferative disease suggests pathogenic diffe
rences between the murine syndrome and human AIDS for which the murine
disease is considered by some to be an animal model.