The induction of delayed type hypersensitivity was demonstrated clearly in mice immunized with viable group A streptococci. Female BALB/c mice were inoculated subcutaneously with 1×10
7 viable cells weekly for 8 weeks and used for experiments 7-10 days after the last immunization. The streptococci inoculated in mice were group A
streptococcus pyogenes types 3 and 12 and non-typable strains and group D streptococci.
Positive foot pad reactions were observed with homologous and heterologous antigens. Reactivity was transferred by immune lymphocytes, but not by ordinary lymphocytes, from normal mice or by sera from infected mice. The infiltration of mononuclear cells was observed among histological changes caused by the foot pad reaction. An increase was demonstrated in
3H-TdR incorporation by lymphocytes obtained from infected mice when homologous and heterologous antigens were added to the cells. When the cells were treated with anti-thymocyte serum and complement, the proliferative response and passive transfer were remarkably reduced in the foot pad reaction.
Crude antigens were prepared from streptococcal cell walls. They were further fractionated by hydroxyl apatite column chromatography and stepwise elution with 0.01, 0.1 and 0.3M sodium phosphate, pH 6.8. The resulting fractions were designated P-1, P-2 and P-3, respectively. All of them, but P-3, showed homologous and heterologous responses in
3H-TdR incorporation. P-3 showed only a homologous response in
3H-TdR uptake. It was suggested that two kinds of cell wall protein might have appeared to cause delayed type hypersensitivity.
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