INTRODU CTIONAscaris suum larval metabolic fluids nave been shown to be good protective antigens when injected into mice, prior to an infection (13,14,15). Because of the complexity of the medium in whicíi the larvae ihave to be grown (23) there m ight bs a dim inution of the immune response due to the presence of competing nonprotective immunogens.It is well known th a t the sim ultaneous exposure of an anim al to several antigens decreases the immune response to some of the antigens in the m ixture (1,2,11, 12). It is, therefore, desirable to separate a complex antigenic m ixture into its components. One of the preferred methods with the least biological damage to the antigens is fractionation on the basis of molecular size differences using filtration through a column of agarose gels. These are more rigid th a n m any other gels and have low compressibility so th a t a good flow rate and reproducible separation migih t bs insured (18).The present paper concerns attem pts to isolate the A. suum metabolic larval intigens from the culture medium using exclusion chrom atography.
MATERIALS AND METHODSAnimais. One hundred and ten albino Swiss mice averaging 22.2 ± 1.5 gm in weight were divided into 11 groups of 10 anim ais ea ch .T h is stu d y w as p e rfo rm e d a t th e D e p a rtm e n t of Zoology, U n iv e rsity of Illin o is, U rb a n a , Illin o is, U .S .A ., u n d e r p a r tia l su p p o rt of g r a n t AI05910 from th e N a tio n a l I n s t it u t o of Allergy a n d In fe c tio u s Diseases. * C e n tro d e P e sq u isa s em F isio lo g ia e Im u n o lo g ia de H elm in to s, D e p a rta m e n to de M icrobiologia e Parasito lo g ia, E scola P a u lis ta de M ed icin a. São P a u lo . B rasil. ** D e p a rtm e n t o f Biology, U n iv ersity of New M exico, A lb u q u erq u e, New M exico. U .S .A . S u b m itte d to p u b lic a tio n on 6.25.73.