Oral tolerance.

Abstract:

:Oral tolerance is the immunologic mechanism by which the mucosal immune system maintains unresponsiveness to the myriad of antigens in the mucosal environment which might otherwise induce untoward immune responses. Recent studies have shown that it is mediated by several distinct, yet interacting mechanisms including the generation of suppressive T cells producing antigen nonspecific cytokines and the induction of clonal deletion and/or anergy. In this review of oral tolerance, we discuss these mechanisms in detail and show how oral tolerance or lack thereof may explain the occurrence of mucosal inflammation. In addition, we discuss how induction of oral tolerance can be used to treat autoimmune states.

journal_name

J Clin Immunol

authors

Strober W,Kelsall B,Marth T

doi

10.1023/a:1023222003039

subject

Has Abstract

pub_date

1998-01-01 00:00:00

pages

1-30

issue

1

eissn

0271-9142

issn

1573-2592

journal_volume

18

pub_type

杂志文章,评审
  • Antibody-dependent cellular cytotoxicity (ADCC)-mediated destruction of human immunodeficiency virus (HIV)-coated CD4+ T lymphocytes by acquired immunodeficiency syndrome (AIDS) effector cells.

    abstract::The acquired immunodeficiency syndrome (AIDS) is defined in clinical terms by the development of Kaposi's sarcoma and/or severe opportunistic infections in persons without predisposing conditions. A hallmark of the syndrome has been a decrease in the number of CD4+ T helper cells. The reduction in the frequency of the...

    journal_title:Journal of clinical immunology

    pub_type: 杂志文章

    doi:10.1007/BF00916950

    authors: Katz JD,Nishanian P,Mitsuyasu R,Bonavida B

    更新日期:1988-11-01 00:00:00

  • gammadelta T lymphocytes-selectable cells within the innate system?

    abstract::Lymphocytes expressing gammadelta T cell receptors (TCR) constitute an entire system of functionally specialized subsets that have been implicated in the regulation of immune responses, including responses to pathogens and allergens, and in tissue repair. The gammadelta TCRs share structural features with adaptive rec...

    journal_title:Journal of clinical immunology

    pub_type: 杂志文章,评审

    doi:10.1007/s10875-007-9077-z

    authors: Born WK,Jin N,Aydintug MK,Wands JM,French JD,Roark CL,O'Brien RL

    更新日期:2007-03-01 00:00:00

  • Catecholamines induce alterations of distribution and activity of human natural killer (NK) cells.

    abstract::Catecholamines have been suggested to be responsible for altered cellular immunity after stress. This study was performed to determine the effects of adrenaline and noradrenaline on lymphocyte subpopulations and NK cell functions. Subjects were given a subcutaneous injection of either NaCl, adrenaline (5 micrograms/kg...

    journal_title:Journal of clinical immunology

    pub_type: 杂志文章

    doi:10.1007/BF00920243

    authors: Schedlowski M,Falk A,Rohne A,Wagner TO,Jacobs R,Tewes U,Schmidt RE

    更新日期:1993-09-01 00:00:00

  • Natural autoantibody to galectin-9 in normal human sera.

    abstract::Antibodies to certain self-antigens are detected in normal individuals as well as in patients with autoimmune diseases. Natural autoantibodies found in normal human sera are thought to act as an immune regulator, a functional controller of specific proteins, or the first-line defense against pathogenic microorganisms....

    journal_title:Journal of clinical immunology

    pub_type: 杂志文章

    doi:10.1023/a:1020599526249

    authors: Suk K,Hwang DY,Lee MS

    更新日期:1999-05-01 00:00:00

  • Antigen-specific expansion of TCR Vbeta3+ CD4+ T cells in the early stage of collagen-induced arthritis and its arthritogenic role in DBA/1J mice.

    abstract::To investigate type II collagen (CII)-specific CD4+ T cell receptors involving in Collagen-induced arthritis (CIA) in DBA/1J mice as a model of rheumatoid arthritis in humans, TCR Vbeta usage in draining lymph nodes (dLNs) was assessed by flow cytometric analysis at 3, 5, and 8 weeks after bovine CII immunizations. In...

    journal_title:Journal of clinical immunology

    pub_type: 杂志文章

    doi:10.1007/s10875-006-9012-8

    authors: Lee JS,Cho ML,Jhun JY,Min SY,Ju JH,Yoon CH,Min JK,Park SH,Kim HY,Cho YG

    更新日期:2006-05-01 00:00:00

  • i.v.IG for autoimmune, fibrosis, and malignant conditions: our experience with 200 patients.

