Abstract
Infection of BALB/c mice with Plasmodium yoelii greatly facilitated the growth of a syngeneic virus-induced transplantable lymphoma, injected subcutaneously over a range of cell doses. A similar but less marked effect could be obtained by giving 200 mg kg−1 cyclophosphamide one day before tumour inoculation. By contrast, P. yoelii infection did not alter the growth of a methylcholanthrene-induced fibrosarcoma (Meth A), given sc in medium or low doses (104 or 102 cells), nor did it prevent the induction of resistance against a subsequent lethal challenge with the same cell line. Following a large sc dose of 106 Meth A cells, tumour growth was actually slower in mice infected with malaria than in uninfected mice.