Abstract Actinobacillus actinomycetemcomitans has frequently been implicated in juvenile periodontitis. The present monoclonal antibodies are specific to Actinobacillus actinomycetemcomitans. The present monoclonal antibodies are typically employed as reagents which include an inert carrier, preferably a liquid, such as buffered saline solution and a preservative. The carrier compositions are suitably selected to provide for the proper dispersal of bacteria, and to preserve the integrity of antigens and supplemental structures. The selection of the proper carrier is especially important in the detection in mixtures which include bacteria which produce large amounts of autolyltic enzymes such as B. gingivalis. The monoclonal antibodies of the present invention are useful in clinical testing and differentiating antigens in the gingival or subgingival sera. The method of testing and differentiating involves the steps of contacting a sample of the bacterial flora from a lesion or other site with a measured amount of monoclonal antibody specific to a single antigen site on Actinobacillus actinomycetemcomitans and subsequently measuring the number of antibody-antigen complexes formed.
A monoclonal antibody reagent useful in determining the presence of pathogens containing at least one monoclonal antibody species specific to the microorganism Actinobacillus actinomycetemcomitans.
Claim 2
Dependent Claim
24 words
A monoclonal antibody reagent useful in determining the presence of pathogens containing at least one monoclonal antibody species specific to the microorganism Actinobacillus actinomycetemcomitans.
Claim 3
Dependent Claim
8 words
Monoclonal antibodies species specific to microorganism Actinobacillus actinomycetemcomitans.
Claim 4
Dependent Claim
8 words
Monoclonal antibodies species specific to microorganism Actinobacillus actinomycetemcomitans.
Claim 5
Independent Claim
65 words
A method of determining the presence of Actinobacillus actinomycetemcomitans in a gingival fluid comprising the steps of: (a) contacting a selected antigenic substance from said pathogens with a monoclonal antibody species specific to said pathogen to form a complex of said antigenic substance and said monoclonal antibody, and (b) measuring the amount of said complex by determining the amount of antibody in said formed complex.
Claim 6
Independent Claim
65 words
A method of determining the presence of Actinobacillus actinomycetemcomitans in a gingival fluid comprising the steps of: (a) contacting a selected antigenic substance from said pathogens with a monoclonal antibody species specific to said pathogen to form a complex of said antigenic substance and said monoclonal antibody, and (b) measuring the amount of said complex by determining the amount of antibody in said formed complex.
Claim 7
Independent Claim
64 words
A method of determining the presence of Actinobacillus actinomycetemcomitans in a biological fluid comprising the steps of: (a) providing an aliquot of the biological fluid to be studied, (b) contacting said aliquot with a measured amount of monoclonal antibodies species specific to distinct antigenic determinants on the surface of the cells of Actinobacillus actinomycetemcomitans, and (c) determining whether any reaction with said antibodies occurs.
Claim 8
Independent Claim
64 words
A method of determining the presence of Actinobacillus actinomycetemcomitans in a biological fluid comprising the steps of: (a) providing an aliquot of the biological fluid to be studied, (b) contacting said aliquot with a measured amount of monoclonal antibodies species specific to distinct antigenic determinants on the surface of the cells of Actinobacillus actinomycetemcomitans, and (c) determining whether any reaction with said antibodies occurs.
Claim 9
Dependent Claim
24 words
The method of claim 4 wherein the antibodies are labeled and said labeled antibodies have a predetermined fluorescence response to a given optical stimulation.
Claim 10
Dependent Claim
21 words
The method of claim 4 wherein the amount of reaction is determined and the presence of periodontopathogens is quantitatively derived therefrom.