Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
1
pubmed:dateCreated
2000-1-19
pubmed:abstractText
CD8+ T cells down-regulate a variety of immune responses. For example, porcine and human insulin do not stimulate Abs in C57BL/6 mice because CD8+ T cells inhibit CD4+ helper T cells. By contrast, bovine insulin induces Ab in C57BL/6 mice, and removal of CD8+ T cells does not alter this response. This raises the question of whether porcine, but not bovine, insulin activates CD8+ T cells or whether both insulins activate CD8+ T cells but CD4+ helper T cells are differentially inhibited by them. In this study, we show that insulin-specific CD8+ CTL can be cultured from C57BL/6 mice primed with either bovine or human insulin in CFA. Thus, exogenous Ags, besides OVA, induce CD8+ CTL when administered in an adjuvant, suggesting this is a typical response. These CTL are H-2Kb restricted and produce IL-5, IL-10, IFN-gamma, and small amounts of IL-4, which is distinct from IFN-gamma and TNF-alpha that are typically secreted by virus-specific CTL. Moreover, the CTL primed with either bovine or human insulin recognize an A-chain peptide that is identical to the mouse insulin sequence. That foreign proteins, which are closely related to self-proteins, activated autoreactive, CD8+ T cells in vivo is a novel finding. It raises the possibility that self-reactive CTL may be activated by cross-reacting Ags and once activated they might participate in autoimmunity. These results also suggest that down-regulation of insulin-specific responses by autoreactive CD8+ T cells is most likely due to the differential sensitivity of bovine and human insulin-specific CD4+ T cells.
pubmed:grant
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
AIM
pubmed:chemical
pubmed:status
MEDLINE
pubmed:month
Jan
pubmed:issn
0022-1767
pubmed:author
pubmed:issnType
Print
pubmed:day
1
pubmed:volume
164
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
86-92
pubmed:dateRevised
2011-11-17
pubmed:meshHeading
pubmed-meshheading:10604997-Amino Acid Sequence, pubmed-meshheading:10604997-Animals, pubmed-meshheading:10604997-Antigens, CD8, pubmed-meshheading:10604997-Cattle, pubmed-meshheading:10604997-Clone Cells, pubmed-meshheading:10604997-Cytokines, pubmed-meshheading:10604997-Cytotoxicity, Immunologic, pubmed-meshheading:10604997-Epitopes, T-Lymphocyte, pubmed-meshheading:10604997-Female, pubmed-meshheading:10604997-Genetic Vectors, pubmed-meshheading:10604997-H-2 Antigens, pubmed-meshheading:10604997-Humans, pubmed-meshheading:10604997-Insulin, pubmed-meshheading:10604997-Lymphocyte Activation, pubmed-meshheading:10604997-Mice, pubmed-meshheading:10604997-Mice, Inbred C57BL, pubmed-meshheading:10604997-Molecular Sequence Data, pubmed-meshheading:10604997-Peptides, pubmed-meshheading:10604997-T-Lymphocytes, Cytotoxic, pubmed-meshheading:10604997-Th1 Cells, pubmed-meshheading:10604997-Th2 Cells, pubmed-meshheading:10604997-Transfection, pubmed-meshheading:10604997-Tumor Cells, Cultured
pubmed:year
2000
pubmed:articleTitle
Bovine and human insulin activate CD8+-autoreactive CTL expressing both type 1 and type 2 cytokines in C57BL/6 mice.
pubmed:affiliation
Department of Ophthalmology, Winship Cancer Center, Department of Cell Biology, Emory University School of Medicine, Atlanta, GA 30322, USA.
pubmed:publicationType
Journal Article, Research Support, U.S. Gov't, P.H.S., Research Support, Non-U.S. Gov't