Subject(s)
Actinomyces , Actinomycosis/genetics , Abdominal Pain , Actinomycosis/diagnostic imaging , Actinomycosis/drug therapy , Ampicillin/therapeutic use , Female , Humans , Mass Spectrometry , Middle Aged , Peritoneal Diseases/diagnostic imaging , Peritoneal Diseases/drug therapy , Peritoneal Diseases/microbiologyABSTRACT
BACKGROUND & AIMS: Diagnostic procedures in Whipple's disease usually focus on the intestine, but symptomatic central nervous system involvement is a major threat for patients. The aim of this study was to determine the diagnostic value of cerebrospinal fluid (CSF) analysis. METHODS: A total of 39 CSF samples and 2 brain biopsy specimens that were obtained from 24 patients with Whipple's disease at various intervals after diagnosis were examined. Five patients presented with neurological symptoms, 3 of them as relapses after therapy. Thirty-two CSF samples were examined by polymerase chain reaction for Tropheryma whippelli and 20 CSF samples by cytology. Brain biopsy specimens were examined histologically. RESULTS: Positive results were obtained in 4 of 5 patients (80%) with neurological symptoms, in 7 of 10 patients (70%) without neurological symptoms examined before therapy, and in 3 of 11 patients (27%) without neurological symptoms studied during or after therapy. Conversion from positive to negative was observed in 4 patients after antibiotic treatment. CONCLUSIONS: Testing of CSF in Whipple's disease yields a high rate of positive results, even in patients without neurological symptoms. Examination of CSF is therefore potentially useful for initial staging and for monitoring of the efficiency of therapy.
Subject(s)
Actinobacteria/genetics , Actinomycetales Infections/pathology , Brain/pathology , Cerebrospinal Fluid/cytology , DNA, Bacterial/cerebrospinal fluid , Whipple Disease/pathology , Actinobacteria/isolation & purification , Actinomycetales Infections/cerebrospinal fluid , Actinomycetales Infections/diagnosis , Actinomycosis/diagnosis , Actinomycosis/genetics , Actinomycosis/pathology , Adult , Base Sequence , Biopsy/methods , Central Nervous System/pathology , Central Nervous System/physiopathology , Cerebrospinal Fluid/microbiology , DNA, Bacterial/genetics , Disease Progression , Electrophoresis, Polyacrylamide Gel , Female , Genes, myc/genetics , Humans , Intestines/chemistry , Intestines/pathology , Male , Middle Aged , Polymerase Chain Reaction , Whipple Disease/cerebrospinal fluid , Whipple Disease/diagnosisABSTRACT
Antibodies reactive with type 1 and type 2 fimbriae from Actinomyces viscosus T14V specifically inhibit the adherence of A. viscosus T14V to salivary pellicle-coated tooth surfaces and other bacteria, and these antibodies are thought to modulate colonization by this microorganism. These studies were done to determine whether previously noted differences in the antibody responses of inbred mice to type 1 and type 2 fimbriae might be under genetic control. The serum immunoglobulin G (IgG) and IgM antibody responses of inbred, F1 hybrid, and H-2 congenic mice, immunized with A. viscosus T14V cells, were analyzed by enzyme-linked immunosorbent assays for antibodies reactive with A. viscosus T14V whole-cell type 1 and type 2 fimbriae. The results confirmed earlier findings and indicated striking variations in the amounts of IgG anti-type 1 (23-fold) and anti-type 2 (48-fold) fimbria antibodies elicited. The responses of the 17 inbred strains tested showed a relatively continuous distribution from high to low, as well as marked differences in the responses of H-2 and Igh-C identical strain pairs. An analysis of the responses of F1 hybrid and H-2 congenic mice indicated dominance of the low-responder gene(s) and control by H-2-linked genes. Antisera from two high-responder strains inhibited in vitro bacterial adherence to a much greater degree than antisera from a low-responding strain. These data suggest polygenic control of the magnitude of the IgG anti-type 1 and anti-type 2 fimbria antibody responses by H-2-linked genes as well as background genes not associated with H-2 or Igh-C loci.