    abstract::Intravenous immunoglobin (i.v.IG) is generated from the plasma of more than 10,000 healthy subjects. Originally i.v.IG was employed to supplement the missing Igs in subjects with immune-deficiencies. Later on it was given successfully to patients with autoimmune conditions, in some of which the benefits were confirmed...

    journal_title:Journal of clinical immunology

    pub_type: 杂志文章,评审

    doi:10.1023/b:joci.0000019809.55787.ec

    authors: Shoenfeld Y,Krause I

    更新日期:2004-03-01 00:00:00

  • Evidence for a correlation between antibody-dependent cellular cytotoxicity-mediating anti-HIV-1 antibodies and prognostic predictors of HIV infection.

    abstract::Using our gp120/41-expressing, NK cell activity-resistant CEM.NKR cell clones as targets in HIV-1-specific antibody-dependent cellular cytotoxicity (ADCC) assays, we demonstrate here that the serum titers of anti-HIV-1 ADCC antibodies bear a significant (P < 0.05) positive correlation with the peripheral blood CD4+ T ...

    journal_title:Journal of clinical immunology

    pub_type: 杂志文章

    doi:10.1023/a:1011087132180

    authors: Ahmad R,Sindhu ST,Toma E,Morisset R,Vincelette J,Menezes J,Ahmad A

    更新日期:2001-05-01 00:00:00

  • Immune function in chronic active Epstein-Barr virus infection.

    abstract::The spectrum of illness attributed to Epstein-Barr virus (EBV) includes patients with symptoms persisting for more than 1 year without any other obvious underlying disease. High titers of antibodies to EBV, either IgG antiviral capsid antigen or anti-early antigen, can be demonstrated. In this study, 13 patients diagn...

    journal_title:Journal of clinical immunology

    pub_type: 杂志文章

    doi:10.1007/BF00915168

    authors: Kibler R,Lucas DO,Hicks MJ,Poulos BT,Jones JF

    更新日期:1985-01-01 00:00:00

  • Flebogamma(®) 5 % DIF Intravenous Immunoglobulin for Replacement Therapy in Children with Primary Immunodeficiency Diseases.

    abstract:PURPOSE:The previous studies with Flebogamma(®) 5 % DIF intravenous immunoglobulin (IVIG) contained insufficient numbers of pediatric subjects to fully warrant a pediatric indication by the FDA. The objective of this study was to evaluate the efficacy, safety, and pharmacokinetics of Flebogamma® 5 % DIF for replacement...

    journal_title:Journal of clinical immunology

    pub_type: 杂志文章,多中心研究

    doi:10.1007/s10875-016-0303-4

    authors: Ballow M,Pinciaro PJ,Craig T,Kleiner G,Moy J,Ochs HD,Sleasman J,Smits W

    更新日期:2016-08-01 00:00:00

  • Ligase-4 Deficiency Causes Distinctive Immune Abnormalities in Asymptomatic Individuals.

    abstract:PURPOSE:DNA Ligase 4 (LIG4) is a key factor in the non-homologous end-joining (NHEJ) DNA double-strand break repair pathway needed for V(D)J recombination and the generation of the T cell receptor and immunoglobulin molecules. Defects in LIG4 result in a variable syndrome of growth retardation, pancytopenia, combined i...

    journal_title:Journal of clinical immunology

    pub_type: 杂志文章

    doi:10.1007/s10875-016-0266-5

    authors: Felgentreff K,Baxi SN,Lee YN,Dobbs K,Henderson LA,Csomos K,Tsitsikov EN,Armanios M,Walter JE,Notarangelo LD

    更新日期:2016-05-01 00:00:00

  • Pineal germinoma in a child with interferon-γ receptor 1 deficiency. case report and literature review.

    abstract::Interferon-γ receptor 1 (IFN-γR1) deficiency is one of the primary immunodeficiencies conferring Mendelian Susceptibility to Mycobacterial Disease (MSMD). Some cases of neoplasms have been recently reported in patients with MSMD, underlying the already known link between immunodeficiency and carcinogenesis. We report ...

    journal_title:Journal of clinical immunology

    pub_type: 杂志文章,评审

    doi:10.1007/s10875-014-0098-0

    authors: Taramasso L,Boisson-Dupuis S,Garrè ML,Bondi E,Cama A,Nozza P,Morana G,Casanova JL,Marazzi MG

    更新日期:2014-11-01 00:00:00

  • Patterns of antibody reactivity to selected human immunodeficiency virus type 1 (HIV-1) gp160 epitopes infected individuals grouped according to CD4+ cell levels.

