Aline Lury Aoki, MD
,
Outpatient Group of Recurrent Infections, Faculty of Medicine ABC, SP, Brazil, Santo Andre, Brazil
Viviana Arruk
,
Outpatient Group of Recurrent Infections, Faculty of Medicine ABC, SP, Brazil, Santo Andre, Brazil
Rosemeire Navickas Constantino-Silva, PhD
,
Laboratory of Clinical Immunology, Center of Research, Faculty of Medicine ABC, Santo Andre - SP, Brazil
Alexandre Campeas
,
Infectious Diseases, Institute of Infectious Diseases Emilio Ribas, SP, Brazil, Brazil
Maria Do Socorro Ferrão
,
Infectious Diseases, Institute of Infectious Diseases Emilio Ribas, SP, Brazil, Brazil
Myriam Raymundo
,
Infectious Diseases, Institute of Infectious Diseases Emilio Ribas, SP, Brazil, Brazil
Fabiane Milena Castro Araújo Pimenta, MD
,
Outpatient Group of Recurrent Infections, Faculty of Medicine ABC, SP, Brazil, Santo Andre, Brazil
Vivian Alves Costa, MD
,
Outpatient Group of Recurrent Infections, Faculty of Medicine ABC, SP, Brazil, Santo Andre, Brazil
Ana Karolinne Burlamaqui Melo, MD
,
Outpatient Group of Recurrent Infections, Faculty of Medicine ABC, SP, Brazil, Santo Andre, Brazil
Sandra Mitie Ueda Palma, MD
,
Outpatient Group of Recurrent Infections, Faculty of Medicine ABC, SP, Brazil, Santo Andre, Brazil
Michael Kirschfink
,
Institute of Immunology, University of Heildelberg, Germany
Anete Grumach, MD, PhD
,
Outpatient Group of Recurrent Infections, Faculty of Medicine ABC, SP, Brazil, Santo Andre, Brazil
Background: Deficiencies of terminal components of complement have been described in patients affected by meningococcal meningitis. The need of routine investigation has to be established. We evaluated patients with confirmed meningitis due to N. meningitides looking for complement system evaluation.
Methods: Prospective study in which data and blood samples of patients with confirmed meningococcal meningitis were collected. Hemolytic assays, CH50 and APH50, for classical and alternative pathways respectively, ELISA for properdin and mannose binding lectin (MBL) were performed. Specific components were evaluated after confirmed impairment of complement system.
Results: A hundred and twenty nine patients (69M:60F) were included in the study. The age of the patients ranged from 2 months (m) up to 64 years old (mean= 96.2m; median=48m). The following serogroups were identified: type C, 36.4%; B, 20.2%; W135, 1.5% and 41.9% had no serogroup identified. CH50 and AP50 values were below the reference levels in 48 patients (37.2%) and 97 patients (75.2%), and the activity was undetectable in 5 and 15 patients, respectively. Levels of CH50 and AP50 were both low in 46 patients (33.65%) and in 8 were both undetectable. Properdin levels were performed in patients with low AP50 (n = 44) and 43.2% had decreased properdin value. MBL values were below 50 micrograms in 2/26 patients evaluated. One patient was diagnosed with C6 deficiency after the second meningitis.
Conclusions: Although high number of patients had low levels of complement evaluation, it probably represents activation of the system due to meningitis. The study suggests the need of complement evaluation but a period after the acute infection would be more reliable to establish real complement defect.
