Publications by authors named "Cristina S Ferreira"

The secretory capacity of Chinese hamster ovary (CHO) cells remains a fundamental bottleneck in the manufacturing of protein-based therapeutics. Unconventional biological drugs with complex structures and processing requirements are particularly problematic. Although engineered vector DNA elements can achieve rapid and high-level therapeutic protein production, a high metabolic and protein folding burden is imposed on the host cell.

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Article Synopsis
  • Inherited genetic defects in immune system-related genes can lead to Inborn Errors of Immunity (IEI), which are challenging to diagnose due to overlapping symptoms, making accurate identification of genetic variants essential for effective treatment and counseling.
  • This study conducted genetic screening on 13 patients from Brazil's public health system to find associations between genetic variants and patient characteristics, using whole exome sequencing (WES) and a computational framework for analysis.
  • The results identified 16 disease-causing variants across nine genes in six different IEI categories, with X-Linked Agammaglobulinemia as the most common disorder in the group.
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Objectives: Inborn error of immunity (IEI) comprises a broad group of inherited immunological disorders that usually display an overlap in many clinical manifestations challenging their diagnosis. The identification of disease-causing variants from whole-exome sequencing (WES) data comprises the gold-standard approach to ascertain IEI diagnosis. The efforts to increase the availability of clinically relevant genomic data for these disorders constitute an important improvement in the study of rare genetic disorders.

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The ongoing coronavirus 2019 (COVID-19) pandemic, triggered by the emerging SARS-CoV-2 virus, represents a global public health challenge. Therefore, the development of effective vaccines is an urgent need to prevent and control virus spread. One of the vaccine production strategies uses the epitope prediction from the virus genome by immunoinformatic approaches, which assist in selecting candidate epitopes for and clinical trials research.

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