FAMILY CASE STUDIES HELP US IDENTIFY host risk factors in periodontal
disease. In this study we examine a family consisting of a mother (40
years old, with rapidly progressive periodontitis), her elder daughter
(14 years old, with localized juvenile periodontitis), and younger da
ughter (13 years old, with simple gingivitis). We examined 1) the peri
pheral neutrophil functions (chemotactic migration, phagocytosis, supe
roxide production); 2) lymphocyte functions (proliferative activity an
d cytokine productivity of T cells, immunoglobulin [Ig] M productivity
of B cells when stimulated with pokeweed mitogen); 3) phenotypic anal
yses of peripheral lymphocyte subpopulations; 4) serum IgG antibody ti
ters against periodontopathic bacteria; and 5) serological type of HLA
class IS. All the subjects exhibited high T4/T8 ratios due to high pe
rcentage of CD4-positive cells, showed high IgG titers to Actinobacill
us actinomycetemcomitans, and had a HLA DQw1 in common. The mother sho
wed a slight deficiency of neutrophil chemotactic migration to N-formy
l methyonyl leucyl phenylalanin (fMLP), raised interleukin-2 productiv
ity of T cell, and high levels of IgG titers to Porphyromonus gingival
is and Fusobacterium nucleatum. Both daughters showed weak T cell prol
iferative response to anti-CD3 monoclonal antibody and low IgM product
ivity. Low lymphocyte responsiveness may be involved in the pathogenes
is of periodontal disease of these daughters; therefore, the lymphocyt
e dysfunctions shown should be considered in relation to the progressi
on of periodontal disease.