Anti-tetanus toroid antibody production and protection against lethal doses of tetanus toxin in hu-PBL-SCID mice
Authors
Naito, S
Okada, Y
Takahashi, M
Kato, H
Taneichi, M
Ami, Y
Suzaki, Y
Oka, T
Okuma, K
Morokuma, K
Onodera, H
Inoue, M
Takahashi, Y
Yamazaki, S
Kimura, H
Komuro, K
Uchida, T
Citation
S. Naito et al., Anti-tetanus toroid antibody production and protection against lethal doses of tetanus toxin in hu-PBL-SCID mice, INT A AL IM, 123(2), 2000, pp. 149-154
Categorie Soggetti
Immunology
Journal title
INTERNATIONAL ARCHIVES OF ALLERGY AND IMMUNOLOGY
SICI code
1018-2438(200010)123:2<149:ATAPAP>2.0.ZU;2-Z
Abstract
Background In this study, severe combined immunodeficiency (SCID) mice, whi
ch permit the survival of lymphoid cells of human origin, were used to stud
y the human anti-tetanus immune response. Methods: Human peripheral blood l
ymphocytes (hu-PBL) obtained from 88 healthy donors (aged from 18 to 62) we
re transplanted into SCID mice, and anti-tetanus toroid (Ttd) antibody prod
uction and protection against lethal doses of tetanus toxin (Ttx) were inve
stigated in the hu-PBL-SCIID mice. Results: The transfer of human PBL evoke
d significant human anti-Ttd IgG antibody production for 37.5% of the donor
s. After in vivo immunization, the percentage of donors with PBL exhibiting
positive anti-TtD IgG production in the mice increased to 54.5%. Mean anti
-Ttd IgG levels in the sera were also significantly elevated in response to
immunization. The mean IgG titer for the mice injected with PBL from donor
s under the age of 40 was significantly higher than that of the mice inject
ed with PBL from donors aged 40 or older. Four weeks after the cell transfe
r, the mice were challenged with Ttx. The induction of protection against T
tx challenge was observed mostly in mice with PBL transferred from donors u
nder the age of 40. In vivo immunization in SCID mice with Ttd increased th
e number of cases of resistance to Ttx. Conclusions: These results suggest
that hu-PBL-SCID mice might serve as a tool for predicting the protective a
bility against pathogens in PBL donors and also for evaluating vaccine effi
cacy. Copyright (C) 2000 S. Karger AG,Basel.