Literature DB >> 11106945

Induction of specific transplantation immunity by oral immunization with allogeneic cells.

V Holán1, A Zajícová, M Krulová, J Plsková, J Fric, M Filipec.   

Abstract

Oral administration of antigen has been shown to be effective for both positive and negative modulation of immune responses. In the present study we characterized changes in the reactivity of the immune system after oral immunization with allogeneic spleen cells. Mice were orally immunized for 10 consecutive days with fresh allogeneic spleen cells, and the phenotype, proliferative response, cytotoxic activity and cytokine production profile of recipient spleen cells were assessed 1 or 7 days after the last immunization dose. Although no significant changes in the proportion of CD4+, CD8+ or CD25+ cells were observed in the spleen of orally immunized mice, significant activation of alloreactivity in spleen cells was found. Cells from orally immunized mice exhibited enhanced proliferation and cytotoxic activity after stimulation with specific allogeneic cells in vitro, and produced considerably higher concentrations of interferon-gamma (IFN-gamma) and significantly less interleukin (IL)-4 than did cells from control mice. The production of IL-2 was essentially unchanged and that of IL-10 was only slightly increased. The systemic allosensitization induced by oral immunization was demonstrated in vivo by increased resistance to the growth of allogeneic tumours induced by subcutaneous inoculation of high doses of tumour cells. In addition, orthotopic corneal allografts in orally immunized recipients were rejected more rapidly (in a second-set manner) than in control, untreated recipients. These data show that oral immunization with allogeneic cells modulates individual components of the immune response and that specific transplantation immunity, rather than tolerance, is induced in the treated recipients.

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Year:  2000        PMID: 11106945      PMCID: PMC2327093          DOI: 10.1046/j.1365-2567.2000.00111.x

Source DB:  PubMed          Journal:  Immunology        ISSN: 0019-2805            Impact factor:   7.397


  33 in total

1.  High dose oral tolerance in ovalbumin TCR-transgenic mice: systemic neutralization of IL-12 augments TGF-beta secretion and T cell apoptosis.

Authors:  T Marth; W Strober; B L Kelsall
Journal:  J Immunol       Date:  1996-09-15       Impact factor: 5.422

2.  The effect of oral immunization on corneal allograft survival.

Authors:  Y G He; J Mellon; J Y Niederkorn
Journal:  Transplantation       Date:  1996-03-27       Impact factor: 4.939

3.  Regulation of IgE responses to inhaled antigen in mice by antigen-specific gamma delta T cells.

Authors:  C McMenamin; C Pimm; M McKersey; P G Holt
Journal:  Science       Date:  1994-09-23       Impact factor: 47.728

4.  Induction of oral tolerance to myelin basic protein in CD8-depleted mice: both CD4+ and CD8+ cells mediate active suppression.

Authors:  Y Chen; J Inobe; H L Weiner
Journal:  J Immunol       Date:  1995-07-15       Impact factor: 5.422

5.  Induction of anergy or active suppression following oral tolerance is determined by antigen dosage.

Authors:  A Friedman; H L Weiner
Journal:  Proc Natl Acad Sci U S A       Date:  1994-07-05       Impact factor: 11.205

Review 6.  Oral tolerance: immunologic mechanisms and treatment of animal and human organ-specific autoimmune diseases by oral administration of autoantigens.

Authors:  H L Weiner; A Friedman; A Miller; S J Khoury; A al-Sabbagh; L Santos; M Sayegh; R B Nussenblatt; D E Trentham; D A Hafler
Journal:  Annu Rev Immunol       Date:  1994       Impact factor: 28.527

7.  Enhanced type 2 and diminished type 1 cytokines in neonatal tolerance.

Authors:  N Chen; E H Field
Journal:  Transplantation       Date:  1995-04-15       Impact factor: 4.939

8.  Distinct lymphokine production by CD4+ T cells isolated from mucosal and systemic lymphoid organs.

Authors:  S L Tonkonogy; S L Swain
Journal:  Immunology       Date:  1993-12       Impact factor: 7.397

9.  Suppression of insulitis in non-obese diabetic (NOD) mice by oral insulin administration is associated with selective expression of interleukin-4 and -10, transforming growth factor-beta, and prostaglandin-E.

Authors:  W W Hancock; M Polanski; J Zhang; N Blogg; H L Weiner
Journal:  Am J Pathol       Date:  1995-11       Impact factor: 4.307

10.  The natural immune response to inhaled soluble protein antigens involves major histocompatibility complex (MHC) class I-restricted CD8+ T cell-mediated but MHC class II-restricted CD4+ T cell-dependent immune deviation resulting in selective suppression of immunoglobulin E production.

Authors:  C McMenamin; P G Holt
Journal:  J Exp Med       Date:  1993-09-01       Impact factor: 14.307

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  1 in total

1.  Augmented production of proinflammatory cytokines and accelerated allotransplantation reactions in heroin-treated mice.

Authors:  V Holán; A Zajícová; M Krulova; V Blahoutová; H Wilczek
Journal:  Clin Exp Immunol       Date:  2003-04       Impact factor: 4.330

  1 in total

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