Cinara Cássia Brandão

Prof. Dr. Cinara Cássia Brandão

Molecular Biology, Faculdade de Medicina de São José do Rio Preto, São José do Rio Prêto, São Paulo, Brazil
orcid

Research Focus & Metrics

Academic Career Length

17Years (2010-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

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1 October 2011 in Experimental Parasitology
Verified
Journal Article
Closed access
IFIsabelle Martins Ribeiro Ferreira
Isabelle Martins Ribeiro Ferreira
JVJose E Vidal
Jose E Vidal
Cinara Cássia BrandãoCinara Cássia Brandão
Cinara Cássia Brandão
LMLuiz Carlos De Mattos
Luiz Carlos De Mattos
DQDaofeng Qu
Daofeng Qu
VPVera Lucia Pereira-Chioccola
Vera Lucia Pereira-Chioccola

1 June 2018 in Clinical Microbiology and Infection
Verified
Journal Article
Closed access
MNMauricio Nogueira
Mauricio Nogueira
Nivison Nery Jr.Nivison Nery Jr.
Nivison Nery Jr.
CEC.F. Estofolete
C.F. Estofolete
ATA.C. Bernardes Terzian
A.C. Bernardes Terzian
GGG.F. Guimarães
G.F. Guimarães
AKA.I. Ko
A.I. Ko

6 September 2016 in Clinical Infectious Diseases
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Journal Article
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ASAntonio Soares de Souza
Antonio Soares de Souza
CDCristiane Moraes Dias
Cristiane Moraes Dias
FBFernanda Del Campo Braojos Braga
Fernanda Del Campo Braojos Braga
ATAna Carolina Bernardes Terzian
Ana Carolina Bernardes Terzian
CECássia Fernanda Estofolete
Cássia Fernanda Estofolete
DVDenise Cristina Mós Vaz-Oliani
Denise Cristina Mós Vaz-Oliani
Zika virus (ZIKV) infection acquired during pregnancy is associated with congenital microcephaly. We describe 2 cases of ZIKV infection in women in their 36th week of pregnancy whose fetuses had preserved head circumference at birth and findings of subependymal cysts and lenticulostriate vasculopathy in postnatal imaging. These represent the first signs of congenital brain injury acquired due to ZIKV in the third trimester.

18 March 2013 in Epidemiology and Infection
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Journal Article
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AFA. I. C. Ferreira
A. I. C. Ferreira
Cinara Cássia BrandãoCinara Cássia Brandão
Cinara Cássia Brandão
FFFábio Batista Frederico
Fábio Batista Frederico
CMC. S. Meira
C. S. Meira
GAG. C. Almeida
G. C. Almeida
LMLuiz Carlos De Mattos
Luiz Carlos De Mattos
SUMMARY: The aim of this study was to investigate risk factors for ocular toxoplasmosis (OT) in patients who received medical attention at a public health service. Three hundred and forty-nine consecutive patients, treated in the Outpatient Eye Clinic of Hospital de Base, São José do Rio Preto, São Paulo state, Brazil, were enrolled in this study. After an eye examination, enzyme-linked immunosorbent assay (ELISA) was used to determine anti-Toxoplasma gondii antibodies. The results showed that 25·5% of the patients were seronegative and 74·5% were seropositive for IgG anti-T. gondii antibodies; of these 27·3% had OT and 72·7% had other ocular diseases (OOD). The presence of cats or dogs [odds ratio (OR) 2·22, 95% confidence interval (CI) 1·24–3·98, P = 0·009] and consumption of raw or undercooked meat (OR 1·77, 95% CI 1·05–2·98, P = 0·03) were associated with infection but not with the development of OT. Age (OT 48·2 ± 21·2 years vs. OOD: 69·5 ± 14·7 years, P < 0·0001) and the low level of schooling/literacy (OT vs. OOD: OR 0·414, 95% CI 0·2231–0·7692, P = 0·007) were associated with OT. The presence of dogs and cats as well as eating raw/undercooked meat increases the risk of infection, but is not associated with the development of OT.

1 January 2014 in Frontiers in Microbiology
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Journal Article
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TGToxoplasma Groups
Toxoplasma Groups
CMCristina S. Meira
Cristina S. Meira
Vera Lucia Pereira-ChioccolaVera Lucia Pereira-Chioccola
Vera Lucia Pereira-Chioccola
JVJose E Vidal
Jose E Vidal
Cinara Cássia BrandãoCinara Cássia Brandão
Cinara Cássia Brandão
LMLuiz Carlos De Mattos
Luiz Carlos De Mattos
This study analyzed the synthesis of IFN-, TNF-α and IL-10 in chronically infected patients which developed the symptomatic disease as cerebral or ocular toxoplasmosis. Blood from 61 individuals were divided into four groups: Cerebral toxoplasmosis/AIDS patients (CT/AIDS group) (n=15), ocular toxoplasmosis patients (OT group) (n=23), chronic toxoplasmosis individuals (CHR group) (n=13) and healthy individuals (HI group) (n=10). OT, CHR and HI groups were HIV seronegative. The diagnosis was made by laboratorial (PCR and ELISA) and clinical subjects. For cytokine determination, peripheral blood mononuclear cells (PBMC) of each patient were isolated and stimulated in vitro with T. gondii antigen. IFN-γ, TNF-α, and IL10 activities were determined by ELISA. Patients from CT/AIDS and OT groups had low levels of IFN- when were compared with those from CHR group. These data suggest the low resistance to develop ocular lesions by the low ability to produce IFN- against the parasite. The same patients, which developed ocular or cerebral toxoplasmosis had higher TNF-α levels than CHR individuals. High TNF-α synthesis contribute to the inflammatory response and damage of the choroid and retina in OT patients and in AIDS patients caused a high inflammatory response as the TNF-α synthesis is not affected since monocytes are the major source this cytokine in response to soluble T. gondii antigens. IL-10 levels were almost similar in CT/AIDS and OT patients but low when compared with CHR individuals. The deviation to Th2 immune response including the production of anti-inflammatory cytokines, such as IL-10 may promote the parasite’s survival causing the tissue immune destruction. IL-10 production in T. gondii-infected brains may support the persistence of parasites as down-regulating the intracerebral immune response. All these indicate that OT and CT/AIDS patients produced low levels of IL10 (Th2 response) and IFN- (Th1 response). They produced high TNF-α suggesting a high inf

1 July 2011 in Diagnostic Microbiology and Infectious Disease
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Journal Article
Closed access
Cinara Cássia BrandãoCinara Cássia Brandão
Cinara Cássia Brandão
CMCristina S. Meira
Cristina S. Meira
AFAna I.C. Ferreira
Ana I.C. Ferreira
FFFábio Batista Frederico
Fábio Batista Frederico
RHRoberto M. Hiramoto
Roberto M. Hiramoto
VPVera L. Pereira-Chioccola
Vera L. Pereira-Chioccola