Active immunity and T-cell populations in pigs intraperitoneally inoculated with baculovirus-expressed transmissible gastroenteritis virus structural proteins.
Active immunity and T-cell populations in pigs intraperitoneally inoculated with baculovirus-expressed transmissible gastroenteritis virus structural proteins.
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DOI:
10.1016/s0165-2427(99)00074-4
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发表时间:
1999-09-20
影响因子:
1.8
通讯作者:
Saif LJ
中科院分区:
文献类型:
--
作者:
Sestak K;Meister RK;Hayes JR;Kim L;Lewis PA;Myers G;Saif LJ
The intraperitoneal inoculation of pigs with baculovirus-expressed transmissible gastroenteritis virus (TGEV) structural proteins (S, N, M) in conjunction with thermolabile Escherichia coli mutant toxin (LT-R192G) in incomplete Freund’s adjuvant (IFA) was tested in an attempt to elicit active immunity to TGEV in gut-associated lymphoid tissues (GALT). Four groups of 63 (1–5-week-old) suckling, TGEV-seronegative pigs were used to assess the efficacy of the recombinant protein vaccine (group 3) in comparison with sham (group 1), commercial vaccine (group 2), and virulent TGEV Miller-strain-inoculated pigs (group 4). The TGEV-specific mucosal and systemic immune responses were measured after in vivo and in vitro stimulation with TGEV-antigens. The major T-cell subset distribution was analyzed in vivo and in vitro after stimulation of mononuclear cells with TGEV (from mesenteric lymph nodes of group 3 inoculated with TGEV-recombinant proteins). Induction of active immunity was assessed by challenge of pigs with virulent TGEV at 27 days of age. Baculovirus-expressed TGEV proteins coadministered with LT-R192G in IFA induced mesenteric lymph node immune responses associated with IgA-antibodies to TGEV and partial protection against TGEV-challenge. The high titers of serum IgG- and virus-neutralizing-antibodies to TGEV in group 3 pigs most likely reflected the dose of TGEV S-protein administered. At the day of TGEV-challenge, the in vitro stimulation of mononuclear cells from the mesenteric lymph nodes of group 3 pigs with inactivated TGEV resulted in an increase in double positive (CD4+CD8+), natural killer (CD2+CD4−CD8+dim) and cytotoxic (CD2+CD4−CD8+bright) T-cell phenotypes, accompanied by increased expression of interleukin-2 receptor and a decrease of the null (CD2−CD4−CD8−/SW6+) cell phenotype.
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影响因子:
5.5
作者:
HUSBAND, AJ
通讯作者:
HUSBAND, AJ
影响因子:
1.1
作者:
HUSBAND, AJ;SEAMAN, JT
通讯作者:
SEAMAN, JT
影响因子:
6.4
作者:
Katz, JM;Lu, XH;Galphin, JC
通讯作者:
Galphin, JC
影响因子:
3.7
作者:
Godet M;Rasschaert D;Laude H
通讯作者:
Laude H
影响因子:
1.8
作者:
BRIM, TA;VANCOTT, JL;SAIF, LJ
通讯作者:
SAIF, LJ