DIFFERENTIAL INDUCTION OF CARRIER ANTIGEN-SPECIFIC IMMUNITY BY SALMONELLA-TYPHIMURIUM LIVE-VACCINE STRAINS AFTER SINGLE MUCOSAL OR INTRAVENOUS IMMUNIZATION OF BALB C MICE/
Kl. Karem et al., DIFFERENTIAL INDUCTION OF CARRIER ANTIGEN-SPECIFIC IMMUNITY BY SALMONELLA-TYPHIMURIUM LIVE-VACCINE STRAINS AFTER SINGLE MUCOSAL OR INTRAVENOUS IMMUNIZATION OF BALB C MICE/, Infection and immunity, 63(12), 1995, pp. 4557-4563
In this study, we constructed strain KR21 (chi 4550 Delta cya Delta cr
p Delta asd/pYA292asd(+)-toxC(+)) and compared it with BRD847 (aroA ar
oD/pnirB-toxC) for the ability to induce humoral and cellular immunity
after a single oral or intravenous immunization in 3- to 4-week-old B
ALB/c mice. ToxC-specific serum immunoglobulin G (IgG) was detectable
in animals orally immunized with either BRD847 or KR21. However, after
intravenous immunization, IgG was detected only in BRD847-immunized a
nimals. Measurement of immunoglobin types IgG1 and IgG2a suggests that
a Th1 cellular response is prominent after immunizations with either
system. ToxC-specific IgA was detected in fecal and vaginal samples of
animals immunized orally and intravenously with BRD847, while those i
mmunized with KR21 failed to show fecal or vaginal IgA responses. Dela
yed-type hypersensitivity was used as a measure of induction of T-cell
responses in vivo. Mice immunized either orally or intravenously with
BRD847 showed significant ear swelling responses after ToxC injection
s, while KR21-immunized animals failed to show a cellular response. Th
ese data indicate that the aroA aroD/pnirB system holds greater potent
ial for inducing global immunity after a single dose when directly com
pared with the balanced lethal system (Delta cya Delta crp Delta asd/p
YA29asd(+)).