    abstract::We examined sera from 160 HIV-infected individuals for antibodies reactive to HIV-1 gp160 epitopes defined by seven synthetic peptides. Seropositive individuals were placed into three groups based upon levels of circulating CD4+ cells. These groups consisted of individuals with (1) more than 400 CD4+ cells, (2) 200-40...

    journal_title:Journal of clinical immunology

    pub_type: 杂志文章

    doi:10.1007/BF00918790

    authors: Warren RQ,Wolf H,Zajac RA,Boswell RN,Kanda P,Kennedy RC

    更新日期:1991-01-01 00:00:00

  • Efficacy and Adverse Events During Janus Kinase Inhibitor Treatment of SAVI Syndrome.

    abstract:OBJECTIVES:Mutations affecting the TMEM173 gene cause STING-associated vasculopathy with onset in infancy (SAVI). No standard immunosuppressive treatment approach is able to control disease progression in patients with SAVI. We studied the efficacy and safety of targeting type I IFN signaling with the Janus kinase inhi...

    journal_title:Journal of clinical immunology

    pub_type: 杂志文章

    doi:10.1007/s10875-019-00645-0

    authors: Volpi S,Insalaco A,Caorsi R,Santori E,Messia V,Sacco O,Terheggen-Lagro S,Cardinale F,Scarselli A,Pastorino C,Moneta G,Cangemi G,Passarelli C,Ricci M,Girosi D,Derchi M,Bocca P,Diociaiuti A,El Hachem M,Cancrini C,To

    更新日期:2019-07-01 00:00:00

  • Lymphotoxin detected in the blister fluid of bullous pemphigoid patients.

    abstract::The role of lymphocytes in the pathogenesis of bullous pemphigoid was examined by assaying the blister fluid obtained from bullous pemphigoid patients for the presence of the lymphokine, lymphotoxin. Blister fluids from six bullous pemphigoid were assayed on L-929 target cells for the presence of cytolytic molecules i...

    journal_title:Journal of clinical immunology

    pub_type: 杂志文章

    doi:10.1007/BF00915284

    authors: Jeffes EW,Yamamoto RS,Ahmed AR,Granger GA

    更新日期:1984-01-01 00:00:00

  • 30-Year Review of Pediatric- and Adult-Onset CVID: Clinical Correlates and Prognostic Indicators.

    abstract:PURPOSE:To evaluate mortality risk factors in pediatric-onset common variable immunodeficiency disorders (CVID), we evaluated the largest single-institution cohort of pediatric-onset CVID patients. Previous publications on CVID have provided valuable descriptive data, but lack risk stratification to guide physicians in...

    journal_title:Journal of clinical immunology

    pub_type: 杂志文章

    doi:10.1007/s10875-019-00674-9

    authors: Baloh C,Reddy A,Henson M,Prince K,Buckley R,Lugar P

    更新日期:2019-10-01 00:00:00

  • Prognostic Value of Blood-Based Inflammatory Biomarkers in Secondary Hemophagocytic Lymphohistiocytosis.

    abstract:PURPOSE:Hemophagocytic lymphohistiocytosis (HLH) is a rare systematic immune disease manifested with excessive activation of lymphocytes and macrophages. This study was designed to explore the feasible prognostic factors of secondary HLH (sHLH). METHOD:We retrospectively analyzed 179 patients with newly diagnosed sHLH...

    journal_title:Journal of clinical immunology

    pub_type: 杂志文章

    doi:10.1007/s10875-020-00801-x

    authors: Huang J,Yin G,Duan L,Tian T,Xu J,Wang J,Gao X,Cheng W,Liu L,Qiu H

    更新日期:2020-07-01 00:00:00

  • Th22, but not Th17 might be a good index to predict the tissue involvement of systemic lupus erythematosus.

    abstract:PURPOSE:T-helper (Th) cells abnormalities are considered to be associated with the pathogenesis of Systemic lupus erythematosus (SLE). Recently, The Th22 cells have been identified and implicated in the pathogenesis of autoimmune diseases such as Rheumatoid arthritis (RA), although therir role in Systemic lupus erythem...

    journal_title:Journal of clinical immunology

    pub_type: 杂志文章

    doi:10.1007/s10875-013-9878-1

    authors: Yang XY,Wang HY,Zhao XY,Wang LJ,Lv QH,Wang QQ

    更新日期:2013-05-01 00:00:00

  • Allotype-associated differences in concentrations of human IgG subclasses.

