Leila Sawada

Dr. Leila Sawada


Research Focus & Metrics

Academic Career Length

13Years (2014-Present)

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

Representative Publications

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25 February 2014 in Virology Journal
Verified
Journal Article
Open access
PDF file
AOAldemir B. Oliveira-Filho
Aldemir B. Oliveira-Filho
LSLeila Sawada
Leila Sawada
LPLaine Pinto
Laine Pinto
DLDaiane Locks
Daiane Locks
SBSantana L Bahia
Santana L Bahia
JLJosé Alexandre R Lemos
José Alexandre R Lemos
Currently, sharing of drug paraphernalia is the main form of HCV transmission worldwide. In South America, consistent findings indicate that shared sniffing equipment is an important factor in the spread of HCV among non-injecting drug users. Epidemiological data on the status of HCV infection in illicit drug users in the Amazon region are scarce, although reports of clinical cases of hepatitis or pathologies associated with HCV infection in other population groups are numerous. Thereby, this study investigated the prevalence, genotype frequency, and epidemiological factors associated with HCV infection in non-injecting drug users in the state of Pará, eastern Amazon.

30 November 2021 in Biomolecules
Verified
Journal Article
Open access
PDF file
LSLeila Sawada
Leila Sawada
Antonio VallinotoAntonio Vallinoto
Antonio Vallinoto
IBIgor Brasil-Costa
Igor Brasil-Costa
Epstein–Barr virus (EBV) is an oncovirus ubiquitously distributed and associated with different types of cancer. The reason why only a group of infected people develop cancer is still unknown. EBV-associated cancers represent about 1.8% of all cancer deaths worldwide, with more than 150,000 new cases of cancer being reported annually. Since EBV-associated cancers are described as more aggressive and more resistant to the usual treatment compared to EBV-negative ones, the recent introduction of monoclonal antibodies (mAbs) targeting immune checkpoints (ICs) in the treatment of cancer patients represents a possible therapy for EBV-associated diseases. However, the current mAb therapies available still need improvement, since a group of patients do not respond well to treatment. Therefore, the main objective of this review is to summarize the progress made regarding the contribution of EBV infection to the expression of the IC indoleamine 2,3-dioxygenase (IDO) thus far. This IC has the potential to be used as a target in new immune therapies, such as mAbs. We hope that this work helps the development of future immunotherapies, improving the prognosis of EBV-associated cancer patients.