REATIVAÇÃO DA DOENÇA DE CHAGAS EM INDIVÍDUOS COINFECTADOS PELO HIV: ASPECTOS HISTOPATOLÓGICOS
Carregando...
Arquivos
Data
Título da Revista
ISSN da Revista
Título de Volume
Editor
DOI
Resumo
Introduction – Reactivation of Chagas disease (CD) has been described in severe
immunocompromised patients by various etiologies, among them those due to
coinfection with HIV. Objective – Perform histopathological and
immunohistochemical evaluation of the brain, myocardium, esophagus and large
bowel of autopsied patients with CD and/or Acquired Immunodeficiency Syndrome
(AIDS) compared with control patients. Material and Methods – A survey of autopsy
reports was conducted in the period from 1998 to 2012 and selected eight adult
subjects who were divided into four groups: Reactivation of Chagas disease (RE)
(n=2), Chagas disease (CH) (n=2), AIDS (AI) (n=2) and Control (CO) (n=2). From
each subject were collected and processed fragments of brain, myocardium,
esophagus and large bowel whose fragments were processed for histological and
immunohistochemical analysis. The histological sections stained with hematoxylin
and eosin, Giemsa and Picrossirius were used to quantify the density of inflammatory
cells, the density of mast cells and the percentage of collagen, respectively.
Immunohistochemical analysis was performed to IL17 and CD31. Results – In the
myocardium the density of mast cells was significantly higher in the CH group when
compared to other groups. In the esophagus and large intestine, the density of mast
cells was significantly higher when compared to other groups. The percentage of
collagen in the esophagus, heart and intestine in the RE group was significantly
lower when compared to the CO group. The CH group had a higher percentage of
collagen in the myocardium and in the large bowel when compared to other groups.
The density of cells immunostained by anti-IL17 was significantly higher in the large
bowel and myocardium in the CH group when compared to the CO group. The
myocardium and esophagus AI group higher density of vessels immunostained by
anti-CD31 when compared to the other groups found. No significant correlations as
the density of mast cells and percentage of collagen in groups RE, CO, CH and AI.
Conclusion – Brain lesions found in patients with reactivation of DC and the highest
density of immunostained cells by anti-IL17 at these sites suggests that this cytokine
was intensifying local inflammation with consequent tissue damage due to
inflammation. In addition, in these subjects, the highest density of mast cells in the
esophagus and intestine suggests that these cells would be exercising relevant
activity in esophageal and intestinal inflammation..