    abstract::The concentrations of seven immunoglobulin isotypes (IgA, IgE, IgM, IgG1, IgG2, IgG3, and IgG4) were measured in the sera of 207 Finnish blood donors, and they were allotyped with anti-Gm antibodies: anti-f, anti-a, anti-x, and anti-n. The above population could be divided into 12 phenotypes, and significant differenc...

    journal_title:Journal of clinical immunology

    pub_type: 杂志文章

    doi:10.1007/BF00918793

    authors: Sarvas H,Rautonen N,Mäkelä O

    更新日期:1991-01-01 00:00:00

  • Endogenously activated interleukin-4 differentiates disease progressors and non-progressors in tuberculosis susceptible families: a 2-year biomarkers follow-up study.

    abstract:OBJECTIVE:Dynamic cytokine profiles from endogenously activated T cells in transit from lymph node to the infected sites via the blood compartment after recent exposure to Mycobacterium tuberculosis may differentiate disease progressors from non-disease progressors in a BCG-vaccinated population. METHODS:Household con...

    journal_title:Journal of clinical immunology

    pub_type: 杂志文章

    doi:10.1007/s10875-011-9566-y

    authors: Hussain R,Talat N,Ansari A,Shahid F,Hasan Z,Dawood G

    更新日期:2011-10-01 00:00:00

  • Changes of natural killer cells during acute psychological stress.

    abstract::Emotional stress is often followed by increased susceptibility to infections. One major role in the immediate immune response to infection is played by natural killer (NK) cells. This study was designed to establish whether acute psychological stress influences cellular immune functions and to elucidate the role of en...

    journal_title:Journal of clinical immunology

    pub_type: 杂志文章

    doi:10.1007/BF00919268

    authors: Schedlowski M,Jacobs R,Stratmann G,Richter S,Hädicke A,Tewes U,Wagner TO,Schmidt RE

    更新日期:1993-03-01 00:00:00

  • Clinical, immunological and molecular characterization of DOCK8 and DOCK8-like deficient patients: single center experience of twenty-five patients.

    abstract:PURPOSE:Autosomal recessive hyper-IgE syndrome is a rare combined immunodeficiency characterized by susceptibility to viral infections, atopic eczema, high serum IgE and defective T cell activation. The genetic etiologies are diverse. Null mutations in DOCK8 and TYK2 are responsible for many cases. This study aims to p...

    journal_title:Journal of clinical immunology

    pub_type: 杂志文章

    doi:10.1007/s10875-012-9769-x

    authors: Alsum Z,Hawwari A,Alsmadi O,Al-Hissi S,Borrero E,Abu-Staiteh A,Khalak HG,Wakil S,Eldali AM,Arnaout R,Al-Ghonaium A,Al-Muhsen S,Al-Dhekri H,Al-Saud B,Al-Mousa H

    更新日期:2013-01-01 00:00:00

  • Lymphocyte phenotype and function in the chronic fatigue syndrome.

    abstract::Lymphocytes of 18 patients meeting the Centers for Disease Control (CDC) case definition for the chronic fatigue syndrome (CFS), 10 similar, chronically fatigued patients not fully conforming to the CDC case definition, and 17 matched, healthy individuals were studied to determine the presence of abnormalities of peri...

    journal_title:Journal of clinical immunology

    pub_type: 杂志文章

    doi:10.1007/BF00920633

    authors: Straus SE,Fritz S,Dale JK,Gould B,Strober W

    更新日期:1993-01-01 00:00:00

  • Identification of an HLA-A0201-restricted CTL epitope generated by a tumor-specific frameshift mutation in a coding microsatellite of the OGT gene.

    abstract::Deficient DNA mismatch repair results in microsatellite instability and might induce shifts of translational reading frames of genes encompassing coding microsatellites. These may be translated in truncated proteins, including neo-peptide tails functioning as tumor rejection antigens, when presented in the context of ...

    journal_title:Journal of clinical immunology

    pub_type: 杂志文章

    doi:10.1023/a:1025329819121

    authors: Ripberger E,Linnebacher M,Schwitalle Y,Gebert J,von Knebel Doeberitz M

    更新日期:2003-09-01 00:00:00

  • I kappa B alpha promoter polymorphisms in patients with systemic lupus erythematosus.

    abstract::To investigate the associations of IkappaBalpha gene polymorphisms with the development and clinical manifestations of systemic lupus erythematosus (SLE), 110 patients with SLE and 120 unrelated healthy controls were enrolled in this study. The IkappaBalpha -881 A/G, -826 C/T, -550 A/T, -519 C/T, and -297 C/T polymorp...

