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1985 Kreshover lecture. Molecular Factors Influencing Neutrophil Defects in Periodontal DiseaseState University of New York at Buffalo, School of Dental Medicine, Department of Oral Biology, and Periodontal Disease Clinical Research Center, Foster Hall, Buffalo, New York 14214
Emory University, School of Dentistry, 1462 Clifton Road, N.E., Atlanta, Georgia 30322
State University of New York at Buffalo, School of Dental Medicine, Department of Oral Biology, and Periodontal Disease Clinical Research Center, Foster Hall, Buffalo, New York 14214
University of Minnesota, School of Medicine, Minneapolis, Minnesota 55455
State University of New York at Buffalo, School of Dental Medicine, Department of Oral Biology, and Periodontal Disease Clinical Research Center, Foster Hall, Buffalo, New York 14214 Major advances in our understanding of the role of the neutrophil in host defense against periodontal organisms have been made through studies of localized juvenile periodontitis (LJP). Several.lines of evidence suggest that LJP is an infectious process closely associated with Actinobacillus (Haemophilus) actinomycetemcomitans as a causative agent, although other organisms may also participate. The immunologic profile of LJP patients suggests that a cell-associated neutrophil locomotory dysfunction is a key underlying immunodeficiency resulting in increased susceptibility to periodontal infection. In addition, LJP patients often exhibit cervical lymphadenopathy and IgG-hypergammaglobulinemia, and a markedly elevated antibody response to the infecting organism, A. actinomycetemcomitans, is found in the serum and crevicular fluid of most patients. Evaluation of the locomotory properties of LJP neutrophils shows that random migration and chemokinesis are normal; however, about 70% of the LJP patients suffer from a defect in chemotaxis, with their neutrophils responding poorly to bacterial chemotaetic factors, synthetic chemotactic peptides, and complement fragments (C5a). Depressed chemotaxis of LJP neutrophils is paralleled by their reduced capacity to bind the synthetic chemotactic peptide N-formylmethionylleucylphenylalanine (FMLP), as well as C5a. Furthermore, there is a reduction in the amount of glycoprotein 110, a neutrophil membrane matrix component and differentiation antigen which is associated with FMLP- and possibly also C5a-mediated chemotaxis. Reduction ofC5a and of FMLP ligand binding, decreased expression of GP-110, and reduced neutrophil chemotaxis are consistent with a stem cell maturation error in LJP patients. This is further supported by studies demonstrating increased expression of CR2, the C3d/EBV receptor, on peripheral blood neutrophils of LJP patients. CR2 receptors are normally present on immature human neutrophils but are lost during the maturation process. These alterations in neutrophil surface components and their reduced chemotaxis may result from a genetically determined abnormality. Studies demonstrating the familial nature of both the neutrophil chemotactic disorder and the clinical entity represented by localized juvenile periodontitis point to a strong role for genetic determinants in the disease which affect neutrophil surface receptors.
Journal of Dental Research, Vol. 65, No. 12,
1379-1391 (1986) This article has been cited by other articles:
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