Modulation of immune responses to periodontal bacteria. 1994

E Gemmell, and G J Seymour
University of Queensland, Brisbane, Australia.

There is little doubt that the interaction between the host immune mechanisms and putative periodontal bacteria is fundamental in the clinical manifestations of the different forms of adult chronic inflammatory periodontal disease. Recent work regarding the function of polymorphonuclear neutrophils indicates that, in addition to their established protective and destructive roles, these cells may have a regulatory function in periodontal disease. Equally, emerging evidence suggests that T-cell responses in adult periodontal disease are antigen specific. Further, the migration and retention of specific T cells in the periodontal tissues appears to be related not to the expression of adhesion molecules but rather to the presence of a specific antigen. T-cell subsets are now characterized on the basis of their cytokine profiles. Type 1 T cells produce interleukin-2 and interferon-gamma, whereas type 2 T cells produce interleukin-4 and interleukin-10. A hypothesis based on this characterization of T cells is presented. According to this hypothesis, susceptible subjects have a type 2 response, whereas nonsusceptible subjects respond predominantly with type 1 T cells. The possible role of interleukin-12 in controlling this response is highlighted, thus demonstrating the marriage of innate and adaptive immune responses in adult periodontal disease.

UI MeSH Term Description Entries
D009504 Neutrophils Granular leukocytes having a nucleus with three to five lobes connected by slender threads of chromatin, and cytoplasm containing fine inconspicuous granules and stainable by neutral dyes. LE Cells,Leukocytes, Polymorphonuclear,Polymorphonuclear Leukocytes,Polymorphonuclear Neutrophils,Neutrophil Band Cells,Band Cell, Neutrophil,Cell, LE,LE Cell,Leukocyte, Polymorphonuclear,Neutrophil,Neutrophil Band Cell,Neutrophil, Polymorphonuclear,Polymorphonuclear Leukocyte,Polymorphonuclear Neutrophil
D010518 Periodontitis Inflammation and loss of connective tissues supporting or surrounding the teeth. This may involve any part of the PERIODONTIUM. Periodontitis is currently classified by disease progression (CHRONIC PERIODONTITIS; AGGRESSIVE PERIODONTITIS) instead of age of onset. (From 1999 International Workshop for a Classification of Periodontal Diseases and Conditions, American Academy of Periodontology) Pericementitis,Pericementitides,Periodontitides
D002908 Chronic Disease Diseases which have one or more of the following characteristics: they are permanent, leave residual disability, are caused by nonreversible pathological alteration, require special training of the patient for rehabilitation, or may be expected to require a long period of supervision, observation, or care (Dictionary of Health Services Management, 2d ed). For epidemiological studies chronic disease often includes HEART DISEASES; STROKE; CANCER; and diabetes (DIABETES MELLITUS, TYPE 2). Chronic Condition,Chronic Illness,Chronically Ill,Chronic Conditions,Chronic Diseases,Chronic Illnesses,Condition, Chronic,Disease, Chronic,Illness, Chronic
D003602 Cytotoxicity, Immunologic The phenomenon of target cell destruction by immunologically active effector cells. It may be brought about directly by sensitized T-lymphocytes or by lymphoid or myeloid "killer" cells, or it may be mediated by cytotoxic antibody, cytotoxic factor released by lymphoid cells, or complement. Tumoricidal Activity, Immunologic,Immunologic Cytotoxicity,Immunologic Tumoricidal Activities,Immunologic Tumoricidal Activity,Tumoricidal Activities, Immunologic
D006090 Gram-Negative Bacteria Bacteria which lose crystal violet stain but are stained pink when treated by Gram's method. Gram Negative Bacteria
D006801 Humans Members of the species Homo sapiens. Homo sapiens,Man (Taxonomy),Human,Man, Modern,Modern Man
D016176 T-Lymphocyte Subsets A classification of T-lymphocytes, especially into helper/inducer, suppressor/effector, and cytotoxic subsets, based on structurally or functionally different populations of cells. T-Cell Subset,T-Cell Subsets,T-Lymphocyte Subset,Subset, T-Cell,Subset, T-Lymphocyte,Subsets, T-Cell,Subsets, T-Lymphocyte,T Cell Subset,T Cell Subsets,T Lymphocyte Subset,T Lymphocyte Subsets
D016207 Cytokines Non-antibody proteins secreted by inflammatory leukocytes and some non-leukocytic cells, that act as intercellular mediators. They differ from classical hormones in that they are produced by a number of tissue or cell types rather than by specialized glands. They generally act locally in a paracrine or autocrine rather than endocrine manner. Cytokine

Related Publications

E Gemmell, and G J Seymour
February 2001, Immunological reviews,
E Gemmell, and G J Seymour
June 2020, Vaccines,
E Gemmell, and G J Seymour
January 1992, Advances in experimental medicine and biology,
E Gemmell, and G J Seymour
April 2022, Pathogens (Basel, Switzerland),
E Gemmell, and G J Seymour
August 2001, Current opinion in immunology,
E Gemmell, and G J Seymour
November 2004, Journal of clinical periodontology,
E Gemmell, and G J Seymour
May 2009, Mucosal immunology,
E Gemmell, and G J Seymour
January 1998, Parasitology,
E Gemmell, and G J Seymour
January 1987, Cancer detection and prevention. Supplement : official publication of the International Society for Preventive Oncology, Inc,
E Gemmell, and G J Seymour
November 1980, Federation proceedings,
Copied contents to your clipboard!