    journal_title:Journal of clinical immunology

    pub_type: 杂志文章

    doi:10.1007/s10875-007-9156-1

    authors: Lin CH,Wang SC,Ou TT,Li RN,Tsai WC,Liu HW,Yen JH

    更新日期:2008-05-01 00:00:00

  • Effect of hyperoxia on pulmonary SIgA and its components, IgA and SC.

    abstract:PURPOSE:Oxygen therapy (hyperoxia) is essential for the treatment of some neonatal critical care conditions. The lung is the primary target for the changes induced by hyperoxia. Secretory immunoglobulin A (SIgA), IgA and secretory component (SC) reflect the local immunity in the respiratory tract induced by hyperoxia. ...

    journal_title:Journal of clinical immunology

    pub_type: 杂志文章

    doi:10.1007/s10875-013-9891-4

    authors: Liu DY,Jiang T,Wang S,Cao X

    更新日期:2013-07-01 00:00:00

  • Efficacy and safety of subcutaneous vivaglobin® replacement therapy in previously untreated patients with primary immunodeficiency: a prospective, multicenter study.

    abstract::Treatment of primary immunodeficiency (PI) is typically initiated with intravenous immunoglobulin (IVIG) loading and then continued with IVIG or subcutaneous IgG (SCIG). This prospective, open-label, multicenter, 6-month study evaluated a new regimen of initiating IgG therapy with SCIG in 18 previously untreated patie...

    journal_title:Journal of clinical immunology

    pub_type: 临床试验,杂志文章,多中心研究

    doi:10.1007/s10875-011-9588-5

    authors: Borte M,Quinti I,Soresina A,Fernández-Cruz E,Ritchie B,Schmidt DS,McCusker C

    更新日期:2011-12-01 00:00:00

  • Macrophage T-cell interaction in man: handling of tetanus toxoid antigen by human monocytes.

    abstract::An absolute requirement for monocytes was demonstrated in the T-cell proliferative response to tetanus toxoid (TT) antigen. Antigen-pulsed monocytes were shown to be effective in triggering T-cell proliferation. Using 125I-radiolabeled TT antigen, uptake by monocytes increased progressively over an 18-hr period, at wh...

    journal_title:Journal of clinical immunology

    pub_type: 杂志文章

    doi:10.1007/BF00915473

    authors: Alpert SD,Jonsen ME,Broff MD,Schneeberger E,Geha RS

    更新日期:1981-01-01 00:00:00

  • A role of fas-associated death domain (FADD) in increased apoptosis in aged humans.

    abstract::Fas-associated death domain (FADD) is an adapter protein that is recruited to the death-inducing signaling complex (DISC) during signaling via death receptors. FADD is a common conduit in both CD95-mediated and TNF-R-mediated apoptosis. In aging, T cells show increased susceptibility to death receptor-induced apoptosi...

    journal_title:Journal of clinical immunology

    pub_type: 杂志文章

    doi:10.1023/B:JOCI.0000018059.56924.99

    authors: Gupta S,Kim C,Yel L,Gollapudi S

    更新日期:2004-01-01 00:00:00

  • B-cell lymphoma in a patient with complete interferon gamma receptor 1 deficiency.

    abstract::Immunosuppression-associated lymphoproliferative disorders can be related to primary as well as acquired immune disorders. Interferon gamma receptor (IFN-γR) deficiency is a rare primary immune disorder, characterized by increased susceptibility to mycobacterial infections. Here we report the first case of an Epstein ...

    journal_title:Journal of clinical immunology

    pub_type: 杂志文章

    doi:10.1007/s10875-013-9907-0

    authors: Bax HI,Freeman AF,Anderson VL,Vesterhus P,Laerum D,Pittaluga S,Wilson WH,Holland SM

    更新日期:2013-08-01 00:00:00

  • Severe combined immunodeficiency (SCID) in Canadian children: a national surveillance study.

    abstract:PURPOSE:Severe Combined Immune Deficiency (SCID) is universally fatal unless treated with hematopoietic stem cell transplantation (HSCT). Following the identification of disseminated Bacille Calmette-Guérin (BCG) infections in Canadian First Nations, Métis and Inuit (FNMI) children with unrecognized primary immune defi...

    journal_title:Journal of clinical immunology

    pub_type: 杂志文章

    doi:10.1007/s10875-013-9952-8

    authors: Rozmus J,Junker A,Thibodeau ML,Grenier D,Turvey SE,Yacoub W,Embree J,Haddad E,Langley JM,Ramsingh RM,Singh VA,Long R,Schultz KR

    更新日期:2013-11-01 00:00:00