RESUMO
Resumen La infección por SARS-CoV-2 promueve un descontrol del sistema inmune con predominio de una respuesta inflamatoria de rápida instauración y el desencadenamiento de una tormenta de citocinas. El objetivo de esta revisión es comprender mejor los mecanismos inmunológicos y su descontrol activados por SARS-CoV-2. La activación de la inmunidad innata, contra la infección, es el factor clave para el control viral o su progresión hacia COVID-19. La respuesta inmune adaptativa, igualmente es perturbada por SARS-CoV-2 con lo cual se posibilita una mayor tasa de infección, así como también el descontrol inmunológico sistémico que puede desencadenar shock y daño tisular en diferentes órganos, muerte por COVID-19 o autoinmunidad post COVID-19.
Abstract The SARS-CoV-2 infection promotes a lack of control of the immune system with a predominance of a rapidly onset inflammatory response and the triggering of a cytokine storm. The objective of this review is to understand better the immune mechanisms and their lack of control activated by SARS-CoV-2. The activation of innate immunity against infection is the key factor for viral control or its progression towards COVID-19. The adaptive immune response is also disturbed by SARS-CoV-2, which enables a higher infection rate, as well as systemic immune lack of control that can trigger shock and tissue damage in different organs, death from COVID-19 or autoimmunity post-COVID-19.
RESUMO
We have analyzed the response to the treatment with benznidazol in newborns and nurslings in the Hospital Materno Infantil Germán Urquidi of Cochabamba, Bolivia, between 1999 and 2002. It is important an integral treatment of the nursling with a subsequent information directed to the family. The response was close to 100% when the treatment was correctly administrated. They were not adverse effects and the detected biochemical alterations did not present clinical significance.
Assuntos
Doença de Chagas/congênito , Doença de Chagas/tratamento farmacológico , Nitroimidazóis/uso terapêutico , Tripanossomicidas/uso terapêutico , Doença de Chagas/sangue , Protocolos Clínicos , Assistência Integral à Saúde , Família , Seguimentos , Humanos , Lactente , Recém-Nascido , Cooperação do Paciente , Estudos Prospectivos , Resultado do TratamentoRESUMO
This study compares the levels of specific antibodies IgM and IgA for Chagas in samples of blood from newborns. Three groups of cord blood samples have been analysed: a group of 42 samples from newborns, displaying positive parasitemia, of seropositive mothers (M+B+), 68 samples from newborns with negative parasitemia whose mothers were seropositive (M+B-) and a group of 45 control newborns coming from mothers with negative serology for Chagas. From the 42 M+B+ samples with congenital Chagas disease, 81 and 82.9% displayed detectable levels of IgM and IgA antibodies, respectively In the M+B- group, 70.6 and 33.8% presented antibodies of IgM and IgA classes, respectively, whereas in the control group M-B-, we detected 6% and 11.1% of IgM and IgA antibodies, respectively. The calculated sensitivity of detection of congenital cases using IgM or IgA antibodies was of 82.9% and 80.9% respectively, whereas the specificity of detection was of 29.4% for IgM antibodies and of 66.1% for IgA antibodies.